Literature DB >> 23560516

Clinical correlates of acute pulmonary events in children and adolescents with sickle cell disease.

Rabindra Paul1, Caterina P Minniti, Mehdi Nouraie, Lori Luchtman-Jones, Andrew Campbell, Sohail Rana, Onyinye Onyekwere, Deepika S Darbari, Olaid Ajayi, Manuel Arteta, Gregory Ensing, Craig Sable, Niti Dham, Gregory J Kato, Mark T Gladwin, Oswaldo L Castro, Victor R Gordeuk.   

Abstract

OBJECTIVES: We aimed to identify risk factors for acute pulmonary events in children and adolescents in the Pulmonary Hypertension and the Hypoxic Response in SCD (PUSH) study.
METHODS: Patients with hemoglobin SS (n = 376) and other sickle cell genotypes (n = 127) aged 3-20 yrs were studied at four centers in a cross-sectional manner. A subgroup (n = 293) was followed for a median of 21 months (range 9-35).
RESULTS: A patient-reported history of one or more acute pulmonary events, either acute chest syndrome (ACS) or pneumonia, was obtained in 195 hemoglobin SS patients (52%) and 51 patients with other genotypes (40%). By logistic regression, history of acute pulmonary events was independently associated with patient-reported history of asthma (P < 0.0001), older age (P = 0.001), >3 severe pain episodes in the preceding 12 months (P = 0.002), higher tricuspid regurgitation velocity (TRV) (P = 0.028), and higher white blood cell (WBC) count (P = 0.043) among hemoglobin SS patients. History of acute pulmonary events was associated with >3 severe pain episodes (P = 0.009) among patients with other genotypes. During follow-up, 43 patients (15%) had at least one new ACS episode including 11 without a baseline history of acute pulmonary events. History of acute pulmonary events (odds ratio 5.0; P < 0.0001) and younger age (odds ratio 0.9; P = 0.007) were independently associated with developing a new episode during follow-up.
CONCLUSIONS: Asthma history, frequent pain, and higher values for TRV and WBC count were independently associated with history of acute pulmonary events in hemoglobin SS patients and frequent pain was associated in those with other genotypes. Measures to reduce pain episodes and control asthma may help to decrease the incidence of acute pulmonary events in SCD.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Year:  2013        PMID: 23560516      PMCID: PMC3689858          DOI: 10.1111/ejh.12118

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  37 in total

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3.  Sickle cell chronic lung disease: prior morbidity and the risk of pulmonary failure.

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Authors:  E P Vichinsky; L D Neumayr; A N Earles; R Williams; E T Lennette; D Dean; B Nickerson; E Orringer; V McKie; R Bellevue; C Daeschner; E A Manci
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Review 10.  Sickle cell disease: wheeze or asthma?

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