Longitudinal impact of screening colonoscopy on greenhouse gas emissions.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 19 03 2024
accepted: 02 07 2024
medline: 19 7 2024
pubmed: 19 7 2024
entrez: 19 7 2024
Statut: epublish

Résumé

Colonoscopy is the gold-standard screening test for colorectal cancer. However, it has come under scrutiny for its carbon footprint and contribution to greenhouse gas (GHG) emissions compared to other medical procedures. Notwithstanding, screening colonoscopies may have a positive effect on GHG emissions that is unknown. This study estimated the carbon emissions prevented by screening colonoscopies in the U.S. Using the reported number of screening colonoscopies performed annually in the U.S. and the absolute risk reduction (ARR) reported in the NorDICC trial, we calculated the expected minimum number of cancer treatment and surveillance visits prevented through screening based on the cancer stage. The average carbon emission averted per mile traveled was computed using the Environmental Protection Agency's (EPA) GHG equivalencies calculator. The final estimate of carbon emissions averted over a decade by screening colonoscopies performed in one year was determined. 6.3 million screening colonoscopies performed in one year prevent 1,134,000 colorectal cancers over a ten-year period. Of these, 38∙3% (434,254) are localized, 38∙8% (440,281) are regional, and 22∙9% (259,465) are metastatic disease. The minimum number of post-diagnosis visits prevented is 11 for stage I, ≥ 21 for stage II, ≥25 for stage III, and ≥ 20 for stage IV disease, comprised of diagnostic, surgical evaluation, chemotherapy, and surveillance visits. The total number of visits prevented by screening is 2,388,397 for stage I, 5,254,421 for stage II, 13,120,369 for stage III, and 9,210,972 for stage IV disease. Approximately 395 million miles of travel and 158,263 metric tons of CO2, equivalent to 177 million pounds of coal burned, 19 billion smartphones charged, or 18 million gallons of gasoline consumed, were saved over ten years through screening. Colorectal cancer screening decreases cancer-related GHG emissions and minimizes the environmental impact of cancer treatment.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
Colonoscopy is the gold-standard screening test for colorectal cancer. However, it has come under scrutiny for its carbon footprint and contribution to greenhouse gas (GHG) emissions compared to other medical procedures. Notwithstanding, screening colonoscopies may have a positive effect on GHG emissions that is unknown. This study estimated the carbon emissions prevented by screening colonoscopies in the U.S.
METHODS METHODS
Using the reported number of screening colonoscopies performed annually in the U.S. and the absolute risk reduction (ARR) reported in the NorDICC trial, we calculated the expected minimum number of cancer treatment and surveillance visits prevented through screening based on the cancer stage. The average carbon emission averted per mile traveled was computed using the Environmental Protection Agency's (EPA) GHG equivalencies calculator. The final estimate of carbon emissions averted over a decade by screening colonoscopies performed in one year was determined.
RESULT RESULTS
6.3 million screening colonoscopies performed in one year prevent 1,134,000 colorectal cancers over a ten-year period. Of these, 38∙3% (434,254) are localized, 38∙8% (440,281) are regional, and 22∙9% (259,465) are metastatic disease. The minimum number of post-diagnosis visits prevented is 11 for stage I, ≥ 21 for stage II, ≥25 for stage III, and ≥ 20 for stage IV disease, comprised of diagnostic, surgical evaluation, chemotherapy, and surveillance visits. The total number of visits prevented by screening is 2,388,397 for stage I, 5,254,421 for stage II, 13,120,369 for stage III, and 9,210,972 for stage IV disease. Approximately 395 million miles of travel and 158,263 metric tons of CO2, equivalent to 177 million pounds of coal burned, 19 billion smartphones charged, or 18 million gallons of gasoline consumed, were saved over ten years through screening.
CONCLUSION CONCLUSIONS
Colorectal cancer screening decreases cancer-related GHG emissions and minimizes the environmental impact of cancer treatment.

Identifiants

pubmed: 39028703
doi: 10.1371/journal.pone.0307133
pii: PONE-D-24-11124
doi:

Substances chimiques

Greenhouse Gases 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0307133

Informations de copyright

Copyright: © 2024 Yusuf et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests: Abhishek Kumar has stocks and stock options in Abbvie, AVEO, Cara Therapeutics, Celgene, Iovance Biotherapeutics, Eli Lilly, Viking Therapeutics, SPDR S and P Biotech ETF, Agenus, Amgen, BioTelemetry, Bristol-Myers Squibb, Bio-Path Holdings, Inc, ChemBio Diagnostic Systems, CRISPR therapeutics, CVS Health, Editas Medicine, Five Prime Therapeutics, Immunomedics, Livongo, Medtronic, Northwest Biotherapeutics, PTC Therapeutics, Regeneron, Teladoc, Trovagene, Vertex, Globus Medical, Acadia Pharmaceuticals, ADMA Biologics, BeyondSpring Pharmaceuticals, Cardiff Oncology, IDEXX Laboratories, AIkido Pharma, Albireo Pharma, Blueprint Medicines, Precision, Biosciences, Novavax, Poseida Therapeutics, Surgalign, AstraZeneca, Contrafect, CryoLife, Geron, Johnson & Johnson/Janssen, Kronos, Ontrak, Spectrum Pharmaceuticals, Uniqure, Renalytix AI PLC, Sierra Oncology, Vericel, Viatris, CUE Biopharma, DermTech, Gevo, Jazz Pharmaceuticals, Purple Biotech, Protagonist Therapeutics, Schrodinger, and Sensei Biotherapeutics. He also received travel and hotel funding for a lecture from the American Society of Clinical Oncology. All other authors have no competing interests.

Auteurs

Hasiya Yusuf (H)

Department of Internal Medicine, Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, New York, United States of America.

Vinita Gupta (V)

Division of Hematology &Oncology, Department of Internal Medicine, Jacobi Medical Center, New York City Health and Hospital Corporation, Bronx, New York, United States of America.

Ikponmwosa Osaghae (I)

Department of Epidemiology, MD Anderson Cancer Center, The University of Texas, Houston, Texas, United States of America.

Abhishek Kumar (A)

Division of Hematology &Oncology, Department of Internal Medicine, Jacobi Medical Center, New York City Health and Hospital Corporation, Bronx, New York, United States of America.
Division of Hematology & Oncology, Department of Internal Medicine, Albert Einstein College of Medicine, Bronx, NY, United States of America.

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