Evidence map›Paper›PMID 22463614›Full record

Trial reportBritish journal of haematology2012

Refining the value of secretory phospholipase A2 as a predictor of acute chest syndrome in sickle cell disease: results of a feasibility study (PROACTIVE).

Lori Styles, Carrie G Wager, Richard J Labotka, Kim Smith-Whitley, Alexis A Thompson, Peter A Lane, Lillian E C McMahon, Robin Miller, Susan D Roseff, Rathi V Iyer and 8 more

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in British journal of haematology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00951808 (Preventing Acute Chest Syndrome by Transfusion Feasibility Study), which is not on this map. Cited by 24 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 5 pooled it
2.4field-weighted citation impact, top 12% 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.

NCT00951808 nacompletednot on this map

Preventing Acute Chest Syndrome by Transfusion Feasibility Study( PROACTIVE Feasibility Study)

TypeinterventionalSponsorCarelon ResearchRan2009 to 2010Enrolled237ConditionsSickle Cell DiseaseArmsSingle blood transfusion, Standard care
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 5 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  6. Trial
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  18. Review
  19. Measuring success: utility of biomarkers in sickle cell disease clinical trials and care.Hematology. American Society of Hematology. Education Program · 2018
    Review
  20. 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

18 authors at 15 institutions in 1 country.

Lori StylesPediatric Sickle Cell Program, Children's Hospital & Research Center Oakland, CA, USA. lstyles@mail.cho.org
Carrie G Wager
Richard J Labotka
Kim Smith-Whitley
Alexis A Thompson
Peter A Lane
Lillian E C McMahon
Robin Miller
Susan D Roseff
Rathi V Iyer
Lewis L Hsu
Oswaldo L Castro
Kenneth I Ataga
Onyinye Onyekwere
Maureen Okam
Rita Bellevue
Scott T Miller
Sickle Cell Disease Clinical Research Network (SCDCRN)
Howard University · USBoston Medical Center · USBrigham and Women's Hospital · USChildren's Healthcare of Atlanta · USChildren's Hospital of Philadelphia · USChildren's National · USCommunity Health Systems - Dupont Hospital · USJackson Memorial Hospital · USLurie Children's Hospital · USNew England Research Institutes · USNewYork–Presbyterian Brooklyn Methodist Hospital · USSUNY Downstate Health Sciences University · USUniversity Health System · USUniversity of Illinois Chicago · USUniversity of North Carolina at Chapel Hill · US

Funding

INSTITUTIONAL CLINICAL AND TRANSLATIONAL SCIENCE AWARDUL1RR024134 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2006 to 2011
$70.4M
UNC CLINICAL AND TRANSLATIONAL SCIENCE AWARD: BPCAUL1RR025747 · NCRR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RUNGE, MARSCHALL S. · 2008 to 2011
$44.6M
WIRELESS CAPSULE ENDOSCOPY TO EVALUATE THE SMALL INTESTINE M01RR002172 · NCRR · CHILDREN'S HOSPITAL BOSTON · PI MANDELL, JAMES WILLIAM · 1985 to 2008
$16.0M
Data Coordinating Center for the Sickle Cell Disease Clinical Research NetworkU10HL083721 · NHLBI · NEW ENGLAND RESEARCH INSTITUTES, INC. · PI MCKINLAY, SONJA M · 2006 to 2008
$12.6M
NCRR NIH HHS MO1-RR02172NCRR NIH HHS U54 RR026076NCRR NIH HHS UL1-RR-024134NCRR NIH HHS UL1RR025747NHLBI NIH HHS U10 HL083721NHLBI NIH HHS U10HL083721
6 · The paper itself

Abstract

Acute chest syndrome (ACS) is defined as fever, respiratory symptoms and a new pulmonary infiltrate in an individual with sickle cell disease (SCD). Nearly half of ACS episodes occur in SCD patients already hospitalized, potentially permitting pre-emptive therapy in high-risk patients. Simple transfusion of red blood cells may abort ACS if given to patients hospitalized for pain who develop fever and elevated levels of secretory phospholipase A2 (sPLA2). In a feasibility study (PROACTIVE; ClinicalTrials.gov NCT00951808), patients hospitalized for pain who developed fever and elevated sPLA2 were eligible for randomization to transfusion or observation; all others were enrolled in an observational arm. Of 237 enrolled, only 10 were randomized; one of the four to receive transfusion had delayed treatment. Of 233 subjects receiving standard care, 22 developed ACS. A threshold level of sPLA2 ≥ 48 ng/ml gave optimal sensitivity (73%), specificity (71%) and accuracy (71%), but a positive predictive value of only 24%. The predictive value of sPLA2 was improved in adults and patients with chest or back pain, lower haemoglobin concentration and higher white blood cell counts, and in those receiving less than two-thirds maintenance fluids. The hurdles identified in PROACTIVE should facilitate design of a larger, definitive, phase 3 randomized controlled trial.

Indexed as

Acute Chest SyndromeAdolescentAdultAnemia, Sickle CellChildFeasibility StudiesFemaleHumansMalePhospholipases A2, SecretoryPrognosisYoung AdultPhospholipases A2, Secretory

Identifiers

PMID22463614
PMCPMC3349768
OpenAlexW1984063009

What OpenQuestion holds

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Registered trials

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.