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Optimizing Inpatient Care for Lung Cancer Patients with Immune Checkpoint Inhibitor- Related Pneumonitis Using a Clinical Care Pathway Algorithm.
Brito-Dellan, Norman; Franco-Vega, Maria Cecilia; Ruiz, Juan Ignacio; Lu, Maggie; Sahar, Hadeel; Rajapakse, Pramuditha; Lin, Heather Y; Peterson, Christine; Alviarez, Daniel Leal; Altay, Haider; Tomy, Sophy; Manzano, Joanna-Grace Mayo.
Afiliación
  • Brito-Dellan N; The University of Texas MD Anderson Cancer Center.
  • Franco-Vega MC; The University of Texas MD Anderson Cancer Center.
  • Ruiz JI; The University of Texas MD Anderson Cancer Center.
  • Lu M; The University of Texas MD Anderson Cancer Center.
  • Sahar H; The University of Texas MD Anderson Cancer Center.
  • Rajapakse P; University of Massachusetts Chan Medical School.
  • Lin HY; The University of Texas MD Anderson Cancer Center.
  • Peterson C; The University of Texas MD Anderson Cancer Center.
  • Alviarez DL; The University of Texas MD Anderson Cancer Center.
  • Altay H; The University of Texas MD Anderson Cancer Center.
  • Tomy S; The University of Texas MD Anderson Cancer Center.
  • Manzano JM; The University of Texas MD Anderson Cancer Center.
Res Sq ; 2024 Apr 12.
Article en En | MEDLINE | ID: mdl-38659939
ABSTRACT

Purpose:

Immune checkpoint inhibitor-related pneumonitis (ICI-P) is a condition associated with high mortality, necessitating prompt recognition and treatment initiation. This study aimed to assess the impact of implementing a clinical care pathway algorithm on reducing the time to treatment for ICI-P.

Methods:

Patients with lung cancer and suspected ICI-P were enrolled, and a multi-modal intervention promoting algorithm use was implemented in two phases. Pre- and post-intervention analyses were conducted to evaluate the primary outcome of time from ICI-P diagnosis to treatment initiation.

Results:

Of the 82 patients admitted with suspected ICI-P, 73.17% were confirmed to have ICI-P, predominantly associated with non-small cell lung cancer (91.67%) and stage IV disease (95%). Pembrolizumab was the most commonly used immune checkpoint inhibitor (55%). The mean times to treatment were 2.37 days in the pre-intervention phase and, 3.07 days (p=0.46), and 1.27 days (p=0.40) in the post-intervention phases 1 and 2, respectively. Utilization of the immunotoxicity order set significantly increased from 0% to 27.27% (p = 0.04) after phase 2. While there were no significant changes in ICU admissions or inpatient mortality, outpatient pulmonology follow-ups increased statistically significantly, demonstrating enhanced continuity of care. The overall mortality for patients with ICI-P was 22%, underscoring the urgency of optimizing management strategies. Notably, all patients discharged on high-dose corticosteroids received appropriate gastrointestinal prophylaxis and prophylaxis against Pneumocystis jirovecii pneumonia infections at the end of phase 2.

Conclusion:

Implementing a clinical care pathway algorithm for ICI-P management standardizes care practices and enhances patient outcomes, underscoring the importance of structured approaches.
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