Evidence map›Paper›PMID 23176402›Full record

Trial reportTransfusion2013

Patients with sickle cell anemia on simple chronic transfusion protocol show sex differences for hemodynamic and hematologic responses to transfusion.

Jon A Detterich, Suvimol Sangkatumvong, Roberta Kato, Ani Dongelyan, Adam Bush, Michael Khoo, Herbert J Meiselman, Thomas D Coates, John C Wood

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Transfusion, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Sex determines cardiac and renal Vulnerability to chronic hemoglobin toxicity.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026
    Article
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Observational
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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

9 authors at 2 institutions in 1 country.

Jon A DetterichDivision of Cardiology, Division of Pediatric Pulmonology, Division of Hematology, Children's Hospital Los Angeles, Los Angeles, California 90027, USA. jdetterich@chla.usc.edu
Suvimol Sangkatumvong
Roberta Kato
Ani Dongelyan
Adam Bush
Michael Khoo
Herbert J Meiselman
Thomas D Coates
John C Wood
Children's Hospital of Los Angeles · USUniversity of Southern California · US

Funding

ZOPOLRESTAT IN NORMOTENSIVE, TYPE 1 DIA WITH INCIPIENT NEPHROPATHYM01RR000043 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZAIA, JOHN A · 1985 to 2010
$76.4M
Southern California Clinical and Translational Science InstituteUL1TR000130 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BUCHANAN, THOMAS A · 2012 to 2015
$36.0M
Childrens Hospital Los Angeles Child Health Research Development AwardK12HD052954 · NICHD · CHILDREN'S HOSPITAL OF LOS ANGELES · PI WILLIAMS, ROBERTA GAY · 2006 to 2017
$4.0M
Sickle Cell Scholar ComponentU54HL090511 · NHLBI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI COATES, THOMAS DUANE · 2008 to 2011
$2.6M
Human models of sickle cell vascular damageR01HL071801 · NHLBI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI COATES, THOMAS DUANE · 2003 to 2006
$1.1M
Iron-mediated vascular disease in sickle cell disease.RC1HL099412 · NHLBI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI WOOD, JOHN C · 2009 to 2010
$995k
NCATS NIH HHS UL1 TR000130NCRR NIH HHS M01 RR000043NCRR NIH HHS NIH RR00043-43NHLBI NIH HHS 5 RC1 HL099412-01NHLBI NIH HHS NIH 1 U54 HL090511-01NHLBI NIH HHS R01 HL071801NHLBI NIH HHS RC1 HL099412NHLBI NIH HHS U54 HL090511NICHD NIH HHS K12 HD052954
6 · The paper itself

Abstract

backgroundChronic transfusion therapy (CTT) is a mainstay for stroke prophylaxis in sickle cell anemia, but its effects on hemodynamics are poorly characterized. Transfusion improves oxygen-carrying capacity, reducing demands for high cardiac output, while decreasing hemoglobin (Hb)S%, reticulocyte count, and hemolysis. We hypothesized that transfusion would improve oxygen-carrying capacity, but that would be counteracted by a decrease in cardiac output due to increased hematocrit (Hct) and vascular resistance, leaving oxygen delivery unchanged. STUDY DESIGN AND

methodsTo test this hypothesis, we examined patients on CTT immediately before transfusion and again 12 to 120 hours after transfusion, using echocardiography and near infrared spectroscopy.

resultsComparable increases in Hb and Hct and decreases in reticulocyte count and HbS with transfusion were observed in all patients, but males had a larger rebound of HbS%, reticulocyte count, and free Hb levels between transfusions. In males, transfusion decreased heart rate by 12%, stroke volume by 15%, and cardiac index by 24% while estimates for pulmonary and systemic vascular resistance increased, culminating in 6% decrease in oxygen delivery. In contrast, stroke volume and cardiac index and systemic and pulmonary vascular resistance did not change in women after transfusion, such that oxygen delivery improved 17%.

conclusionIn our sample population, males exhibit a paradoxical reduction in oxygen delivery in response to transfusion because the increase in vascular resistance is larger than the increase in oxygen capacity. This may result from an inability to adequately suppress their HbS% between transfusion cycles.

Indexed as

Blood TransfusionHemodynamicsAdolescentAdultAnemia, Sickle CellBiomarkersBlood Cell CountChildClinical ProtocolsCross-Sectional StudiesEchocardiographyFemaleHematocritHemoglobin, SickleHumansLinear ModelsBiomarkersHemoglobin, Sickle

Identifiers

PMID23176402
PMCPMC3957479
OpenAlexW2117154557

What OpenQuestion holds

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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.