Evidence map›Paper›PMID 36602417›Full record

Trial reportEuropean journal of haematology2023

Time to pain relief: A randomized controlled trial in the emergency department during vaso-occlusive episodes in sickle cell disease.

Paula Tanabe, Hayden B Bosworth, Regina D Crawford, Jeffrey Glassberg, Christopher N Miller, Judith A Paice, Susan Silva

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in European journal of haematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. A comparison of the effect of patient-specific versus weight-based protocols to treat vaso-occlusive episodes in the emergency department.Academic emergency medicine : official journal of the Society for Academic Emergency Medicine · 2023
    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

7 authors at 4 institutions in 1 country.

Paula TanabeSchool of Nursing, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-9933-6425
Hayden B BosworthSchool of Nursing, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-6188-9825
Regina D CrawfordSchool of Medicine, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0003-3981-1591
Jeffrey GlassbergEmergency Medicine, Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Christopher N MillerDepartment of Emergency Medicine, University of Cincinnati, Cincinnati, Ohio, USA.ORCID https://orcid.org/0000-0003-0286-9212
Judith A PaiceHematology Oncology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-7534-1756
Susan SilvaSchool of Nursing, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-6368-4732
Duke University · USIcahn School of Medicine at Mount Sinai · USNorthwestern University · USUniversity of Cincinnati · US

Funding

Comparing Acute Pain Management Protocols for Patients with Sickle Cell DiseaseR34HL121224 · NHLBI · DUKE UNIVERSITY · PI TANABE, PAULA · 2014 to 2015
$745k
National Heart and Lung InstituteNHLBI NIH HHS R34 HL121224NHLBI NIH HHS R34 RHL121224A
6 · The paper itself

Abstract

objectiveCompare time to pain relief (minimum of a 13 mm and 30% reduction) during an Emergency Department (ED) visit among patients with sickle cell disease (SCD) experiencing severe pain associated with a vaso-occlusive episode who were randomized to receive either an individualized or weight-based pain protocol.

methodsA randomized controlled trial in two EDs. Adults with sickle cell disease. Research staff recorded pain scores every 30 min during an ED visit (up to 6 h in the ED) using a 0-100 mm visual analogue scale. Analysis included 122 visits, representing 49 patients (individualized: 61 visits, 25 patients; standard: 61 visits, 24 patients).

resultsPain reduction across 6-h was greater for the individualized compared to the standard protocol (protocol-by-time: p = .02; 6-h adjusted pain score comparison: Individualized: M = 29.2, SD = 38.8, standard: M = 45.3, SD = 35.6; p = .03, Cohen d = 0.43). Hazards models indicated a greater probability of 13 mm (HR = 1.54, 95% CI = 1.05, 2.27, p = .03) and 30% (HR = 1.71, 95% CI = 1.11, 2.63, p = .01) reduction in the individualized relative to the standard protocol.

conclusionsPatients who received treatment with an individualized protocol experienced a more rapid reduction in pain, including a 13 mm and 30% reduction in pain scores when compared to those that received weight-based dosing.

Indexed as

Anemia, Sickle CellPain ManagementAdultEmergency Service, HospitalHumansPainemergencypainsickle cellvaso-occlusive episodes

Identifiers

PMID36602417
PMCPMC10073280
OpenAlexW4313544476

What OpenQuestion holds

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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.