A study on paracetamol cardiotoxicity
© The Author(s). 2016
Received: 17 November 2015
Accepted: 1 July 2016
Published: 14 July 2016
Sri Lanka has a high suicide rate, with more than 40 % of poisoning admissions due to overdose of drugs with Paracetamol being the commonest. Data regarding cardiotoxicity to paracetamol is very minimal though hepatotoxicity following poisoning is well studied. Paracetamol cardiotoxicity has rarely been clinically significant and may have well been overlooked. The possibility that paracetamol overdose might be directly cardiotoxic has been the subject of a few reports. Unexplained deaths and electrocardiographic changes associated with paracetamol poisoning have also been reported in which cardiac origin cannot be clearly ruled out. Although some studies state that paracetamol poisoning has no direct cardiotoxic effect, electrocardiographic changes due to metabolic derangement of hepatotoxicity have been shown in certain studies. Thus, we conducted this study to assess in detail the cardiotoxic effect of paracetamol poisoning.
This is a cross sectional descriptive study done on those with confirmed paracetamol poisoning. Serum paracetamol levels, Electrocardiogram, Echocardiogram, troponin I, and other basic investigations were done.
Paracetamol ingestion is more common among teenagers and the young population in Sri Lanka. Although several cases of paracetamol poisoning induced cardiotoxicity has been described in the past, this study demonstrated no electrocardiographic, echocardiographic or cardiac biomarkers changes of myocardial toxicity.
Though literature review support cardiotoxicity following paracetamol poisoning, our study does not provide enough evidence for this. Continuous cardiac monitoring, serial troponin and echocaediogram assessment would be voluble adjunct in its management. Further experiments and research in this subject would be useful with a larger number of samples to further evaluate this important problem.
Sri Lanka has a very high suicide rate, mainly due to acute poisoning with pesticides. Since 1995 the suicide rate in Sri Lanka has declined to 23 per 100,000 population in 2006, and is attributed to a drop in case fatality due to the reduction in toxicity of accessible pesticides, and the implication of regulations to restrict the accessibility of toxic pesticides . Ingestion of pesticides as a method of self-harm has become less frequent in recent years in Sri Lanka. In urban districts in Sri Lanka, more than 40 % of poisoning admissions were due to the overdose of drugs, medicaments and biological substances but this trend is not restricted to urban areas alone. However, though there is a shift of substances used in self-poisoning from pesticides to medicinal drugs, there is a steep rise in rates of self-poisoning in most districts, which is a serious issue . Over the past few years paracetamol poisoning has shown a marked increase. It is the most widely used over-the -counter analgesic/antipyretic. The main reason for paracetamol to be the commonest drug responsible for self-poisoning is that it is readily available [3–6]. It was the commonest drug responsible for deliberate self-harm in the National Hospital Sri Lanka in 2003 [4, 5]. It was also the commonest drug responsible for self-poisoning in the United Kingdom, with 25 000 admissions from paracetamol being recorded in 2001 alone .
Paracetamol is predominantly metabolised to glucuronide and sulphate conjugates, which are excreted in the urine. Hepatotoxicity is related to the conversion of a small proportion of the ingested dose to N-acetyl-p-benzoquinoneimine. In therapeutic doses, N-acetyl-p-benzoquinoneimine is detoxified by conjugation with glutathione in the liver, but hepatic and renal damage may ensue once the protective intracellular glutathione stores are depleted. N-acetylcysteine and methionine replenish glutathione stores in the liver and kidney. Methionine is given orally whereas N-acetylcysteine is available in oral and intravenous form. There is also some evidence that N- acetylcysteine reduces mortality in paracetamol induced liver failure, although the drug acts via a different mechanism from glutathione repletion [8–13].
Evidence of cardiotoxicity in paracetamol overdose
Evidence of cardiotoxicity in Paracetamol overdose
Acute myocardial necrosis
Patchy myocardial necrosis in left ventricular wall
Transient interventricular septal thickenning
ST/T wave inversions
Flatten T waves
Multifocal ventricular ectopics
Dilated left ventricle
Acute severe left ventricular failure
Congestive heart failure
The above evidence would justify paracetamol cardiotoxicity being studied in detail amongst our patients. We carried out a study on patients presenting to the Toxicology Unit of the Teaching Hospital Peradeniya. We selected this unit of the Teaching Hospital Peradeniya as all acute poisoning patients are admitted here.
The objective of our study was to assess the demographic and clinical patterns of paracetamol poisoning induced cardiotoxicity in the Sri Lankan population. The study population included all patients with a history of Paracetamol poisoning presenting to the toxicology unit of the Teaching Hospital Peradeniya over a period of one year. All patients who were clinically diagnosed to have paracetamol poisoning after detailed history at the time of presentation were included in this study. Those patients with multiple drug poisoning and those who refused to participate were excluded from the study. Ethical clearance was obtained from the Ethical Review Committee of the Faculty of Medicine, University of Peradeniya, and informed written consent was obtained from all subjects prior to data collection.
All patients presenting with paracetamol poisoning to the Toxicology Unit of the Teaching Hospital Peradeniya were assessed by detailed history and examination by investigators recruited to the study. The patients who were confirmed to have a paracetamol poisoning were selected for the study. The toxic dose of paracetamol for adults is considered to be either a single dose of 7.5–10 g, which is equivalent to 20 tablets of 500 mg each, or repeated sub-therapeutic doses exceeding 100 mg/kg/day. As for healthy children aged between 1 and 6 years the toxic dose is considered to be between 150 and 200 mg/kg. This toxic dose is defined by the occurrence of hepatotoxicity which is the main toxic effect of paracetamol poisoning, and the cardiotoxic dose has not yet been determined. All the subjects of this study were above the age of 15, therefore all subjects who had consumed more than 20 paracetamol tablets were considered to have paracetamol poisoning.
Liver functions and renal functions were assessed daily over the next few days. Daily 12 leads ECG was taken, and was interpreted by a Consultant Physician specialized in Cardiology. Serum Troponin I level was measured at 4 h after ingestion of paracetamol in patients who were found to have detectable serum paracetamol levels. In addition basic demographic data was also obtained. Data was collected using a comprehensive data collection sheet and was analyzed using the SPSS (Statistical package for social sciences) 20.0 software.
Basic socio-demographic data
Age and sex Distribution
Number Total = 68
Reason for Paracetamol ingestion
Reason for Paracetamol ingestion
Number of patients
Clinical data on admission
Number of patients
Out of 68 patients, 58(85.3 %) were Sinhalese, 9(13.2 %) were Muslims and 1(1.5 %) patient was Christian; 16(23.5 %) patients were regular smokers and 18(26.5 %) were regular alcohol users.
Among the Studied population, 44(64.7 %) only completed their primary education (Ordinary level), 21(30.9 %) educated up to Advanced level and only 3(4.4 %) completed tertiary education.
Out of 68, 47(69.12 %) answered the source of paracetamol as Home and 21(30.88 %) patients were taken Paracetamol over the counter.
All the patients had ingested paracetamol tablets and the mean number of paracetamol tablets was 37+/- 18.36 (Range20–96) (19 g); 2(2.9 %) of them ingested alcohol with paracetamol and 3(4.4 %) ingested cholropheniramine with paracetamol.
Of the 68 subject, 27 (39.70 %) had detectable paractamol levels in serum, and 21 (30.88 %) had Alanine Transaminase levels (ALT) ≥ 1000 IU/L.
Out of studied sample (68), 9 (13.2 %) had a past history of Depression, 11(16.2 %) had a chronic illness, and only 10(14.7 %) had a history of previous suicidal attempts. Eight(11.8 %) had family history of suicide and 6(9 %) had family history of depression.
Electrocardiogram findings of the sample
Echocardiogram was done on all the patients and did not reveal any significant abnormality. All of them had normal ejection fraction and there were no any regional wall motion abnormalities. There were no hypokinetic or akinetic segments.
Cardiac Biomarker Troponin I was done only in patients who had detectable serum paracetamol levels (27 Patients). Surprisingly Troponin I was negative in all of them.
The average time taken for hospital admission following paracetamol ingestion was 3.25 ± 2.27 h.
Paracetamol is the most commonly encountered drug leading to toxicity due to overdose and can lead to severe complications and even result in death. The commonest organ system involved in toxicity of paracetamol is the liver.(H,I) A few previous studies have reported cases of paracetamol toxicity affecting organs other than the liver, including the heart, which was assessed in detail by this study [10, 15, 17–19].
Currently there are a few hypothesized mechanisms for the occurrence of the previous reported cases of cardiotoxicity due to paracetamol overdose, which could either be a direct or indirect effect. A few studies have shown the Acetaminophen moiety to have a direct toxic effect on the heart [9, 14, 20–23]. One hypothesis for the direct toxic effect on the heart suggests that myocardial injury occurs due to a similar mechanism which causes hepatic damage, with paracetamol partly converted to a toxic metabolite, N-acetyl-p-benzoquinonimine, which is normally inactivated by reduction with glutathione and acts as a direct toxin on the myocardium . Paracetamol has shown to bind covalently to proteins in both the liver and cardiac tissue which results in the alteration of protein structure and function, potentially precipitating cytokine release and tissue injury [22, 23]. Another hypothesis is one resulting in ischemia due to paracetamol, which can be due to the depletion of sulfydryl groups. Acetaminophen can deplete sulfydryl groups, which interferes with nitric oxide production, which results in coronary ischaemia [9, 20]. This sulfydryl deficit also may interfere with endothelium derived vascular relaxing factor, which leads to functional coronary ischemia [9, 20].
The most commonly postulated hypothesis for the mechanism for cardiotoxicty in paracetamol poisoning is metabolic derangements such as hyperkalemia, metabolic acidosis and increase in serum fatty acid levels, resulting by hepatic failure, which could lead to arrythmias [9, 12]. Previously reported cases of paracetamol poisoning with cardiac tissue damage has almost always been associated with hepatotoxicity. Lesna et al. stated that there have been no cases of cardiac arrest so far in the absence of hepatotoxicity, which further justifies the hypothesis which states that cardiac tissue damage in paracetamol poisoning occurs following metabolic derangements due to hepatotoxicity [18, 24–27]. Similarly, in this study 30.88 % had ALT ≥ 1000 IU/L indicating hepatic tissue injury, but all had negative Troponin I, echocardiogram and ECG, indicating the absence of cardiac tissue injury in any of the subjects. A case of myocardial damage following acute paracetamol poisoning by Ohtani et al. reported heart failure to occur 2 weeks following hepatic injury, and had return of hepatic function tests to normal and had no elevated levels of serum paracetamol by that time, which shows that though there may be no features of cardiac tissue injury or impairment at the time there is hepatic damage, but cardiac toxicity could occur at a later stage even in the absence of features of hepatic tissue injury at that stage [28–32]. Mi Jin et al. in their experiment have demonstrated that paracetamol induced cytotoxicity and altered gene expression in cultures cardiomyocytes of H9C2 cells . This study was plan to identify the alterations in gene expression in cultured cardiomyocytes;H9C2 cells, which are rat cardiomyocytes, were treated with paracetamol, to evaluate the possible toxic mechanism in the heart. During this study authors have demonstrated some of the DNA damage and upregulation of genes including those associated with oxidative stress, DNA damage and apoptosis . During this study to examine toxic effects of paracetamol,H9C2 rat cardiomyocytes were incubated with different concentratins of paracetamol and viability was determined at different time intervals and showed H9C2 cells viability was decreased by treatment with paracetamol in a time- and dose-dependant manner . Another laboratory study done by Inoue et al. to study cardiotoxicity and hepatotoxicity of different compounds using neonatal rat heart cells and rat hepatocytes confirmed that paracetamol was cardiotoxic in significant overdose .
Previous studies have shown that cardiotoxicity following paracetamol poisoning may be either immediate or delayed [20, 21], similar to the case reported by Ohtani et al. which showed a delay in onset of cardiac involvement . The average time taken for hospital admission following paracetamol ingestion in this study was 3.25 ± 2.27 h. Probably if these patients were followed up weeks later, some of them may have developed cardiac toxicity and showed cardiac tissue damage by elevated troponin I, or positive echocardiogram or ECG changes. Since the cardiotoxicity due to paracetamol poisoning is believed to be either immediate or delayed, it is of paramount importance to administer N-acetylcysteine (NAC) as early as possible because it may be beneficial in reducing the functional coronary ischaemia as well as the direct toxic effects, irrespective of the time of ingestion [34–40]. Since a majority of 81 % of subjects were treated with NAC, and since the time taken for hospital admission following paracetamol ingestion was short, effective treatment with NAC would’ve been protective against the development of cardiotoxicity in this sample. Gastric aspiration or lavage should be carried out, or emesis induced within 4 h of ingestion of 100 mg/kg of paracetamol to reduce absorption, and this has been carried out in 39 % of patients. Activated charcoal and cholestyramine reduce absorption of paracetamol if given within 1 h of ingestion [24–26]. 42.1 % of the patients underwent treatment with charcoal, but since it was done after 1 h of ingestion, the protective effect from this measure would have been minimal or absent. However, other effective measures for the treatment of paracetamol poisoning may be the reason for cardiotoxicity not to develop in these patients.
In contrast to the believed toxic potential of paracetamol on the heart, literature has also demonstrated paracetamol to have a cardioprotective potential in ischaemia reperfusion syndrome. At concentrations of 45–50 mg/ml, well below the clinically toxic dose of 300 mg/ml, paracetamol can reduce tissue injury by preventing the opening of the mitochondrial permeability transition pore and reducing apoptosis [27, 28]. This dose dependent cardioprotective effect has a different mechanism from that of the cardiotoxic effect [41, 42]. However, the mean amount of paracetamol ingested by this study sample was 19 g, accounting to about 315 mg/kg, indicating that this cardioprotective effect of paracetamol is quite unlikely in this sample according to the facts stated in literature.
In patients with severe paracetamol poisoning, the ECG often reveals minor nonspecific ST changes and T wave flattening with U waves during the first 48 h, which is likely to be related to hyperkalaemia, but not due to direct cardiotoxicity . Nonspecific ECG changes and elevated serum creatine kinase has been reported without clinical evidence of toxic myocarditis [30, 31]. A post mortem analysis of 20 fatal cases of paracetamol poisoning showed that there was no evidence of cardiomyopathy. Some degree of focal necrotizing myopathy has been found to occur in patients with fatal massive hepatic necrosis of diverse etiology [32, 33]. Serious cardiovascular complications in paracetamol overdose are not heard of in the absence of hepatic failure, and cardiac abnormalities reported in certain fatal cases are due to the profound metabolic disturbances of acute liver failure rather than paracetamol itself.
In contrast, there have been a few very rare cases of paracetamol overdose reported with abnormal ECG patterns in the absence of hepatotoxicity, metabolic derangement or encephalopathy [32, 43]. A similar case of a 29 year old man with significant paracetamol overdose was found to have an abnormal ECG in the absence of hepatic encephalopathy .
Approximately 35.3 % ingested paracetamol overdose by impulsive action, 20.6 % for deliberate self-harm, and 44.1 % for suicide. 11.8 % had a family history of suicide and 9 % had a family history of depression. Considering these facts, there is also a possibility that a certain number of patients may have mentioned an exaggerated number of paracetamol tablets ingested, and some may also not be very sure of the time and details of ingestion of the overdose. There is also the possibility that paracetamol tablets may have a more diluted concentration of the drug in its composition with a hindrance of quality, resulting in a lower level of serum paracetamol than expected compared to the number of tablets ingested.
Cardiotoxicity is not a common presentation in paracetamol poisoning. It further justifies certain previous studies which state that if at all any cardiac tissue damage only occurs due to metabolic derangements following hepatotoxicity.
ALT, Alanine Transaminase levels; ECG, Electrocardiograph; NAC, N-acetylcysteine
We all express our gratitude to all participants who consented to take part in this study.
Faculty of Medicine, University of Peradeniya has made this study possible through Earned Funds Research Grant (No: RG/EF/2013/12) offered to UR.
Availability of data and materials
The raw datasets supporting this article can be made available by emailing the corresponding author.
UR conceived the research idea and guided it. Data collection, analysis and interpretation of data and literature review were done by UR, KPJ, and EMME.UR and AMSDMD guided the other authors in data analysis, interpretation and corrected the final manuscript. All authors were involved in the study and read and approved the final manuscript.
UR [MBBS, MD, MRCP (UK), FRCP (London)] is a Senior Lecturer and Consultant Physician, Department of Medicine, University of Peradeniya. KPJ [MBBS] and EMME [MBBS] are Temporary Lecturers and Research Assistants, Department of Medicine, University of Peradeniya, Sri Lanka. AMSDMD [MBBS, D.Path (Colombo), MD-Heamatology (Colombo), PhD (London)] is a Professor, Department of Pathology, Faculty of Medicine, University of Peradeniya.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Ethical approval for the research work has been obtained from the Ethical review committee, Faculty of Medicine, University of Peradeniya, Sri Lanka. All the data were collected from the participants after obtaining written consent.
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