Evidence map›Paper›PMID 19255296›Full record

ArticleChest2009

Soluble p-selectin and the risk of primary graft dysfunction after lung transplantation.

Steven M Kawut, Jeffrey Okun, Daichi Shimbo, David J Lederer, Joao De Andrade, Vibha Lama, Ashish Shah, Aaron Milstone, Lorraine B Ware, Ann Weinacker and 3 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Chest, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Genetic variation in the prostaglandin E2 pathway is associated with primary graft dysfunction.American journal of respiratory and critical care medicine · 2014
    Trial
  2. Lung rehabilitation using xenogeneic cross-circulation does not lead to hyperacute rejection in a human lung transplantation model.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2025
    Article
  3. Article
  4. Review
  5. Risk of primary graft dysfunction following lung transplantation in selected adults with connective tissue disease-associated interstitial lung disease.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2021
    Article
  6. Article
  7. Review
  8. Protein biomarkers associated with primary graft dysfunction following lung transplantation.American journal of physiology. Lung cellular and molecular physiology · 2017
    Review
  9. Article
  10. Article
  11. Primary graft dysfunction.Seminars in respiratory and critical care medicine · 2013
    Review
  12. Clinical risk factors for primary graft dysfunction after lung transplantation.American journal of respiratory and critical care medicine · 2013
    Article
  13. Update on lung transplantation: programmes, patients and prospects.European respiratory review : an official journal of the European Respiratory Society · 2012
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Elevated plasma clara cell secretory protein concentration is associated with high-grade primary graft dysfunction.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2011
    Article
  19. 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

13 authors at 7 institutions in 1 country.

Steven M KawutDepartment of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA. Electronic address: kawut@mail.med.upenn.edu.
Jeffrey OkunDepartment of Medicine, Columbia University College of Physicians and Surgeons, New York City, NY.
Daichi ShimboDepartment of Medicine, Columbia University College of Physicians and Surgeons, New York City, NY.
David J LedererDepartment of Medicine, Columbia University College of Physicians and Surgeons, New York City, NY.
Joao De AndradeDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL.
Vibha LamaDepartment of Medicine, University of Michigan, Ann Arbor, MI.
Ashish ShahDepartment of Surgery, Johns Hopkins University, Baltimore, MD.
Aaron MilstoneDepartment of Medicine, Vanderbilt University, Nashville, TN.
Lorraine B WareDepartment of Medicine, Vanderbilt University, Nashville, TN.
Ann WeinackerDepartment of Medicine, Stanford University, Stanford, CA.
Ejigayehu DemissieDepartment of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA.
Jason D ChristieDepartment of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA.
Lung Transplant Outcomes Group
Columbia University · USUniversity of Pennsylvania · USVanderbilt University · USJohns Hopkins University · USStanford University · USUniversity of Alabama at Birmingham · USUniversity of Michigan–Ann Arbor · US

Funding

Clinical Risk Factors for Primary Graft DysfunctionR01HL087115 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHRISTIE, JASON D · 2007 to 2017
$7.1M
Biomarker Profiles in the Diagnosis/Prognosis of ARDSU01HL081332 · NHLBI · VANDERBILT UNIVERSITY · PI WARE, LORRAINE B · 2005 to 2008
$6.0M
Genetics of primary graft dysfunctionR01HL081619 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHRISTIE, JASON D · 2007 to 2011
$3.9M
RISK FACTORS &BIOMARKERS OF OX STRESS IN GRAFT FAILUREK23HL004243 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHRISTIE, JASON D · 2000 to 2004
$652k
Neurohormonal Activation in Pulmonary HypertensionK23HL067771 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KAWUT, STEVEN M · 2001 to 2005
$641k
NHLBI NIH HHS HL04243NHLBI NIH HHS HL067771NHLBI NIH HHS HL081332NHLBI NIH HHS HL081619NHLBI NIH HHS HL087115NHLBI NIH HHS K23 HL067771NHLBI NIH HHS L30 HL086095NHLBI NIH HHS R01 HL081619NHLBI NIH HHS R01 HL087115NHLBI NIH HHS U01 HL081332
6 · The paper itself

Abstract

backgroundPlatelet activation with subsequent neutrophilic adherence to the vasculature initiates ischemia-reperfusion injury. We hypothesized that higher plasma P-selectin levels reflecting platelet activation would therefore be associated with primary graft dysfunction (PGD) after lung transplantation.

methodsIn a prospective, multicenter cohort study of 376 patients who had undergone lung transplantation between 2002 and 2007, we measured soluble P-selectin levels before lung transplantation and at 6 and 24 h after lung reperfusion in 20 patients with grade III PGD (Pao(2)/fraction of inspired oxygen, < 200 mm Hg [with alveolar infiltrates seen on chest radiographs]) at 72 h after transplantation and 61 control subjects without PGD.

resultsHigher postoperative soluble P-selectin levels were associated with an increased risk of PGD at 72 h after transplantation (odds ratio [OR] per 1 natural log increase in soluble P-selectin at 6 h after lung allograft reperfusion, 3.5; 95% confidence interval [CI], 1.01 to 11.8; p = 0.048) and at 24 h after lung allograft reperfusion (OR, 4.8; 95% CI, 1.4 to 16.1; p = 0.01). Higher preoperative mean pulmonary artery pressure and the use of cardiopulmonary bypass were also associated with an increased risk of PGD.

conclusionHigher postoperative soluble P-selectin levels were associated with an increased risk of PGD at 72 h following lung transplantation.

Indexed as

AdultAgedCase-Control StudiesCohort StudiesFemaleHumansLogistic ModelsLung DiseasesLung TransplantationMaleMiddle AgedPlatelet ActivationPrimary Graft DysfunctionP-SelectinRisk FactorsP-Selectin

Identifiers

PMID19255296
PMCPMC2821286
OpenAlexW1600451925

What OpenQuestion holds

Textmetadata
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.