Evidence map›Paper›PMID 39703275›Full record

ArticleCureus2024

Clinical Profile and Outcomes of Pediatric Snakebite Envenomation: A Three-Year Retrospective Study From a Rural Tertiary Care Center in South India.

Tamilarasan Muniyapillai, Maniprabhu S, Abinaya R, Karthikeyan Kulothungan, Sriranganathan Thirunavukkarasu, Neethu George

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Vipera Snakebite in Children: A Focus on Europe.Children (Basel, Switzerland) · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Tamilarasan MuniyapillaiCommunity Medicine, Dhanalakshmi Srinivasan Medical College and Hospital, Perambalur, IND.
Maniprabhu SCommunity Medicine, K.A.P. Viswanatham Medical College, Trichy, IND.
Abinaya RCommunity Medicine, Panimalar Medical College Hospital and Research Institute, Chennai, IND.
Karthikeyan KulothunganCommunity Medicine, Dhanalakshmi Srinivasan Medical College and Hospital, Perambalur, IND.
Sriranganathan ThirunavukkarasuCommunity Medicine, Srinivasan Medical College and Hospital, Trichy, IND.
Neethu GeorgeCommunity Medicine, Dhanalakshmi Srinivasan Medical College and Hospital, Perambalur, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Snakebite envenomation remains a significant public health challenge in tropical countries, particularly affecting the pediatric population. Children are especially vulnerable because of their smaller body mass, outdoor activities, and delayed presentation to healthcare facilities. This study aimed to analyze the clinical profile, demographic patterns, and envenomation characteristics of snakebites in children aged 1-16 years presenting to a tertiary care center. Additionally, the study sought to evaluate the spectrum of complications and clinical outcomes in pediatric snakebite cases while assessing the mortality rate and associated risk factors in pediatric snakebite envenomation. Methodology A retrospective medical record review was conducted analyzing all snakebite cases in children aged below 16 years admitted to the Department of Pediatrics, Dhanalakshmi Srinivasan Medical College and Hospital, Perambalur, Tamil Nadu (southern state in India), between January 2021 and December 2023. Data extracted included demographics, bite characteristics, clinical manifestations, time to healthcare presentation, and treatment details. Management protocols followed World Health Organization (WHO) guidelines for snakebite envenomation, including the administration of polyvalent anti-snake venom (ASV) when indicated. Results Among 202 pediatric snakebite cases, children aged 9-12 years constituted the majority (n = 110, 54.5%), with significant male predominance (n = 148, 73.3%). Unidentified snakes were responsible for the highest proportion of bites (n = 72, 35.6%), followed by vipers (n = 65, 32.2%) and cobras (n = 53, 26.2%). Lower limb bites were most frequent (n = 108, 53.5%), and seasonal analysis revealed peak incidence during January-April (n = 106, 52.5%). Common clinical manifestations included hematuria (n = 112, 55.4%), oliguria (n = 102, 50.5%), and renal failure (n = 80, 39.6%). Most patients (n = 120, 59.4%) received antivenom within six hours, with 46.6% (n = 94) requiring 5-10 vials. The overall mortality rate was 9.9% (n = 20). Statistical analysis revealed significant associations between mortality and snake species identification (p = 0.0014), with the highest mortality in unidentified snakebites (n = 15, 20.8%). Anatomical bite site (p = 0.042), renal failure (p = 0.001), respiratory paralysis (p = 0.001), and ptosis (p = 0.001) were also significantly associated with mortality. Time to antivenom administration significantly impacted survival (p = 0.001), with mortality rates of 0.8% (n = 1) for treatment within six hours, increasing to 38.5% (n = 10) for delays beyond 12 hours. Demographics and local manifestations showed no significant correlation with mortality. Conclusion Our study reveals distinct patterns in pediatric snakebites, predominantly affecting male children in pre-adolescent age. The high proportion of unidentified snakes remains challenging. With renal and hematological manifestations being frequent, mortality is significantly influenced by delayed treatment, respiratory paralysis, and renal failure. Early antivenom administration, proper snake identification, and prompt medical intervention remain crucial factors in improving outcomes and reducing mortality.

Indexed as

anti-snake venomneuroparalyticoutcome assessmentsnakebitesnakebite envenomingvasculotoxic

Identifiers

PMID39703275
PMCPMC11656267

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.