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PLoS One. 2014 May 30;9(5):e97462. doi: 10.1371/journal.pone.0097462. eCollection 2014.

Severe nocturnal and postexercise hypoxia in children and adolescents with sickle cell disease.

Author information

1
Pediatric Emergency Department, Hospital Necker, APHP, Paris, France.
2
Paris Descartes University, Paris, France; Department of Biostatistics, Hospital Necker, APHP, Paris, France.
3
Pediatrics Department and Sickle Cell Clinic, Hospital Necker, AP-HP, Paris, France.
4
Pediatric Pneumology and Allergology Department, Hospital Necker, APHP, Paris, France.
5
Paris Descartes University, Paris, France; Pediatric Cardiology Department, M3C-Necker, AP-HP, Paris, Paris Descartes University, France.
6
Paris Descartes University, Paris, France; Pediatrics Department and Sickle Cell Clinic, Hospital Necker, AP-HP, Paris, France.

Abstract

Hypoxia is a common feature in children with sickle cell disease (SCD) that is inconsistently associated with painful crises and acute chest syndrome. To assess the prevalence and risk factors of hypoxia, we recorded daytime, nocturnal, and postexercise pulse oximetry (SpO2) values in 39 SCD patients with a median age of 10.8 years. Median daytime SpO2 was 97% (range, 89%-100%), and 36% of patients had daytime hypoxia defined as SpO2<96%. Median nocturnal SpO2 was 94.7% (range, 87.7%-99.5%), 50% of patients had nocturnal hypoxia defined as SpO2≤93%, and 11(37%) patients spent more than 10% of their total sleep time with SpO2<90%. Median postexercise SpO2 was 94% (range, 72%-100%) and 44.7% of patients had postexercise hypoxia defined as an SpO2 decrease ≥3% after a 6-minute walk test. Among patients with normal daytime SpO2, 35% had nocturnal and 42% postexercise hypoxia. Compared to 9 patients without daytime, nocturnal, or postexercise hypoxia, 25 patients with hypoxia under at least one of these three conditions had greater anemia severity (P = 0.01), lower HbF levels (P = 0.04), and higher aspartate aminotransferase levels (P = 0.03). Males predominated among patients with postexercise hypoxia (P = 0.004). Hypoxia correlated neither with painful crises nor with acute chest syndrome. Of 32 evaluable patients, 6 (18.8%) had a tricuspid regurgitation velocity ≥2.6 m/s, and this feature was associated with anemia (P = 0.044). Median percentage of the predicted distance covered during a 6-minute walk test was 86% [46-120]; the distance was negatively associated with LDH (P = 0.044) and with a past history of acute chest syndrome (P = 0.009). In conclusion, severe episodes of nocturnal and postexercise hypoxia are common in children with SCD, even those with normal daytime SpO2.

PMID:
24878576
PMCID:
PMC4039516
DOI:
10.1371/journal.pone.0097462
[Indexed for MEDLINE]
Free PMC Article

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