Kwadwo Darko , Sonia Pulido , Muhammad Ammar Haider , Milan Sivakumar , Bernice Limann , Pearl Tenkorang , Okikioluwa Odesanya , Peace Odiase , Mark Farid , Umaru Barrie , Bruno P. Braga , Mabel Banson , Teddy Totimeh
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引用次数: 0
Abstract
Objective
Craniosynostosis is a congenital skull deformity that impacts development and quality of life of children if left untreated. This study aimed to evaluate literature regarding presentation, treatment, and outcomes of craniosynostosis in Africa.
Methods
A systematic review of the literature using PubMed/MEDLINE, Scopus, Web of Science, and Google Scholar databases was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines.
Results
Fourteen retrospective/prospective studies with 620 patients and 14 case reports involving 27 cases (8 countries) were included. In 12 articles, 56.6% of patients (317/560) were males, with a mean age of 2.4 years (confidence interval [CI]: 1.1–3.7). Abnormal head shape was the most reported presentation in 77.8% of cases (332/427, 8 articles). Syndromic craniosynostosis was seen in 25.2% (CI: 13.7%–36.6%). Common phenotypes were trigonocephaly in 31.5% (CI: 3.6%–59.4%), anterior plagiocephaly in 23.2% (CI: 5.1%–41.3%), and scaphocephaly in 22.1% (CI: 13.5%–30.8%). Five hundred seventy eight patients, 99.5% (CI: 99.0%–100.0%), underwent surgical treatment. Vault remodeling was performed in 72.9% patients (CI: 47.4%–98.6%). Postoperative complications included cerebrospinal fluid leaks 5.4% (CI: 0.0%–11.6%) and surgical site infections 4.5% (CI: 0.0%–10.8%). Follow-up ranged between 0.2 and 40.9 months; 95.6% of cases (CI: 90.1%–100.0%) exhibited improved deformity and neurological deficits at last follow-up. The mortality rate was 3.1% (CI: 0.0%–6.9%, 2 articles).
Conclusions
Few studies on craniosynostosis in Africa highlight the need for more research. Treatment with open techniques yields few complications and a low mortality rate. Early diagnosis and collaborative data reporting will enhance understanding of its burden and variations across Africa.
期刊介绍:
World Neurosurgery has an open access mirror journal World Neurosurgery: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
The journal''s mission is to:
-To provide a first-class international forum and a 2-way conduit for dialogue that is relevant to neurosurgeons and providers who care for neurosurgery patients. The categories of the exchanged information include clinical and basic science, as well as global information that provide social, political, educational, economic, cultural or societal insights and knowledge that are of significance and relevance to worldwide neurosurgery patient care.
-To act as a primary intellectual catalyst for the stimulation of creativity, the creation of new knowledge, and the enhancement of quality neurosurgical care worldwide.
-To provide a forum for communication that enriches the lives of all neurosurgeons and their colleagues; and, in so doing, enriches the lives of their patients.
Topics to be addressed in World Neurosurgery include: EDUCATION, ECONOMICS, RESEARCH, POLITICS, HISTORY, CULTURE, CLINICAL SCIENCE, LABORATORY SCIENCE, TECHNOLOGY, OPERATIVE TECHNIQUES, CLINICAL IMAGES, VIDEOS