Time-related decrease in diffusion capacity in HIV-infected patients with impaired immune function

Scand J Infect Dis. 1992;24(1):29-34. doi: 10.3109/00365549209048397.

Abstract

The purpose of this study was to investigate acute and time-related changes in lung function, i.e. forced expiratory volume in 1 second (FEV1), vital capacity (VC) and transfer factor (KCO) in HIV-infected patients with CD4 cell counts less than 400 x 10(6)/l. 66 males with no history of HIV-related pulmonary symptoms participated in a prospective lung function study for 9 months with 3-month intervals between examinations. 15/66 patients (23%) developed acute pulmonary symptoms, i.e. dyspnea (n = 12), cough (n = 13), fever greater than 38 degrees C (n = 13) and interstitial infiltrates on the X-ray (n = 9). Among the 51 asymptomatic patients, a significant time-related decrease in KCO (median decrease of 7%) was found, whereas no significant change in FEV1 or VC was observed during the study. Baseline KCO, i.e. KCO at entry, was found to be significantly higher in the asymptomatic patients (102% predicted (pred.) than in those patients who developed pneumonia (88% pred.). Development of pulmonary symptoms was both followed by a significant decrease in KCO (median decrease 17%), FEV1 and VC. We therefore conclude that HIV-infected patients with impaired immune function have in the absence of pulmonary symptoms a decrease in KCO. In case of pneumonia an acute decrease in both KCO, FEV1 and VC occurs.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Bronchoscopy
  • CD4-Positive T-Lymphocytes
  • Forced Expiratory Volume
  • HIV Infections / complications
  • HIV Infections / immunology*
  • HIV Infections / physiopathology
  • Humans
  • Leukocyte Count
  • Lung Volume Measurements
  • Male
  • Middle Aged
  • Pneumonia / complications
  • Pneumonia / physiopathology
  • Prospective Studies
  • Pulmonary Diffusing Capacity
  • Respiratory Function Tests*
  • Time Factors
  • Transfer Factor / analysis
  • Vital Capacity

Substances

  • Transfer Factor