Integrating health status and survival data: the palliative effect of lung volume reduction surgery. Academic Article uri icon

Overview

abstract

  • RATIONALE: In studies that address health-related quality of life (QoL) and survival, subjects who die are usually censored from QoL assessments. This practice tends to inflate the apparent benefits of interventions with a high risk of mortality. Assessing a composite QoL-death outcome is a potential solution to this problem. OBJECTIVES: To determine the effect of lung volume reduction surgery (LVRS) on a composite endpoint consisting of the occurrence of death or a clinically meaningful decline in QoL defined as an increase of at least eight points in the St. George's Respiratory Questionnaire total score from the National Emphysema Treatment Trial. METHODS: In patients with chronic obstructive pulmonary disease and emphysema randomized to receive medical treatment (n = 610) or LVRS (n = 608), we analyzed the survival to the composite endpoint, the hazard functions and constructed prediction models of the slope of QoL decline. MEASUREMENTS AND MAIN RESULTS: The time to the composite endpoint was longer in the LVRS group (2 years) than the medical treatment group (1 year) (P < 0.0001). It was even longer in the subsets of patients undergoing LVRS without a high risk for perioperative death and with upper-lobe-predominant emphysema. The hazard for the composite event significantly favored the LVRS group, although it was most significant in patients with predominantly upper-lobe emphysema. The beneficial impact of LVRS on QoL decline was most significant during the 2 years after LVRS. CONCLUSIONS: LVRS has a significant effect on the composite QoL-survival endpoint tested, indicating its meaningful palliative role, particularly in patients with upper-lobe-predominant emphysema.

publication date

  • May 29, 2009

Research

keywords

  • Health Status
  • Palliative Care
  • Pneumonectomy
  • Pulmonary Disease, Chronic Obstructive
  • Pulmonary Emphysema

Identity

PubMed Central ID

  • PMC2724716

Scopus Document Identifier

  • 67749119775

Digital Object Identifier (DOI)

  • 10.1164/rccm.200809-1383OC

PubMed ID

  • 19483114

Additional Document Info

volume

  • 180

issue

  • 3