Evidence map›Paper›PMID 30251637›Full record

Observational studyThe Journal of pediatrics2018

Targeted Hydroxyurea Education after an Emergency Department Visit Increases Hydroxyurea Use in Children with Sickle Cell Anemia.

Lydia H Pecker, Sarah Kappa, Adam Greenfest, Deepika S Darbari, Robert Sheppard Nickel

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in The Journal of pediatrics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Design and Refinement of CyberCellJournal of medical extended reality · 2025
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Efficient Clinical Counseling for Sickle Cell Disease.Journal of the National Medical Association · 2021
    Review
  7. Article
  8. 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

5 authors at 3 institutions in 1 country.

Lydia H PeckerDivision of Hematology, Department of Pediatrics, Johns Hopkins University, Baltimore, MD.
Sarah KappaDivision of Hematology, Children's National Health System, Washington, DC.
Adam GreenfestGeorge Washington University School of Medicine and Health Sciences, Washington, DC.
Deepika S DarbariDivision of Hematology, Children's National Health System, Washington, DC; George Washington University School of Medicine and Health Sciences, Washington, DC.
Robert Sheppard NickelDivision of Hematology, Children's National Health System, Washington, DC; George Washington University School of Medicine and Health Sciences, Washington, DC. Electronic address: rnickel@childrensnational.org.
Children's National · USGeorge Washington University · USJohns Hopkins University · US

Funding

Rationale for the Pediatric Hematology and Transfusion Medicine Multidisciplinary Research Training Award (PHTMMRT) at Children?s NationalT32HL110841 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI Catherine M. Bollard, NAOMI L LUBAN · 2012 to 2026
$2.0M
NHLBI NIH HHS T32 HL110841
6 · The paper itself

Abstract

objectiveTo evaluate the impact of an initiative to increase hydroxyurea use among children with sickle cell anemia (SCA) who presented to the emergency department (ED). STUDY

designThis observational cohort study included children with SCA not taking hydroxyurea who presented to the ED with pain or acute chest syndrome and then attended a Quick-Start Hydroxyurea Initiation Project (Q-SHIP) session. A Q-SHIP session includes a hematologist-led discussion on hydroxyurea, a video of patients talking about hydroxyurea, and a direct offer to start hydroxyurea.

resultsOver 64 weeks, 112 eligible patients presented to the ED and 59% (n = 66) participated in a Q-SHIP session a median of 6 days (IQR 2, 20 days) after ED or hospital discharge; 55% of participants (n = 36) started hydroxyurea. After a median follow-up of 49 weeks, 83% (n = 30) of these participants continued hydroxyurea. Laboratory markers of hydroxyurea adherence were significantly increased from baseline: median mean corpuscular volume +8.6 fL (IQR 5.0, 17.7, P < .0001) and median hemoglobin F +5.7% (IQR 2.5, 9.8, P = .0001). Comparing Q-SHIP participants to nonparticipants, 12 weeks after ED visit, participants were more likely to have started hydroxyurea than nonparticipants (53% vs 20%, P = .0004) and to be taking hydroxyurea at last follow-up (50% vs 20%, P = .001). Two years after the implementation of Q-SHIP the overall proportion of eligible patients on hydroxyurea presenting to our ED increased from 56% to 80%, P = .0069.

conclusionsParticipation in a clinic to specifically address starting hydroxyurea after a SCA complication increases hydroxyurea use.

Indexed as

AdolescentAnemia, Sickle CellAntisickling AgentsChildChild, PreschoolEmergency Service, HospitalFemaleFollow-Up StudiesHumansHydroxyureaMalePatient Education as TopicRetrospective StudiesAntisickling AgentsHydroxyureahydroxyureapatient educationpediatricssickle cell disease

Identifiers

PMID30251637
PMCPMC6159227
OpenAlexW2811165539

What OpenQuestion holds

Textmetadata
LicenceTDM
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.