The impact of the California state lockdown during the COVID-19 pandemic on management of patients with pancreatic ductal adenocarcinoma.

COVID‐19 healthcare access lockdown pancreatic cancer pandemic

Journal

Journal of surgical oncology
ISSN: 1096-9098
Titre abrégé: J Surg Oncol
Pays: United States
ID NLM: 0222643

Informations de publication

Date de publication:
18 Jun 2024
Historique:
received: 06 05 2024
accepted: 12 05 2024
medline: 19 6 2024
pubmed: 19 6 2024
entrez: 19 6 2024
Statut: aheadofprint

Résumé

The SARS-COVID-19 pandemic significantly limited healthcare access. We sought to evaluate whether California's lockdown in March 2020 affected staging and time to treatment of pancreatic ductal adenocarcinoma (PDAC). We hypothesized that patients diagnosed after the lockdown would have longer time to treatment and higher stage at presentation. We retrospectively identified and categorized 1294 patients presenting to five University of California healthcare systems with a new diagnosis of PDAC into "pre-lockdown" and "post-lockdown" groups based on timing of pathologic diagnosis. In the 12 months pre-lockdown, 835 patients were diagnosed with PDAC, and 459 patients in the 6 months post-lockdown. Demographics, staging, and treatment type were similar between eras. There was a decreased male:female ratio post- versus pre-lockdown (0.97 vs. 1.25; p = 0.03). Time from symptom onset to first treatment was significantly increased among females post-lockdown (p = 0.001). However, overall time from diagnosis to first treatment was shorter in the post-lockdown era (median 23 vs. 26 days, p < 0.001). The COVID-19 lockdown did not significantly delay initial presentation, diagnosis, or treatment of newly diagnosed PDAC patients. Time from diagnosis to first treatment was shorter post-lockdown. Reduced healthcare utilization for minor complaints and increased telehealth utilization may have contributed.

Sections du résumé

BACKGROUND AND OBJECTIVES OBJECTIVE
The SARS-COVID-19 pandemic significantly limited healthcare access. We sought to evaluate whether California's lockdown in March 2020 affected staging and time to treatment of pancreatic ductal adenocarcinoma (PDAC). We hypothesized that patients diagnosed after the lockdown would have longer time to treatment and higher stage at presentation.
METHODS METHODS
We retrospectively identified and categorized 1294 patients presenting to five University of California healthcare systems with a new diagnosis of PDAC into "pre-lockdown" and "post-lockdown" groups based on timing of pathologic diagnosis.
RESULTS RESULTS
In the 12 months pre-lockdown, 835 patients were diagnosed with PDAC, and 459 patients in the 6 months post-lockdown. Demographics, staging, and treatment type were similar between eras. There was a decreased male:female ratio post- versus pre-lockdown (0.97 vs. 1.25; p = 0.03). Time from symptom onset to first treatment was significantly increased among females post-lockdown (p = 0.001). However, overall time from diagnosis to first treatment was shorter in the post-lockdown era (median 23 vs. 26 days, p < 0.001).
CONCLUSIONS CONCLUSIONS
The COVID-19 lockdown did not significantly delay initial presentation, diagnosis, or treatment of newly diagnosed PDAC patients. Time from diagnosis to first treatment was shorter post-lockdown. Reduced healthcare utilization for minor complaints and increased telehealth utilization may have contributed.

Identifiants

pubmed: 38894577
doi: 10.1002/jso.27695
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
Pays : United States

Informations de copyright

© 2024 The Author(s). Journal of Surgical Oncology published by Wiley Periodicals LLC.

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Auteurs

Parisa Oviedo (P)

University of California San Diego, Moores Cancer Center, La Jolla, California, USA.

Shohei Burns (S)

University of California San Francisco, San Francisco, California, USA.

Wen-Pin Chen (WP)

University of California Irvine, Irvine, California, USA.

Hanna K Mandl (HK)

University of California Los Angeles, Los Angeles, California, USA.

Claudia Rosso (C)

University of California Irvine, Irvine, California, USA.

Niloofar Radgoudarzi (N)

University of California San Diego, Moores Cancer Center, La Jolla, California, USA.

Anna Crosetti (A)

University of California San Francisco, San Francisco, California, USA.

Steven Zamora (S)

University of California San Diego, Moores Cancer Center, La Jolla, California, USA.

Lauren M Perry (LM)

University of California Davis, Davis, California, USA.

Richard J Bold (RJ)

Mayo Clinic Comprehensive Cancer Center, Phoenix, Arizona, USA.

Amanda N Labora (AN)

University of California Los Angeles, Los Angeles, California, USA.

Timothy R Donahue (TR)

University of California Los Angeles, Los Angeles, California, USA.

Ajay Maker (A)

University of California San Francisco, San Francisco, California, USA.

Jennifer B Valerin (JB)

University of California Irvine, Irvine, California, USA.

Jason A Zell (JA)

University of California Irvine, Irvine, California, USA.

Rebekah R White (RR)

University of California San Diego, Moores Cancer Center, La Jolla, California, USA.

Classifications MeSH