Evidence map›Paper›PMID 39427500›Full record

ArticleThe American journal of emergency medicine2024

Trends and hospital practice variation for analgesia for children with sickle cell disease with vaso-occlusive pain episodes: An 11-year analysis.

Mohamed Eltorki, Matt Hall, Sriram Ramgopal, Pradip P Chaudhari, Oluwakemi Badaki-Makun, Chris A Rees, Kelly R Bergmann, Daniel J Shapiro, Frank Gonzalez, Timothy Phamduy and 1 more

Abstract read
In one paragraph

Article in The American journal of emergency medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

11 authors.

Mohamed EltorkiSection of Pediatric Emergency Medicine, Department of Pediatrics, Cumming School of Medicine, Alberta Children's Hospital Research Institute, University of Calgary, 28 Oki Drive NW, Calgary, Alberta T3B 6A8, USA; Division of Pediatric Emergency Medicine, Department of Pediatrics, Faculty of Health Sciences, McMaster University, 1200 Main St W, Hamilton, Ontario L8S 4L8, Canada. Electronic address: mmeltork@ucalgary.ca.
Matt HallChildren's Hospital Association, 6803 W 64th St, Overland Park, Kansas 66202, USA.
Sriram RamgopalDivision of Emergency Medicine, Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Ann & Robert H. Lurie Children's Hospital, 225 E Chicago Ave, Chicago, IL 60611, USA.
Pradip P ChaudhariDivision of Emergency and Transport Medicine, Children's Hospital Los Angeles, Department of Pediatrics, Keck School of Medicine of the University of Southern California, Children's Hospital Los Angeles, 4650 Sunset Blvd, Los Angeles, California 90027, USA.
Oluwakemi Badaki-MakunDivision of Pediatric Emergency Medicine, Department of Pediatrics, Johns Hopkins University School of Medicine, Center for Data Science in Emergency Medicine, Johns Hopkins University, Johns Hopkins Hospital, 1800 Orleans St, Baltimore, MD 21287, USA.
Chris A ReesDivision of Pediatric Emergency Medicine, Emory University School of Medicine, Children's Healthcare of Atlanta at Egleston, 1405 Clifton Rd NE, Atlanta, GA 30322, USA.
Kelly R BergmannDepartment of Emergency Medicine, Children's Minnesota, 915 E 25th St, Minneapolis, MN, USA.
Daniel J ShapiroDivision of Pediatric Emergency Medicine, University of California, UCSF Benioff Children's Hospital, 1825 Fourth St, San Francisco, California 94158, USA.
Frank GonzalezDivision of Emergency and Transport Medicine, Children's Hospital Los Angeles, Department of Pediatrics, Keck School of Medicine of the University of Southern California, Children's Hospital Los Angeles, 4650 Sunset Blvd, Los Angeles, California 90027, USA.
Timothy PhamduyDivision of Pediatric Emergency Medicine, Dayton Children's Hospital, Department of Pediatrics, Wright State University, Dayton Children's Hospital, 1 Children's Plaza, Dayton, OH 45404, USA.
Mark I NeumanDivision of Emergency Medicine, Boston Children's Hospital, 300 Longwood Ave, Boston, MA 02115, USA.

Funding

Advancing Approaches to Identify Young Children at Risk for Post-Discharge MortalityK23HL173694 · NHLBI · EMORY UNIVERSITY · PI Christopher A. Rees · 2024 to 2026
$585k
NHLBI NIH HHS K23 HL173694
6 · The paper itself

Abstract

This cross-sectional analysis of 86,111 visits for sickle cell disease and vaso-occlusive episodes (VOE) in U.S. pediatric emergency departments between 2013 and 2023 shows increased use of NSAIDs, ketamine, and acetaminophen, with unchanged opioid use. Hospitals with a higher volume of VOE visits more frequently administered opioids.

backgroundVaso-occlusive episodes (VOEs) are a hallmark of sickle cell disease (SCD), leading to frequent emergency department (ED) visits. Effective pain management is crucial, with guidelines recommending routine use of non-steroidal anti-inflammatory drugs (NSAIDs) with opioids, and emerging evidence supporting ketamine use. However, these recommendations are based on low-certainty evidence, and the impact of these guidelines on analgesia use over time remains unclear.

objectiveThis study aimed to analyze trends in analgesia use over an 11-year period in pediatric SCD patients presenting to U.S. EDs with VOE and assess variations in treatment across hospitals.

methodsA cross-sectional study was conducted using data from the Pediatric Health Information System covering 34 U.S. children's hospitals from January 1, 2013, to December 31, 2023. The primary outcomes were the proportions of visits where opioids, NSAIDs, acetaminophen, and/or ketamine were administered on the first calendar day of the initial visit. Secondary outcomes included the co-administration of NSAIDs with opioids. Logistic and linear regression models were used to assess trends and hospital-level variations.

resultsA total of 86,111 ED visits for VOE were analyzed. Opioids were administered in 82 % of encounters, NSAIDs in 72 %, acetaminophen in 17 %, and ketamine in 1 %. Co-administration of NSAIDs with opioids occurred in 59 % of the visits. Among discharged patients, there was a positive trend for NSAID use (slope: 1.68 %/year, 95 % CI: 0.91 %, 2.45 %) and NSAID-opioid co-administration (slope: 1.03 %/year, 95 % CI: 0.37 %, 1.69 %) over time. Acetaminophen use also increased over the study period (slope: 0.99 %/year, 95 % CI: 0.80 %, 1.17 %). In hospitalized patients, there was a significant upward trend for acetaminophen (slope: 1.29 %/year, 95 % CI: 0.69 %, 1.89 %) and ketamine (slope: 0.36 %/year, 95 % CI: 0.27 %, 0.45 %), while opioid use remained unchanged. Significant hospital-level variations were observed, with larger hospitals more likely to administer opioids but less likely to co-administer NSAIDs with opioids compared to medium-volume hospitals.

conclusionOver the past decade, the use of NSAIDs, acetaminophen, and ketamine has increased in the management of VOE in pediatric SCD patients, while opioid use remains consistent. The co-administration of NSAIDs and opioids has also increased, reflecting guideline adherence. Variations in analgesia practices across hospitals underscore the need for standardizing pain management strategies in this population.

Indexed as

AcetaminophenAnalgesics, OpioidAnemia, Sickle CellAnti-Inflammatory Agents, Non-SteroidalEmergency Service, HospitalKetaminePain ManagementPractice Patterns, Physicians'AdolescentAnalgesiaAnalgesicsChildChild, PreschoolCross-Sectional StudiesFemaleHumansAcetaminophenAnalgesicsAnalgesics, OpioidAnti-Inflammatory Agents, Non-SteroidalKetamineAnalgesic trendsHospital practice patternsMultimodal analgesiaNon-steroidal anti-inflammatory drugs (NSAIDs)Opioid usePain managementPediatric emergency medicineVaso-occlusive crisis

Identifiers

PMID39427500
PMCPMC12925324

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.