Title
Author
DOI
Article Type
Special Issue
Volume
Issue
QT interval prolongation during carbon monoxide poisoning is a predictor of late cardiac and neurological complications
1Department of Emergency Medicine, Istanbul Haydarpasa Numune Training and Research Hospital, 34668 Istanbul, Turkey
2Department of Emergency Medicine, Istanbul Bagcilar Training and Research Hospital, 34200 Istanbul, Turkey
3Department of Emergency Medicine, Istanbul Sisli Etfal Training and Research Hospital, 34396 Istanbul, Turkey
4Department of Emergency Medicine, Istanbul Gaziosmanpasa Training and Research Hospital, 34255 Istanbul, Turkey
5Department of Emergency Medicine, Istanbul Sancaktepe Sehit Prof. Dr. İlhan Varank Training and Research Hospital, 34785 Istanbul, Turkey
DOI: 10.22514/sv.2025.154
Submitted: 03 June 2025 Accepted: 10 July 2025
Online publish date: 13 October 2025
*Corresponding Author(s): Abuzer Coskun E-mail: abuzer.coskun@sbu.edu.tr
Background: Carbon monoxide (CO) poisoning late complications and deaths are mainly associated with myocardia and central nervous system damage. The aim of this study was to examine how serum carboxyhemoglobin levels relate to acute QT interval prolongation (QTc) on electrocardiograms, delayed cardiac syndrome (DCS), delayed neuropsychiatric issues (DNS), and death in acute carbon monoxide poisoning. Methods: In this retrospective analysis, 1924 patients who presented to the emergency department with a preliminary diagnosis of CO poisoning between 2018 and 2023 were included in the study. Patients’ QTc, serum carboxyhemoglobin, and late complications of CO poisoning were recorded. Additionally, DNS, DCS, and 30-day and one-year mortality rates were assessed. Results: The mean (standard deviation) age of the 1924 patients included in the study was 45 (14.7) years, and 837 (43.5%) were female. Troponin I was 0.3 (0.6) ng/dL, glucose was 125.1 (37.0) mg/dL, and the mean carboxyhemoglobin was 31.0 (10.5%) (p < 0.001). The QTc was 404.4 (38.3) ms in the group without complications of CO poisoning, 494.9 (23.9) ms in the DCS group, 481.2 (16.3) ms in the DNS group, and 497.0 (15.4) ms in the patients who died (p < 0.001). All-cause 30-day mortality rate was 127 (6.6%) (p = 0.006), while the 180-day mortality rate was 179 (9.3%). At a multivariate regression analysis, the QTc was an independent predictor of late complications and mortality due to CO poisoning, (p < 0.001). The ability to correctly identify DCS, DNS, and death in patients with a prolonged QTc was 90.3–92.7 (Area Under Curve (AUC): 0.93, 95% CI: 0.91–0.95), 89.6–90.8 (AUC: 0.87, 95% CI: 0.85–0.89), and 94.1–96.4 (AUC: 0.94, 95% CI: 0.92–0.95), respectively (p < 0.001). Conclusions: QTc in the acute phase of carbon monoxide poisoning may be an important in predicting late cardiac complications and neuropsychiatric sequelae.
Carbon monoxide poisoning; Emergency department; Cardiac complications; Neuropsychiatric sequelae; QT interval prolongation
Mustafa Ahmet Afacan,Abuzer Coskun,Burak Demirci,Ertugrul Altinbilek,Mustafa Calik,Derya Ozturk,Burcu Bayramoglu. QT interval prolongation during carbon monoxide poisoning is a predictor of late cardiac and neurological complications. Signa Vitae. 2025.doi:10.22514/sv.2025.154.
[1] Mattiuzzi C, Lippi G. Worldwide epidemiology of carbon monoxide poisoning. Human & Experimental Toxicology. 2020; 39: 387–392.
[2] Öz E, Küçükkelepçe O, Kurt O, Vural A. Carbon monoxide poisoning: beyond survival—mortality, morbidities, and risk factors, a Turkey sample. PeerJ. 2023; 11: e16093.
[3] Nazari J, Dianat I, Stedmon A. Unintentional carbon monoxide poisoning in Northwest Iran: a 5-year study. Journal of Forensic and Legal Medicine. 2010; 17: 388–391.
[4] McMahon K, Launico MV. Carbon monoxide toxicity. StatPearls: Treasure Island (FL). 2025.
[5] Rose JJ, Wang L, Xu Q, McTiernan CF, Shiva S, Tejero J, et al. Carbon monoxide poisoning: pathogenesis, management, and future directions of therapy. American Journal of Respiratory and Critical Care Medicine. 2017; 195: 596–606.
[6] Uysal C, Celik S, Duzgun Altuntas A, Kandemir E, Kaya M, Karapirli M, et al. Carbon monoxide-related deaths in Ankara between 2001 and 2011. Inhalation Toxicology. 2013; 25: 102–106.
[7] Cho DH, Thom SR, Son JW, Ko SM, Cha YS. Practical recommendations for the evaluation and management of cardiac injury due to carbon monoxide poisoning. JACC: Heart Failure. 2024; 12: 1343–1352.
[8] Savioli G, Gri N, Ceresa IF, Piccioni A, Zanza C, Longhitano Y, et al. Carbon monoxide poisoning: from occupational health to emergency medicine. Journal of Clinical Medicine. 2024; 13: 2466.
[9] Eroglu M, Uz O, Isilak Z, Yalcin M, Yildirim AO, Kardesoglu E. Carbon monoxide poisoning increases Tpeak-Tend dispersion and QTc dispersion. Cardiovascular Journal of Africa. 2014; 25: 106–109.
[10] Olatunde O, Raj V, Tambe V, Szombathy T. Carbon monoxide poisoning and its effect on QTc prolongation. Journal of Cardiology Cases. 2020; 22: 19–21.
[11] Al-Busaidi S, Al Shandoudi L, Al-Ghafri M, Shoaib M. The unusual presentation of non-ST elevation myocardial infarction following acute carbon monoxide poisoning in an elderly female: a case report. Journal of the Oman Medical Association. 2024; 1: 81–86.
[12] Stephenson L, Tiemensma M, Van Den Heuvel C, Byard RW. The spectrum of presentations of unintentional carbon monoxide poisoning. Medicine, Science and the Law. 2024; 64: 310–318.
[13] Afzal M, Agarwal S, Elshaikh RH, Babker AMA, Choudhary RK, Prabhakar PK, et al. Carbon monoxide poisoning: diagnosis, prognostic factors, treatment strategies, and future perspectives. Diagnostics. 2025; 15: 581.
[14] Ran T, Nurmagambetov T, Sircar K. Economic implications of unintentional carbon monoxide poisoning in the United States and the cost and benefit of CO detectors. The American Journal of Emergency Medicine. 2018; 36: 414–419.
[15] Bleecker ML. Carbon monoxide intoxication. Handbook of Clinical Neurology. 2015; 131: 191–203.
[16] Kim H, Choi S, Park E, Yoon E, Min Y, Lampotang S. Serum markers and development of delayed neuropsychological sequelae after acute carbon monoxide poisoning: anion gap, lactate, osmolarity, S100B protein, and interleukin-6. Clinical and Experimental Emergency Medicine. 2018; 5: 185–191.
[17] Hydzik P, Francik R, Francik S, Gomółka E, Eker ED, Krośniak M, et al. The critical assessment of oxidative stress parameters as potential biomarkers of carbon monoxide poisoning. International Journal of Molecular Sciences. 2023; 24: 10784.
[18] Kuroda H, Fujihara K, Kushimoto S, Aoki M. Novel clinical grading of delayed neurologic sequelae after carbon monoxide poisoning and factors associated with outcome. Neurotoxicology. 2015; 48: 35–43.
[19] Freitas C, Salazar L, Duarte-Costa S, Fraga C, Monteiro S, Camacho Ó. Hyperbaric medicine in pediatrics—reality of a Portuguese reference center. Paulista Journal of Pediatrics. 2024; 43: e2023230.
[20] Liao SC, Mao YC, Hung YM, Lee CH, Yang CC. Predictive role of QTc prolongation in carbon monoxide poisoning-related delayed neuropsychiatric sequelae. BioMed Research International. 2018; 2018: 2543018.
[21] Thygesen K, Alpert JS, Jaffe AS, Chaitman BR, Bax JJ, Morrow DA, et al.; Executive Group on behalf of the Joint European Society of Cardiology (ESC)/American College of Cardiology (ACC)/American Heart Association (AHA)/World Heart Federation (WHF) Task Force for the Universal Definition of Myocardial Infarction. Fourth Universal definition of myocardial infarction (2018). Journal of the American College of Cardiology. 2018; 72: 2231–2264.
[22] Graber ML, Olson APJ, Barnett T. Learning from tragedy—the Jessica Barnett story: challenges in the diagnosis of long QT syndrome. Diagnosis. 2021; 8: 392–397.
[23] Choi S, Nah S, Han S. Correlation between time to hyperbaric oxygen therapy and delayed neurological sequelae in acute carbon monoxide poisoning patients. Diagnostics. 2024; 14: 186.
[24] Mirvis MD, Goldberger LA. Electrocardiografía. In Braunwald E (ed.) Tratado de Cardiología (pp. 107–149). 7th edn. Elsevier: Madrid, Spain. 2006.
[25] Mantri N, Lu M, Zaroff JG, Risch N, Hoffmann T, Oni-Orisan A, et al. QT interval dynamics and cardiovascular outcomes: a cohort study in an integrated health care delivery system. Journal of the American Heart Association. 2021; 10: e018513.
[26] Sut N, Ajredani M, Koçak Z. Importance of sample size calculation and power analysis in scientific studies: an example from the Balkan Medical Journal. Balkan Medical Journal. 2022; 39: 384–385.
[27] Huang CC, Ho CH, Chen YC, Hsu CC, Lin HJ, Wang JJ, et al. Effects of hyperbaric oxygen therapy on acute myocardial infarction following carbon monoxide poisoning. Cardiovascular Toxicology. 2020; 20: 291–300.
[28] Ansari Ramandi MM, Valizadeh N, Moezzi A, Ghoddusi M, Hatami F. Chest pain in a young male with carbon monoxide poisoning and substance abuse: a case report and literature review. ARYA Atherosclerosis Journal. 2023; 19: 58–62.
[29] Lippi G, Rastelli G, Meschi T, Borghi L, Cervellin G. Pathophysiology, clinics, diagnosis and treatment of heart involvement in carbon monoxide poisoning. Clinical Biochemistry. 2012; 45: 1278–1285.
[30] Cevik Y, Tanriverdi F, Delice O, Kavalci C, Sezgen S. Reversible increases in QT dispersion and P wave dispersion during carbon monoxide intoxication. Hong Kong Journal of Emergency Medicine. 2010; 17: 441–450.
[31] Wang T, Zhang Y. Mechanisms and therapeutic targets of carbon monoxide poisoning: a focus on reactive oxygen species. Chemico-Biological Interactions. 2024; 403: 111223.
[32] Figueiredo-Pereira C, Villarejo-Zori B, Cipriano PC, Tavares D, Ramírez-Pardo I, Boya P, et al. Carbon monoxide stimulates both mitophagy and mitochondrial biogenesis to mediate protection against oxidative stress in astrocytes. Molecular Neurobiology. 2023; 60: 851–863.
[33] Stucki D, Stahl W. Carbon monoxide—beyond toxicity? Toxicology Letters. 2020; 333: 251–260.
[34] Szponar J, Kołodziej M, Majewska M, Zaleski K, Lewandowska-Stanek H. Myocardial injury in the course of carbon monoxide poisoning. Jagiellonian Medical Review. 2012; 69: 528–534. (In Polish)
[35] Wronska A, Kurkowska-Jastrzebska I, Santulli G. Application of microRNAs in diagnosis and treatment of cardiovascular disease. Acta Physiologica. 2015; 213: 60–83.
[36] Lee FY, Chen WK, Lin CL, Kao CH. Carbon monoxide poisoning and subsequent cardiovascular disease risk: a nationwide population-based cohort study. Medicine. 2015; 94: e624.
[37] Kaya H, Coşkun A, Beton O, Zorlu A, Kurt R, Yucel H, et al. COHgb levels predict the long-term development of acute myocardial infarction in CO poisoning. The American Journal of Emergency Medicine. 2016; 34: 840–844.
[38] Karaman S, Coskun A. Risk of late appearance of acute myocardial infartion after carbon monoxide (CO) intoxication. Medical Journal of Chile. 2019; 147: 1128–1135.
[39] Kassa BD, Yigzaw AA, Kassie YG, Kedimu MW, Mekuanint YF, Moges N. Delayed neuropsychiatric sequelae due to long-term effects of carbon monoxide poisoning in Ethiopia: a case report. Toxicology Reports. 2023; 11: 36–39.
[40] Oh S, Choi SC. Acute carbon monoxide poisoning and delayed neurological sequelae: a potential neuroprotection bundle therapy. Neural Regeneration Research. 2015; 10: 36–38.
[41] Bielecka-Papierz G, Poleszak E, Serafko A. Mephedrone—a synthetic derivative of cathinone. Current Issues in Pharmacy and Medical Sciences. 2023; 36: 54–64.
[42] Bandeira GA, Lucato LT. Toxic leukoencephalopathies. Handbook of Clinical Neurology. 2024; 204: 455–486.
[43] Ruth-Sahd LA, Zulkosky K, Fetter ME. Carbon monoxide poisoning: case studies and review. Dimensions of Critical Care Nursing. 2011; 30: 303–314.
[44] Heo KS, Phan LP, Le NTT, Jin Y. Mechanistic insights and emerging therapeutic strategies targeting endothelial dysfunction in cardiovascular diseases. Archives of Pharmacal Research. 2025; 48: 305–332.
[45] Karabacak M, Varol E, Türkdogan KA, Duman A, Akpinar O, Karabacak P. Mean platelet volume in patients with carbon monoxide poisoning. Angiology. 2014; 65: 252–256.
[46] Garg J, Krishnamoorthy P, Palaniswamy C, Khera S, Ahmad H, Jain D, et al. Cardiovascular abnormalities in carbon monoxide poisoning. American Journal of Therapeutics. 2018; 25: e339–e348.
[47] Karakus H, Bulbul O, Kulaber A, Yaman H, Pasli S, Imamoglu M, et al. Evaluation of the neuroprotective effects of idebenone in an experimental carbon monoxide poisoning model. Journal of Applied Toxicology. 2025; 45: 659–668.
[48] Beppu T. The role of MR imaging in assessment of brain damage from carbon monoxide poisoning: a review of the literature. American Journal of Neuroradiology. 2014; 35: 625–631.
[49] arid NA, Harruff RC. Globus pallidus necrosis unrelated to carbon monoxide poisoning: retrospective analysis of 27 cases of basal ganglia necrosis. Journal of Forensic Sciences. 2015; 60: 1484–1487.
[50] Chang CC, Hsu JL, Chang WN, Huang SH, Huang CW, Chang YT, et al. Metabolic covariant network in relation to nigrostriatal degeneration in carbon monoxide intoxication-related parkinsonism. Frontiers in Neuroscience. 2016; 10: 187.
[51] Coşkun A, Eren FA, Eren ŞH, Korkmaz İ. Predicting of neuropsychosis in carbon monoxide poisoning according to the plasma troponin, COHb, RDW and MPV levels: neuropsychoses in carbon monoxide poisoning. The American Journal of Emergency Medicine. 2019; 37: 1254–1259.
[52] Caballero-Bermejo AF, Ruiz-Antoran B, Ramio-Lluch C, Dueñas-Ruiz A, Pineda Torcuato Á, Homar-Amengual C, et al. Clinical features and predictors of delayed neurological syndrome in carbon monoxide poisoning: the AMICO study. Emergencias. 2024; 36: 116–122. (In Spanish)
[53] Drew BJ, Ackerman MJ, Funk M, Gibler WB, Kligfield P, Menon V, et al.; American Heart Association Acute Cardiac Care Committee of the Council on Clinical Cardiology, the Council on Cardiovascular Nursing, and the American College of Cardiology Foundation. Prevention of torsade de pointes in hospital settings: a scientific statement from the American Heart Association and the American College of Cardiology Foundation. Circulation. 2010; 121: 1047–1060.
[54] Ye M, Zhang JW, Liu J, Zhang M, Yao FJ, Cheng YJ. Association between dynamic change of QT interval and long-term cardiovascular outcomes: a prospective cohort study. Frontiers in Cardiovascular Medicine. 2021; 8: 756213.
[55] Beinart R, Zhang Y, Lima JA, Bluemke DA, Soliman EZ, Heckbert SR, et al. The QT interval is associated with incident cardiovascular events: the MESA study. Journal of the American College of Cardiology. 2014; 64: 2111–2119.
[56] Rajvanshi S, Nath R, Kumar M, Gupta A, Pandit N. Correlation of corrected QT interval with quantitative cardiac troponin-I levels and its prognostic role in non-ST-elevation myocardial infarction. International Journal of Cardiology. 2017; 240: 55–59.
[57] Dallas ML, Yang Z, Boyle JP, Boycott HE, Scragg JL, Milligan CJ, et al. Carbon monoxide induces cardiac arrhythmia via induction of the late Na+ current. American Journal of Respiratory and Critical Care Medicine. 2012; 186: 648–656.
[58] Yelken B, Tanriverdi B, Cetinbaş F, Memiş D, Süt N. The assessment of QT intervals in acute carbon monoxide poisoning. Anadolu Kardiyol Derg. 2009; 9: 397–400.
[59] Hancı V, Ayoğlu H, Yurtlu S, Yıldırım N, Okyay D, Erdoğan G, et al. Effects of acute carbon monoxide poisoning on the P-wave and QT interval dispersions. The Anatolian Journal of Cardiology. 2011; 11: 48–52.
[60] Buchelli Ramirez H, Fernández Alvarez R, Rubinos Cuadrado G, Martinez Gonzalez C, Rodriguez Jerez F, Casan Clara P. Elevated carboxyhemoglobin: sources of carbon monoxide exposure. Archivos de Bronconeumología. 2014; 50: 465–468. (In Spanish)
[61] Roderique JD, Josef CS, Feldman MJ, Spiess BD. A modern literature review of carbon monoxide poisoning theories, therapies, and potential targets for therapy advancement. Toxicology. 2015; 334: 45–58.
[62] Jung MH, Lee J, Oh J, Ko BS, Lim TH, Kang H, et al. Effectiveness of initial troponin I and brain natriuretic peptide levels as biomarkers for predicting delayed neuropsychiatric sequelae in patients with CO poisoning: a retrospective multicenter observational study. Journal of Personalized Medicine. 2023; 13: 921.
[63] Gao X, Wei W, Yang GD. Clinical factors for delayed neuropsychiatric sequelae from acute carbon monoxide poisoning: a retrospective study. Frontiers in Medicine. 2024; 11: 1333197.
[64] Wen T, Liang J, Wei Y, Lin W, Pan L. Analysis of prognosis of neurological sequelae in children with carbon monoxide poisoning. Scientific Reports. 2025; 15: 16007.
[65] Szponar J, Goliszek S, Kujawa A, Tchórz M, Sutkowska A, Radoniewicz-Tchórz A, et al. Echocardiographic and clinical patterns in patients with acute carbon monoxide poisoning without cardiovascular and other chronic diseases. Clinical Toxicology. 2025; 63: 246–252.
[66] Patel B, Omeh J, Tackling G, Gupta R, Sahadeo T, Villcant V, et al. The clinical association between carbon monoxide poisoning and myocardial injury as measured by elevated troponin I levels. Journal of Clinical Medicine. 2023; 12: 5529.
[67] Lisbona CF, Hamnett HJ. Epidemiological study of carbon monoxide deaths in Scotland 2007–2016. Journal of Forensic Sciences. 2018; 63: 1776–1782.
[68] Kinoshita H, Türkan H, Vucinic S, Naqvi S, Bedair R, Rezaee R, et al. Carbon monoxide poisoning. Toxicology Reports. 2020; 7: 169–173.
[69] Osborne J, Sobh M, Trudel G. Carbon monoxide as a clinical marker of hemolysis. American Journal of Hematology. 2023; 98: 1127–1159.
[70] Weaver LK. Carbon monoxide poisoning. Undersea & Hyperbaric Medical Society. 2020; 47: 151–169.
[71] Heyboer M III, Sharma D, Santiago W, McCulloch N. Hyperbaric oxygen therapy: side effects defined and quantified. Advances in Wound Care. 2017; 6: 210–224.
[72] Marcinkowska AB, Mankowska ND, Kot J, Winklewski PJ. Impact of hyperbaric oxygen therapy on cognitive functions: a systematic review. Neuropsychology Review. 2022; 32: 99–126.
Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,200 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.
Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.
Chemical Abstracts Service Source Index The CAS Source Index (CASSI) Search Tool is an online resource that can quickly identify or confirm journal titles and abbreviations for publications indexed by CAS since 1907, including serial and non-serial scientific and technical publications.
Index Copernicus The Index Copernicus International (ICI) Journals database’s is an international indexation database of scientific journals. It covered international scientific journals which divided into general information, contents of individual issues, detailed bibliography (references) sections for every publication, as well as full texts of publications in the form of attached files (optional). For now, there are more than 58,000 scientific journals registered at ICI.
Geneva Foundation for Medical Education and Research The Geneva Foundation for Medical Education and Research (GFMER) is a non-profit organization established in 2002 and it works in close collaboration with the World Health Organization (WHO). The overall objectives of the Foundation are to promote and develop health education and research programs.
Scopus: CiteScore 1.3 (2024) Scopus is Elsevier's abstract and citation database launched in 2004. Scopus covers nearly 36,377 titles (22,794 active titles and 13,583 Inactive titles) from approximately 11,678 publishers, of which 34,346 are peer-reviewed journals in top-level subject fields: life sciences, social sciences, physical sciences and health sciences.
Embase Embase (often styled EMBASE for Excerpta Medica dataBASE), produced by Elsevier, is a biomedical and pharmacological database of published literature designed to support information managers and pharmacovigilance in complying with the regulatory requirements of a licensed drug.
Top