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1.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2018; 28 (3): 214-217
Dans Anglais | IMEMR | ID: emr-163441

Résumé

Objective: To compare the efficacy of Saccharomyces boulardii and lactic acid producing probiotics in addition to usual treatment regimen to cure diarrhea among children [6 months to 5 years of age]


Study Design: Randomized controlled trial


Place and Duration of Study: Department of Pediatrics, Sheikh Zayed Hospital, Lahore, from February to July 2015


Methodology: Children suffering from acute diarrhea were orally administered Saccharomyces boulardii and lactic acid producing probiotics for 5 days. The efficacy of administered probiotics was monitored. Patients were given Saccharomyces boulardii and lactic acid producing probiotics randomly to remove the bias


Results: Two hundred patients randomly selected for trials; out of which, 100 were treated with Saccharomyces boulardii while the other 100 were supplemented with lactic acid concomitantly along with conventional diarrhea treatment. Results indicated that Saccharomyces boulardii treatment group has significantly higher efficacy rate [45%] compared to lactic acid producing probiotics [26%]


Conclusion: This study concluded that Saccharomyces boulardii has a better efficacy compared to lactic acid and may be adopted as a probiotic of choice


Sujets)
Humains , Mâle , Femelle , Nourrisson , Enfant d'âge préscolaire , Diarrhée du nourrisson/traitement médicamenteux , Probiotiques/usage thérapeutique , Saccharomyces boulardii , Acide lactique , Résultat thérapeutique , Maladie aigüe
2.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2017; 27 (1): 13-17
Dans Anglais | IMEMR | ID: emr-185673

Résumé

Objective: To compare the effectiveness of per rectal misoprostol over oxytocin in primary postpartum haemorrhage [PPH]


Study Design: Randomised controlled trial study


Place and Duration of Study: Gynaecology and Obstetrics Department, Unit IV, Bolan Medical Complex Hospital, Quetta, from September 2013 to February 2014


Methodology: Emergency obstetric patients receiving per rectal misoprostol [800 micro gm] were named as group 'A' and those receiving 10 units oxytocin intramuscularly were labelled as group 'B'. The patients were followed within 24 hours of spontaneous vaginal deliveries. Pads soaked were used to assess the amount of blood loss


Results: A total of 1,678 patients were included in the study. The mean age of patients in group-A was 29.11 years while the mean age of patients in group-B was 29.16 years. One hundred and twenty-three [14.66%] patients in group-A and 120 [14.31%] patients in group-B had PPH. Among the total 1,678 patients, 243 [14.49%] had postpartum haemorrhage among whom 24 [9.88%] had major haemorrhage with a blood loss >/=1000 mL. Among the sub-group [839 patients] administered misoprostol had 123 [14.66%] patients with blood loss greater than 500 mL and the rest 716 patients [85.34%] had blood loss less than 500 mL. The sub-group administered oxytocin have 120 [14.31%] out of 839 patients with postpartum haemorrhage while 719 [85.69%] had blood loss less than 500 mL


Conclusion: Active management of 3rd stage of labour with per rectal misoprostol administration was as effective as intramuscular oxytocin. Both were equally effective to reduce PPH and the subsequent need for surgical interventions


Sujets)
Humains , Femelle , Adolescent , Jeune adulte , Adulte , Hémorragie de la délivrance/traitement médicamenteux , Misoprostol/administration et posologie , Ocytocine/administration et posologie , Pakistan
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