Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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We report a case of a term neonate presenting with anomalous origin of the right coronary artery from the pulmonary trunk, an aortopulmonary window, interrupted aortic arch type A, and an atrial septal defect within the oval fossa. The infant, admitted in cardiogenic shock, was stabilized with fluid resuscitation, intubation, and inotropic support. Comprehensive imaging revealed the complex cardiac anomalies. Surgical intervention successfully addressed all the lesions. The patient showed excellent postoperative recovery, with no complications at 6 months. Our experience underscores the critical need for detailed preoperative assessment in managing complex congenital heart defects.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12348722 | PMC |
http://dx.doi.org/10.4103/apc.apc_171_24 | DOI Listing |