47 results on '"Tullu M. S."'
Search Results
2. Contribution of Indian publications to research in telemedicine.
- Author
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Tullu M. S.
- Subjects
PUBLISHING ,TELEMEDICINE ,MEDICAL research - Abstract
The author offers observation on research contribution of India on telemedicine. Topics discussed include findings of the study by P. K. Behera and colleagues, titled "Mapping and visualizing the research contribution of India on telemedicine: A scientometric study," role played by the Covid-19 pandemic in the popularity and acceptance of telemedicine, and applications for the use of telemedicine.
- Published
- 2023
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3. Success in Publishing: Selecting an Appropriate Journal and Braving the Peer-review Process.
- Author
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Tullu, M. S. and Karande, S.
- Subjects
AUTHORS ,AUTHORSHIP ,DECISION making ,MANUSCRIPTS ,PROFESSIONAL peer review ,PUBLISHING ,SERIAL publications - Abstract
The article offers tips on how prospective research authors can get published in appropriate peer-reviewed journals. It discusses the need to select the right journal in the internet before drafting a manuscript, to informally have the same read for grammar and content before submission, and to ensure that the journal selected is regularly published with its own website and electronic versions. Also noted is the need to have the work independently reviewed by peers.
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- 2018
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4. Writing a model research paper: A roadmap.
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Tullu, M. S. and Karande, S.
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AUTHORSHIP ,MANUSCRIPTS ,MEDICAL writing ,PUBLISHING - Abstract
The author offers tips on preparing a model research paper for successful publication in eminent peer-reviewed biomedical journals. Topics covered include the components of the basic Introduction, Methods, Results, and Discussions (IMRaD) structure of a manuscript, how to create the different sections, like methods section, results section and discussion section, of the research paper, and the importance of adhering to the instructions to authors.
- Published
- 2017
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5. "FISHed" out the diagnosis: A case of DiGeorge syndrome.
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Bajaj, S., Thombare, T. S., Tullu, M. S., and Agrawal, M.
- Subjects
HEART disease genetics ,DIGEORGE syndrome ,COLD (Temperature) ,COUGH ,DYSPNEA ,CHILDREN ,DIAGNOSIS - Abstract
Our patient presented with congenital heart disease (CHD: Tetralogy of Fallot), hypocalcemia, hypoparathyroidism, and facial dysmorphisms. Suspecting DiGeorge syndrome (DGS), a fluorescence in situ hybridization (FISH) analysis for 22q11.2 deletion was made. The child had a hemizygous deletion in the 22q11.2 region, diagnostic of DGS. Unfortunately, the patient succumbed to the heart disease. DGS is the most common microdeletion syndrome, and probably underrecognized due to the varied manifestations. This case stresses the importance of a detailed physical examination and a high index of suspicion for diagnosing this genetic condition. Timely diagnosis can help manage and monitor these patients better and also offer prenatal diagnosis in the next pregnancy. [ABSTRACT FROM AUTHOR]
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- 2016
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6. When potion becomes poison! A case report of flecainide toxicity.
- Author
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Bajaj S., Tullu M. S., Khan Z. A. H., and Agrawal M.
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SEIZURES (Medicine) ,ELECTROCARDIOGRAPHY ,FLECAINIDE ,SPASMS ,SUPRAVENTRICULAR tachycardia - Abstract
"We report a 48-day-old female infant, who developed cardiac conduction abnormalities and seizures secondary to supratherapeutic doses of oral flecainide. Flecainide was started in this infant for treatment of supraventricular tachycardia. The drug was withdrawn with successful normalization of the QRS complex and no further recurrence of seizures. The Naranjo probability score for adverse drug reaction was 8, making the causality ""probable."" The case restates an important message that physicians should be aware of the side effects of the drugs that they prescribe, especially of those drugs which have a narrow therapeutic window." [ABSTRACT FROM AUTHOR]
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- 2017
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7. Quality research in Indian medical colleges and teaching institutions: The need of the hour.
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Tullu, M. S. and Karande, S.
- Subjects
ACADEMIC medical centers ,EDUCATORS ,MEDICAL schools ,MEDICAL school faculty ,QUALITY assurance ,RESEARCH ,OCCUPATIONAL roles - Abstract
The editor stresses the need for quality research in Indian medical colleges and teaching institutions. He cites reasons for this need including the current Indian population and the mixed and varied population in India that can influence the profile and manifestations of a disease and its response to therapy. He challenges medical teachers to develop independent, creative and critical thinking to do quality research and to undergo training in research methodology.
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- 2016
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8. A rare case of nephrotic syndrome: 'Nailed' the diagnosis.
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Agarwal, S., Divecha, C., Tullu, M. S., and Deshmukh, C. T.
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NEPHROTIC syndrome diagnosis ,EDEMA ,FUROSEMIDE ,NEPHROTIC syndrome ,SPIRONOLACTONE ,ENALAPRIL ,NAIL-patella syndrome ,PREDNISOLONE ,DISEASE complications ,DIAGNOSIS - Abstract
An 18-month-old female child presented to us with clinical features suggestive of nephrotic syndrome. Her physical examination and detailed family history highlighted the familial occurrence of abnormal nails, suggesting a diagnosis of the Nail-Patella syndrome. Nail-Patella syndrome is a rare cause of nephrotic syndrome in children. This case highlights the importance of a detailed history, including pedigree and a thorough examination of the patient. [ABSTRACT FROM AUTHOR]
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- 2014
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9. Colistin: Re-emergence of the 'forgotten' antimicrobial agent.
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Dhariwal, A. K. and Tullu, M. S.
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ANTI-infective agents ,ANTIBIOTICS ,DRUG interactions ,DRUG resistance in microorganisms ,GRAM-negative bacterial diseases ,PEDIATRICS ,COLISTIN ,PHARMACODYNAMICS ,THERAPEUTICS - Abstract
The treatment of the emerging multidrug resistant (MDR) gram-negative organisms is a challenge. The development of newer antibiotics has recently slowed down. This has led to the re-emergence of the 'old forgotten' antibiotic "Colistin", whose use had almost stopped (after 1970's) due to the high incidence of nephrotoxicity and neurotoxicity. Colistin (polymyxin E) is a polypeptide antibiotic belonging to polymyxin group of antibiotics with activity mainly against the gram-negative organisms. Use of colistin has been increasing in the recent past and newer studies have shown lesser toxicity and good efficacy. Colistin acts on the bacterial cell membrane resulting in increased cell permeability and cell lysis. Colistin can be administered orally, topically, by inhalational route, intramuscularly, intrathecally, and also intravenously. Parenteral Colistin (in the form of colistimethate sodium) has been used to treat ventilator-associated pneumonia (VAP) and bacteremia caused by MDR bacteria such as Pseudomonas aeruginosa, Klebsiella pneumoniae, and Acinetobacter baumannii. Inhaled Colistin is used for treating pneumonia/VAP due to MDR gram-negative organisms and also used prophylactically in patients with cystic fibrosis. This manuscript is a brief review of Colistin and its clinical applications in the pediatric population. [ABSTRACT FROM AUTHOR]
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- 2013
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10. An unusual cause of central cyanosis in a nine-year-old boy.
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Shobi, A., Tullu, M. S., Bhatia, S., and Agrawal, M.
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ANGIOGRAPHY ,CHEST X rays ,CYANOSIS ,DIFFERENTIAL diagnosis ,ECHOCARDIOGRAPHY ,THERAPEUTIC embolization ,ARTERIOVENOUS malformation ,DISEASE complications ,CHILDREN ,THERAPEUTICS - Abstract
Pulmonary arteriovenous malformations are rare vascular anomalies which rarely present in childhood. We discuss a nine-year-old male child who presented with the classical triad of exertional dyspnea, cyanosis and clubbing since six years of age. Pulmonary arteriovenous malformation was suspected on chest radiography and was later confirmed on computed tomography scan. A bubble contrast echocardiography showed the presence of an extracardiac shunt. Pulmonary angiography was done to delineate the anatomy of the pulmonary vasculature and to plan embolization. The child has undergone two sittings of transcatheter coil embolization with improvement in oxygenation. [ABSTRACT FROM AUTHOR]
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- 2012
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11. An unusual recurrence of antitubercular drug induced hepatotoxicity in a child.
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Bhatia, S., Tullu, M. S., Kannan, S., Gogtay, N. J., Thatte, U. M., and Lahiri, K. R.
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DRUG therapy for tuberculosis ,HEPATOTOXICOLOGY ,ANTITUBERCULAR agents ,CHEST X rays ,LIVER function tests ,DISEASE relapse ,DIAGNOSIS - Abstract
The article presents a case study of a two-and-a-half-year-old child who was admitted at the hospital due to a six-day fever and a dry spasmodic cough for 4 days. It notes that the patient started her respiratory problems at the age of 6 months when she was admitted for bronchiolitis. The article discusses hepatoxicity related to antitubercular drug therapy.
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- 2011
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12. Idiopathic pulmonary hemosiderosis: Alveoli are an answer to anemia.
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Bhatia, S., Tullu, M. S., Vaideeswar, P., and Lahiri, K. R.
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LUNG disease diagnosis ,TOMOGRAPHY ,BIOPSY ,DYSPNEA ,FEVER ,HEMOSIDEROSIS ,LUNGS ,LUNG diseases ,PREDNISOLONE ,DIAGNOSIS - Abstract
Idiopathic pulmonary hemosiderosis (IPH) is a rare disorder (triad of iron-deficiency anemia, hemoptysis, and alveolar infiltrates). A 3-year-old male presented with mild fever, breathlessness, dry cough, and bluish nail discoloration for 8 days. He had required five blood transfusions in the past 1 year (last transfusion was given 4 months ago). He had a respiratory rate of 58/min with respiratory distress, cyanosis, and grade III clubbing. Respiratory system examination was normal. Several previous reports of hemoglobin were as low as 3.6 g/dl with hypochromic and microcytic anemia. There were transient increases in the hemoglobin and normalization of red cell morphology with blood transfusions. Serum iron, G6PD enzyme assay, hemoglobin electrophoresis, the sickling test, Coomb's test, stool and urine analysis, and a Meckel's scan were normal. HIV antibody and dsDNA were negative. The chest radiograph revealed symmetrical patchy infiltrates sparing lung apices (confirmed on high-resolution computed tomography). Lung biopsy diagnosed pulmonary hemosiderosis (interstitial lung disease with hemosiderin-laden macrophages scattered in the alveoli and areas of fibrosis in the alveolar septa). The patient showed marked clinical improvement in 10 days of therapy with prednisolone. IPH should be listed in the differential diagnosis of a child presenting with unexplained hypochromic, microcytic anemia and respiratory symptoms. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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13. Research publications for academic career advancement: An idea whose time has come. But is this the right way?
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Bavdekar, S. B. and Tullu, M. S.
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AUTHORSHIP ,MEDICAL school faculty ,MEDICAL research ,EMPLOYEE promotions ,PUBLISHING - Abstract
The article focuses on the Circular of the Medical Council of India in 2015 requiring publication of original research articles by medical teachers to be promoted as Associate Professor or Professor in medical colleges. It discusses arguments against the Circular for not including other scholarly responsibilities such as mentoring students for research, reviewing of manuscripts for journals and editorial work. It also questions MCI's qualification of original research articles.
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- 2016
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14. Oseltamivir.
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Tullu, M. S.
- Subjects
FEVER ,INFLUENZA ,NEURAMINIDASE ,VIRUSES ,DRUG resistance - Abstract
Oseltamivir, a selective neuraminidase enzyme inhibitor, has gained worldwide attention in view of Influenza A (H1N1) pandemic. It is one of the most important drugs effective against the novel influenza virus. Oseltamivir is used for the treatment of uncomplicated acute illness due to influenza infection. Early initiation of treatment with the drug provides greater clinical benefits. The drug can also be effectively used for prophylaxis. Oseltamivir is readily absorbed from the gastrointestinal tract and is converted to the active metabolite- oseltamivir carboxylate, which has a wider distribution in the body. Oseltamivir carboxylate is eliminated in the urine with a half-life of 6-10 h. The drug is generally well-tolerated and does not have many clinically significant drug interactions. Nausea and vomiting are the commonest adverse effects associated with its use. The standard adult dose for treatment is 75 mg twice a day for five days and the dose for prophylaxis is 75 mg once daily for at least seven days following contact with an infected individual. The dose needs to be adjusted in patients with renal failure but no adjustments are required in patients with hepatic impairment. Although most of the influenza virus strains are sensitive to oseltamivir, development of drug resistance may limit the clinical utility of the drug in the future. [ABSTRACT FROM AUTHOR]
- Published
- 2009
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15. Pulmonary arteriovenous malformations.
- Author
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Tullu, Milind, Mahajan, Murlidhar, Ramchandani, Captain, Deshmukh, Chandrahas, Kamat, Jaishree, Vaswani, Rajwanti, Pahuja, Prem, Rangarajan, Venkatesh, Tullu, M S, Mahajan, M D, Ramchandani, S, Deshmukh, C T, Kamat, J R, Vaswani, R K, Pahuja, P K, and Rangarajan, V
- Abstract
Pulmonary arteriovenous malformations rarely present in childhood. Two cases are presented in this report. Both the cases presented clinically with cyanosis and clubbing without a cardiac murmur. The second case had cerebral abscess in addition. Both the cases underwent a contrast-enhanced echocardiography which suggested the presence of pulmonary arteriovenous malformations. The first case also underwent 99mTc radionuclide scan and pulmonary angiography. The cases are being reported for their characteristic clinical features and for emphasizing the role of non-invasive modalities like contrast-enhanced echocardiography and radionuclide scan in reaching the diagnosis. [ABSTRACT FROM AUTHOR]
- Published
- 2001
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16. Glanzmann's thrombasthenia.
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Tullu, Milind, Dixit, Prashant, Nair, Sona, Kamat, Jaishree, Vaswani, Rajwanti, Shetty, Shrimati, Pawar, Aruna, Tullu, M S, Dixit, P S, Nair, S B, Kamat, J R, Vaswani, R K, Shetty, S D, and Pawar, A R
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GENETIC disorder diagnosis ,BLOOD coagulation disorders ,DIFFERENTIAL diagnosis ,FLOW cytometry ,GENETIC disorders ,GLYCOPROTEINS ,HEMORRHAGIC diseases ,MENTAL health surveys ,DIAGNOSIS - Abstract
Glanzmann's thrombasthenia (GT) is an uncommon cause of bleeding in children. We diagnosed two siblings as having GT on the basis of flow cytometric studies. Both had cutaneous bleedings and epistaxis since early childhood. Hematological investigations revealed prolonged bleeding time and a normal platelet count. Both the patients had absence of aggregation of platelets with the agonist adenosine diphosphate. Absence of the GPIIb/IIIa receptor was confirmed by flow cytometry. A short review of the disorder is presented. [ABSTRACT FROM AUTHOR]
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- 2001
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17. Colloid Cyst of the Third Ventricle: A Cause of Sudden Death in a Child.
- Author
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Kava, M. P., Tullu, M. S., Deshmukh, C. T., and Shenoy, A.
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- 2003
18. Congenital left ventricular diverticula
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Tullu, M. S., Vaideeswar, P., and Deshmukh, C. T.
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- 2000
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19. Dorfman-Chanarin syndrome: A rare neutral lipid storage disease
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Tullu, M. S., Muranjan, M. N., Save, S. U., Deshmukh, C. T., SHAILA KHUBCHANDANI, and Bharucha, B. A.
20. Success in publishing: The answer lies in training and improving research infrastructure.
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Bavdekar, S. B. and Tullu, M. S.
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COLLEGE teachers ,MEDICAL research ,STUDY & teaching of medicine ,EMPLOYEE promotions ,PUBLISHING - Abstract
A letter to the editor is presented in April 2016 which discusses the need to provide training and better research infrastructure to medical teachers to enable them to produce good quality research as required by the Medical Council of India's (MCI) circular before being considered for promotion.
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- 2016
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21. Comments on Jordans' anomaly.
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Tullu, M S, Muranjan, M N, and Deshmukh, C T
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- 2000
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22. The art of referencing: Well begun is half done!
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Divecha CA, Tullu MS, and Karande S
- Abstract
Competing Interests: None
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- 2023
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23. Lane-Hamilton syndrome - Is it really a needle in a haystack?
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Mondkar SA, Tullu MS, Sathe P, and Agrawal M
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- Child, Child, Preschool, Female, Humans, Pallor, Syndrome, Hemosiderosis, Pulmonary, Anemia, Celiac Disease, Hemosiderosis, Lung Diseases
- Abstract
Introduction: The association of pulmonary hemosiderosis with celiac disease (Lane-Hamilton syndrome) is extremely rare., Case Details: A five-year-old female child presented with fever, cough, breathlessness, and pallor for 20 days, without any previous history of recurrent lower respiratory tract infections, tuberculosis, or cardiac disease. There was no history of pica, chronic diarrhea, bleeding, or personal or family history of repeated blood transfusions. She had tachycardia, tachypnea, severe pallor, stunting, rickets, and bilateral fine lung crepitations. Peripheral smear and blood indices revealed dimorphic anemia. Anti-tissue transglutaminase IgA antibody levels were high (>200 U/mL) and the upper gastrointestinal endoscopy with duodenal biopsy confirmed the diagnosis of celiac disease. The child was discharged on a gluten-free diet (GFD) and oral hematinic, but her dietary compliance was poor. Interestingly, the child had persistent bilateral pulmonary infiltrates, which was initially attributed to congestive cardiac failure (CCF), which persisted even despite treatment. HRCT chest revealed interstitial thickening and bilateral alveolar shadows and bronchoalveolar lavage showed a few inflammatory cells. The child was readmitted four times with similar complaints and was given packed red cell transfusions. In the fourth admission, a lung biopsy was done, which revealed extensive pulmonary hemosiderosis. The patient was given a course of oral steroids for 6 weeks, with a gluten-free diet, following which both the anemia and the pulmonary infiltrates resolved., Conclusion: Pulmonary hemosiderosis is an important cause of anemia in cases of celiac disease and may be misdiagnosed as CCF due to severe anemia. A strict GFD, with or without corticosteroids, can reverse the clinical and radiological picture., Competing Interests: None
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- 2022
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24. Published a research paper? What next??
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Divecha CA, Tullu MS, and Karande S
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- Humans, Publications
- Abstract
Competing Interests: None
- Published
- 2021
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25. The predictors of outcome and progression of pediatric sepsis and septic shock: A prospective observational study from western India.
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Shah S, Deshmukh CT, and Tullu MS
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- Bacterial Infections mortality, Child, Preschool, Female, Fever etiology, Humans, India epidemiology, Infant, Intensive Care Units, Male, Malnutrition, Mortality, Multiple Organ Failure etiology, Multiple Organ Failure mortality, Prevalence, Prospective Studies, Sepsis etiology, Sepsis microbiology, Shock, Septic etiology, Shock, Septic microbiology, Survival Analysis, Systemic Inflammatory Response Syndrome diagnosis, Systemic Inflammatory Response Syndrome microbiology, Bacterial Infections epidemiology, Sepsis mortality, Shock, Septic mortality, Systemic Inflammatory Response Syndrome mortality
- Abstract
Introduction: There is a paucity of studies on the progression and outcome of Systemic Inflammatory Response Syndrome (SIRS) with its determinants., Aims and Objectives: To determine the predictors of the outcome and progression of pediatric sepsis and septic shock., Materials and Methods: Prospective observational study of children fulfilling criteria of SIRS and their progression to sepsis, severe sepsis, and septic shock (clinically and biochemically) was conducted at a tertiary care center., Results: Totally, 200 children were recruited over a period of 21 months (from February 2016 to October 2017). Most cases (80, 40%) were infants. Of the total, 188 (94%) cases were of an infective etiology (mostly respiratory system). Temperature and heart rate were the two commonest SIRS parameters which were deranged. Blood cultures were positive in only 25 (12.5%) cases. Out of the total 200 children, 108 progressed to sepsis, of which 26 progressed to severe sepsis, of which 22 progressed to septic shock. Abnormal leukocyte count, culture positivity and severe acute malnutrition were significantly associated with progression of SIRS patients to septic shock (P = 0.001, 0.00001 and 0.002, respectively). Factors associated with mortality were positive blood culture, multiorgan dysfunction, late hospital admissions, severe acute malnutrition, and requirement of supportive care (P values-<0.0001, <0.0001, 0.03, <0.0001 and <0.0001, respectively)., Conclusions: SIRS can progress to septic shock if not identified early. The predictors of mortality were positive blood cultures, multiorgan dysfunction, late hospital admissions, severe acute malnutrition, and requirement of supportive care. The predictors of progression to septic shock were abnormal leukocyte count, culture positivity, and severe acute malnutrition., Competing Interests: None
- Published
- 2020
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26. Peer reviewing an original research paper.
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Tullu MS and Karande S
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- Humans, Publications standards, Peer Review, Research, Periodicals as Topic
- Abstract
Competing Interests: None
- Published
- 2020
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27. Beta-thalassemia major complicated by intracranial hemorrhage and critical illness polyneuropathy.
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Sanju S, Tullu MS, Karande S, Muranjan MN, and Parekh P
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- Child, Humans, Male, Intracranial Hemorrhages etiology, Polyneuropathies etiology, beta-Thalassemia complications
- Abstract
Intracranial hemorrhage (ICH) is rarely seen in patients with thalassemia. A seven-year-old male, known case of beta-thalassemia major, on irregular packed cell transfusions (elsewhere) and non-compliant with chelation therapy, presented with congestive cardiac failure (Hb-3 gm/dl). He received three packed red cell transfusions over 7 days (cumulative volume 40 cc/kg). On the 9th day, he developed projectile vomiting and two episodes of generalized tonic-clonic convulsions with altered sensorium. He had exaggerated deep tendon reflexes and extensor plantars. CT-scan of brain revealed bilateral acute frontal hematoma with diffuse subarachnoid hemorrhage (frontal and parietal). Coagulation profile was normal. CT-angiography of brain showed diffuse focal areas of reduced caliber of anterior cerebral, middle cerebral, and basilar and internal carotid arteries (likely to be a spasmodic reaction to subarachnoid hemorrhage). He required mechanical ventilation for 4 days and conservative management for the hemorrhage. However, on the 18th day, he developed one episode of generalized tonic-clonic convulsion and his sensorium deteriorated further (without any new ICH) and required repeat mechanical ventilation for 12 days. On the 28th day, he was noticed to have quadriplegia (while on a ventilator). Nerve conduction study (42nd day) revealed severe motor axonal neuropathy (suggesting critical illness polyneuropathy). He improved with physiotherapy and could sit upright and speak sentences at discharge (59th day). The child recovered completely after 3 months. It is wise not to transfuse more than 20 cc/kg of packed red cell volume during each admission and not more than once in a week (exception being congestive cardiac failure) for thalassemia patients., Competing Interests: There are no conflicts of interest.
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- 2019
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28. Pseudomonas sepsis with Noma: an association?
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Vaidyanathan S, Tullu MS, Lahiri KR, and Deshmukh CT
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- Child Nutrition Disorders complications, Child, Preschool, Humans, Male, Noma microbiology, Noma complications, Pseudomonas Infections complications, Sepsis complications
- Abstract
We report here a 2.5-year-old male child with community-acquired Pseudomonal sepsis showing the characteristic lesions of ecthyma gangrenosum. The child had development of gangrenous changes of the nose and face - the 'cancrum oris' or 'Noma'. We highlight the possible association of Pseudomonas sepsis and Noma, with malnutrition playing a central role in causing both the diseases.
- Published
- 2005
29. An infant with pericardial effusion.
- Author
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Tullu MS, Vaideeswar P, Deshmukh CT, Lahiri KR, Pandit SP, and Chaturvedi RA
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- Edema etiology, Fatal Outcome, Female, Heart Arrest etiology, Humans, Infant, Hemangioma diagnosis, Mediastinal Neoplasms diagnosis, Pericardial Effusion etiology
- Published
- 2004
30. An unusual case of biliary atresia.
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Tullu MS, Hanchate VG, Hira PR, Kamat JR, Vaswanti RK, and Chaubal NG
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- Abdomen diagnostic imaging, Arteriovenous Fistula complications, Arteriovenous Fistula diagnosis, Biliary Atresia complications, Caroli Disease diagnosis, Cholestasis complications, Cholestasis diagnosis, Diagnosis, Differential, Echocardiography, Humans, Infant, Male, Pulmonary Artery abnormalities, Radiography, Abdominal, Biliary Atresia diagnosis
- Abstract
Intrahepatic biliary cysts are rarely seen in the patients with biliary atresia. We describe a ten-month-old child with biliary atresia in whom the abdominal imaging studies (ultrasonography, computed tomographic scan and magnetic resonance cholangiopancreatography) revealed multiple intrahepatic biliary cysts ('bile lakes'). The child also had intrapulmonary shunting of blood due to pulmonary arteriovenous fistulae, which were demonstrated on contrast-enhanced echocardiography. Both these findings, 'bile lakes' and pulmonary arteriovenous fistulae occur rarely in biliary atresia.
- Published
- 2002
31. Congenital heart disease with rheumatic fever and rheumatic heart disease: a coincidence or an association?
- Author
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Bokhandi SS, Tullu MS, Shaharao VB, Bavdekar SB, and Kamat JR
- Subjects
- Age Distribution, Child, Child, Preschool, Comorbidity, Heart Defects, Congenital diagnosis, Heart Defects, Congenital surgery, Humans, India epidemiology, Infant, Male, Prevalence, Prognosis, Retrospective Studies, Rheumatic Fever diagnosis, Rheumatic Heart Disease diagnosis, Rheumatic Heart Disease epidemiology, Rheumatic Heart Disease surgery, Risk Assessment, Sampling Studies, Heart Defects, Congenital epidemiology, Rheumatic Fever epidemiology
- Published
- 2002
32. Infantile tremor syndrome and zinc deficiency.
- Author
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Vora RM, Tullu MS, Bartakke SP, and Kamat JR
- Subjects
- Humans, Infant, Male, Syndrome, Tremor diagnosis, Tremor therapy, Tremor etiology, Zinc deficiency
- Abstract
Infantile tremor syndrome is characterized by coarse tremors, mental and physical retardation, light colored brown hair, skin pigmentation and anemia. Amongst the theories proposed for the etilogy of the disorder, the nutritional theory is most accepted. In this case report, we have presented a fourteen-month-old male child with ITS and documented zinc deficiency. Though most of the previous workers have proposed vitamin-B12 deficiency as the etimology for ITS, our report suggests that zinc deficiency could also have a causative role.
- Published
- 2002
33. Molluscum contagiosum and Job's syndrome.
- Author
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Martins MN, Tullu MS, and Mahajan SA
- Subjects
- Child, Preschool, Humans, Job Syndrome therapy, Male, Molluscum Contagiosum therapy, Job Syndrome complications, Job Syndrome pathology, Molluscum Contagiosum complications, Molluscum Contagiosum pathology
- Published
- 2001
34. Morgagni hernia with Down syndrome: a rare association -- case report and review of literature.
- Author
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Parmar RC, Tullu MS, Bavdekar SB, and Borwankar SS
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- Abnormalities, Multiple diagnosis, Hernia, Diaphragmatic complications, Hernia, Diaphragmatic diagnostic imaging, Humans, Infant, Male, Radiography, Respiratory Insufficiency etiology, Down Syndrome, Hernias, Diaphragmatic, Congenital
- Abstract
Morgagni hernia is a rare diaphragmatic hernia accounting for only 2% of the congenital diaphragmatic defects. A case of Morgagni hernia was diagnosed radiologically in a 12-months-old male with Down syndrome, with recurrent respiratory distress and chest deformity. The 2-dimensional echocardiography was normal. The diagnosis of Morgagni hernia was confirmed by barium studies. The patient underwent a corrective surgery at 18 months of age following which his symptoms subsided. Literature review revealed only 18 cases of Morgagni hernia with Down syndrome reported till date, with age of presentation varying from neonatal age group to 12 years of age. The mode of presentations varied from asymptomatic detection to severe respiratory distress. The possible mechanism of association and its clinical implication has been discussed. The case emphasises a need for diaphragmatic hernia to be looked for as a possible cause of respiratory distress in Down syndrome.
- Published
- 2001
35. Ovarian dysgenesis with balanced autosomal translocation.
- Author
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Tullu MS, Arora P, Parmar RC, Muranjan MN, and Bharucha BA
- Subjects
- Adolescent, Amenorrhea genetics, Chromosomes, Human, Pair 1 genetics, Chromosomes, Human, Pair 11 genetics, Female, Humans, Karyotyping, Gonadal Dysgenesis genetics, Ovary abnormalities, Translocation, Genetic genetics
- Abstract
Autosomal translocations are rare in the patients with ovarian dysgenesis. An 18-year-old female who presented with primary amenorrhoea had hypergonadotropic hypogonadism and streak ovaries with hypoplastic uterus. Karyotype analysis revealed a balanced autosomal translocation involving chromosomes 1 and 11. The probable role of autosomal translocations in ovarian dysgenesis has been discussed.
- Published
- 2001
36. Krabbe disease--clinical profile.
- Author
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Tullu MS, Muranjan MN, Kondurkar PP, and Bharucha BA
- Subjects
- Age Distribution, Child, Child, Preschool, Developing Countries, Female, Humans, Incidence, India epidemiology, Infant, Magnetic Resonance Imaging methods, Male, Prognosis, Retrospective Studies, Risk Factors, Sex Distribution, Leukodystrophy, Globoid Cell diagnosis, Leukodystrophy, Globoid Cell epidemiology
- Abstract
Objective: To study clinical features and investigations of children with Krabbe Disease (KD)., Design: Retrospective., Setting: Genetic Clinic of a tertiary care teaching hospital., Methods: Hospital records of patients with enzymatically confirmed KD were analyzed with respect to their clinical features and investigations including neuroimaging (CT-scan and/or MRI). Galactocerebrosidase (GALC) activity was estimated photometrically in the peripheral blood leukocytes., Results: Nine children (age ranging from 2 1/2 months to 8 years) were studied, of which 5 had the classical infantile disease, 3 had late infantile form and one was diagnosed as juvenile KD. GALC levels in peripheral blood leukocytes were low or absent in all. Most of the children with infantile disease presented with neurodegeneration, seizures or fever. Optic atrophy was uncommon in our series (present only in a single case). Majority of the cases had elevated cerebrospinal fluid (CSF) protein levels and peripheral neuropathy on nerve conduction (NC) studies. Findings typical of KD were noted in 7 patients who underwent magnetic resonance imaging (MRI). The sole patient with juvenile disease presented with developmental delay and progressive spastic quadriparesis., Conclusion: Krabbe disease should be considered in the differential diagnosis of early infantile onset of neurodegeneration with seizures. Likewise, older children with progressive ataxia or spastic quadriparesis in whom the etiology remains obscure, must be investigated for Krabbe disease. MRI can be diagnostic in absence of availability of enzyme diagnosis.
- Published
- 2000
37. Experience of pediatric tetanus cases from Mumbai.
- Author
-
Tullu MS, Deshmukh CT, and Kamat JR
- Subjects
- Child, Child, Preschool, Female, Humans, India epidemiology, Infant, Male, Retrospective Studies, Risk Factors, Treatment Outcome, Tetanus complications, Tetanus etiology, Tetanus mortality, Tetanus therapy
- Published
- 2000
38. Paediatrics in India.
- Author
-
Tullu MS and Kamat JR
- Subjects
- History, 20th Century, History, Ancient, Humans, India, Pediatrics history
- Published
- 2000
39. Neurofibromatosis-Noonan syndrome or LEOPARD Syndrome? A clinical dilemma.
- Author
-
Tullu MS, Muranjan MN, Kantharia VC, Parmar RC, Sahu DR, Bavdekar SB, and Bharucha BA
- Subjects
- Humans, Infant, Male, Neurofibromatoses complications, Neurofibromatoses diagnosis, Noonan Syndrome complications, Noonan Syndrome diagnosis
- Abstract
Neurofibromatosis (NF), Noonan syndrome (NS), and LEOPARD syndrome are all autosomal dominant conditions, each being a distinct clinical entity by itself. Rarely, one encounters cases with features of NF and NS and is termed as the 'Neurofibromatosis-Noonan syndrome' (NF-NS). The authors report a clinical dilemma with major clinical features of the NF-NS syndrome and LEOPARD syndrome co-existing in the same patient. Also, features of Noonan syndrome and LEOPARD syndrome are compared with the case reported.
- Published
- 2000
40. Dorfman-Chanarin syndrome: a rare neutral lipid storage disease.
- Author
-
Tullu MS, Muranjan MN, Save SU, Deshmukh CT, Khubchandani SR, and Bharucha BA
- Subjects
- Female, Humans, Infant, Liver pathology, Male, Neutrophils pathology, Skin pathology, Syndrome, Vacuoles pathology, Abnormalities, Multiple, Ichthyosis diet therapy, Ichthyosis pathology, Lipid Metabolism, Inborn Errors diet therapy, Lipid Metabolism, Inborn Errors pathology
- Published
- 2000
41. Bacterial nosocomial pneumonia in Paediatric Intensive Care Unit.
- Author
-
Tullu MS, Deshmukh CT, and Baveja SM
- Subjects
- Chi-Square Distribution, Child, Child, Preschool, Female, Humans, Incidence, Infant, Length of Stay, Male, Microbial Sensitivity Tests, Probability, Risk Factors, Time Factors, Cross Infection etiology, Intensive Care Units, Pediatric, Intubation, Intratracheal adverse effects, Pneumonia etiology, Respiration, Artificial adverse effects
- Abstract
Aims: To determine the incidence, risk factors, mortality and organisms causing nosocomial pneumonia (NP) in intubated patients in Paediatric Intensive Care Unit (PICU)., Materials & Methods: All patients with endotracheal (ET) tube with or without mechanical ventilation (MV) in a PICU of a tertiary care teaching hospital were included in this prospective study. Clinical parameters and investigations were evaluated in patients who developed nosocomial pneumonia (NP). Colonisation of the ET tube tip was studied by culture and the antibiotic susceptibility pattern of the isolates was determined., Results: Sixty-nine patients had an ET tube inserted and fifty-nine of these underwent MV. ET tube tip colonisation was seen in 70 out of 88 ET tubes inserted. The incidence of NP in patients with ET tube was 27.54% (7.96/100 days of ET intubation). NP developed only in patients undergoing MV. The main risk factors for developing NP were - duration of MV and duration of stay in the PICU. Age, sex, immunocompromised status and altered sensorium did not increase the risk of NP. The mortality in cases with NP was 47. 37%. E. coli and Klebsiella were the commonest organisms isolated from the ET tube tip cultures with maximum susceptibility to amikacin and cefotaxime., Conclusions: NP developed only in patients undergoing MV. Duration of MV and duration of stay in the PICU increased the risk of developing NP.
- Published
- 2000
42. Mediastinal yolk sac tumor--a rare presentation.
- Author
-
Tullu MS, Deshmukh CT, Vaideeswar P, Bharucha BA, and Arora PK
- Subjects
- Child, Preschool, Fatal Outcome, Humans, Male, Endodermal Sinus Tumor diagnosis, Mediastinal Neoplasms diagnosis
- Published
- 1999
43. Superior sagittal sinus thrombosis: a rare complication of nephrotic syndrome.
- Author
-
Tullu MS, Deshmukh CT, Save SU, Bhoite BK, and Bharucha BA
- Subjects
- Child, Preschool, Humans, Male, Sagittal Sinus Thrombosis diagnostic imaging, Tomography, X-Ray Computed, Nephrotic Syndrome complications, Sagittal Sinus Thrombosis etiology
- Abstract
A two and half year-old-male child, known case of steroid responsive nephrotic syndrome presented with fever and vomiting of acute onset. He was diagnosed to have superior sagittal sinus thrombosis on a contrast computerised tomographic scan of brain. Recovery was complete without anticoagulant therapy. Superior sagittal sinus thrombosis is an extremely rare complication of nephrotic syndrome.
- Published
- 1999
44. Benzathine penicillin induced immune haemolytic anaemia.
- Author
-
Tullu MS, Arora P, Deshmukh CT, Muranjan MN, and Bharucha BA
- Subjects
- Anemia, Hemolytic immunology, Child, Female, Humans, Anemia, Hemolytic chemically induced, Penicillin G Benzathine adverse effects, Penicillins adverse effects
- Abstract
Penicillin-induced immune haemolytic anaemia is very rare. A ten year-old-female with rheumatic mitral stenosis on benzathine penicillin prophylaxis presented with features of haemolytic anaemia and investigations supported the diagnosis of immune haemolytic anaemia. Patient responded to discontinuation of the drug and therapy with oral prednisolone. This is first such case reported from India.
- Published
- 1999
45. Cri-du-chat syndrome: clinical profile and prenatal diagnosis.
- Author
-
Tullu MS, Muranjan MN, Sharma SV, Sahu DR, Swami SR, Deshmukh CT, and Bharucha BA
- Subjects
- Chromosomes, Human, Pair 5, Cri-du-Chat Syndrome genetics, Fatal Outcome, Female, Genetic Counseling, Humans, Infant, Male, Pregnancy, Cri-du-Chat Syndrome diagnosis, Prenatal Diagnosis
- Abstract
Prenatal diagnosis of cri-du-chat syndrome is described in 2 pregnancies. In Case 1, the mother was a balanced translocation carrier and had 2 previously affected off springs. Prenatal diagnosis by chorion villus sampling and cordocentesis was successful in diagnosing an affected conceptus and the pregnancy was electively terminated. Case 2 was referred for nonimmune foetal hydrops and cordocentesis revealed deletion 5p. This second case was noteworthy for the fact that deletion 5p has not been reported to cause foetal hydrops.
- Published
- 1998
46. Urinary catheter related nosocomial infections in paediatric intensive care unit.
- Author
-
Tullu MS, Deshmukh CT, and Baveja SM
- Subjects
- Anti-Bacterial Agents therapeutic use, Bacteria isolation & purification, Chi-Square Distribution, Child, Child, Preschool, Cross Infection microbiology, Cross Infection mortality, Female, Humans, Incidence, Infant, Intensive Care Units, Pediatric, Male, Microbial Sensitivity Tests, Prospective Studies, Risk Factors, Time Factors, Urine microbiology, Cross Infection etiology, Urinary Catheterization adverse effects
- Abstract
The present prospective study was carried out in the Paediatric Intensive Care Unit (PICU) of a tertiary care teaching hospital in Mumbai. The objective was to determine the incidence, risk factors, mortality and organisms responsible for urinary catheter related infections (UCRI). Colonization and/or bacteriuria was labelled as urinary catheter related infection (UCRI). Forty-four patients with 51 urinary catheters were studied. Incidence of UCRI was 47.06%. Age, female sex and immunocompromised status did not increase the risk of UCRI. Duration of catheter in-situ and duration of stay in the PICU were associated with higher risk of UCRI. The mortality was not increased by UCRI. Commonest organism isolated in UCRI was E. coli, which had maximum susceptibility to nitrofurantoin and amikacin.
- Published
- 1998
47. Bacterial profile and antimicrobial susceptibility pattern in catheter related nosocomial infections.
- Author
-
Tullu MS, Deshmukh CT, and Baveja SM
- Subjects
- Anti-Bacterial Agents therapeutic use, Catheterization, Central Venous adverse effects, Cross Infection drug therapy, Cross Infection etiology, Drug Resistance, Microbial, Humans, Intubation, Intratracheal adverse effects, Prospective Studies, Urinary Catheterization adverse effects, Cross Infection microbiology
- Abstract
This prospective study was carried out over a period of 6 months in the Paediatric Intensive Care Unit (PICU) of a tertiary care teaching hospital. The aim of the study was to determine the organisms causing catheter related nosocomial infections in the PICU and to study their antimicrobial susceptibility pattern. Patients with endotracheal intubation, indwelling urinary catheters and central venous catheters (CVC)/venous cutdown catheters were included in the study. Colonization of the endotracheal tube, urinary catheter related infections (UCRI) and colonization of the CVC/venous cutdown catheters was studied. E. coli was the commonest organism colonizing the endotracheal tube tip with maximum susceptibility to cefotaxime and amikacin. E. coli was also was the commonest organism causing UCRI with maximum susceptibility to nitrofurantoin and amikacin. Acinetobacter was the commonest organism colonizing the CVC/venous cutdown catheters with maximum susceptibility to ciprofloxacin. All these sites of catheter related infections considered together, E. coli and Klebsiella were the commonest nosocomial organisms. Both had maximum susceptibility to amikacin. Methicillin resistant Staphylococcus aureus (MRSA) was isolated only from one culture. All the organisms had a poor susceptibility to cefazolin and amoxycillin. A knowledge of the resident microbial flora and their antimicrobial susceptibility pattern is necessary for formulating a rational antibiotic policy in an ICU.
- Published
- 1998
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