کوندرودیسپلازی متافیزال معرفی دو بیمار مبتلا به نوع Schmid

Authors

  • اسپندار, رامین
  • بغدادی, تقی
Abstract:

Typhoid fever is an endemic disease in Iran and other developing countries. This disease has gradually become resistant to the first line of drugs, and because of this resistancy we have studied a new alternative drug (cefixime) on typhoid fever patients and compared it's effectiveness with chloramphenicol. For this purpose, by a randomized clinical trial in Emam Khomeini hospital between 1995-2000, we allocated 44 uncomplicated patient with established typhoid fever (positive blood or bone marrow culture) and by random selection, 24 patient were given cefixime (400 mg PO bid) and 20 patient received chloramphenicol (500 mg po Q6h). The duration of therapy were 10 and 14 days for chloramphenicol and cefixime group respectively. Median fever clearance times were 5±1.9 for cefixime recipients and 3.8±1.2 days for chloramphenicol treated patients, but for improvement in other clinical and laboratory findings, there were not any significant difference. Bacteriologic and clinical cure rate for cefixime was 100 and 92 percents respectively. Though, even cefixime like other betalactam drugs is slow in helping the fever disappearance but our study suggests that oral cefixime is effective and can be used as an alternate treatment of typhoid fever.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

معرفی یک بیمار مبتلا به سندرم مافوچی

Introduction: Maffucci syndrome is a rare clinical entity (approximately 200 cases have been reported in the medical literature) with a combination occurrence of multiple enchodroma and vascular tumors. Case Report: Our patient was an 18 year old girl born in a non-consanguineous marriage with finger and toe bones disorders (enchondroma) causing deformity of fingers and toes with multiple vas...

full text

معرفی یک بیمار مبتلا به سندرم ایکتیوزلاملار

Introduction: Ichthyosis lamellar syndrome is a rare genodermatosis and in most families is inherited as an autosomal recessive trait because of transglutaminase-1 deficiency. Case Report: Our patient was a 6 year old girl and she was the result of consanguinity. She had large plate-like scales. The scales had mosaic-like pattern and erythroderma was absent. Tautness of her facial skin was as...

full text

معرفی بیمار مبتلا به رتینوبلاستومای پیش‌رفته

هدف: معرفی بیمار مبتلا به رتینوبلاستوم پیش‌رفته و مراجعه دیرهنگام. معرفی بیمار: دختر 6 ساله با توده اربیت از 6 ماه قبل به درمانگاه چشم بیمارستان امام حسین (ع) مراجعه کرد. با تشخیص احتمالی رتینوبلاستوم و با توجه به وسعت ضایعه، ابتدا شیمی‌درمانی و سپس عمل جراحی برداشت کامل ضایعه (exentration) صورت پذیرفت. تشخیص رتینوبلاستوم در بررسی آسیب‌شناسی تایید شد و حاشیه ضایعه سالم بود. نتیجه‌گیری: با و...

full text

معرفی یک بیمار مبتلا به هیستیوسیتوزیس ایکس از نوع Hand Schuller Christian disease

The term histiocytosis refers to a group of idiopathic clinics entities characterized by diffuse proliferation of mature histiocytes associated with tumorlike masses of foamy reticuloendothelial cells containing lipoid droplets with variable number of eosinophiles and connective tissue. This cells causes tumorlike masses in the bones and other vicera in the body thus it may have very different ...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 59  issue None

pages  19- 22

publication date 2001-05

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

No Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023