Abstract

Clozapine is associated with increased risk of myocarditis. However, many common side-effects of clozapine overlap with the clinical manifestations of myocarditis. As a result, there is uncertainty about which signs, symptoms and investigations are important in distinguishing myocarditis from benign adverse effects of clozapine. Clarity on this issue is important, since missing a diagnosis of myocarditis or discontinuing clozapine unnecessarily may both have devastating consequences. To examine the clinical characteristics of clozapine-induced myocarditis and to identify which signs and symptoms distinguish true myocarditis from other clozapine adverse effects. A retrospective analysis of the record database for 247 621 patients was performed. A natural language processing algorithm identified the instances of patients in which myocarditis was suspected. The anonymised case notes for the patients of each suspected instance were then manually examined, and those whose instances were ambiguous were referred for an independent assessment by up to three cardiologists. Patients with suspected instances were classified as having confirmed myocarditis, myocarditis ruled out or undetermined. Of 254 instances in 228 patients with suspected myocarditis, 11.4% (n = 29 instances) were confirmed as probable myocarditis. Troponin and C-reactive protein (CRP) had excellent diagnostic value (area under the curve 0.975 and 0.896, respectively), whereas tachycardia was of little diagnostic value. All confirmed instances occurred within 42 days of clozapine initiation. Suspicion of myocarditis can lead to unnecessary discontinuation of clozapine. The 'critical period' for myocarditis emergence is the first 6 weeks, and clinical signs including tachycardia are of low specificity. Elevated CRP and troponin are the best markers for the need for further evaluation.

Highlights

  • BackgroundMany common side-effects of clozapine overlap with the clinical manifestations of myocarditis

  • Clozapine is associated with increased risk of myocarditis

  • Troponin and C-reactive protein (CRP) had excellent diagnostic value, whereas tachycardia was of little diagnostic value

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Summary

Background

Clozapine is the ‘gold-standard’ drug in the management of treatment-resistant schizophrenia (TRS)[1,2] defined as inadequate response to at least two trials of antipsychotic medication of adequate dose and duration.[3]. The variability of clinical presentation and frequently insidious onset of symptoms make the true incidence and prevalence of CIM difficult to determine,[11] and benign cases of CIM may go undetected and remit without the need to stop clozapine treatment.[12] Current studies report a range between 0.2% and 3.4%,5,13 with distinguishably higher rates reported by Australian studies. Some authors have attributed this variation in incidence rates to better monitoring and case identification in Australia.[12] As preventative measures, current guidelines suggest a gradual dose titration, serial ECG and a high level of suspicion for non-specific symptoms of myocarditis (such as malaise, chest pain, palpitation).[14] Avoiding concomitant valproate use has been proposed to reduce the risk of developing CIM.[15]

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