Low-Dose Morphine for Dyspnea in Terminally Ill Patients with Idiopathic Interstitial Pneumonias

Yoshinobu Matsuda1,2,3, Isseki Maeda4, Kazunobu Tachibana1,3

  • 11 Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center , Osaka, Japan .

Abstract

Insights

Continuous subcutaneous morphine effectively reduced dyspnea in terminally ill patients with idiopathic interstitial pneumonias (IIPs). This treatment improved breathing comfort without negatively impacting respiratory rate, offering a potential palliative option.

Area of Science:

  • Pulmonology
  • Palliative Care
  • Pharmacology

Background:

  • Dyspnea is a common and debilitating symptom in patients diagnosed with idiopathic interstitial pneumonias (IIPs).
  • Effective management of dyspnea is crucial for improving the quality of life in terminally ill patients with IIPs.

Purpose of the Study:

  • To evaluate the efficacy and safety of continuous subcutaneous morphine administration for managing dyspnea.
  • To assess the impact of morphine on dyspnea severity and respiratory rate in terminally ill IIP patients.

Main Methods:

  • Retrospective review of terminally ill idiopathic interstitial pneumonia patients receiving continuous subcutaneous morphine for dyspnea.
  • Dyspnea severity assessed via Numerical Rating Scale (NRS) and respiratory rate (RR) recorded pre-treatment and at 2 and 4 hours post-initiation.
  • Subgroup analysis conducted for patients with and without noninvasive positive pressure ventilation (NPPV).

Main Results:

  • Dyspnea NRS scores significantly decreased at 4 hours post-morphine initiation (p=0.04) compared to baseline.
  • Respiratory rate (RR) did not show significant changes at 2 or 4 hours post-treatment.
  • Patients not using NPPV experienced significant dyspnea improvement, while NPPV users did not show significant improvement.

Conclusions:

  • Continuous subcutaneous morphine may be a beneficial option for alleviating dyspnea in terminally ill IIP patients.
  • The observed benefits occurred without a significant reduction in respiratory rate, suggesting a favorable safety profile.
  • Further research may be warranted to explore optimal use in patients requiring ventilatory support.

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