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Can Red Blood Cell and Platelet Transfusions Have a Pathogenic Role in Bronchopulmonary Dysplasia?
Bahr, Timothy M; Snow, Gregory L; Christensen, Thomas R; Davenport, Patricia; Henry, Erick; Tweddell, Sarah M; Ilstrup, Sarah J; Yoder, Bradley A; Ohls, Robin K; Sola-Visner, Martha C; Christensen, Robert D.
Affiliation
  • Bahr TM; Division of Neonatology, Department of Pediatrics, University of Utah, Salt Lake City, UT; Department of Neonatology, Intermountain Health, Murray, UT. Electronic address: tim.bahr@imail.org.
  • Snow GL; Office of Research, Intermountain Health, Murray, UT.
  • Christensen TR; Division of Neonatology, Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Davenport P; Division of Newborn Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA.
  • Henry E; Department of Neonatology, Intermountain Health, Murray, UT.
  • Tweddell SM; Division of Neonatology, Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Ilstrup SJ; Transfusion Services and Department of Pathology, Intermountain Health, Murray, UT.
  • Yoder BA; Division of Neonatology, Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Ohls RK; Division of Neonatology, Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Sola-Visner MC; Division of Newborn Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA.
  • Christensen RD; Division of Neonatology, Department of Pediatrics, University of Utah, Salt Lake City, UT; Department of Neonatology, Intermountain Health, Murray, UT.
J Pediatr ; 265: 113836, 2024 Feb.
Article in En | MEDLINE | ID: mdl-37992802
OBJECTIVE: To evaluate whether transfusions in infants born preterm contribute to the pathogenesis of bronchopulmonary dysplasia (BPD). STUDY DESIGN: We conducted a multihospital, retrospective study seeking associations between red blood cell or platelet transfusions and BPD. We tabulated all transfusions administered from January 2018 through December 2022 to infants born ≤29 weeks or <1000 g until 36 weeks postmenstrual age and compared those with BPD grade. We performed a sensitivity analysis to assess the possibility of a causal relationship. We then determined whether each transfusion was compliant with restrictive guidelines, and we estimated effects fewer transfusions might have on future BPD incidence. RESULTS: Eighty-four infants did not develop BPD and 595 did; 352 developed grade 1 (mild), 193 grade 2 (moderate), and 50 grade 3 (severe). Transfusions were given at <36 weeks to 7% of those who did not develop BPD, 46% who did, and 98% who developed severe BPD. For every transfusion the odds of developing BPD increased by a factor of 2.27 (95% CI, 1.59-3.68; P < .001). Sensitivity analyses suggested that transfusions might contribute to BPD. Fifty-seven percent of red blood cell transfusions and 68% of platelet transfusions were noncompliant with new restrictive guidelines. Modeling predicted that complying with restrictive guidelines could reduce the transfusion rate by 20%-30% and the moderate to severe BPD rate by ∼4%-6%. CONCLUSIONS: Transfusions were associated with BPD incidence and severity. Lowering transfusion rates to comply with current restrictive guidelines might result in a small but meaningful reduction in BPD rates.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bronchopulmonary Dysplasia Limits: Humans / Infant / Newborn Language: En Journal: J Pediatr Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bronchopulmonary Dysplasia Limits: Humans / Infant / Newborn Language: En Journal: J Pediatr Year: 2024 Document type: Article Country of publication: United States