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Indian Pediatrics

, Volume 52, Issue 2, pp 125–127 | Cite as

Slower rise of exhaled breath temperature in cystic fibrosis

  • Geetanjali Bade
  • Sumita Gupta
  • Sushil Kumar Kabra
  • Anjana TalwarEmail author
Research Paper

Abstract

Objective

To measure exhaled breath temperature in patients with cystic fibrosis.

Methods

17 patients (6–18 years) with cystic fibrosis and 15 age- and gender-matched healthy controls were recruited in this cross sectional study. Exhaled breath temperature was measured in subjects recruited in both the groups with a device X-halo and analyzed as plateau temperature achieved and rate of temperature rise.

Results

Patients with cystic fibrosis showed no significant difference in plateau temperature [34.4(32.3–34.6) versus 33.9 (33.0–34.4)°C; P=0.35] while mean (SEM.) rate of temperature rise was significantly less in patients [0.09 (0.01) versus 0.14 (0.02) Δ°C/s ; P=0.04] as compared to controls.

Conclusion

There was a slower rise of exhaled breath temperature in patients with cystic fibrosis whereas plateau temperature was not significantly different from controls.

Keywords

Cystic fibrosis Exhaled breath temperature Inflammation 

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Copyright information

© Indian Academy of Pediatrics 2015

Authors and Affiliations

  • Geetanjali Bade
    • 1
  • Sumita Gupta
    • 2
  • Sushil Kumar Kabra
    • 2
  • Anjana Talwar
    • 1
    Email author
  1. 1.Department of PhysiologyAll India Institute of Medical SciencesNew DelhiIndia
  2. 2.Department of PediatricsAll India Institute of Medical SciencesNew DelhiIndia

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