22 results on '"Torregrosa S"'
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2. Mathematical modelling of frailty, dependency and mortality in a 70-year-old general population.
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Camacho Torregrosa, S., Santamaría Navarro, C., and Albert Ros, X.
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Due to the ageing of the world population, a better functional capacity for the elderly is needed. Hence the importance of detecting people at risk of frailty, dependence and death to fulfil an individualized approach. There are models that uses frailty indices, but none that use the Frail-VIG Index, based on the comprehensive geriatric assessment. Three predictive models of frailty, dependency and mortality for 70-year-old in the general population are presented. The risk factors for developing frailty or dependency are female gender, chronicity level 2 or 3, and marriage. For mortality, the risk factors are male gender, low educational level and being frail according to frail-VIG index. In conclusion, the health actions to prevent frailty and dependence should focus on reducing the chronicity level, especially in women. To delay mortality, an individualized approach should be implemented in frail people. Further studies are needed to determine other health and social risk factors. [ABSTRACT FROM AUTHOR]
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- 2023
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3. Correction to: Switching to Preservative-Free Tafluprost/Timolol Fixed-Dose Combination in the Treatment of Open-Angle Glaucoma or Ocular Hypertension: Subanalysis of Data from the VISIONARY Study According to Baseline Monotherapy Treatment (Advances in Therapy, (2022), 39, 8, (3501-3521), 10.1007/s12325-022-02166-6)
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Oddone, F., Kirwan, J., Lopez-Lopez, F., Zimina, M., Fassari, C., Hollo, G., Faschinger, C., Chen, E., Nemeth, G., Bator, G., Tsorbatzoglou, A., Acs, T., Ferencz, M., Sohajda, Z., Toth, J., Volner, V., Vogt, G., Biro, Z., Facsko, A., Nemes, J., Berta, A., Elek, I., Ng, E., Rossi, G., Rossetti, L., Vetrugno, M., Iester, M., Marchini, G., Scorcia, V., Staurenghi, G., Cagini, C., Salgarello, T., Bettin, P., Figus, M., Scuderi, G. L., De Cilla, S., Grundmane, I., Linavska, N., Volksone, L., Laganovska, G., Baumane, K., Lemij, H., Gundersen, K. G., Erichev, V., Adbulaeva, E., Karlova, E., Zakharova, E., Panova, I., Malyugin, B., Rodriguez-Agirretxe, I., Valladares, A. M., del Castillo, J. B., Gimenez, R., Vallejo, M. P., Garcia-Medina, J. J., Lopez, A. A., Torregrosa, S., Loscos, J., Kolko, M., Ansari, E., Broadway, D., Claridge, K., Ruben, S., Nita, A., Smith, M., Moosavi, A., King, A. J. W., and Kinsella, M.
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Pharmacology (medical) ,General Medicine - Abstract
The authors would like to acknowledge missing data for all prior latanoprost users as a whole. The following sentence has been added to the manuscript (page 8, first paragraph): Mean (SD) reduction from baseline at Month 6 for users of all latanoprost formulations (preserved and PF) was 6.1 (4.25) mmHg (25.9%; p\0.0001). The authors have also prepared a table to summarise the change in intraocular pressure following a switch to the preservative-free tafluprost/timolol fixed-dose combination from all latanoprost formulations (preserved and preservative-free formulations). See Table 1 below.(Table Preseneted.) .The original article has been corrected.
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- 2022
4. Switching to Preservative-Free Tafluprost/Timolol Fixed-Dose Combination in the Treatment of Open-Angle Glaucoma or Ocular Hypertension: Subanalysis of Data from the VISIONARY Study According to Baseline Monotherapy Treatment
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Oddone, F., Kirwan, J., Lopez-Lopez, F., Zimina, M., Fassari, C., Hollo, G., Faschinger, C., Chen, E., Nemeth, G., Bator, G., Tsorbatzoglou, A., Acs, T., Ferencz, M., Sohajda, Z., Toth, J., Volner, V., Vogt, G., Biro, Z., Facsko, A., Nemes, J., Berta, A., Elek, I., Ng, E., Rossi, G., Rossetti, L., Vetrugno, M., Iester, M., Marchini, G., Scorcia, V., Staurenghi, G., Cagini, C., Salgarello, T., Bettin, P., Figus, M., Scuderi, G. L., De Cilla, S., Grundmane, I., Linavska, N., Volksone, L., Laganovska, G., Baumane, K., Lemij, H., Gundersen, K. G., Erichev, V., Adbulaeva, E., Karlova, E., Zakharova, E., Panova, I., Malyugin, B., Rodriguez-Agirretxe, I., Valladares, A. M., del Castillo, J. B., Gimenez, R., Vallejo, M. P., Garcia-Medina, J. J., Lopez, A. A., Torregrosa, S., Loscos, J., Kolko, M., Ansari, E., Broadway, D., Claridge, K., Ruben, S., Nita, A., Smith, M., Moosavi, A., King, A. J. W., and Kinsella, M.
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Adult ,Hyperemia ,Tafluprost/timolol fixed-dose combination ,Ocular hypertension ,VISIONARY study ,Travoprost ,Preservative-free topical medication ,Prostaglandin analogue monotherapy ,Humans ,Pharmacology (medical) ,Prospective Studies ,Chronic ,Open-angle glaucoma ,Antihypertensive Agents ,Intraocular Pressure ,Real-world evidence ,Prostaglandins A ,Fatigue Syndrome, Chronic ,Prostaglandins F ,Glaucoma ,General Medicine ,Beta-blocker monotherapy ,Fatigue Syndrome ,Drug Combinations ,Bimatoprost ,Open-Angle ,Timolol ,Latanoprost ,Glaucoma, Open-Angle - Abstract
Introduction: The VISIONARY study demonstrated statistically significant intraocular pressure (IOP) reductions with the preservative-free fixed-dose combination of tafluprost 0.0015% and timolol 0.5% (PF tafluprost/timolol FC) in open-angle glaucoma (OAG) or ocular hypertension (OHT) patients, sub-optimally controlled with topical prostaglandin analogue (PGA) or beta-blocker monotherapy. Current subanalyses have examined these data according to the baseline monotherapy. Methods: A European, prospective, observational study included adults (aged ≥ 18 years) with OAG or OHT, who were switched to the PF tafluprost/timolol FC from PGA or beta-blocker monotherapy. Treatment outcomes were reported according to prior monotherapy subgroup: beta-blocker, preserved latanoprost, PF-latanoprost, bimatoprost, tafluprost, and travoprost. Endpoints included the mean change from baseline regarding IOP, conjunctival hyperemia, and corneal fluorescein staining (CFS) at Week 4 and Week 12, and at Month 6. Results: The subanalysis included 577 patients. All prior monotherapy subgroups demonstrated statistically significant IOP reductions from baseline at Week 4, that were maintained through Month 6 (p
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- 2022
5. Treatment of Open-Angle Glaucoma and Ocular Hypertension with Preservative-Free Tafluprost/Timolol Fixed-Dose Combination Therapy: The VISIONARY Study
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Oddone, F., Tanga, L., Kothy, P., Hollo, G., Faschinger, C., Chen, E., Nemeth, G., Bator, G., Tsorbatzoglou, A., Acs, T., Ferencz, M., Sohajda, Z., Toth, J., Volner, V., Vogt, G., Biro, Z., Facsko, A., Nemes, J., Berta, A., Elek, I., Ng, E., Rossi, G., Rossetti, L., Vetrugno, M., Iester, M., Marchini, G., Scorcia, V., Staurenghi, G., Cagini, C., Salgarello, T., Bettin, P., Figus, M., Scuderi, G. L., De Cilla, S., Grundmane, I., Linavska, N., Volksone, L., Laganovska, G., Baumane, K., Lemij, H., Gundersen, K. G., Zimina, M., Erichev, V., Karlova, E., Zakharova, E., Panova, I., Malyugin, B., Aguirrec, I. R., Lopez-Lopez, F., Valladares, A. M., del Castillo, J. B., Gimenez, R., Vallejo, M. P., Medina, J. G., Lopez, A. A., Torregrosa, S., Loscos, J., Kolko, M., Ansari, E., Broadway, D., Claridge, K., Ruben, S., Kirwan, J., Nita, A., Smith, M., Moosavi, A., King, A. J. W., and Kinsella, M.
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Male ,030213 general clinical medicine ,Intraocular pressure ,genetic structures ,Ocular hypertension ,Timolol ,Glaucoma ,0302 clinical medicine ,Prostaglandins, Synthetic ,Medicine ,Pharmacology (medical) ,Prospective Studies ,Open-angle glaucoma ,media_common ,Original Research ,Aged, 80 and over ,Fixed-dose combination ,General Medicine ,Middle Aged ,Drug Combinations ,Tolerability ,030220 oncology & carcinogenesis ,Female ,Glaucoma, Open-Angle ,medicine.drug ,medicine.medical_specialty ,medicine.drug_class ,Tonometry, Ocular ,03 medical and health sciences ,Preservative-free topical medication ,Ophthalmology ,Humans ,media_common.cataloged_instance ,European union ,Antihypertensive Agents ,Intraocular Pressure ,Aged ,business.industry ,Preservatives, Pharmaceutical ,Prostaglandins F ,Tafluprost ,Correction ,medicine.disease ,eye diseases ,sense organs ,Prostaglandin analogue ,business - Abstract
Introduction: A non-interventional, multicenter, European, prospective evaluation of the effectiveness, tolerability, and safety of a topical preservative-free tafluprost (0.0015%) and timolol (0.5%) fixed-dose combination (PF tafluprost/timolol FC) in adults with open-angle glaucoma (OAG) and ocular hypertension (OHT) demonstrating insufficient response to topical beta-receptor blockers or prostaglandin analogue (PGA) monotherapy. Methods: Mean intraocular pressure (IOP) change from baseline was measured at study visits following a switch to PF tafluprost/timolol FC. Primary endpoint was absolute mean IOP change at month 6. Change from baseline concerning ocular signs and symptoms was also explored. Results: Analyses included 577 patients (59.6% female). Mean age (SD) was 67.8 (11.67) years. Mean (SD) IOP reduction from baseline was significant at all study visits; 5.4 (3.76) mmHg (23.7%) at week 4, 5.9 (3.90) mmHg (25.6%) at week 12, and 5.7 (4.11) mmHg (24.9%) at month 6 (p < 0.0001 for all visits). At month 6, 69.2%, 53.6%, 40.0%, and 25.8% were responders based on ≥ 20%, ≥ 25%, ≥ 30%, and ≥ 35% cutoff values for mean IOP, respectively. Significant reductions were observed concerning corneal fluorescein staining (p < 0.0001), dry eye symptoms, irritation, itching, and foreign body sensation (p < 0.001 for each parameter). Conjunctival hyperemia was significantly reduced at all study visits (p < 0.0001 at each visit). Overall, 69 treatment-related adverse events (AEs) were reported, one of which was serious (status asthmaticus). Most AEs were mild to moderate in severity, and the majority had resolved or were resolving at the end of the study period. Conclusion: In clinical practice, PF tafluprost/timolol FC provided statistically and clinically significant IOP reductions in patients with OAG and OHT insufficiently controlled on or intolerant to PGA or beta-receptor blocker monotherapy. The full IOP reduction appeared at week 4 and was maintained over the 6-month study period. Key symptoms of ocular surface health improved. Trial Registration: European Union electronic Register of Post-Authorisation Studies (EU PAS) register number, EUPAS22204.
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- 2020
6. Correction to: Treatment of Open-Angle Glaucoma and Ocular Hypertension with Preservative-Free Tafluprost/Timolol Fixed-Dose Combination Therapy: The VISIONARY Study (Advances in Therapy, (2020), 37, 4, (1436-1451), 10.1007/s12325-020-01239-8)
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Oddone, F., Tanga, L., Kothy, P., Hollo, G., Faschinger, C., Chen, E., Nemeth, G., Bator, G., Tsorbatzoglou, A., Acs, T., Ferencz, M., Sohajda, Z., Toth, J., Volner, V., Vogt, G., Biro, Z., Facsko, A., Nemes, J., Berta, A., Elek, I., Ng, E., Rossi, G., Rossetti, L., Vetrugno, M., Iester, M., Marchini, G., Scorcia, V., Staurenghi, G., Cagini, C., Salgarello, T., Bettin, P., Figus, M., Scuderi, G. L., De Cilla, S., Grundmane, I., Linavska, N., Volksone, L., Laganovska, G., Baumane, K., Lemij, H., Gundersen, K. G., Zimina, M., Erichev, V., Karlova, E., Zakharova, E., Panova, I., Malyugin, B., Aguirrec, I. R., Lopez-Lopez, F., Valladares, A. M., del Castillo, J. B., Gimenez, R., Vallejo, M. P., Garcia-Medina, J. J., Lopez, A. A., Torregrosa, S., Loscos, J., Kolko, M., Ansari, E., Broadway, D., Claridge, K., Ruben, S., Kirwan, J., Nita, A., Smith, M., Moosavi, A., King, A. J. W., and Kinsella, M.
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- 2020
7. Evaluation of the retinal nerve fiber layer thickness in smokers
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Escrivá Pastor, E., Sanz Gonzalez, S.M., Torregrosa, S., Pinazo Durán, M.D., Benítez-del-Castillo, J., Ramírez-Sebastián, A.I., and Zanón Moreno, V.
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- 2019
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8. New horizons for the treatment of glaucoma. I: Neuroinflammation and inflammasomes
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Zanon-Moreno, V., Raga-Cervera, J., García-Medina, J.J., Benitez-del-Castillo, J., Vinuesa-Silva, I., Torregrosa, S., and Pinazo-Durán, M.D.
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- 2018
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9. Oral vaccination of animals with antigens encapsulated in alginate microspheres
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Bowersock, T.L, Hogenesch, H, Suckow, M, Guimond, P, Martin, S, Borie, D, Torregrosa, S, Park, H, and Park, K
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- 1999
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10. Recomendaciones conjuntas sobre el manejo del paciente con osteoporosis y/o fracturas por fragilidad durante y después de la pandemia por COVID-19 de la SEIOMM, SEFRAOS, SER, SEMI, SEGG, SEMG, SEMERGEN y SEEN
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Caeiro Rey JR, Guañabens Gay N, Torregrosa Suau O, Cuadra Llopart L, Bastida Calvo JC, Micó Pérez R, and Rozas Moreno P
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Medicine ,Osteopathy ,RZ301-397.5 - Published
- 2022
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11. Paniculitis mesentérica asociada al uso de bifosfonatos: ¿son estos más proinflamatorios de lo que sabemos?
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Torregrosa Suau O, Guilló Quiles E, and Mora Rufete A
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paniculitis mesentérica ,bifosfonatos ,Medicine ,Osteopathy ,RZ301-397.5 - Abstract
La paniculitis mesentérica se caracterizada por una inflamación crónica inespecífica del tejido adiposo del mesenterio intestinal, y su etiología es desconocida. Se ha relacionado con malignidad, vasculitis, enfermedades reumáticas y con determinados fármacos. Presentamos un caso de paniculitis mesentérica asociada a la toma de bifosfonatos, no descrita previamente en la literatura, apoyando así el concepto de sus potenciales efectos secundarios proinflamatorios.
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- 2017
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12. TP62 223. Terapia vacuum assisted closure como tratamiento de mediastinitis en pacientes sometidos a cirugía cardíaca
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Hernández, C., Heredia, T., Bel Mínguez, A., Doñate, L., Pérez, M., Valera, F., Margarit, J., Torregrosa, S., and Montero, A.
- Abstract
Introducción y objetivoLa mediastinitis poscirugía cardía-ca, aunque infrecuente, continúa siendo una patología con una elevada mortalidad pese a su manejo de forma agresiva. Según algunas series publicadas previamente, la mortalidad se sitúa en torno al 30–40% de los afectados que son tratados de forma convencional. En este estudio queremos mostrar nuestros resultados y experiencia en el manejo de esta patología con la utilización de la terapia vacuum assisted closure (VAC).Material y métodosDesde abril de 2006 - diciembre de 2011 se utilizó la terapia VAC en 63 pacientes con diagnóstico establecido de mediastinitis. De forma retrospectiva se recogieron datos pre, intra y postoperatorio que se analizaron en SPSS.ResultadosLa edad media fue de 64 años (19–82), siendo el 73% varones. El 58,9% eran diabéticos y el 45% eran obesos. La media de días con tratamiento VAC fue de 28. La distribución por etiologías fue: cirugía coronaria (BPAC) 48%, cirugía valvular 18%, combinado 12%, trasplante 10%, congénitos 6%, y aorta ascendente 6%. En el 80% de los pacientes la infección fue polimicrobiana, destacando el S. aureus, que se aisló hasta en el 65% de los cultivos. La estancia media hospitalaria fue de 59 días. La mortalidad hospitalaria fue de 9 pacientes (14,2%).ConclusionesEn nuestro estudio evidenciamos que la terapia VAC disminuye significativamente la mortalidad y estancia hospitalaria de las mediastinitis poscirugía cardíaca comparada con las series publicadas con el tratamiento convencional. Estos resultados nos animan a continuar con este tratamiento.
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13. TP63 278. Terapia vacuum assisted closure como tratamiento de mediastinitis en pacientes que se han sometido a trasplante cardíaco
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Schuler, M., Heredia, T., Bel Mínguez, A., Doñate, L., Hernández, C., Pérez, M., Valera, F., Margarit, J., Torregrosa, S., and Montero, A.
- Abstract
Introducción y objetivoLa mediastinitis es una complicación devastadora en aquellos pacientes que deben ser sometidos a tratamiento inmunosupresor. El objetivo es presentar nuestra experiencia con el uso de la terapia vacuum assisted closure (VAC) para el manejo de esta patología en pacientes sometidos a trasplante cardíaco.Material y métodosDesde abril de 2006 - diciembre de 2011, 5 pacientes sometidos a trasplante cardíaco presentaron mediastinitis y se utilizó la terapia VAC como tratamiento de base. Estudio retrospectivo y análisis con software SPSS 17.0.ResultadosSe analizaron 5 pacientes (3 varones – 2 mujeres) con edad media de 49 años. Todos los cultivos fueron positivos para el S. aureus (aislado en el 100%), en el 60% la infección fue polimicrobiana. La media de días con terapia VAC fue de 30 y la estancia hospitalaria media fue 57 días. El tratamiento definitivo al cual fueron sometidos fue cierre por segunda intención en 2 casos y plastia de pectorales en 3.ConclusionesNo hubo ningún caso de muerte hospitala-ria. En todos los pacientes se evidenció una evolución satisfactoria con la utilización de la terapia VAC que permitió la resolución definitiva de la herida sin ser necesaria en ningún caso una reducción en la terapia inmunosupresora.
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14. CO66 222. Experiencia con el dispositivo oxigenador de membrana extracorpórea en el tratamiento del shock poscardiotomía refractario
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Hernández, C.E., Heredia, T., Bel, A.M., Doñate, L., Schuler, M., Pérez, M., Torregrosa, S., Valera, F.J., Margarit, J.A., and Montero, J.A.
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Introducción y objetivoLa incidencia de shock poscardio-tomía refractario (SPCR) a tratamiento convencional se sitúa en torno al 1%. La implantación de oxigenador de membrana extracorpórea (ECMO) de forma temporal como puente a la recuperación o a la utilización de otras medidas terapéuticas está ampliamente aceptada, pese a que los resultados no han sido satisfactorios según algunas series. En esta serie queremos mostrar nuestros resultados con el uso de la asistencia circulatoria de corta duración para el tratamiento de pacientes con SPCR.Material y métodosEstudio sobre una serie de casos en los que se implantó dispositivo ECMO por fallo en el destete de la circulación extracorpórea (CEC) o por desarrollo posterior del cuadro.ResultadosEntre diciembre de 2006 – diciembre de 2011 se implantaron un total de 14 dispositivos en pacientes con SPCR, siendo 5 (35,7%) en enfermos sometidos a revascularización coronaria. En 7 casos se inició la asistencia tras el destete de la CEC. El tiempo medio de asistencia fue de 177,6h. En el 78,6% de la muestra se utilizó balón intraaórtico de contrapulsación previamente. La complicación más frecuente fue la hemorragia mediastínica con reintervención hasta en el 42,8% de los pacientes. La mortalidad hospitalaria fue de un 57,1%, sin detectar muertes tardías.ConclusiónEstos resultados han hecho que el tratamiento con ECMO sea considerado en nuestro centro como una medida de primer orden para el tratamiento de los pacientes con fallo cardíaco tras la cirugía, a pesar de la alta mortalidad del proceso, que en algunas series es superior al 70%.
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15. Extracorporeal membrane oxygenation in lung transplantation.
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Vicente R, Moreno I, Soria A, Ramos F, and Torregrosa S
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- Humans, Postoperative Care, Preoperative Care, Extracorporeal Membrane Oxygenation methods, Lung Transplantation
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The use of extracorporeal techniques in cardiopulmonary support has spread in the last 20 years. ECMO (extracorporeal membrane oxygenation) devices are the most commonly employed option, and have been used for years in lung transplant programs. Nevertheless, few articles on the results of ECMO involving large numbers of cases have been published to date. The use of ECMO in respiratory failure affords immediate oxygen support in patients with severe hypoxia and/or acidosis, and moreover provides pulmonary protection, since it allows an instantaneous decrease in the ventilator pressure and FiO2 needs. The complications of ECMO have been minimized thanks to the technological improvements found in the latest devices, though renal failure, infections, bleeding, and vascular and mechanical complications are still reported in many studies. At present there is less controversy regarding the use of cardiorespiratory assists with ECMO as an alternative in decompensated patients who are on the waiting list, referred to the intra- and postoperative periods of lung transplantation., (Copyright © 2012 Elsevier España, S.L. and SEMICYUC. All rights reserved.)
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- 2013
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16. Transfemoral stent-graft of distal aortic arch complicated with retrograde dissection.
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Torregrosa S, Montes H, Pérez M, Castelló A, Mata D, Valera F, and Montero A
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- Humans, Male, Middle Aged, Aortic Dissection surgery, Aorta, Thoracic surgery, Aortic Aneurysm, Thoracic surgery, Stents
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- 2006
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17. Long-term outcome after valve replacement with the omnicarbon prosthesis.
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di Summa M, Poletti G, Brero L, Centofanti P, La Torre M, Patanè F, Raggio JM, Sanchez FG, Maroñas JM, Torregrosa S, Valera FJ, and Caffarena J Jr
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- Adult, Aged, Aortic Valve physiopathology, Aortic Valve surgery, Cohort Studies, Female, Follow-Up Studies, Heart Valve Diseases diagnosis, Heart Valve Diseases mortality, Humans, Linear Models, Male, Middle Aged, Mitral Valve physiopathology, Probability, Prospective Studies, Prosthesis Failure, Reoperation, Survival Analysis, Treatment Outcome, Bioprosthesis, Heart Valve Diseases surgery, Heart Valve Prosthesis, Mitral Valve surgery, Postoperative Complications mortality, Quality of Life
- Abstract
Background and Aim of the Study: The study aim was to determine whether long-term prognosis was affected by valve replacement with a tilting-disc prosthesis., Methods: Surgical data were recorded prospectively for all (n = 153) valve replacement cases with the Omnicarbon prosthesis during the period February 1985 to January 1986. A rheumatic valvular pathology was present in 105 patients (68.6%). There were 78 (51%) aortic (AVR), 51 (33%) mitral (MVR) and 24 (16%) double (DVR) valve replacements. The follow up was 99% complete (n = 151)., Results: Mean follow up was 10.2+/-4.4 years (total 1,472 patient-years (pt-yr)). Survival at 10 years was 68+/-4% (71+/-5% AVR, 61+/-7% MVR), and this fell to 57+/-4% at 14 years. No structural failure was observed. Thromboembolic and hemorrhagic events were rare, with actuarial freedom from thromboembolism of 94+/-2% and 91+/-3% at 10 and 14 years, respectively. This low incidence of thromboembolism encouraged an ease in anticoagulation; hence the AVR and MVR cohorts had a median INR of 2.8, but a higher INR (3.4) was maintained in DVR patients. All prostheses had acceptable hemodynamic performance. No cases of hemolytic anemia were detected, and mean blood counts were within normal ranges. Lactate dehydrogenase values indicated minimal hemolysis, and were lowest after AVR (median LDH 93% normal) and highest after DVR (median LDH 136% normal). Functional evaluation showed an improvement in NYHA class that remained stable over 14 years. At follow up, 95% (75/79) of patients were in NYHA class I or II., Conclusion: Survival and quality of life after Omnicarbon valve implantation exceeded the authors' expectations. Functional capacity remains good, and valve-related complication rates are low. The Omnicarbon tilting-disc valve has been shown to provide reliable and satisfactory service in the long term.
- Published
- 2002
18. Increased expression of type 2 cytokines in chronic proliferative dermatitis (cpdm) mutant mice and resolution of inflammation following treatment with IL-12.
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HogenEsch H, Torregrosa SE, Boggess D, Sundberg BA, Carroll J, and Sundberg JP
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- Animals, Cells, Cultured, Chronic Disease, Cytokines biosynthesis, Dermatitis pathology, Eosinophilia etiology, Hypersensitivity, Delayed etiology, Interferon-gamma biosynthesis, Interleukin-11 therapeutic use, Interleukin-13 biosynthesis, Interleukin-5 biosynthesis, Mice, Mice, Mutant Strains, Skin immunology, Skin metabolism, Skin pathology, Spleen immunology, Spleen metabolism, Th2 Cells metabolism, Transcriptional Activation, Cytokines genetics, Dermatitis drug therapy, Dermatitis immunology, Interleukin-12 therapeutic use, Th2 Cells immunology
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Chronic proliferative dermatitis (cpdm) is a spontaneous mutation that results in eosinophilic inflammation in multiple tissues, including the skin. To determine the mechanisms underlying the eosinophilic inflammation, the expression of cytokines in the skin was determined. There was increased expression of IL-4, IL-5, IL-13, and granulocyte-macrophage colony-stimulating factor in the skin of cpdm/cpdm mice, and no change in IL-10 and TNF expression. Supernatants of cultured spleen cells of cpdm/cpdm mice contained an increased amount of IL-5 and IL-13, and a decreased amount of IFN-gamma. The ability of the cpdm/cpdm mice to mount a delayed-type hypersensitivity response was greatly reduced. These data are consistent with impaired type 1 and excessive type 2 cytokine production in cpdm/cpdm mice. The significance of this imbalanced cytokine production was evident in the efficacy of systemic treatment of cpdm/cpdm mice with IL-12. Mutant mice treated for 3 weeks with IL-12 had minimal changes in the skin as opposed to the severe dermatitis in mice treated with the vehicle. Treatment with IL-11, which opposes the effect of IL-12, had no effect.
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- 2001
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19. Long-term clinical experience with the Omnicarbon prosthetic valve.
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Torregrosa S, Gómez-Plana J, Valera FJ, Caffarena J, Maroñas JM, García-Sánchez F, Peris J, Frías R, and Caffarena JM
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- Adolescent, Adult, Aged, Anemia, Hemolytic etiology, Anticoagulants adverse effects, Child, Child, Preschool, Endocarditis etiology, Female, Follow-Up Studies, Humans, Male, Middle Aged, Postoperative Complications, Postoperative Hemorrhage chemically induced, Prosthesis Failure, Reoperation, Survival Rate, Thromboembolism etiology, Heart Valve Prosthesis, Heart Valve Prosthesis Implantation adverse effects, Heart Valve Prosthesis Implantation mortality
- Abstract
Background: From February 1985 to December 1994, 781 Omnicarbon valve prostheses were implanted in 647 patients. These were 357 male and 290 female patients with a mean age of 53.5+/-10.5 years (range, 4 to 78 years). Before operation, 81% of the patients were in New York Heart Association class III or IV, 16% were in class II, and only 3% were in class I., Methods: There were 227 aortic valve replacements (AVR) (35%), 286 mitral valve replacements (MVR) (44%), and 134 double-valve replacements (DVR) (21%) (AVR + MVR). Follow-up was 96.3% complete and consisted of 2,746 patient-years (mean follow-up, 4.6 years, and maximum follow-up, 10.7 years)., Results: Hospital mortality rates were 7.0% for AVR, 8.0% for MVR, and 8.2% for DVR. The annualized rate of anticoagulant-related hemorrhage was 0.8% per patient-year, and thromboembolism occurred at a rate of 0.7% per patient-year. No structural failure was observed during 10-year follow-up. Twenty-one instances of nonstructural dysfunction (two, pannus growth, and 19, dehiscence) of the Omnicarbon valve occurred in 20 patients, an incidence of 0.8% per patient-year. Hemolytic anemia was observed only in the presence of valvular dehiscence (6 of 19). Eight patients (0.3% per patient-year) had development of prosthetic valve endocarditis (4, AVR; 2, MVR; and 2 DVR). At the end of 10 years of follow-up, 91% of the survivors were in New York Heart Association class I or II. The overall survival rate at 10 years was 82.5%+/-2.6% (85.0%+/-3.9%, AVR; 81.0%+/-4.1%, MVR; and 82.5%+/-2.6%, DVR). Considering only valve-related deaths, the survival rate at 10 years was 91.9%+/-2.4% (90.0%+/-2.7%, AVR; 93.1%+/-3.8%, MVR; and 90.0%+/-1.8%, DVR)., Conclusions: Clinical results over a 10-year follow-up are excellent with the Omnicarbon prosthesis.
- Published
- 1999
- Full Text
- View/download PDF
20. Induction of pulmonary immunity in cattle by oral administration of ovalbumin in alginate microspheres.
- Author
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Bowersock TL, HogenEsch H, Torregrosa S, Borie D, Wang B, Park H, and Park K
- Subjects
- Animals, Cattle, Female, Glucuronic Acid, Hexuronic Acids, Microspheres, Administration, Oral, Alginates, Bronchoalveolar Lavage Fluid immunology, Ovalbumin immunology
- Abstract
Respiratory infectious diseases are an important cause of economic losses to the cattle industry. There is a need for an effective, easy to administer vaccine to the critical bacterial pathogens that cause pneumonia in cattle. An orally administered vaccine could be given to a large number of animals without significant stress to the animals and with minimal labor. The purpose of this study was to determine whether the oral administration of a model antigen (ovalbumin) in alginate microspheres could induce pulmonary immunity in cattle. Calves were vaccinated orally with ovalbumin (OVA) following either a subcutaneous (s.c.) or oral priming dose of OVA. Calves primed and boostered by oral administration (oral/oral) of OVA encapsulated in alginate microparticles had increased numbers of antigen-specific IgA ASCs (ASCs) in bronchoalveolar lavage (BAL) fluids. Calves that received a s.c. priming followed by an oral booster inoculation (s.c./oral) of OVA in alginate microspheres had a greater number of anti-OVA IgA, IgG1 and IgG2 ASCs in BALF. S.c./oral calves also had increased numbers of anti-OVA IgG1 ASCs in peripheral blood whereas oral/oral calves had none. S.c./oral calves had increased anti-OVA IgG1, IgG2, and IgA titers in BALF, and IgG1 and IgG2 in serum compared to both oral/oral and sham vaccinated calves. These results indicate that oral administration of antigen encapsulated in alginate microspheres results in a mucosal immune response in the respiratory tract of cattle. Furthermore, s.c. priming both enhanced the IgA response and stimulated an IgG1 and IgG2 response not seen in oral/oral calves. The difference in antibody isotype results suggest that design of the vaccination protocol can direct antibody responses as needed for a specific immunization program.
- Published
- 1998
- Full Text
- View/download PDF
21. Systemic and pulmonary immune response to intrabronchial administration of ovalbumin in calves.
- Author
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HogenEsch H, Torregrosa SE, Borie D, Gaskell C, and Bowersock TL
- Subjects
- Animals, Antibody-Producing Cells metabolism, Bronchoalveolar Lavage Fluid immunology, Cattle, Epitopes immunology, Female, Immunization veterinary, Immunoglobulins biosynthesis, Immunoglobulins blood, Injections, Subcutaneous, Bronchi immunology, Lung immunology, Ovalbumin administration & dosage, Ovalbumin immunology
- Abstract
Local immunization of the respiratory tract may be the best way to achieve protection against respiratory pathogens. In order to do so successfully, it is important to fully understand how the immune response to antigen administered via the respiratory route develops. We studied the respiratory and systemic immune response after subcutaneous (SC) and intrabronchial (IB) inoculation of calves with ovalbumin (OVA). Eight calves received two SC inoculations of OVA and eight other calves received two SC and three additional IB inoculations of OVA. The occurrence of OVA-specific antibodies and antibody-secreting cells (ASC) was measured over time using isotype-specific enzyme linked immunosorbent assay (ELISA) and ELISPOT. SC immunization of calves did not result in OVA-specific IgA in bronchoalveolar lavage (BAL) fluid. Subcutaneous priming followed by intrabronchial challenge caused an initial IgG1 response in the bronchoalveolar lavage fluid, followed by a large IgA response. The presence of IgG1-ASCs indicated that the IgG1 was at least partially locally produced. Most of the OVA-specific IgA in the BAL fluid was secreted by pulmonary ASCs as indicated by the large number of IgA-ASCs in BAL samples and the low serum level of OVA-specific IgA. Antigen-specific IgG1 ASCs were detectable among peripheral mononuclear cells after culture with OVA.
- Published
- 1996
- Full Text
- View/download PDF
22. Should supraclavicular brachial plexus block be avoided in pregnancy?
- Author
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Gazmuri RR, Torregrosa SA, Dagnino JA, and Iniguez FG
- Subjects
- Adult, Bupivacaine adverse effects, Carpal Tunnel Syndrome surgery, Clavicle, Female, Humans, Pregnancy, Respiratory Paralysis etiology, Brachial Plexus, Cough etiology, Dyspnea etiology, Nerve Block adverse effects, Pregnancy Complications etiology
- Abstract
Unilateral phrenic nerve block is common after supraclavicular brachial plexus block techniques, although it is rarely symptomatic in patients without respiratory disease. A 24-weeks-pregnant woman was scheduled for a carpal tunnel release because of intractable pain. After a perivascular subclavian brachial plexus block with 30 ml of 0.33% plain bupivacaine was performed, the patient developed a right phrenic nerve block manifested by acute dyspnea and cough. No deleterious consequences followed, but surgery was canceled. Respiratory changes produced by pregnancy might compromise ventilatory reserve. Thus, we suggest avoiding supraclavicular approaches to brachial plexus block in pregnant women, since they may be as prone to developing respiratory embarrassment, secondary to phrenic block, as patients with pulmonary pathology.
- Published
- 1992
- Full Text
- View/download PDF
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