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1.
Article | IMSEAR | ID: sea-213327

ABSTRACT

Background: Acute pancreatitis is an inflammatory process with a highly variable clinical course. The present study was conducted to assess severity of acute pancreatitis.Methods: The present study was conducted on 53 patients of acute pancreatitis of both genders. A thorough clinical examination was performed. Ranson’s score (RS), Glasgow score (GS), acute physiology and chronic health evaluation (APACHE-II) score, APACHE-O score and Balthazar’s computed tomography severity index (CTSI) score was recorded.Results: Out of 53 patients, males were 47 and females were 6. Patients were divided into acute pancreatitis (32) and severe pancreatitis (21). Results of the bivariate analysis of Ranson scoring system in mild periodontitis was 0.84 in severe was 2.95, Glasgow score was 0.66 in mild and 2.48 in severe, APACHE-II had 6.94 in mild and 10.33 in severe, APACHE-O had 7.34 in mild and 11 in severe and CTSI had 1.9 in mild and 6.15 in severe.Conclusions: Authors found that all the scoring systems are useful in assessing the severity of acute pancreatitis.

2.
Article | IMSEAR | ID: sea-213294

ABSTRACT

Background: Acute pancreatitis (AP) is a sudden inflammatory condition of the pancreas. The present study recorded independent risk factors of acute pancreatitis.Methods: The present study was conducted on 50 patients of acute pancreatitis of both genders. A detailed general and systemic examination was done in all patients. History of smoking, alcoholism, hypertension, weight, obesity and diabetes was taken.Results: Out of 50 patients, males were 45 and females were 5. There was history of smoking in 20 patients, alcoholism in 15, weight >70 kg in 38, hypertension in 10, diabetes in 24 patients and obesity in 12 patients. The difference found to be significant (p<0.05).Conclusions: Authors found that smoking, alcoholism, hypertension, diabetes, weight >70 kg and obesity as independent risk factors of acute pancreatitis.

3.
Indian Pediatr ; 2009 Feb; 46(2): 133-6
Article in English | IMSEAR | ID: sea-12619

ABSTRACT

OBJECTIVE: To compare the effectiveness of tepid sponging and antipyretic drug versus only antipyretic drug among febrile children. DESIGN: Randomized controlled trial. SETTING: Tertiary care hospital. PARTICIPANTS: 150 children 6 mo - 12 yr age with axillary temperature 101F. INTERVENTION: Tepid sponging and antipyretic drug (Paracetamol) (n=73) or only antipyretic drug (Paracetamol) (n=77). MAIN OUTCOME MEASURES: Reduction of body temperature and level of comfort. RESULTS: The reduction of body temperature in the tepid sponging and antipyretic drug group was significantly faster than only antipyretic group; however, by the end of 2 hours both groups had reached the same degree of temperature. The children in tepid sponging and antipyretic drug had significantly higher discomfort than only antipyretic group, but the discomfort was mostly mild. CONCLUSION: Apart from the initial rapid temperature reduction, addition of tepid sponging to antipyretic administration does not offer any advantage in ultimate reduction of temperature; moreover it may result in additional discomfort.


Subject(s)
Analgesics, Non-Narcotic/therapeutic use , Baths , Body Temperature , Child , Child, Preschool , Combined Modality Therapy , Female , Fever/prevention & control , Fever/therapy , Humans , Infant , Male , Treatment Outcome
4.
J Cancer Res Ther ; 2008 Oct-Dec; 4(4): 173-7
Article in English | IMSEAR | ID: sea-111400

ABSTRACT

AIM: To evolve a fast dose verification method for high-dose-rate (HDR) brachytherapy treatment plans and to demonstrate its applicability in different clinical cases. MATERIALS AND METHODS: We developed a software tool in VC++ for the Varisource HDR unit for HDR dosimetry plan verification using TG-43 parameters. HDR treatment dosimetry of a number clinical cases using Varisource was verified by comparison with the treatment planning system (TPS). RESULTS: A number of different types of clinical cases treated by Varisource were evaluated. TPS calculated dose values and verification code calculated dose values were found to agree to within 3% for most of the dose calculation points. CONCLUSIONS: We have validated with clinical cases a fast and independent dose verification method of the dosimetry at selected points for HDR brachytherapy treatments plan using TG-43 parameters. This can be used for the verification of the TPS calculated dose at various points. The code is written to work with Varisource, but it can conceivably be modified for other sources also by using the fitted constant of the respective source.


Subject(s)
Anisotropy , Brachytherapy/methods , Humans , Models, Statistical , Monte Carlo Method , Probability , Programming Languages , Radiometry/methods , Radiotherapy Dosage , Radiotherapy Planning, Computer-Assisted/methods , Radiotherapy, High-Energy/methods , Software
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