← Back to all signals
RESEARCH PAPER ANALYSIS

Epidemiology of cerebrospinal fluid shunt surgery in Australia and New Zealand (2017-2024).

AI interpretation is pending for this paper.

Open original publication →
PMID41202569
JournalJournal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
Publication Date2025-11-06
Ingested2026-08-02 12:05 AM
EXECUTIVE SUMMARY

What the AI sees

Not AI summarized yet.

WHY IT MATTERS

Research significance

Pending deeper interpretation.

ABSTRACT

Source abstract

BACKGROUND: Hydrocephalus-related procedures constitute approximately one-third of neurosurgical interventions annually, with incidence rates ranging from 30 to 300 per 100,000 population, varying by region, age and aetiology. Despite advancements in surgical techniques and shunt devices, cerebrospinal fluid (CSF) shunts exhibit high complication and failure rates, necessitating frequent revisions due to issues such as overdrainage, underdrainage, infections and mechanical failures. This study leverages data from the Australasian Shunt Registry (ASR) to define the epidemiology of shunt surgery in Australia and Aotearoa New Zealand, addressing a critical gap in regional data. METHODS: A retrospective, multicentre, registry-based study analysed 8 years of data (January 2017-December 2024) from the ASR, established in 2016 by the Neurosurgical Society of Australasia. The study included 7238 procedures across 5220 patients from 63 sites (37 public, 26 private), encompassing primary insertions, revisions, and other shunt-related procedures. Incidence rates were calculated per 100,000 person-years using population estimates (Australia ∼ 25.8 million, New Zealand ∼ 5 million), stratified by age (infants < 1 year, children 1-<18 years, adults ≥ 18 years). Survival analysis employed Kaplan-Meier estimation and Cox regression to assess revision risks related to operator role and surgery duration, with analyses conducted using R (version 4.4.1). RESULTS: The overall incidence of primary shunt insertions was 1.64 per 100,000 person-years, with age-specific rates of 15.8 (infants), 1.3 (children), and 1.5 (adults). Revisions accounted for 35.5 % of procedures, with one-year and 90-day revision rates at 9.3 % and 5.6 %, respectively. Common diagnoses included haemorrhage (44.6 % infants), tumours (32.4 % children), and idiopathic normal pressure hydrocephalus (26.2 % adults). Surgery durations exceeding 2 h doubled revision risk (HR 2.06, p < 0.001), potentially linked to increased infection risk. CONCLUSIONS: This first ASR report defines the epidemiology of shunt surgery across Australia and Aotearoa New Zealand compared to UK and Norwegian benchmarks. It contributes to the knowledge base of this complex patient population, ultimately aiding clinical outcomes and economic burden reduction.

SUPPORTING PAPER SET

32 more papers to review

Ranked by current scoring engine
1 Retinoblastoma Metastatic to Bone: Case Series and Literature Review. Journal of radiology case reports 53.4 2 Pediatric Plantar Malignant Melanoma, Subungual Melanoma, and Spitzoid Melanoma: A Case Series of Rare Pediatric Melanomas. The Journal of clinical and aesthetic dermatology 48.5 3 Inborn errors of immunity and mortality: 10 years of single-center experience. Allergologia et immunopathologia 60.5 4 Regional Diversity of Human Papillomavirus Genotypes in Southeastern Brazil: Implications for Cervical Cancer Screening. Journal of medical virology 61.0 5 Epidemiology and Survival Determinants of Monomorphic Epitheliotropic T-Cell Lymphoma: A Pooled Patient-Level Dataset Analysis. Hematological oncology 74.52 6 Knowledge, attitudes, and practices regarding Helicobacter pylori-induced gastric ulcers and cancers among Saudi residents: a nationwide web-based survey. Frontiers in public health 70.4 7 Adult psychological outcomes among women with different adolescent PCOS presentations. Frontiers in endocrinology 59.5 8 Computational insights into synergistic mechanisms of PD-901 and 5-azacitidine targeting PTPN11 (SHP2) E76K mutation in juvenile myelomonocytic leukemia. Frontiers in bioinformatics 62.85 9 Clinical evidence and biological mechanisms linking obesity to adverse outcomes in pediatric and adolescent acute lymphoblastic leukemia. Frontiers in oncology 68.95 10 [Comparison of inpatient disease statistics based on two coding rules]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi 61.9 11 Serum HMGB3 and PCSK9 Levels as Predictors of Early Treatment Response in Pediatric Mycoplasma pneumoniae Pneumonia: A Single-Center Prospective Cohort Study. International journal of general medicine 79.26 12 Prevalence and penetrance of heritable retinoblastoma in two adult population cohorts: implications for genomic newborn screening. European journal of human genetics : EJHG 65.5 13 A mixed methods study of adolescent and young adult cancer survivors and their utilization of a survivorship clinic: Barriers and facilitators. Journal of cancer survivorship : research and practice 65.9 14 Perinatal Characteristics of Japanese Children With Infantile Hemangioma: A Questionnaire-Based Case-Control Study. The Journal of dermatology 67.0 15 Efficacy of celecoxib and methotrexate-vinblastine regimen in desmoid-type fibromatosis: A retrospective cohort study. Medicine 76.0 16 The safety and efficacy of different anti-tuberculosis regimens containing Lzd for RR/MDR/Pre-XDR-TB patients in China. Medicine 68.2 17 Nursing care of a pediatric patient with anti-NMDAR encephalitis complicated by secondary epilepsy: A case report. Medicine 61.1 18 Cardiac involvement in neurofibromatosis type 1: real-world baseline and follow-up findings from a tertiary single-center cohort. European journal of pediatrics 62.9 19 Multimodal clinical-radiomic-deep learning model for preoperative classification of pediatric pineal region tumors. Neuroradiology 70.4 20 Precision medicine for pediatric gliomas. Current opinion in oncology 80.34 21 Parental distress - a predictor of treatment adherence in pediatric neuroblastoma: a cross-sectional study of chinese families. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 62.24 22 Integrating optimal patient-centered care: patient- and family-reported experiences after complex treatment for rare diseases. World journal of pediatrics : WJP 63.94 23 [Guidelines for the diagnosis and treatment of hemophagocytic lymphohistiocytosis (2026 edition)]. Zhonghua yi xue za zhi 73.84 24 Cranial MRI in Girls With Central Precocious Puberty: Clinical Characteristics and Predictors of Abnormal Findings. Saudi medical journal 69.8 25 Diffuse midline glioma, H3 K27-altered, forming a suprasellar mass: A case report. Radiology case reports 51.9 26 Integrating immunophenotyping and morphology in the diagnosis of acute leukemia at the National Oncology Center, Sana'a, Yemen. The Libyan journal of medicine 61.0 27 Not Just a Pediatric Condition: Down Syndrome Across the Lifespan. Missouri medicine 54.0 28 The incidence of thyroid cancer in Danish children, adolescents and young adults. Danish medical journal 56.0 29 Cancer in Young Women: Late-Stage Breast Cancer Registry Analysis of a 24-Year Nationwide Retrospective Cohort of 52,734 Patients in Brazil (CLARA Study). Clinical breast cancer 71.0 30 Pediatric Familial Cerebral Cavernous Malformation Associated With a Novel KRIT1 Initiation-Region Frameshift Variant. Molecular genetics & genomic medicine 56.0 31 Social Inequalities, Geographical Accessibility to Care, and Excess Mortality for Patients With Hematological Malignancies in France: Results From French Cancer Registries. Hematological oncology 65.2 32 Bibliometric and clinical trial landscape of hepatoblastoma (2000-2024): a multi-database analysis of global research. Frontiers in oncology 77.1
PATIENT-FRIENDLY SUMMARY

Epidemiology of cerebrospinal fluid shunt surgery in Australia and New Zealand (2017-2024).

For education only—not personal medical advice.

Before you continue

AI-assisted research information

Neurocompute uses AI to summarize scientific papers, interpret research signals, and suggest relevant reference links. AI-generated content can be incomplete, misleading, or wrong, and generated links may be irrelevant or unavailable.

Our reviewed outputs have performed strongly to date, but past accuracy is not a guarantee. Verify summaries, scores, claims, and links against the original publication before relying on them.

This platform is for research and education only. It does not provide medical advice, diagnosis, treatment recommendations, or clinical guidance.

Pediatric cancer research intelligence graphic
PEDIATRIC CANCER VISUAL SYSTEM

Open the Research Intelligence Map

Explore the active pediatric oncology analysis view.

Expand Intelligence View →
Full Pediatric cancer research intelligence graphic