Risk factors of congenital hydrocephalus: a case-control study in a lower-middle-income country (Egypt)
Author:
Ali Taher M.1, Elwy Reem1, Abdelrazik Bassante2, Soliman Mohamed A. R.134, Alsawy Mohamed F.1, Abdullah Ahmed1, Ahmed Eman15, Zaki Shurouk1, Salem Amany A.6, Katri Mohamed A.1, Elhamaky Mostafa1, Kandel Haitham1, Marei Ahmed A.1, Menabbawy Ahmed Al17, Ghoul Ahmed M. F.1, Hafez Ahmed A.1, Abdelbar Sarah1, Moharam Reham Khaled1, Hany Ayman8, Hasanin Ahmed9, Marx Sascha7, Fleck Steffen7, Baldauf Jörg7, Schroeder Henry W. S.7, Refaee Ehab El17, Zohdi Ahmed1
Affiliation:
1. Departments of Neurosurgery, 2. Heidelberg Institute of Global Health, Heidelberg University, Heidelberg, Germany; 3. Department of Neurosurgery, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, New York; 4. Department of Neurosurgery, Buffalo General Medical Center, Kaleida Health, Buffalo, New York; 5. Faculty of Biotechnology, Badr University in Cairo, Egypt; and 6. Public Health, 7. Department of Neurosurgery, University Medicine Greifswald, Germany 8. Obstetrics and Gynecology, and 9. Anaesthesiology, Faculty of Medicine, Cairo University, Cairo, Egypt;
Abstract
OBJECTIVE
Hydrocephalus is the most common brain disorder in children and is more common in low- and middle-income countries. Research output on hydrocephalus remains sparse and of lower quality in low- and middle-income countries compared with high-income countries. Most studies addressing hydrocephalus epidemiology are retrospective registry studies entailing their inherent limitations and biases. This study aimed to investigate child-related, parental, and socioeconomic risk factors of congenital hydrocephalus (CH) in a lower-middle-income country.
METHODS
An investigator-administered questionnaire was used to query parents of patients with CH and controls who visited the authors’ institution from 2017 until 2021. Patients with secondary hydrocephalus and children older than 2 years of age at diagnosis were excluded. Uni- and multivariable logistic regression was performed to identify the factors affecting CH development.
RESULTS
Seven hundred forty-one respondents (312 cases and 429 controls) were included in this study. The authors showed that maternal diseases during pregnancy (OR 3.12, 95% CI 1.96–5.03), a lack of periconceptional folic acid intake (OR 1.92, 95% CI 1.32–2.81), being a housewife (OR 2.66, 95% CI 1.51–4.87), paternal illiteracy (OR 1.65, 95% CI 1.02–2.69), parental consanguinity (OR 3.67, 95% CI 2.40–5.69), a history of other CNS conditions in the family (OR 2.93, 95% CI 1.24–7.34), conceiving a child via assisted fertilization techniques (OR 3.93, 95% CI 1.57–10.52), and the presence of other congenital anomalies (OR 2.57, 95% CI 1.38–4.87) were associated with an independent higher odds of a child having CH. Conversely, maternal hypertension (OR 0.22, 95% CI 0.09–0.48), older maternal age at delivery (OR 0.93, 95% CI 0.89–0.97), and having more abortions (OR 0.80, 95% CI 0.67–0.95) were negatively correlated with CH.
CONCLUSIONS
Multiple parental, socioeconomic, and child-related factors were associated with higher odds for developing CH. These results can be utilized to guide parental counseling and management, and direct social education and prevention programs.
Publisher
Journal of Neurosurgery Publishing Group (JNSPG)
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