124 results on '"Daniela Francescato Veiga"'
Search Results
2. Quality of breast reconstruction service at a university hospital as assessed by the patients
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Carlos Eduardo de Oliveira, José da Conceição Carvalho Júnior, Ricardo Beckhauser Kuhnen, Ana Laura Batista Coelho, Isabella Scavariello Zicari Di Monte, Lydia Masako Ferreira, and Daniela Francescato Veiga
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Breast Neoplasms ,Mammaplasty ,Patient Satisfaction ,Health Services Administration ,Surgery ,RD1-811 - Abstract
ABSTRACT Purpose: To evaluate the quality of breast reconstruction service at a university hospital, as assessed by the patients. Methods: This cross-sectional study enrolled adult women who underwent immediate or delayed breast reconstruction by any technique performed at a university hospital between 1 and 24 months before the assessment. The Brazilian version of the Health Service Quality Scale (HSQS) was self-applied to the participants. The HSQS produces percentage scores, which are expressed in values ranging from 0 to 10 for each domain of the scale, and into an overall percentage quality score. The management team was asked to establish a minimum satisfactory score for the breast reconstruction service. Results: Ninety patients were included. The management team considered 8.00 the minimum satisfactory score for the service. The overall percentage score was 93.3%. Only one domain, ‘Support,’ had an average score lower than that considered satisfactory (7.22 ± 3.0); while the others had higher scores. The domain that scored highest was ‘Qualification’ (9.94 ± 0.3), followed by ‘Result’ (9.86 ± 0.4). There was a positive correlation between ‘type of oncologic surgery’ and ‘intentions of loyalty to the service’ (ρ = 0.272; p = 0.009) and a negative correlation between ‘education’ and ‘quality of the environment’ (ρ = –0.218; p = 0.039). The higher the patient’s level of education, the higher the score attributed to ‘relationship’ (ρ = 0.261; p = 0.013) and the lower the score of ‘aesthetics and functionality’ (ρ = –0.237; p = 0.024). Conclusions: The quality of the breast reconstruction service was considered satisfactory, but there is a demand for structural improvements, better interpersonal relationships, and a stronger support network for patients.
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- 2023
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3. Patient-Reported Outcomes after Subpectoral Breast Augmentation with Microtextured or Macrotextured Implants Using the BREAST-Q
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Alice Teixeira Leite, Miguel Sabino-Neto, Vanessa Contato Lopes Resende, Daniela Francescato Veiga, and Lydia Masako Ferreira
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mammaplasty ,breast implants ,plastic surgery ,patient-reported outcome measures ,patient satisfaction ,Surgery ,RD1-811 - Abstract
Background Breast augmentation with implants is the most commonly performed cosmetic plastic surgery in Brazil and worldwide. The aim of this study was to assess patient satisfaction and quality of life following subpectoral breast augmentation with either microtextured or macrotextured implants, using the BREAST-Q. Methods A prospective study was conducted with 40 women with hypomastia undergoing subpectoral breast augmentation. The patients were randomly allocated to two groups to receive either microtextured or macrotextured breast implants. All participants were assessed preoperatively (baseline) and after 2 and 4 months of surgery for quality of life and patient satisfaction with the surgical results, using the BREAST-Q augmentation module, a patient-reported outcome measure. Results The patients had a mean age of 28.9 ± 6.45 years. The microtextured (n = 20) and macrotextured (n = 20) groups were homogeneous for sex, age, education level, marital status, and number of children (p > 0.05). Both groups showed significant improvement in satisfaction with breasts (p
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- 2022
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4. Mammoplasty: steps for safe surgery. Evidence from literature
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Paulo Rogério Quieregatto do Espirito Santo, Daniela Francescato Veiga, Ricardo Frota Boggio, Felipe Lehmann Coutinho, Anne Groth, Adriano Guimarães Brasolin, and Lydia Masako Ferreira
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mammoplasty ,postoperative complications ,plastic surgery ,patient safety ,mama ,Surgery ,RD1-811 - Abstract
Introduction: Mammoplasty is one of the most performed surgeries by plastic surgeons. Like every procedure, it is not free of risks or complications. Objectives: Discuss controversial issues and complications in breast surgery and main treatments. Methods: Four full members of the SBCP with extensive experience in breast plastic surgery participated in the discussion, in addition to the regent of the mammoplasty chapter. Factors that presented the greatest controversy in mammoplasties were evaluated: use of antibiotics; preoperative infiltration; association of mammoplasty with breast implants; large mammary ptoses; masculinizing mammoplasty; flaps for the elevation of the nippleareola complex (NAC); use of drains; dressings in mammoplasties and fat grafting. Results: The literature and discussion among specialists generated the observations: there is robust evidence of the effectiveness in the use of perioperative antibiotics of reducing mammoplasties, but there is no evidence of benefits in maintaining use for more than 24 hours; preoperative infiltration with vasoconstrictor solutions does not reduce the incidence of hematoma; in mammoplasty associated with implants there was no consensus on the best technique, plane or texture of the implant; there was no consensus on the best technique in the elevation of NAC in large ptoses, whether grafts or flaps; masculinizing mammoplasty does not present complications different from those found in the literature; there is no specific protocol for conduct when there is suffering from the NAC; dressings can be removed on the first postoperative day or kept longer, and there should be parsimony in the fat graft. Conclusion: The present study concluded that mammoplasty is safe surgery, but continued studies are needed to minimize complications.
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- 2021
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5. Single dose versus 24 h antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial
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Daniela Francescato Veiga, Edgard da Silva Garcia, José Wilson Moreira-Filho, Evelyne Borges de Mattos Andrade, Yara Juliano, Joel Veiga-Filho, and Lydia Masako Ferreira
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Plastic surgery ,Mammaplasty ,Anti-bacterial agents ,Prophylaxis ,Wound infection ,Medicine (General) ,R5-920 - Abstract
Abstract Background Reduction mammaplasty is among the most commonly performed procedures in plastic surgery. Antibiotics are widely prescribed, on an empirical basis, to prevent surgical site infections. However, there is a lack of evidence to support its use. This trial aims to compare the influence of the use of prophylatic antibiotics as a single dose or for 24 h on surgical site infection rates following reduction mammaplasty. Methods Randomized trial of non-inferiority, with two parallel groups. A total of 146 breast hypertrophy patients, with reduction mammaplasty already scheduled, will be enrolled. Patients will be randomly allocated to the placebo group that will receive antibiotics only at the anesthesia induction (n = 73) or to the antibiotics group that will receive antibiotics at the anesthesia induction and for 24 h (n = 73). None of the patients will receive antibiotics after hospital discharge. Patients will be followed-up weekly, for 30 days, regarding surgical site infection. The Centers for Disease Control and Prevention criteria will be applied. A statistical analysis of the data will be performed. Discussion Previous studies have demonstrated a decrease in infection rates after reduction mammaplasty when antibiotic prophylaxis was used, compared to the use of no antibiotics. However, the duration of antibiotic prophylaxis remains a point to be clarified. This study will test the hypothesis that maintaining the use of antibiotics for 24 h does not reduce infection rates compared to the use of a single preoperative dose. Trial registration Clinicaltrials.gov NCT04079686 . Registered on September 6, 2019.
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- 2020
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6. Quality of randomized clinical trials published by plastic surgeons: a long-term follow-up study
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Thiago Bezerra Morais, Daniela Francescato Veiga, Miguel Sabino, and Lydia Masako Ferreira
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randomized controlled trials as a subject ,evidencebased medicine ,statistical analysis ,random distribution ,plastic surgery ,Surgery ,RD1-811 - Abstract
Introduction: In two previous studies, the quality of randomized clinical trials (RCTs) with the participation of at least one plastic surgeon was assessed in two periods: from 1966 to 2003 and from 2004 to 2008. The objective is to evaluate the evolution of the quality of RCTs published by plastic surgeons in the subsequent five-year period, from 2009 to 2013. Methods: RCTs published from 2009 to 2013, in English, with the participation of at least one plastic surgeon, were identified by an electronic search and classified according to allocation concealment by two independent evaluators. The quality of the studies with adequate allocation concealment was evaluated by two evaluators using the Delphi List and the Jadad Scale. Results: Of the 6,997 identified studies, 261 were classified according to allocation concealment. Of these, 43 (16.47%) had adequate allocation concealment. According to an assessment conducted using the Delphi List, there was an improvement in the items "most important characteristics of the prognosis" (p < 0.001), "use of an independent evaluator" (p = 0.0029), and "measures of variability and estimation of points for the primary variable" (p = 0.0057) compared to the 1966-2003 assessment ; there was no difference in the assessment of the same items from 2004-2008. Regarding the Jadad Scale, there was an increase in the scores from 2009 to 2013 compared to the 1996-2003 period (p < 0.0004); however, there was no significant difference in the 2004-2008 period. Conclusion: There was no difference in the quality of the RCTs published by plastic surgeons in the 2009-2013 period compared to the previous five-year period (2004 to 2008). However, both periods indicated higher quality compared to the 1966-2003 period.
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- 2019
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7. Alcohol (70%) versus alcoholic chlorhexidine solution (0.5%) in skin antisepsis for neuraxial blocks: a randomized clinical trial
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LUIZ CARLOS SOUZA TOSTES, ANA BEATRIZ ALKMIM TEIXEIRA LOYOLA, ADILSON DE OLIVEIRA FRAGA, LETÍCIA AZEVEDO GAZZI, LUIZ FRANCISLEY DE PAIVA, YARA JULIANO, and DANIELA FRANCESCATO VEIGA
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Antisepsis ,Chlorhexidine ,Ethanol ,Anesthesia Spinal ,Anestesia Epidural ,Surgery ,RD1-811 - Abstract
ABSTRACT Objective: to compare the use of 0.5% alcoholic chlorhexidine and 70% alcohol in skin antisepsis for neuraxial blocks. Method: this is a non-inferiority randomized clinical trial, with two parallel arms. Seventy patients who were candidates for neuraxial block were randomly allocated to group A (n = 35), in whom antisepsis was performed with 0.5% alcoholic chlorhexidine, or to group B (n = 35), in whom we used 70% hydrated ethyl alcohol. Swabs were harvested for culture at three times: before antisepsis, two minutes after application of the antiseptic, and immediately after puncture. The samples were sown in three culture media and the number of colony forming units (CFU) per cm² was counted. Results: there was no difference between the groups regarding age, sex, body mass index, time to perform the block or type of block. There were no differences between groups in the CFU/cm² counts before antisepsis. There was less bacterial growth in group B two minutes after application of the antiseptic (p = 0.048), but there was no difference between the groups regarding the number of CFU/cm² at the end of the puncture. Conclusion: 70% alcohol was more effective in reducing the number of CFU/cm² after two minutes, and there was no difference between the two groups regarding skin colonization at the end of the procedure. These results suggest that 70% alcohol may be an option for skin antisepsis before neuraxial blocks. Trial registration: ClinicalTrials.gov, NCT02833376.
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- 2021
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8. Bioactive and biocompatible cement as a single element in pulpotomy of deciduous teeth: a randomized clinical trials
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Fernanda Valadão MOYSÉS, Daniela Francescato VEIGA, Marcelo Junqueira PEREIRA, Matheus Henrique Lopes DOMINGUETE, Camila Alessandra PAZZINI, Ana Carla Junqueira PEREIRA, and José Dias da SILVA NETO
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Pediatric dentistry ,Pulpotomy ,Biocompatible materials ,Dentistry ,RK1-715 - Abstract
ABSTRACT Objective: Pulpotomy in deciduous teeth maintains the integrity and health of deciduous teeth and supporting tissues until a permanent tooth has erupted. PBS HD CIMMO® cement was evaluated in deciduous teeth pulpotomies as base material and restoration. A randomized clinical trial was performed Methods: This study was approved by the Ethics Committee of (Universidade Vale do Sapucaí) UNIVÁS with Certificate of Presentation for Ethical Consideration, protocol number is: 1.771.929. 60 deciduous molar teeth from 32 healthy children were selected. These teeth were divided into two groups: G1 with 30 teeth, in which the classictreatment with formocresol was used, and G2 with 30 teeth, in which PBS HD CIMMO® cement was used as base and simultaneous final restoration. The evaluation was performed 12 months after the intervention through clinical and radiographic exams. Fisher’s exact test was performed to correlate the clinical and radiographic aspects in both groups Results: There was no significant difference (p= 0.090) in the clinical-radiographic evaluation. PBS HD CIMMO® cement is option to be used as a single element in pulpotomies of deciduous teeth Conclusion: Longitudinal studies should be performed in order to demonstrate a significant association between these groups. The study was enrolled in clinical trials (clinical trials.gov) with registration NCT03200938.
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- 2020
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9. Antibiotic prophylaxis in breast cancer surgery. A randomized controlled trial
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Rubens Murilo de Athayde Prudencio, Fabíola Soares Moreira Campos, Ana Beatriz Alkmim Teixeira Loyola, Ivanildo Archangelo Junior, Neil Ferreira Novo, Lydia Masako Ferreira, and Daniela Francescato Veiga
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Antibiotic Prophylaxis ,Breast Neoplasms ,Postoperative Care ,Surgical Wound Infection ,Surgery ,RD1-811 - Abstract
Abstract Purpose To assess the effect of antibiotic prophylaxis on surgical site infection (SSI) rates in women undergoing breast cancer surgery in two tertiary hospitals in Brazil. Methods This was a randomized, double-blind, placebo-controlled, parallel-group clinical trial. A total of 124 women without independent risk factors for SSI were randomly assigned to receive either cefazolin (antibiotic group, n = 62) or placebo (control group, n = 62) as preoperative prophylaxis. After surgery, all surgical wounds were examined once a week, for four weeks, according to the Centers for Disease Control and Prevention definitions and classifications for SSI. Results Baseline characteristics were homogeneous between the two groups. Only one patient in the antibiotic group developed SSI, which was classified as superficial incisional. The overall SSI rate was low, with no significant difference between groups. Conclusion Antibiotic prophylaxis had no significant effect on reducing SSI rates in women without independent risk factors for SSI undergoing breast cancer surgery.
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- 2020
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10. Cross-cultural validation of the FACE-Q Satisfaction with Facial Appearance Overall Scale (FACE-Q SFAOS) in Brazilian rhytidoplasty patients
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José Teixeira Gama, Luís Antônio Rossetto, Nathalya Botelho Brito, Daniela Francescato Veiga, and Lydia Masako Ferreira
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Validation Studies ,Surveys and Questionnaires ,Rhytidoplasty ,Plastic Surgery ,Medicine (General) ,R5-920 - Abstract
OBJECTIVES: This study aimed to culturally validate the FACE-Q - Satisfaction with Facial Appearance Overall Scale (Face-Q SFAOS) in a population of Brazilian rhytidoplasty patients. METHOD: Authorization for the translation and validation of the questionnaire was obtained from the FACE-Q SFAOS distribution rights holders. The FACE-Q SFAOS was translated and then back-translated. For cultural validation, a total of 57 women were selected 5 to 8 months after undergoing rhytidoplasty. Twenty of them participated in the cultural adaptation, 30 participated in the reproducibility analysis, and 57 participated in the construct validation. RESULTS: The analysis identified two factors (general appearance and face geometry) that exhibited excellent internal consistency. The total satisfaction score, which comprised nine items, also presented excellent internal consistency. Good reproducibility was found for Overall Appearance, Geometry and Total. There was a difference in the satisfaction means (total and factors) between procedure locations; patients undergoing frontal, upper eyelid and lower eyelid procedures were less satisfied than those who did not undergo such procedures. Satisfaction was higher with geometry than with overall face appearance. CONCLUSION: The FACE-Q SFAOS was adapted to the cultural context of Brazilian rhytidoplasty patients and was reproducible, and the scale exhibited face, content and construct validity.
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- 2020
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11. Bioceramic cement in the filling of bone defects in rats
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Christiano Cândido Zerbinatti, Daniela Francescato Veiga, Monique Amanda Bastista Oliveira, Fiorita Gonzales Lopes Mundim, Rodrigo Machado Pereira, Francisco Azevedo, Taylor Brandão Schnaider, and José Dias da Silva Neto
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Dental Implants ,Immediate Dental Implant Loading ,Guided Tissue Regeneration, Periodontal ,Bone Substitutes ,Rats ,Surgery ,RD1-811 - Abstract
Abstract Purpose To evaluate PBS®MCIMMO cement in the filling of bone defects. Methods Thirty-six adult male Wistar rats were divided into three groups of twelve individuals each (group 1, group 2 and group 3). In all groups, a bone failure in the femur was induced, 2.0 mm wide and 7.0 mm deep. In group 1, the PBS®MCIMMO cement was applied to the bone defect produced and a titanium implant (CONNECTION®) 1.5 mm thick and 6 mm long was installed. In group 2, only the PBS® CIMMO cement was installed. In group 3, only bone failure was performed. Kruskal Wallis tests were performed to compare the mean area among the three groups. Results In all comparisons, significance was observed for group 2 (p = 0.0014–0.0026). Conclusion The PBS®CIMMO cement induced bone neoformation, and integration between the newly formed bone, cement, and implant was observed.
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- 2019
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12. Work ability and productivity in patients with diabetic foot
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Helga dos Santos Cabeceira, Diba Maria Sebba Tosta de Souza, Yara Juliano, and Daniela Francescato Veiga
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Diabetes Mellitus ,Diabetic Foot ,Efficiency ,Absenteeism ,Work ,Medicine (General) ,R5-920 - Abstract
OBJECTIVE: To assess work ability and productivity in patients with diabetic foot. METHODS: This investigation was a cross-sectional controlled study. A total of 117 individuals were selected from March to June 2014 and allocated to group A (patients without diabetes, n=43), group B (diabetes patients without foot ulcers, n=43), or group C (patients with diabetic foot, n=31). Two validated instruments, the Work Limitations Questionnaire (WLQ) and the Work Productivity and Activity Impairment Questionnaire General Health v2.0 (WPAI-GH), were used to assess work ability and productivity. RESULTS: The groups were homogeneous regarding age and sex; however, patients in group C had a lower education level than the other participants (p=0.006). The median WLQ scores for groups A, B, and C were 0.0121, 0.0146, and 0.0852, respectively (p
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- 2019
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13. The use of a biocompatible cement in endodontic surgery. A randomized clinical trial 1
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Sérgio Ribeiro da Silva, José Dias da Silva Neto, Taylor Brandão Schnaider, Daniela Francescato Veiga, Neil Ferreira Novo, Marcos Mesquita Filho, and Lydia Masako Ferreira
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Apicoectomy ,Biocompatible Materials ,Dental Cements. ,Surgery ,RD1-811 - Abstract
ABSTRACT PURPOSE: To evaluate the clinical applicability of Pozzolana Biologic Silva cement (PBS(r)) in endodontic surgery. METHODS: Persistent apical periodontitis was diagnosed in 30 teeth of 12 patients by cone-beam computed tomography (CT). All patients had 2 or 4 affected teeth and underwent endodontic surgery with root-end filling. Patients with 2 affected teeth had one tooth (control) treated with mineral trioxide aggregate (MTA-Angelus(r)) as a root-end filling material, and the other tooth treated with PBS (experiment). When the patient had four affected teeth, two of them were treated with MTA and two with PBS. Six months after surgery, all patients were assessed by CT scan. Between-group comparisons of measurements were performed using the Wilcoxon test. RESULTS: Periradicular tissue regeneration was observed in all cases. Significant within-group differences in long axes of the lesion were found in the bucco-palatal direction (PBS group, p=0.0012; MTA group, p=0.024) and coronal-apical direction (PBS group, p=0.0007; MTA group, p=0.0015) between pre- and postoperative measurements. CONCLUSIONS: Pozzolana Biologic Silva cement can be used in the treatment of persistent periradicular lesions. The clinical use of PBS as a root-end filling material may be an alternative to MTA. PBS has additives, which provide enhanced strength.
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- 2016
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14. Outcomes analysis of breast reduction in Brazilian women using the BREAST-Q® questionnaire: a cross-sectional controlled study
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Adriana Corbolan Andrade, Daniela Francescato Veiga, Isabella de Carvalho Aguiar, Yara Juliano, Miguel Sabino-Neto, and Lydia Masako Ferreira
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Breast ,Mammoplasty ,Patient’s Satisfaction ,Evaluation of Results ,Quality of Life ,Medicine (General) ,R5-920 - Abstract
OBJECTIVE: The aim of this study was to analyse patient-reported outcomes of reduction mammoplasty among Brazilian women. METHODS: A total of 100 women were enrolled in this cross-sectional controlled study, 50 with breast hypertrophy (Hypertrophy Group) and 50 who had undergone breast reduction at least six and up to 12 months before (Mammoplasty Group). The Brazilian version of the BREAST-Q® was applied to assess patient-reported outcomes. The module reduction/mastopexy was used, and the preoperative and postoperative versions were applied to the hypertrophy and mammoplasty groups, respectively. RESULTS: The mammoplasty group presented higher scores for the subscales satisfaction with breasts, psychosocial well-being, sexual well-being and physical well-being (p=0.0001 for all of these subscales). CONCLUSION: These results suggest that patients submitted to reduction mammoplasty are satisfied with the outcomes and present better quality of life scores compared with women with breast hypertrophy.
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- 2018
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15. Antimicrobial activity of Melaleuca sp. oil against clinical isolates of antibiotics resistant Staphylococcus aureus
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Sávia Perina Portilho Falci, Manoel Araujo Teixeira, Pablo Ferreira das Chagas, Beatriz Bertolaccini Martinez, Ana Beatriz Alkmim Teixeira Loyola, Lydia Masako Ferreira, and Daniela Francescato Veiga
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Phytotherapy ,Tea Tree oil ,Staphylococcus aureus ,In Vitro Techniques ,Injuries ,Surgery ,RD1-811 - Abstract
PURPOSE: To extract the Melaleuca sp. oil and to assess its in vitro inhibitory effect against Staphylococcus aureus isolates obtained from lower limb wounds and resistant to several antibiotics. METHODS: A total of 14 test-tubes containing Mueller-Hinton broth were used to determine the Minimum Inhibitory Concentration (MIC). The following concentrations of the Melaleuca sp. oil were added to the first 11 tubes: 8; 4; 2; 1; 0.5; 0.2; 0.1; 0.05; 0.025; 0.0125 and 0.00625%. The 12th and 13th tubes, with and without oil, were used as the positive and negative controls, respectively. The experimental study was carried out in triplicate at 37ºC for 18 hours. The Minimum Bactericidal Concentration (MBC), able of killing all the microorganisms, was also determined. Two S. aureus isolates were obtained from lower limb wounds of female patients and the identification of the microorganisms (Staphylococcus aureus) and the test for susceptibility to the antimicrobial agents were carried out by automation using the apparatus MicroScan(r). After identification, the isolates were preserved in liquid Trypticase Soy medium, and inoculated for determination of the MIC and MBC. RESULTS: The MIC was 0.2% and the MBC was 0.4%. CONCLUSION: The Melaleuca sp. oil showed antimicrobial properties in vitro against strains isolated from lower limb wounds which were resistant to multiple antibiotics.
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- 2015
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16. Portland cement versus MTA as a root-end filling material. A pilot study
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Sérgio Ribeiro da Silva, José Dias da Silva Neto, Daniela Francescato Veiga, Taylor Brandão Schnaider, and Lydia Masako Ferreira
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Apicoectomy ,Oral Surgery ,Biocompatible Materials ,Dental Cements ,Translational Medical Research ,Surgery ,RD1-811 - Abstract
PURPOSE: To assess periradicular lesions clinically and by computed tomography (CT) after endodontic surgery using either Portland cement or mineral trioxide aggregate (MTA) as a root-end filling material. METHODS: Three patients diagnosed with periradicular lesions by cone-beam CT underwent endodontic surgery with root-end filling. Patient A was treated with MTA as the root-end filling material, patient B was treated with Portland cement and patient C had two teeth treated, one with MTA and the other with Portland cement. Six months after surgery, the patients were assessed clinically and by CT scan and the obtained results were compared. RESULTS: Periradicular tissue regeneration was observed in all cases, with no significant differences in bone formation when comparing the use of MTA and Portland cement as root-end filling materials. CONCLUSION: Both mineral trioxide aggregate and Portland cement were successful in the treatment of periradicular lesions.
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- 2015
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17. Quality of life and self-esteem in patients submitted to surgical treatment of skin carcinomas: long-term results
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Paula Curitiba Maciel, Joel Veiga-Filho, Marcelo Prado de Carvalho, Fernando Elias Martins Fonseca, Lydia Masako Ferreira, and Daniela Francescato Veiga
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Quality of life ,Self concept ,Skin neoplasms ,Dermatology ,RL1-803 - Abstract
BACKGROUND: Cancer is a multifactorial disease and skin carcinomas are the most common type of cancer. Assessing quality of life and self-esteem outcomes in skin cancer patients is important because these are indicators of the results of the treatment, translating how patients face their lives and their personal relationships. OBJECTIVE: To assess the late impact of the surgical treatment of head and/or neck skin carcinomas on quality of life and self-esteem of the patients. METHODS: Fifty patients with head or neck skin carcinomas were enrolled. Their age ranged between 30 and 75 years, 27 were men and 23 were women. Patients were assessed with regard to quality of life and self-esteem, preoperatively and five years postoperatively. Validated instruments were used: the MOS 36-item Short-form Health Survey (SF-36) and the Rosenberg Self-esteem/EPM-UNIFESP Scale. The Wilcoxon signed-rank test was used for the statistical analysis. RESULTS: Twenty-two patients completed the five-year follow-up, 54.5% women and 45.5% men. Compared to the preoperative assessment, patients had an improvement in mental health (p=0.011) and in self-esteem (p=0.002). There was no statistical difference with regard to the other domains of the SF-36. CONCLUSION: Patients submitted to surgical treatment of skin carcinoma improved mental health and self-esteem in the late postsurgical testing.
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- 2014
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18. Health economics and health preference concepts to orthopedics practitioners
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Carlos Delano Mundim Araújo, Daniela Francescato Veiga, Bernardo Hochman, Luiz Eduardo Felipe Abla, Neil Ferreira Novo, and Lydia Masako Ferreira
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Quality of life ,Quality-adjusted life years ,Cost-benefit analysis ,Medicine ,Orthopedic surgery ,RD701-811 - Abstract
The aim of this study was to describe concepts of health economics in order to update and provide the orthopedic practitioner decision making parameters based on preferences. Four basic types of studies of economical evaluation were presented (cost minimization analysis, cost-benefit, cost-effectiveness and cost-utility), as well as the origin, the concept, advantages and disadvantages of using QALY and utility. It was discussed the importance of costs and of SF-6D, an instrument able to get through the utility data from the Medical Outcomes Study 36-item Short Form Health Survey (SF-36). Physicians, especially orthopedic practitioners, are increasingly using technologies which are progressively expensive, thus, they should be able to understand health economics concepts, the importance of utility in clinical decision making process and economic analysis in health.09+
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- 2014
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19. Abstract: Post-Operative Intravenous Iron Sucrose Versus Post-Operative Oral Iron to Treat Post-Bariatric Abdominoplasty Anaemia (ISAPA): A Prospective, Open-Label, Randomised Controlled Trial
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Juan Carlos Montano-Pedroso, MD, PhD, Elvio Bueno Garcia, MD, PhD, Mariana Alcantara Rodrigues de Moraes, MD, Daniela Francescato Veiga, PhD, and Lydia Masako Ferreira, PhD
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Surgery ,RD1-811 - Published
- 2018
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20. Surgical research in the north and northeast of Brazil Pesquisa cirúrgica no norte e nordeste do Brasil
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Rafael Silva de Araújo, Felipe Nunes Brito, Yan Chaves, Daniela Francescato Veiga, and Lydia Masako Ferreira
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Academic Medical Centers ,Faculty, Medical ,Program Accreditation ,General Surgery ,Research ,Centros Médicos Acadêmicos ,Docentes de Medicina ,Acreditação de Programas ,Cirurgia Geral ,Pesquisa ,Surgery ,RD1-811 - Abstract
PURPOSE: To evaluate the scientific production from the surgical areas from the State University of Para (UEPA), Federal Universities of Para (UFPA) and of Paraiba (UFPB), Brazil. METHODS: The scientific productions of professors in the last five years were classified according to the Qualis system of CAPES-Medicine III (http://qualis.capes.gov.br/webqualis/publico/pesquisaPublicaClassificacao.seam?conversationPropagation=begin) and it was computed the number of guidance of students scientific projects. RESULTS: Seventy-four professors were included, 31 with Master and 43 with PhD degrees. UFPA presented more publications (49% out of the total), which 32% of them in Journals B1 or higher. Otorhinolaryngology presented the greatest number of publications (29% out of the total); however, 98% of them in B3 or lower. Gastroenterological Surgery, which is responsible for 23% out of the total, had 57% of its publications in B1 or higher. The most frequent type of guidance was the one about scientific work of completion of undergraduate course (63%). Gynecology and Obstetrics presented the greatest number of student's guidance (35% out of the total) and Gastroenterological Surgery the largest number of Master's degree and PhD degree supervisions. CONCLUSIONS: The specialties Gynecology and Obstetrics and Gastroenterological Surgery from the State University of Para (UEPA), Federal Universities of Para (UFPA) and of Paraiba (UFPB) presented the greatest number of professors with academic degrees. Gastroenterological Surgery presented the largest scientific productions at higher strata of WebQualis CAPES classification and also the largest number of Master and PhD directed.OBJETIVO: Avaliar titulação e produção de docentes da área cirúrgica das Universidades Estadual do Pará (UEPA), Federal do Pará (UFPA) e Federal da Paraíba (UFPB). MÉTODOS: A produção dos docentes nos últimos cinco anos foi classificada segundo o Qualis da Medicina III da CAPES (http://qualis.capes.gov.br/webqualis/publico/pesquisaPublicaClassificacao.seam?conversationPropagation=begin), e computou-se o número de orientações concluídas. RESULTADOS: Foram incluídos 74 docentes, 31 mestres e 43 doutores. A UFPA apresentou maior produção científica (49% do total de publicações), com 32% destas em periódicos Qualis B1 ou superior. A especialidade com maior número de publicações foi a Otorrinolaringologia (29% do total); entretanto, 98% destas em Qualis B3 ou inferior. Já a Cirurgia Gastroenterológica, responsável por 23% do total, teve 57% de suas publicações em Qualis B1 ou superior. O tipo mais frequente de orientação foi a de trabalhos de conclusão de cursos de graduação (63%). Ginecologia e Obstetrícia apresentou o maior número de orientações concluídas (35% do total), e Cirurgia Gastroenterológica o maior número de orientações de mestrado e doutorado. CONCLUSÕES: As especialidades Ginecologia e Obstetrícia e Cirurgia Gastroenterológica apresentaram o maior número de docentes titulados. A Cirurgia Gastroenterológica apresentou a maior produção nos extratos do Qualis-CAPES, e também o maior número de orientações concluídas de mestrado e doutorado.
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- 2013
21. Unripe Musa sapientum peel in the healing of surgical wounds in rats
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Dênia Amélia Novato Castelli Von Atzingen, Alfredo Gragnani, Daniela Francescato Veiga, Luis Eduardo Felipe Abla, Lorraine Lorene Felix Cardoso, Thiago Ricardo, Adriana Rodrigues dos Anjos Mendonça, and Lydia Masako Ferreira
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Musa sapientum ,Wound Healing ,Phytotherapy ,Rats ,Surgery ,RD1-811 - Abstract
PURPOSE: To assess the effects of unripe Musa sapientum peel on the healing of surgical wounds in rats. METHODS: One hundred and twenty Wistar rats were divided into two treatment groups of 60 animals each: the control group (gel without the active ingredient) and experimental group (4% Musa sapientum peel gel). A 4 x 4 cm surgical wound was created on the back of each animal. The wound was cleaned daily with 0.9% saline, treated with 4% gel or natrosol gel (control), and covered with gauze. Animals from both groups were sacrificed after seven, 14 and 21 days of treatment; the tissue from the wound site was removed together with a margin of normal skin for histological analysis. RESULTS: No significant differences in wound contraction rates (p=0.982) were found between time points (seven, 14 and 21 days of treatment) in both groups. However, a significantly higher wound contraction rate was observed in the control group on day 21 compared with the experimental group (p=0.029). There were no significant differences in histomorphological features between groups. The experimental group showed an increased number of polymorphonuclear cells on day 7, with a significant reduction on day 21 (p=0.026). CONCLUSION: The use of 4% unripe Musa sapientum peel gel on surgical wounds in rats resulted in an increased number of polymorphonuclear cells on day 7, reduced wound contraction, reduced vascular proliferation and increased concentration of collagen fibers on day 21.
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- 2013
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22. Dressing Wear Time after Breast Reconstruction: A Randomized Clinical Trial.
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Daniela Francescato Veiga, Carlos Américo Veiga Damasceno, Joel Veiga-Filho, Luiz Francisley Paiva, Fernando Elias Martins Fonseca, Isaías Vieira Cabral, Natália Lana Larcher Pinto, Yara Juliano, and Lydia Masako Ferreira
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Medicine ,Science - Abstract
The evidence to support dressing standards for breast surgery wounds is empiric and scarce.This two-arm randomized clinical trial was designed to assess the effect of dressing wear time on surgical site infection (SSI) rates, skin colonization and patient perceptions.A total of 200 breast cancer patients undergoing breast reconstruction were prospectively enrolled. Patients were randomly allocated to group I (dressing removed on the first postoperative day, n = 100) or group II (dressing removed on the sixth postoperative day, n = 100). SSIs were defined and classified according to criteria from the Centers for Disease Control and Prevention. Samples collected before placing the dressing and after 1 day (group I) and 6 days (both groups) were cultured for skin colonization assessments. Patients preferences and perceptions with regard to safety, comfort and convenience were recorded and analyzed.A total of 186 patients completed the follow-up. The global SSI rate was 4.5%. Six patients in group I and three in group II had SSI (p = 0.497). Before dressing, the groups were similar with regard to skin colonization. At the sixth day, there was a higher colonization by coagulase-negative staphylococci in group I (p
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- 2016
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23. Oncoplastic approach in the conservative treatment of breast cancer: analysis of costs
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Débora Eleotério de Lima, Joel Veiga Filho, Leda Marques Ribeiro, Thiago Bezerra de Morais, Luiz Roberto Martins Rocha, Yara Juliano, Daniela Francescato Veiga, and Lydia Masako Ferreira
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Breast Neoplasms ,Mastectomy, Segmental ,Surgery, Plastic ,Surgical Flaps ,Health Care Costs ,Surgery ,RD1-811 - Abstract
PURPOSE: To analyze the direct costs of conservative surgical treatment of breast cancer, performed in a university hospital, to the Brazilian National Health Care Public System (SUS), checking the impact of the oncoplastic approach on these costs. METHODS: One hundred thirty eight breast cancer patients who had undergone conservative treatment with oncoplastic approach (n=36) or not (control group, n=102), in the period from 2005 to 2010, were enrolled. Sociodemographic and clinical data were recorded. The direct costs of the surgical procedure were obtained and analyzed. RESULTS: Groups did not differ in regard to age (p=0.963), and patients in oncoplastic group had a longer time of hospital stay (p=0.000). The median direct cost for the oncoplastic group was R$461.00 and for the control group was R$229.00 (p=0.000). CONCLUSION: The oncoplastic approach has generated higher direct costs in conservative surgical treatment of breast cancer to SUS.
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- 2012
24. Effect of zafirlukast on capsular contracture around silicone implants in rats Efeito do zafirlukast na contratura capsular ao redor de implantes de silicone em ratos
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Érika Malheiros Bastos, Miguel Sabino Neto, Élvio Bueno Garcia, Daniela Francescato Veiga, Yuri Anna Han, Rafael Denadai, Rafael de Almeida Santos, and Lydia Masako Ferreira
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Implantes de Mama ,Contratura Capsular em Implantes ,Antagonistas de Leucotrienos ,Ratos ,Breast Implants ,Implant Capsular Contracture ,Leukotriene Antagonists ,Rats ,Surgery ,RD1-811 - Abstract
PURPOSE: To evaluate the effect of zafirlukast on capsular contracture around silicone implants by measuring the pressure within the implant, using a rat experimental model. METHODS: Forty adult female Wistar rats were used. Each one received two silicone implants, one with smooth-surface and the other with textured-surface. They were randomly divided into four groups (n=10). The rats of control group I were sacrificed after the implants. The remaining animals were subjected to a daily regimen of intra-peritoneal injection for a period of 90 days and they were distributed as follows: control group II received 0.9% physiological saline solution; experimental group I received zafirlukast 1.25 mg/kg; and experimental group II received zafirlukast 5 mg/kg. The measurement of intra-implant pressure of control group I was determined on the surgery day and in other groups on the ninetieth day, after being sacrificed. RESULTS: In the evaluation of textured implants there was an increase of internal pressure in the control group II, and there was no increase in the experimental groups. Compared to the controls there were not significant differences in smooth implants. CONCLUSION: Zafirlukast reduced the risk of developing capsular contracture around silicone implants with textured surface.OBJETIVO: Avaliar o efeito do zafirlukast na contratura capsular ao redor de implantes de silicone, através da aferição da pressão intra-implante, utilizando-se um modelo experimental de ratos. MÉTODOS: Quarenta ratos fêmeas Wistar foram utilizados. Cada um recebeu dois implantes de silicone, sendo um com superfície lisa e outro texturizada. Foram divididos aleatoriamente em quatro grupos (n=10). Os ratos do grupo controle I foram sacrificados após o implante. O restante dos animais foi submetido a um regime diário de injeção intraperitoneal por um período de 90 dias e foram distribuídos: grupo controle II recebeu solução salina fisiológica 0,9%, grupo experimental I recebeu zafirlukast 1,25 mg/kg, e grupo experimental II recebeu zafirlukast 5 mg/kg. O grupo controle II recebeu solução salina; grupo experimental I, 1,25 mg/kg/dia de zafirlukast; grupo experimental II, 5mg/kg/dia de zafirlukast. A aferição da pressão intra-implante do grupo controle I foi averiguada no dia do ato operatório, e nos outros grupos no nonagésimo dia, após serem sacrificados. RESULTADOS: Na avaliação dos implantes texturizados houve aumento da pressão interna no grupo controle II e, não se observou aumento nos grupos experimentais. Na comparação com os controles não foram observadas diferenças significativas nos implantes lisos. CONCLUSÃO: O Zafirlukast reduziu o risco de desenvolver contratura capsular em torno de implantes de silicone com superfície texturizada.
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- 2012
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25. Gel from unripe Musa sapientum peel to repair surgical wounds in rats Gel da casca de Musa sapientum verde no reparo de lesões operatórias em ratos
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Dênia Amélia Novato Castelli Von Atzingen, Alfredo Gragnani, Daniela Francescato Veiga, Luis Eduardo Felipe Abla, Adriana Rodrigues dos Anjos Mendonça, Clayton Aparecido de Paula, Yara Juliano, José Carlos Correa, Marcio Raimundo de Faria, and Lydia Masako Ferreira
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Musa sapientum ,Cicatrização ,Ratos ,Wound Healing ,Rats ,Surgery ,RD1-811 - Abstract
PURPOSE: To determine the optimum concentration of a gel obtained from unripe banana (Musa sapientum) peel for wound treatment in rats. METHODS: A randomized triple blind study was conducted with 40 Wistar rats, which were divided into 4 groups: CG, control group; G2%, 2% gel concentration group; G4%, 4% gel concentration group; and G10%, 10 % gel concentration group. The banana peel gel was applied daily, for 7 days, to a 4-cm² wound created on the back of each animal of all groups. After this period, the wounds were biopsied. Statistical analysis was carried out using the Kruskal-Wallis test complemented by the Student-Newman-Keuls test. RESULTS: Macroscopic examination revealed that partial epithelialization occurred in all groups. Wound contraction was also observed in all groups and ranged from 1.38 to 1.57 mm in the study groups, and from 1.03 to 1.10 mm in the control group, with significant differences (p < 0.05) between the groups: CG and G10%, G2% and G4%, G2% and G10%. The interquartile deviation was smaller between the groups CG and G4%. CONCLUSION: The 4% gel obtained from unripe banana peel (G4%) resulted in better epithelialization of wounds healed by secondary intention compared with other gel concentrations.OBJETIVO: Avaliar a concentração ideal do gel da casca de Musa sapientum verde no tratamento de feridas em ratos. MÉTODOS: Estudo randomizado, triplo cego, com 40 ratos da linhagem Wistar divididos em quatro grupos: GC controle, G2% gel a 2%, G4% gel a 4%, G10% gel a 10%. Realizou-se aplicação diária do gel nas diferentes concentrações, durante sete dias, em uma ferida de 4 cm² realizada no dorso de cada rato. Após este período, as lesões foram biopsiadas. Para analise dos dados utilizou-se o teste de Kruskal-Wallis complementado pelo teste de Student-Newman-Keuls. RESULTADOS: Os achados macroscópicos demonstraram reepitelização parcial em todos os grupos. A contração da área da ferida variou entre 1,38 a 1,57 mm nos grupos de estudo, e entre 1,03 a 1,10 mm no grupo controle. Houve diferença significante (p < 0,05) entre os grupos: GC e G10%, G2% e G4%, G2% e G10%, sendo o desvio interquartílico menor entre os grupos GC e G4%. CONCLUSÃO: O gel a 4% da casca de M. sapientum verde promoveu maior área de epitelização em feridas com cicatrização por segunda intenção, em relação ao gel nas outras concentrações testadas.
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- 2011
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26. Mastectomy versus conservative surgical treatment: the impact on the quality of life of women with breast cancer Mastectomia versus tratamento cirúrgico conservador: impacto na qualidade de vida de mulheres com câncer mamário
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Daniela Francescato Veiga, Fabíola Soares Moreira Campos, Leda Marques Ribeiro, Ivanildo Archangelo Junior, Joel Veiga Filho, Yara Juliano, Miguel Sabino Neto, and Lydia Masako Ferreira
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Neoplasias da mama ,Mastectomia ,Mastectomia segmentar ,Qualidade de vida ,Breast neoplasms ,Mastectomy ,Segmental Mastectomy ,Quality of life ,Gynecology and obstetrics ,RG1-991 - Abstract
OBJECTIVES: to compare the impact of mastectomy and conservative surgery on the quality of life of patients with breast cancer. METHODS: an assessment was made of the quality of life of patients undergoing mastectomy or segmentary mastectomy, at the Pouso Alegre Clinical Hospital, in the Brazilian State of Minas Gerais, using SF-36. The patients were grouped by age (50 years) and years of schooling (8 years). The Mann-Whitney test was used to compare the groups with regard to the age and schooling domains of SF-36. RESULTS: a significant difference between the two groups was found in the domains of "physical functioning" (p=0.04) and "pain" (p=0.01): with the patients undergoing a mastectomy registering the worst scores. Young patients who had undergone a mastectomy displayed the worst quality of life in terms of "physical functioning" (p=0.03), "pain" (p=0.01) and "social functioning" (p=0.01); those undergoing conservative surgery aged over 50 years scored worst on "role emotional" (p=0.05). Patients undergoing a mastectomy with lower levels of schooling scored lower in "physical functioning" (p=0.01), "role physical" (p=0.05) and "pain" (p=0.05). Among those who had attended school for more than eight years, those having undergone a mastectomy scored less in the "pain" domain (p=0.04). CONCLUSIONS: patients who had undergone a mastectomy had worse results in the physical component of the evaluation of quality of life and this negative impact was more strongly felt among younger patients and those with lower levels of schooling.OBJETIVOS: comparar o impacto da mastectomia e da cirurgia conservadora na qualidade de vida de pacientes com câncer mamário. MÉTODOS: avaliou-se qualidade de vida de pacientes submetidas à mastectomia ou à mastectomia segmentar, no Hospital das Clínicas de Pouso Alegre, Minas Gerais, Brasil, utilizando-se o SF-36. As pacientes foram estratificadas quanto à idade (50 anos) e escolaridade (8 anos). Aplicou-se o teste de Mann-Whitney para comparar os grupos quanto aos domínios do SF-36, idade e escolaridade. RESULTADOS: observou-se diferença significante entre os grupos nos domínios "capacidade funcional" (p=0,04) e "dor" (p=0,01): as pacientes mastectomizadas com piores resultados. Pacientes mastectomizadas mais jovens apresentaram pior qualidade de vida em "capacidade funcional" (p=0,03), "dor" (p=0,01) e "aspectos sociais" (p=0,01); as submetidas à cirurgia conservadora, com mais de 50 anos, resultado pior em "aspectos emocionais" (p=0,05). Pacientes mastectomizadas com menor escolaridade apresentaram escores menores em "capacidade funcional" (p=0,01), "aspectos físicos" (p=0,05) e "dor" (p=0,05). Entre as que frequentaram a escola por mais de oito anos, as mastectomizadas pontuaram menos no domínio "dor" (p=0,04). CONCLUSÕES: pacientes mastectomizadas apresentaram piores resultados no componente físico da qualidade de vida, e este impacto negativo foi mais acentuado entre pacientes mais jovens e com menor escolaridade.
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- 2010
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27. Ultrasonography for measuring rectus abdominis muscles diastasis Ultra-sonografia para medir a diástase dos músculos retos do abdome
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Denise de Almeida Mendes, Fábio Xerfan Nahas, Daniela Francescato Veiga, Fernando Vilela Mendes, Ricardo Góes Figueiras, Heitor Carvalho Gomes, Pedro Bins Ely, Neil Ferreira Novo, and Lydia Masako Ferreira
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Parede Abdominal ,Músculos Abdominais ,Ultra-sonografia ,Diagnóstico por Imagem ,Cirurgia Plástica ,Reto do Abdome ,Abdominal Wall ,Abdominal Muscles ,Ultrasonography ,Diagnostic Imaging ,Surgery, Plastic ,Rectus Abdominis ,Surgery ,RD1-811 - Abstract
PURPOSE: Preoperative imaging evaluation may be useful for determining the position of recti abdominis muscles before their correction. The purpose of this study is to evaluate the accuracy of ultrasonography to measure the width of rectus abdominis muscle diastasis. METHODS: Rectus diastasis was measured by ultrasonography preoperatively in 20 females. Rectus diastasis was measured in seven levels along the anterior rectus sheath by ultrasound after sustained deep inspiration and after expiration. Rectus diastasis, at the same levels, was also measured after its exposition during abdominoplasty by two independent observers, using a surgical compass. These values were compared using Wilcoxon's statistical text, for non independent values. RESULTS: There was no significant difference between the values obtained by ultrasound and those measured during surgery in the supra-umbilical levels and at the level of the umbilicus. However, below the umbilicus these values differed significantly, showing smaller values in the imaging evaluation. CONCLUSION: Ultrasonography is an accurate method to measure rectus diastasis above the umbilicus and at the umbilical level.OBJETIVO: Estudos radiológicos pré-operatórios podem ser úteis para determinar a posição dos músculos retos do abdome antes de sua correção. O objetivo deste estudo é avaliar a acurácia da ultra-sonografia para medir a largura da diástase dos músculos retos do abdome. MÉTODOS: A diástase dos músculos retos foi medida pela ultra-sonografia, no pré-operatório em 20 mulheres. A diástase dos retos foi medida em sete níveis da bainha anterior dos retos foram examinados com ultra-som após inspiração profunda sustentada e após expiração. A diástase dos retos, nos mesmos níveis, foi também medida após sua exposição durante a abdominoplastia, por dois observadores independentes, usando compasso cirúrgico. As medidas foram comparadas usando o teste estatístico de Wilcoxon para dados não independentes. RESULTADOS: Não houve diferença significante entre as medidas ultra-sonográficas e intra-operatórias nos níveis supra-umbilicais e na cicatriz umbilical. Todavia, inferiormente à cicatriz umbilical, essas medidas diferiram significantemente sendo as ultra-sonográficas menores nestes pontos. CONCLUSÃO: A ultra-sonografia é um método acurado para medir a diástase de retos na região supra- umbilical e no nível do umbigo.
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- 2007
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28. Influência da hipertrofia mamária na capacidade funcional das mulheres Influence of breast hypertrophy in the women's functional capacity
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Carlos Delano Mundim Araújo, Heitor Carvalho Gomes, Daniela Francescato Veiga, Bernardo Hochman, Paulo Magalhães Fernandes, Neil Ferreira Novo, and Lydia Masako Ferreira
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mama ,questionários ,postura ,hipertrofia ,dor nas costas ,breast ,questionnaires ,posture ,hypertrophy ,back pain ,Diseases of the musculoskeletal system ,RC925-935 - Abstract
OBJETIVO: investigar a influência da hipertrofia mamária no sistema musculoesquelético por meio da avaliação da capacidade funcional das mulheres. MÉTODO: foram avaliadas 50 mulheres com hipertrofia mamária, e os resultados foram comparados com os de 50 mulheres com mamas normais. Para avaliação da capacidade funcional, utilizou-se o STANFORD HEALTH ASSESSMENT QUESTIONNAIRE 20 (HAQ-20), que consiste de 20 questões sobre atividades do cotidiano em que a entrevistada tem quatro opções de resposta, que são pontuadas. Quanto menor a pontuação, melhor a capacidade funcional. RESULTADOS: a média dos escores do grupo-controle foi 0,10 e do grupo-hipertrofia foi igual a 0,71. Esses escores submetidos ao teste de Mann-Whitney mostraram que o grupo-hipertrofia apresentou valores significantemente maiores do que o grupo-controle (p < 0,00). CONCLUSÃO: mulheres com hipertrofia mamária apresentam menor capacidade funcional, ou seja, mais dificuldade para realizar atividades comuns da vida diária.OBJECTIVE: to investigate the influence of breast hypertrophy in the musculoskeletal-system through the evaluation of the functional capacity in women. METHOD: 50 women with breast hypertrophy were studied and the results were compared to the 50 women without breast hypertrophy. The STANFORD HEALTH ASSESSMENT QUESTIONNAIRE 20 (HAQ-20) was applied to assess the functional capacity. It contains 20 questions about daily activities in which the patient has four answer options, which are scored. Lower scores indicate better functional capacity. RESULTS: the mean score in the control group was 0.10, while in the breast hypertrophy group it was 0.71. When Mann-Whitney test was run, hypertrophy group showed statistically higher scores (p < 0.00). CONCLUSION: breast hypertrophy patients have more difficulties to perform common activities of the daily life.
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- 2007
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29. Dores na coluna: avaliação em pacientes com hipertrofia mamária Back pain: an assessment in breast hypertrophy patients
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Paulo Magalhães Fernandes, Miguel Sabino Neto, Daniela Francescato Veiga, Luis Eduardo Felipe Abla, Carlos Delano Araújo Mundim, Yara Juliano, and Lydia Masako Ferreira
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Dor nas costas ,Qualidade de vida ,Cervicalgia ,Mama ,Back pain ,Quality of life ,Neck pain ,Breast ,Medicine ,Orthopedic surgery ,RD701-811 - Abstract
OBJETIVO: Avaliar a influência da hipertrofia mamária sobre as dores na coluna e o quanto poderão comprometer as atividades habituais das pacientes. MÉTODOS: Realizou-se estudo transversal analítico em pacientes dos ambulatórios de Ortopedia e Cirurgia Plástica do Hospital Universitário Samuel Libânio, Pouso Alegre - MG. Foram examinadas 100 mulheres, 50 com hipertrofia mamária (grupo estudo) e 50 com mamas normais (grupo controle). O tamanho das mamas foi classificado conforme critérios de Sacchini.. A Escala Numeral Analógica (NRS) e o questionário de Roland-Morris foram utilizados para avaliar a intensidade das dores na coluna e as limitações resultantes destes sintomas. Realizado teste estatístico comparando os grupos em relação as variáveis analisadas. RESULTADOS: A média da idade das pacientes do grupo estudo e controle foram de 32,2 anos e de 32,7 anos respectivamente, e o IMC foi maior no grupo estudo. Os escores do NRS e do Roland-Morris foram maiores no grupo de estudo em relação ao grupo controle com significância estatística. CONCLUSÃO: Os resultados obtidos mostraram que as dores nas costas são mais intensas e determinaram maior limitação das atividades habituais em pacientes portadoras de hipertrofia mamária.OBJECTIVE: To evaluate the influence of breast hypertrophy on the incidence of back pain and how much they can interfere in patients' daily activities. METHODS: This was a cross-sectional analytic study in patients examined at the Outpatient Orthopedics and Plastic Surgery Departments at Samuel Libânio University Hospital in Pouso Alegre, MG. 100 women were examined, 50 presenting breast hypertrophy (study group) and 50 with normal breast size (control group). Breasts were classified according to Sacchini's criteria. The Numerical Rating Scale (NRS) and the Roland-Morris questionnaire were used in order to evaluate the magnitude of back pain and the limitations arising from these symptoms. RESULTS: The mean age of the patients in the study group was 32.2 years and 32.7 for the control group. The scores in the NRS scale and Roland- Morris Questionnaire were higher in the study group when compared to the control group. CONCLUSION: The results achieved showed that back pain is more severe and determined more extensive limitations in the daily activities for patients presenting breast hypertrophy.
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- 2007
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30. Brazilian version of the Body Dysmorphic Disorder Examination
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Renata Trajano Borges Jorge, Miguel Sabino Neto, Jamil Natour, Daniela Francescato Veiga, Anamaria Jones, and Lydia Masako Ferreira
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Body image ,Somatoform disorders ,Evaluation ,Plastic surgery ,Questionnaires ,Medicine - Abstract
CONTEXT AND OBJECTIVE: Body image improvement is considered to be the main reason for undergoing plastic surgery. The objective was to translate the Body Dysmorphic Disorder Examination (BDDE) into Brazilian Portuguese and to adapt and validate this questionnaire for use in Brazil. DESIGN AND SETTING: Cross-sectional survey, at the Department of Plastic Surgery of Universidade Federal de São Paulo. METHODS: The BDDE was first translated into Portuguese and then back-translated into English. These translations were then discussed by healthcare professionals in order to establish the final Brazilian version. In a second stage, the validity and reliability of the BDDE were assessed. For this, patients were initially interviewed by two interviewers and subsequently, by only one of these interviewers. On the first occasion, in addition to the BDDE, the body shape questionnaire (BSQ) and the Rosenberg self-esteem scale were also applied. These questionnaires were applied to 90 patients. RESULTS: Six questions were modified during the assessment of cultural equivalence. Cronbach's alpha was 0.89 and the intraclass correlation coefficients for interobserver and test-retest reliability were 0.91 and 0.87, respectively. Pearson's coefficient showed no correlation between the BDDE and the Rosenberg self-esteem scale (0.22), whereas there was a moderate correlation between the BDDE and the BSQ (0.64). CONCLUSIONS: The BDDE was successfully translated and adapted, with good internal consistency, reliability and construct validity.
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31. Auto-estima em pacientes com carcinomas de pele
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Marcelo Prado de Carvalho, Renato Santos de Oliveira Filho, Heitor Carvalho Gomes, Daniela Francescato Veiga, Yara Juliano, and Lydia Masako Ferreira
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Skin neoplasms ,Carcinoma, basal cell ,Carcinoma, squamous cell ,head and neck neoplasms ,Quality of life ,Self concept ,Surgery ,RD1-811 - Abstract
OBJETIVO: Avaliar a auto-estima de pacientes com carcinomas de pele da face e do pescoço. MÉTODOS: Foram estudados 100 pacientes, com idades entre 30 e 90 anos (mediana = 55 anos), sendo 44 eram do gênero masculino e 56 do gênero feminino. O Grupo Estudo foi composto por 50 pacientes portadores de carcinomas de pele na face e no pescoço, com tamanho igual ou maior a 10 mm no seu maior eixo e com diagnóstico confirmado por biópsia prévia. O Grupo Controle consistiu de 50 indivíduos da população geral. Para avaliação da auto-estima, utilizou-se a Escala de Auto-estima de Rosenberg / UNIFESP-EPM. A análise estatística utilizou com o teste de Mann-Whitney e a Análise de Variância de Kruskal Wallis. RESULTADOS: Os pacientes portadores de câncer de pele e os da população geral não apresentaram diferenças significantes em relação à idade (p=0,331), gênero e escolaridade. O tamanho médio do tumor foi 20,9 + 2 mm. Os pacientes com câncer de pele apresentaram auto-estima significantemente mais baixa, com escore médio de 6,84 e 3,90 para o Grupo Controle (p=0,002). CONCLUSÃO: Os pacientes com câncer de pele na face e no pescoço apresentaram auto-estima menor do que os pacientes sem câncer.
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32. Patient satisfaction with breast reconstructionusing musculocutaneous flap from latissimus dorsiversus from rectus abdominis: a cross-sectional study
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Lilian Baldan Záccaro Augustinho, Miguel Sabino Neto, Daniela Francescato Veiga, Luiz Eduardo Felipe Abla, Yara Juliano, and Lydia Masako Ferreira
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plastic ,Mammaplasty ,Breast neoplasms ,Health ,Medicine - Abstract
ABSTRACT BACKGROUND: Breast cancer is the second most frequent type of cancer worldwide and the most common type among women. The treatment for this condition has evolved over recent decades with therapeutic and technological advances. Breast reconstruction techniques using musculocutaneous flaps from the latissimus dorsi and rectus abdominis have aroused interest regarding patients’ quality of life. Our goal here was to compare patients’ satisfaction scores after they underwent breast reconstruction using musculocutaneous flaps from either the latissimus dorsi or the rectus abdominis. DESIGN AND SETTING: Primary, clinical, analytical, observational and cross-sectional study conducted in a federal university and a public hospital. METHODS: Demographic and clinical data were collected. The Mini-Mental State Examination was then applied, with testing for specificity and sensitivity. Lastly, a breast evaluation questionnaire was applied to evaluate breast satisfaction among 90 women, who were divided into three groups: mastectomy (control; n = 30); breast reconstruction using flap from the latissimus dorsi (n = 30); and reconstruction using flap from the rectus abdominis (n = 30). RESULTS: The groups were homogeneous regarding the main demographic data and the questionnaire responses (P < 0.05). Compared with the control group, the reconstruction groups showed significant improvement in satisfaction (P < 0.0002) after one year. CONCLUSION: Within our sample, women who underwent breast reconstruction with flaps from either the latissimus dorsi or the rectus abdominis had similar satisfaction scores.
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33. Tratamento cirúrgico de carcinomas cutâneos pelo Sistema Único de Saúde: análise de custos
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Karine Helena Bócoli, Daniela Francescato Veiga, Isaías Vieira Cabral, Marcelo Prado de Carvalho, Neil Ferreira Novo, Joel Veiga Filho, and Lydia Masako Ferreira
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Skin neoplasms ,Carcinoma ,Surgery, plastic ,Fees and charge ,Unified health system ,Surgery ,RD1-811 - Abstract
OBJETIVO: analisar os custos do tratamento cirúrgico de carcinomas cutâneos, realizado em serviço de Cirurgia Plástica de hospital universitário, em pacientes do Sistema Único de Saúde (SUS). MÉTODOS:setenta e um pacientes foram incluídos e registrados seus dados sociodemográficos e da operação. Para análise de custos diretos foi considerado o período de internação do paciente, incluindo custos materiais e humanos. RESULTADOS: o custo material médio por procedimento foi R$.324,70, e o valor médio da taxa de serviço hospitalar, segundo a tabela do SUS, foi R$.193,66. Com isso, obteve-se um custo total médio de R$.518,36 por procedimento. Entretanto, o valor médio repassado pelo SUS ao hospital por procedimento foi R$.429,19. CONCLUSÃO: o tratamento cirúrgico dos carcinomas cutâneos gerou para o hospital, um déficit médio de R$.89,16 reais por procedimento.
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34. DEVELOPMENT OF METRICS FOR PROTOCOLS AND OTHER TECHNICAL PRODUCTS
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Daniela Francescato Veiga and Lydia Masako Ferreira
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Protocols ,Handbooks ,Classification ,Education, graduate ,Surgery ,RD1-811 - Abstract
Objective: To develop a proposal for metrics for protocols and other technical products to be applied in assessing the Postgraduate Programs of Medicine III - Capes. Methods: The 2013 area documents of all the 48 Capes areas were read. From the analysis of the criteria used by the areas at the 2013's Triennal Assessment, a proposal for metrics for protocols and other technical products was developed to be applied in assessing the Postgraduate Programs of Medicine III. This proposal was based on the criteria of Biological Sciences I and Interdisciplinary areas. Results: Only seven areas have described a scoring system for technical products. The products considered and the scoring varied widely. Due to the wide range of different technical products which could be considered relevant, and that would not be punctuated if they were not previously specified, it was developed, for the Medicine III, a proposal for metrics in which five specific criteria to be analyzed: Demand, Relevance/Impact, Scope, Complexity and Adherence to the Program. Based on these criteria, each product can receive 10 to 100 points. Conclusion: This proposal can be applied to the item Intellectual Production of the evaluation form, in subsection "Technical production, patents and other relevant production". The program will be scored as Very Good when it reaches mean ≥150 points/permanent professor/quadrennium; Good, mean between 100 and 149 points; Regular, mean between 60 and 99 points; Weak mean between 30 and 59 points; Insufficient, up to 29 points/permanent professor/quadrennium.
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35. METRICS DEVELOPMENT FOR PATENTS
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Daniela Francescato Veiga and Lydia Masako Ferreira
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Intellectual property ,Patents ,Classification ,Licensure ,Surgery ,RD1-811 - Abstract
Objective: To develop a proposal for metrics for patents to be applied in assessing the postgraduate programs of Medicine III - Capes. Methods: From the reading and analysis of the 2013 area documents of all the 48 areas of Capes, a proposal for metrics for patents was developed to be applied in Medicine III programs. Results: Except for the areas Biotechnology, Food Science, Biological Sciences III, Physical Education, Engineering I, III and IV and Interdisciplinary, most areas do not adopt a scoring system for patents. The proposal developed was based on the criteria of Biotechnology, with adaptations. In general, it will be valued, in ascending order, the deposit, the granting and licensing/production. It will also be assigned higher scores to patents registered abroad and whenever there is a participation of students. Conclusion: This proposal can be applied to the item Intellectual Production of the evaluation form, in subsection Technical Production/Patents. The percentage of 10% for academic programs and 40% for Masters Professionals should be maintained. The program will be scored as Very Good when it reaches 400 points or over; Good, between 200 and 399 points; Regular, between 71 and 199 points; Weak up to 70 points; Insufficient, no punctuation.
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36. Sexuality, depression and body image after breast reconstruction
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Silvania de Cassia Vieira Archangelo, Miguel Sabino Neto, Daniela Francescato Veiga, Elvio Bueno Garcia, and Lydia Masako Ferreira
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Breast Reconstruction ,Mastectomy ,Sexuality ,Body image ,Depression ,Medicine (General) ,R5-920 - Abstract
OBJECTIVES: To evaluate the impact of breast reconstruction after mastectomy on sexual function, body image, and depression. METHODS: This cross-sectional, comparative, controlled study was conducted with 90 women between 18 and 65 years of age who had undergone either mastectomy alone (mastectomy group, n=30) or mastectomy combined with breast reconstruction (mastectomy-reconstruction group, n=30) at least one year prior to the study or who had no breast cancer (control group, n=30). Patients were assessed for sexual function, depression, and body image using the validated Brazilian-Portuguese versions of the Female Sexual Function Index, the Beck Depression Inventory, and the Body Dysmorphic Disorder Examination, respectively. RESULTS: The three groups were homogeneous for age, marital status, body mass index, and education level. The women in the mastectomy group reported significantly worse sexual function, greater depressive symptoms, and lower body image than those in the mastectomy-reconstruction and control groups. In the mastectomy group, the frequency of sexual dysfunction was significantly greater among patients without a marital partner and those with a higher level of education than among patients in the other two groups with the same characteristics. CONCLUSION: Patients who had undergone breast reconstruction after mastectomy reported better sexual function and body image and fewer depressive symptoms than patients who had undergone mastectomy alone. Sexual dysfunction was associated with the absence of a marital partner and a higher level of education and was more frequent in the mastectomy group.
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37. Prototype sensor system for analyzing frailty in older people: a pilot study
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Jorge Luiz de Carvalho Mello, Daniela Francescato Veiga, Vitor Ângelo Carlucio Galhardo, Lydia Masako Ferreira, Carlos Minoru Tamaki, Alexandre Carlos Brandão Ramos, and Diba Maria Sebba Tosta de Souza
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General Earth and Planetary Sciences ,General Environmental Science - Abstract
Introduction: Frailty syndrome is characterized by reduced physical and cognitive reserves, making older people vulnerable to adverse events. This study describes a prototype sensor system developed for assessing frailty through physiological parameters and frailty markers. Methods: A prototype combining four sensors in network and a software package was developed and tested in four long-term care facility senior residents of both sexes, aged 60 and older, showing no locomotive syndrome or severe cognitive impairment. Three of them were frail and able to walk without aid (P1), holding onto the wall (P2) or with a cane (P3), and a non-frail participant (P4) walked without aid. Results: Regarding mean acceleration, P1 and P4 showed the lowest and highest values, respectively, on the antero-posterior axis; P4 had the lowest value on the medio-lateral axis; and P3 presented the highest value on the vertical axis. All participants showed similar roll angular velocity; P4 presented the lowest pitch angular velocity; and P1 and P4 had the highest mean yaw angular velocity. A sarcopenic participant (P2) exhibited the lowest force of muscle contraction. Conclusion: The device has potential to detect frailty markers for adverse outcomes in older people, such as postural instability and increased risk of falls.
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- 2023
38. Mammoplasty: steps for safe surgery. Evidence from literature
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Ricardo Frota Boggio, Daniela Francescato Veiga, Adriano Guimarães Brasolin, Anne Karoline Groth, Paulo Rogério Quieregatto do Espirito Santo, Lydia Masako Ferreira, and Felipe Lehmann Coutinho
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medicine.medical_specialty ,business.industry ,medicine ,Surgery ,Mammoplasty ,Safe surgery ,business - Published
- 2021
39. Translation and cross-cultural adaptation of the Brazilian version of BREAST-Q©: breast reconstruction expectations module
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Iara Gama Esteves de Oliveira, Miguel Sabino Neto, Luciana Chamone Amaro, Henrique Kenji Uehara, Lydia Masako Ferreira, and Daniela Francescato Veiga
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Cross-Cultural Comparison ,Quality of life ,Motivation ,Validation studies ,Mammaplasty ,education ,Humans ,Reproducibility of Results ,General Medicine ,Middle Aged ,Breast neoplasms ,Surveys and questionnaires ,Brazil - Abstract
SUMMARY OBJECTIVE: This study aimed to translate the BREAST-Q© — Breast Reconstruction Expectations Module (preoperative) 2.0 into Portuguese and adapt it to the Brazilian cultural context. METHODS: Authorization for translation and cross-cultural adaptation of the questionnaire was obtained from the holders of the instrument's distribution rights. The questionnaire was translated and retro-translated. For cultural adaptation, the instrument was applied to 40 patients who had breast reconstruction surgery scheduled. Cronbach's alpha was used to assess the internal consistency. RESULTS: The mean age of the patients was 53.5 years, and the majority (72.5%) was undergoing reconstruction with implants. Good and excellent internal consistencies were observed for the Coping and Appearance expectations scales (Cronbach's alpha values of 0.878 and 0.909, respectively). For the Pain scale, the internal consistency was moderate (0.738), and it was acceptable (0.587) for the Medical team. CONCLUSION: The BREAST-Q© — Breast Reconstruction Expectations Module (preoperative) 2.0 was successfully translated and adapted to the Brazilian context.
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- 2022
40. Controvérsia sobre a Doença do Implante de Silicone Mamário: Uma revisão sistemática sobre o tema
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Marco Aurélio Guidugli dos Santos, José Manuel Amarante, Daniela Francescato Veiga, and Elvio Bueno Garcia
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medicine.medical_specialty ,business.industry ,General Chemical Engineering ,General surgery ,Silicone implant ,Cancer detection ,Scientific evidence ,chemistry.chemical_compound ,Plastic surgery ,Patient safety ,Silicone ,chemistry ,medicine ,business - Abstract
Introdução: Atualmente, existem evidências esmagadoras para apoiar a segurança dos implantes mamários de silicone. A decisão obter, manter ou remover os implantes mamários é escolha da paciente. Se uma paciente optar por remover os implantes mamários, é importante encontrar um cirurgião plástico certificado pela Sociedade Brasileira de Cirurgia Plástica. Objetivos: O objetivo deste artigo é apresentar o estado atual das evidências científicas relacionadas à segurança dos implantes mamários de silicone. Os estudos em andamento são fortemente incentivados em todas as áreas, da detecção do câncer à doença auto-imune, cabendo ao profissional cirurgião plástico (a), o esforço necessário para melhorar a segurança, a conscientização e a educação do paciente. Metodologia: Foi pesquisado o termo “Silicone Implant Illness” nos portais de indexação Google Acadêmico, Scopus e Web of Sciences e foram selecionados 102 artigos com maior fator de impacto e citações. Conclusão: Até o presente momento, não existem estudos concretos ou baseados em evidências ou dados revisados por pares sobre a formação de uma nova síndrome.
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- 2020
41. CIMENTO PBS®CIMMO EM PREENCHIMENTO DE FALHAS ÓSSEAS: ESTUDO EXPERIMENTAL EM RATOS: PARTE I
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Christiano Cândido Zerbinati, José Dias da Silva Neto, Daniela Francescato Veiga, and Taylor Brandão Schnaider
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As extrações dentárias originam falhas ósseas, alvéolos frescos. Condições clínicas que exigem abordagem com instalação de implantes e reabilitação estética através de próteses sobre os implantes. Este procedimento reabilitador chama-se carga imediata e a condição para que seja possível ser realizada é a estabilidade primária dos implantes. Objetivo: Avaliar cimento PBS®CIMMO no preenchimento de falhas ósseas. Métodos: Trinta e seis ratos Wistar adultos machos foram organizados em três Grupos de doze indivíduos cada (Grupo 1, Grupo 2 e Grupo 3). Aprovação CEUA parecer 265/17. Em todos os Grupos realizou-se uma falha óssea no fêmur com as dimensões de 2,0 mm de largura por 7,0 mm de profundidade. No Grupo 1, aplicou-se o cimento PBS®CIMMO na falha óssea produzida e instalou-se implante de titânio (CONEXÃO®) medindo 1,5mm de espessura e 6mm de comprimento na cavidade. No Grupo 2, aplicou-se o cimento PBS®CIMMO na cavidade. No Grupo 3 realizou-se apenas a falha óssea. Resultados: Realizou-se os testes de Kruskal Wallis para cada área e comparou-se a média dos três Grupos. Foi aplicado o teste Dunn que comparou a média de cada Grupo entre si: Grupo 1 com Grupo 2, Grupo 1 com Grupo 3 e Grupo 2 com Grupo 3. Em todas as comparações ocorreu significância para o Grupo 2 p = 0,0014. Conclusão: O cimento PBS®CIMMO induziu neoformação óssea e observou-se integração osso neoformado, cimento e parafuso de titânio.
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- 2021
42. Brazilian version of the Breast‐Q © —Breast‐Conserving Therapy Module 2.0: Translation, cross‐cultural adaptation, and reproducibility
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Felipe Andreotta Cavagna, Tatiane de Sousa Schunck, Sabino Neto M, Daniela Francescato Veiga, Lydia Masako Ferreira, and Grisotto Jr Le
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medicine.medical_specialty ,business.industry ,medicine.medical_treatment ,Quality of life (healthcare) ,Oncology ,Breast q ,Internal Medicine ,Cross-cultural ,Medicine ,Surgery ,Medical physics ,business ,Adaptation (computer science) ,Mastectomy - Published
- 2020
43. Quality of randomized clinical trials published by plastic surgeons: a long-term follow-up study
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Daniela Francescato Veiga, Thiago Bezerra de Morais, Lydia Masako Ferreira, and Miguel Sabino Neto
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medicine.medical_specialty ,Randomized controlled trial ,Long term follow up ,law ,business.industry ,media_common.quotation_subject ,Physical therapy ,medicine ,Surgery ,Quality (business) ,business ,law.invention ,media_common - Published
- 2019
44. Reply: Postoperative Antibiotic Prophylaxis in Reduction Mammaplasty: A Randomized Controlled Trial
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Daniela Francescato Veiga, Edgard da Silva Garcia, Isaías Vieira Cabral, Lydia Masako Ferreira, Joel Veiga-Filho, Miguel Sabino-Neto, Natália Lana Larcher Pinto, and Neil Ferreira Novo
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medicine.medical_specialty ,Blinding ,medicine.drug_class ,medicine.medical_treatment ,Mammaplasty ,Antibiotics ,030230 surgery ,Placebo ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,Randomized controlled trial ,law ,medicine ,Humans ,Surgical Wound Infection ,Antibiotic prophylaxis ,Surgical team ,business.industry ,Antibiotic Prophylaxis ,Surgery ,030220 oncology & carcinogenesis ,Female ,business ,Body mass index - Abstract
BACKGROUND Reduction mammaplasty is a well-established procedure. Studies have shown benefits of using antibiotics in this procedure. Nevertheless, there is no solid evidence to support postoperative antibiotic prophylaxis. The authors evaluated the influence of postoperative antibiotic delivery on infection rates after reduction mammaplasty. METHODS The authors conducted a randomized trial of noninferiority, with two parallel groups, with triple blinding. The participants were 124 women with breast hypertrophy, with reduction mammaplasty already scheduled, selected consecutively. All patients underwent reduction mammaplasty, performed by the same surgical team, using the superomedial pedicle technique for ascending the nipple-areola complex. All patients received cephalothin (1 g) intravenously at the anesthetic induction and every 6 hours for 24 hours. At hospital discharge, they were assigned randomly to either the placebo (n = 62) or antibiotic group (n = 62) and were instructed to take identical capsules containing 500 mg of cephalexin or placebo, respectively, every 6 hours, for 7 days. Patients were assessed weekly, for 4 weeks, regarding the occurrence of surgical-site infection, by a surgeon who was unaware of the allocation. The criteria and definitions of the Centers for Disease Control and Prevention were adopted. RESULTS There was no statistical difference between groups regarding age, body mass index, or resected breast tissue weight. The overall surgical-site infection rate was 0.81 percent. Only one patient, allocated to the antibiotic, presented infection, classified as superficial incisional (p = 1.00). In the placebo group, surgery time was higher (p = 0.003). CONCLUSION The maintenance of antibiotics in the postoperative period of reduction mammaplasty did not influence the rates of surgical-site infection. CLINICAL QUESTION/LEVEL OF EVIDENCE Therapeutic, I.
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- 2020
45. Antibiotic prophylaxis in breast cancer surgery. A randomized controlled trial
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Neil Ferreira Novo, Lydia Masako Ferreira, Ana Beatriz Alkmim Teixeira Loyola, Fabíola Soares Moreira Campos, Daniela Francescato Veiga, Rubens Murilo de Athayde Prudencio, and Ivanildo Archangelo Junior
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medicine.medical_specialty ,RD1-811 ,medicine.medical_treatment ,Cefazolin ,Breast Neoplasms ,Placebo ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,Breast cancer ,Double-Blind Method ,Randomized controlled trial ,law ,medicine ,Humans ,Surgical Wound Infection ,Clinical Investigation ,Antibiotic prophylaxis ,Mastectomy ,Postoperative Care ,business.industry ,Surgical wound ,Antibiotic Prophylaxis ,medicine.disease ,United States ,Surgery ,Clinical trial ,030220 oncology & carcinogenesis ,Female ,030211 gastroenterology & hepatology ,business ,Brazil ,medicine.drug - Abstract
Purpose To assess the effect of antibiotic prophylaxis on surgical site infection (SSI) rates in women undergoing breast cancer surgery in two tertiary hospitals in Brazil. Methods This was a randomized, double-blind, placebo-controlled, parallel-group clinical trial. A total of 124 women without independent risk factors for SSI were randomly assigned to receive either cefazolin (antibiotic group, n = 62) or placebo (control group, n = 62) as preoperative prophylaxis. After surgery, all surgical wounds were examined once a week, for four weeks, according to the Centers for Disease Control and Prevention definitions and classifications for SSI. Results Baseline characteristics were homogeneous between the two groups. Only one patient in the antibiotic group developed SSI, which was classified as superficial incisional. The overall SSI rate was low, with no significant difference between groups. Conclusion Antibiotic prophylaxis had no significant effect on reducing SSI rates in women without independent risk factors for SSI undergoing breast cancer surgery.
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- 2020
46. Brazilian version of the Breast-Q
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Tatiane de Sousa, Schunck, Daniela Francescato, Veiga, Felipe Andreotta, Cavagna, Grisotto, Jr LE, Sabino, Neto M, and Lydia Masako, Ferreira
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Cross-Cultural Comparison ,Surveys and Questionnaires ,Quality of Life ,Humans ,Reproducibility of Results ,Breast Neoplasms ,Female ,Translations ,Brazil - Published
- 2020
47. Effectiveness of Brazilian national health policy for mammogram screening in women aged over 50 years
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Fabíola Soares Moreira Campos, Lydia Masako Ferreira, Renata Bites Ferreira Amorim, Daniela Francescato Veiga, Leonardo Larrubia Silveira, Ivanildo Archangelo Junior, and Neil Ferreira Novo
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medicine.medical_specialty ,Mammogram screening ,business.industry ,Health Policy ,Breast Neoplasms ,Oncology ,Family medicine ,Internal Medicine ,medicine ,National health policy ,Humans ,Mass Screening ,Surgery ,Female ,business ,Brazil ,Early Detection of Cancer ,Mammography - Published
- 2020
48. Single dose versus 24 h antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial
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Yara Juliano, Lydia Masako Ferreira, José Wilson Moreira-Filho, Daniela Francescato Veiga, Edgard da Silva Garcia, Evelyne Borges de Mattos Andrade, and Joel Veiga-Filho
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Plastic surgery ,medicine.medical_specialty ,medicine.drug_class ,medicine.medical_treatment ,Mammaplasty ,Wound infection ,Antibiotics ,Medicine (miscellaneous) ,030230 surgery ,law.invention ,03 medical and health sciences ,Study Protocol ,0302 clinical medicine ,Randomized controlled trial ,law ,Anti-bacterial agents ,Internal medicine ,medicine ,Humans ,Surgical Wound Infection ,Pharmacology (medical) ,Antibiotic prophylaxis ,Reduction (orthopedic surgery) ,Randomized Controlled Trials as Topic ,Protocol (science) ,lcsh:R5-920 ,business.industry ,Prophylaxis ,Antibiotic Prophylaxis ,030220 oncology & carcinogenesis ,Female ,lcsh:Medicine (General) ,business ,Surgical site infection ,Brazil - Abstract
Background Reduction mammaplasty is among the most commonly performed procedures in plastic surgery. Antibiotics are widely prescribed, on an empirical basis, to prevent surgical site infections. However, there is a lack of evidence to support its use. This trial aims to compare the influence of the use of prophylatic antibiotics as a single dose or for 24 h on surgical site infection rates following reduction mammaplasty. Methods Randomized trial of non-inferiority, with two parallel groups. A total of 146 breast hypertrophy patients, with reduction mammaplasty already scheduled, will be enrolled. Patients will be randomly allocated to the placebo group that will receive antibiotics only at the anesthesia induction (n = 73) or to the antibiotics group that will receive antibiotics at the anesthesia induction and for 24 h (n = 73). None of the patients will receive antibiotics after hospital discharge. Patients will be followed-up weekly, for 30 days, regarding surgical site infection. The Centers for Disease Control and Prevention criteria will be applied. A statistical analysis of the data will be performed. Discussion Previous studies have demonstrated a decrease in infection rates after reduction mammaplasty when antibiotic prophylaxis was used, compared to the use of no antibiotics. However, the duration of antibiotic prophylaxis remains a point to be clarified. This study will test the hypothesis that maintaining the use of antibiotics for 24 h does not reduce infection rates compared to the use of a single preoperative dose. Trial registration Clinicaltrials.gov NCT04079686 . Registered on September 6, 2019.
- Published
- 2020
49. Alcohol (70%) versus alcoholic chlorhexidine solution (0.5%) in skin antisepsis for neuraxial blocks: a randomized clinical trial
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Adilson De Oliveira Fraga, Ana Beatriz Alkmim Teixeira Loyola, Daniela Francescato Veiga, Luiz Francisley de Paiva, Luiz Carlos Souza Tostes, LetÍcia Azevedo Gazzi, and Yara Juliano
- Subjects
Anesthesia, Epidural ,RD1-811 ,medicine.drug_class ,Anestesia Epidural ,Neuraxial blockade ,Alcohol ,Antisepsis ,Anesthesia, Spinal ,Group B ,law.invention ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Antiseptic ,Randomized controlled trial ,Antissepsia ,030202 anesthesiology ,law ,Raquianestesia ,medicine ,Humans ,Surgical Wound Infection ,030212 general & internal medicine ,Trial registration ,Skin ,Álcool Etílico ,Ethanol ,business.industry ,Chlorhexidine ,Clorexidina ,chemistry ,Anesthesia Spinal ,Anesthesia ,Anti-Infective Agents, Local ,Surgery ,business ,medicine.drug - Abstract
Objective: to compare the use of 0.5% alcoholic chlorhexidine and 70% alcohol in skin antisepsis for neuraxial blocks. Method: this is a non-inferiority randomized clinical trial, with two parallel arms. Seventy patients who were candidates for neuraxial block were randomly allocated to group A (n = 35), in whom antisepsis was performed with 0.5% alcoholic chlorhexidine, or to group B (n = 35), in whom we used 70% hydrated ethyl alcohol. Swabs were harvested for culture at three times: before antisepsis, two minutes after application of the antiseptic, and immediately after puncture. The samples were sown in three culture media and the number of colony forming units (CFU) per cm² was counted. Results: there was no difference between the groups regarding age, sex, body mass index, time to perform the block or type of block. There were no differences between groups in the CFU/cm² counts before antisepsis. There was less bacterial growth in group B two minutes after application of the antiseptic (p = 0.048), but there was no difference between the groups regarding the number of CFU/cm² at the end of the puncture. Conclusion: 70% alcohol was more effective in reducing the number of CFU/cm² after two minutes, and there was no difference between the two groups regarding skin colonization at the end of the procedure. These results suggest that 70% alcohol may be an option for skin antisepsis before neuraxial blocks. Trial registration: ClinicalTrials.gov, NCT02833376. RESUMO Objetivo: comparar o uso de solução alcoólica de clorexidina 0,5% e de álcool 70% na antissepsia da pele para bloqueios do neuroeixo. Método: ensaio clínico randomizado de não inferioridade, com dois braços paralelos. Foram selecionados 70 pacientes candidatos à bloqueio do neuroeixo, randomicamente alocados para o grupo A (n=35), em que a antissepsia foi realizada com clorexidina alcoólica 0,5%, ou para o grupo B (n=35), em que se utilizou álcool etílico hidratado 70%. Foram coletadas, com swab, amostras para cultura em três momentos: antes da antissepsia, dois minutos após aplicação do antisséptico, e imediatamente após a punção. As amostras foram semeadas em três meios de cultura e foi contabilizado o número de unidades formadoras de colônias (UFC) por cm². Resultados: não houve diferença entre os grupos quanto à idade, ao sexo, ao índice de massa corporal, ao tempo para realização do bloqueio ou tipo de bloqueio. Também não houve diferenças entre os grupos na contagem de UFC/cm² antes da antissepsia. Constatou-se menor crescimento bacteriano no grupo B dois minutos após aplicação do antisséptico (p=0,048), mas não houve diferença entre os grupos quanto ao número de UFC/cm² ao final da punção. Conclusão: o álcool 70% mostrou-se mais efetivo em reduzir o número de UFC/cm² após dois minutos, e não houve diferença entre os dois grupos quanto à colonização da pele ao final do procedimento. Esses resultados sugerem que o álcool 70% pode ser opção para antissepsia da pele antes de bloqueios do neuroeixo. Registro ensaio clínico: ClinicalTrials.gov, NCT02833376.
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- 2020
50. Cimento bioativo e biocompatível como elemento único em pulpotomia de dentes decíduos: ensaio clínico randomizado
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Marcelo Junqueira Pereira, José Dias da Silva Neto, Fernanda Valadão Moysés, Matheus Henrique Lopes Dominguete, Daniela Francescato Veiga, Camila Alessandra Pazzini, and Ana Carla Junqueira Pereira
- Subjects
Molar ,Pediatric dentistry ,Pulpotomy ,Dentistry ,Single element ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,stomatognathic system ,Randomized controlled trial ,law ,Deciduous teeth ,Medicine ,Biocompatible materials ,General Dentistry ,Cement ,Pulpotomia ,business.industry ,030206 dentistry ,Clinical trial ,stomatognathic diseases ,Odontopediatria ,Deciduous ,medicine.anatomical_structure ,Materiais biocompatíveis ,030211 gastroenterology & hepatology ,business - Abstract
Objective: Pulpotomy in deciduous teeth maintains the integrity and health of deciduous teeth and supporting tissues until a permanent tooth has erupted. PBS HD CIMMO® cement was evaluated in deciduous teeth pulpotomies as base material and restoration. A randomized clinical trial was performed Methods: This study was approved by the Ethics Committee of (Universidade Vale do Sapucaí) UNIVÁS with Certificate of Presentation for Ethical Consideration, protocol number is: 1.771.929. 60 deciduous molar teeth from 32 healthy children were selected. These teeth were divided into two groups: G1 with 30 teeth, in which the classictreatment with formocresol was used, and G2 with 30 teeth, in which PBS HD CIMMO® cement was used as base and simultaneous final restoration. The evaluation was performed 12 months after the intervention through clinical and radiographic exams. Fisher’s exact test was performed to correlate the clinical and radiographic aspects in both groups Results: There was no significant difference (p= 0.090) in the clinical-radiographic evaluation. PBS HD CIMMO® cement is option to be used as a single element in pulpotomies of deciduous teeth Conclusion: Longitudinal studies should be performed in order to demonstrate a significant association between these groups. The study was enrolled in clinical trials (clinical trials.gov) with registration NCT03200938. RESUMO Objetivos: A pulpotomia em dentes decíduos mantém a integridade e a saúde dos dentes decíduos e dos tecidos de suporte, até a erupção de um dente permanente. O cimento PBS HD CIMMO® foi avaliado em pulpotomias de dentes decíduos como material de base e restauração. Um ensaio clínico randomizado foi realizado. Métodos: Este estudo foi aprovado pelo Comitê de Ética da Universidade Vale do Sapucaí, UNIVÁS, com Certificado de Apresentação para Consideração Ética, número do protocolo: 1.771.929. Foram selecionados 60 dentes molares decíduos de 32 crianças saudáveis. Esses dentes foram divididos em dois grupos: G1 com 30 dentes, no qual foi utilizado o tratamento clássico com formocresol e G2 com 30 dentes, no qual o cimento PBS HD CIMMO® foi utilizado como base e restauração final simultânea. A avaliação foi realizada 12 meses após a intervenção através de exames clínicos e radiográficos. O teste exato de Fisher foi utilizado para correlacionar os aspectos clínicos e radiográficos nos dois grupos. Resultados: Não houve diferença significativa (p = 0,090) na avaliação clínico-radiográfica. O cimento PBS HD CIMMO® é uma opção para ser usado como um elemento único em pulpotomias de dentes decíduos. Conclusão: Estudos longitudinais devem ser realizados para demonstrar uma associação significativa entre esses grupos. O estudo foi inscrito em ensaios clínicos (Clinical Trials.gov) com o registro NCT03200938.
- Published
- 2020
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