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Epidemiology of Endocrine Dysfunctions in Pediatric Patients with Previous Central Nervous System Infection: A
Giorgio Sodero1, Clelia Cipolla2, Laura Martino1
1Institute of Pediatrics, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Insights
Pediatric central nervous system (CNS) infections can lead to endocrine issues. This review highlights the need for multidisciplinary follow-up and screening for hypopituitarism in children post-CNS infection.
Area of Science:
- Pediatric Endocrinology
- Infectious Diseases
- Neuroscience
Background:
- Endocrine sequelae following pediatric central nervous system (CNS) infections are not well-documented.
- Previous studies have not systematically assessed the incidence of endocrinological alterations in children with a history of CNS infections.
Purpose of the Study:
- To conduct a scoping review assessing the incidence of endocrinological alterations in pediatric patients with prior CNS infections.
- To identify specific endocrine comorbidities associated with CNS infections like meningitis and encephalitis.
Main Methods:
- Included randomized and non-randomized controlled trials, along with prospective and retrospective observational studies.
- Conducted a comprehensive screening process to identify relevant literature on pediatric CNS infections and endocrine outcomes.
- Synthesized data from ten studies involving 211 pediatric patients.
Main Results:
- Meningitis and encephalitis were the most frequently reported CNS infections.
- Hypopituitarism was identified as a consequence of CNS infections, particularly those caused by Mycobacterium tuberculosis.
- Specific deficiencies included growth hormone, gonadotropin, and corticotropin deficiencies, with some patients exhibiting hyperprolactinemia.
Conclusions:
- Standardized, multidisciplinary follow-up is crucial for pediatric patients with a history of CNS infections.
- Endocrinological evaluation and monitoring of auxological parameters are recommended for early detection of hypopituitarism.
- Establishing endocrinological screening protocols can facilitate timely intervention and appropriate care for affected children.
Abstract:
Purpose The incidence of endocrine sequelae following central nervous system (CNS) infections in pediatric age is not known. We conducted this scoping review to assess the incidence of endocrinological alterations in patients with prior CNS infections in pediatric age. Methods Our screening process included both randomized and non-randomized controlled trials. All types of observational studies, prospective and retrospective, have been included. Results Ten studies were included in our review. The cumulative number of patients in all of the studies was 211, the mean age of the population study was 4.9 (±5 years). The included papers described the following acute CNS infections: meningitis (nine studies reported eighty-five cases) and encephalitis (three studies described sixty-five cases). Two case reports and one retrospective study reported hypopituitarism as a consequence of Mycobacterium tuberculosis CNS infection. In five studies the patients developed endocrine comorbidities at the time of infection. Another study analyzed 49 young adults who previously had tuberculous meningitis at a mean age of 5.9 ± 5.0 years: seven patients had growth hormone deficiency, four of whom also had gonadotropin deficiency; the other three had gonadotropin deficiency, corticotropin deficiency, and mild hyperprolactinemia. Conclusion Standardized multidisciplinary follow-up and research of patients with prior CNS infection is crucial. Although pituitary reserve screening is not commonly performed in these patients, clinical and research centers should set up an endocrinological evaluation with monitoring of auxological parameters to detect the signs and symptoms of hypopituitarism early and to initiate the appropriate care in children with previous CNS infections.
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