Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Purpose Of The Study: In Benin, the etiological diagnosis of serious hip disorders is often difficult and satisfactory epidemiological data are lacking. The purpose of this study was to establish the relative frequencies of pathological conditions leading to serious hip disorders in Benin.
Material And Methods: We report 180 cases of severe hip disorders in 170 children hospitalized over a 7-year period from January 1, 1992 through December 31, 1998. The prospective study was based on clinical and conventional radiological findings, laboratory results and clinical course.
Results: The annual frequency of new cases was: septic arthritis of the hip 18.8 (73.3%), legg-Calvé-Perthus disease 2.9 cases (11%), aseptic osteoarthritis of the femoral head 2.3 cases (8.9%), superior femoral epiphysiolysis 0.9 cases (3.3%), coxalgia 0.9 cases (3.3%), accounting for 25.7 new cases of serious hip disorders per year.
Discussion: Sickle-cell disease or trait (SS or SC hemoglobin) was the cause of aseptic osteonecrosis of the femoral head in 83% of the cases. For the other serious hip disorders, 30% were observed in sickle-cell trait patients and only 2.7% in patients with sickle-cell disease (SS or SC). These rates are similar to those in the general Benin population.
Conclusion: These data offer a better perception of the causes of serious hip disorders observed in children in Benin. Further studies are needed to obtain precise data by nosological entity. Legg-Calvé-Perthes disease, unknown in Benin up to 1992, now is the second leading cause of severe hip disorders and their sequelae.
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