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Record W2946993905 · doi:10.1093/pch/pxz066.115

116 Hyoscine butylbromide (Buscopan) for abdominal pain in children: a randomized controlled trial

2019· article· en· W2946993905 on OpenAlexaff
Naveen Poonai, Sharlene Elsie, Kriti Kumar, Kamary Coriolano, Shaily Brahmbhatt, Emily Dzongkowski, Holly Stevens, Priti Gupta, Michael R. Miller, Dhandapani Ashok, Gary Joubert, Andreana Bütter, Samina Ali

Bibliographic record

VenuePaediatrics & Child Health · 2019
Typearticle
Languageen
FieldMedicine
TopicPediatric Pain Management Techniques
Canadian institutionsUniversity of AlbertaWestern University
Fundersnot available
KeywordsMillerClassicsLibrary scienceMedia studiesMedicineHistorySociologyComputer science

Abstract

fetched live from OpenAlex

Abdominal pain is one of the most frequent reasons for an emergency department (ED) visit. Most cases are functional and no therapy has proven effective. The purpose of this study is to identify an effective therapeutic agent for children who present to the ED with presumed functional abdominal pain. We sought to determine if hyoscine butylbromide (HBB) (BuscopanTM) is effective for children who present to the ED with functional abdominal pain. We conducted a randomized, blinded, superiority trial comparing HBB 10 mg plus acetaminophen placebo to oral acetaminophen 15 mg/kg (max 975 mg) plus HBB placebo using a double-dummy approach. We included children 8–17 years presenting to the ED with colicky abdominal pain rated > 40 mm on a 100 mm visual analog scale (VAS). The primary outcome was VAS pain score at 80 minutes post-administration. Secondary outcomes included adverse effects; caregiver satisfaction with pain management using a five-item Likert scale; recidivism and missed surgical diagnoses within 24-hours of discharge. Analysis was based on intention to treat. 236 participants were randomized (116 acetaminophen; 120 HBB). The mean (SD) age was 12.4 (3.0) years and 153/236 (64.8%) were female. The median (IQR) duration of pain prior to enrollment was 2 (4.5) hours and analgesia was provided to 129/236 (54.7%) of participants. The mean (SD) pre-intervention pain scores in the acetaminophen and HBB groups were 62.3 (16.5) mm and 60.3 (17.9) mm, respectively. At 80 minutes, the mean (SD) pain scores in the acetaminophen and HBB groups were 30.1 (28.8) mm and 29.4 (26.4) mm, respectively and there were no significant differences adjusting for pre-intervention scores (p=0.96). The median (IQR) caregiver satisfaction was high in the acetaminophen [5 (2)] and HBB [5 (1)] groups (p=0.79). The median (IQR) length of stay between acetaminophen [236 (99.75)] and HBB [230.5 (102.5)] was not significantly different (p=0.91). In the acetaminophen and HBB groups, 6 and 8 participants returned to a health provider, of which 4/6 and 6/8 returned with abdominal pain, respectively. There were no missed surgical diagnoses. The most common adverse effect was nausea (9% per group) and there were no significant differences in adverse effects between acetaminophen (28/116, 24.1%) and HBB (32/120, 26.7%) (p=0.57). For children with presumed functional abdominal pain who present to the ED, both acetaminophen and HBB produce a clinically important (VAS <30 mm) reduction in pain and should be routinely considered in this clinical setting.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.009
Threshold uncertainty score0.029

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.003
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0040.002
Bibliometrics0.0010.001
Science and technology studies0.0000.001
Scholarly communication0.0010.001
Open science0.0010.000
Research integrity0.0020.002
Insufficient payload (model declined to judge)0.0090.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.008
GPT teacher head0.280
Teacher spread0.272 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designRandomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2019
Admission routes1
Has abstractyes

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