4.6 Article

Increased Risk of Congestive Heart Failure Following Carbon Monoxide Poisoning

Journal

CIRCULATION-HEART FAILURE
Volume 14, Issue 4, Pages -

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCHEARTFAILURE.120.007267

Keywords

animals; carbon monoxide poisoning; echocardiography; epidemiology; heart failure

Funding

  1. Ministry of Health and Welfare, Taiwan R.O.C. [MOHW108-TDU-B-212-124014]
  2. Ministry of Science and Technology, Taiwan, R.O.C. [MOST 109-2314-B-384-005-MY3, MOST 108-2314-B-384010, MOST 108-2238-B-006-001-MY2]
  3. Chi Mei Medical Center [CMFHR10753]

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This study found an association between carbon monoxide poisoning (COP) and congestive heart failure (CHF) through epidemiological data from Taiwan and animal research, showing that COP patients have a higher risk of developing CHF, even persisting after 2 years, and these findings were supported by the animal model.
Background: Carbon monoxide poisoning (COP) is an important public health issue around the world. It may increase the risk of myocardial injury, but the association between COP and congestive heart failure (CHF) remains unclear. We conducted a study incorporating data from epidemiological and animal studies to clarify this issue. Methods: Using the National Health Insurance Database of Taiwan, we identified patients with COP diagnosed between 1999 and 2012 and compared them with patients without COP (non-COP cohort) matched by age and the index date at a 1:3 ratio. The comparison for the risk of CHF between the COP and non-COP cohorts was made using Cox proportional hazards regression. We also established a rat model to evaluate cardiac function using echocardiography and studied the pathological changes following COP. Results: The 20 942 patients in the COP cohort had a higher risk for CHF than the 62 826 members in the non-COP cohort after adjusting for sex and underlying comorbidities (adjusted hazard ratio, 2.01 [95% CI, 1.74-2.32]). The increased risk of CHF persisted even after 2 years of follow-up (adjusted hazard ratio, 1.85 [95% CI, 1.55-2.21]). In the animal model, COP led to a decreased left ventricular ejection fraction on echocardiography and damage to cardiac cells with remarkable fibrotic changes. Conclusions: Our epidemiological data showed an increased risk of CHF was associated with COP, which was supported by the animal study. We suggest close follow-up of cardiac function for patients with COP to facilitate early intervention and further studies to identify other long-term effects that have not been reported in the literature.

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