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Medication management during electroconvulsant therapy

Authors Zolezzi M

Received 20 November 2015

Accepted for publication 27 January 2016

Published 19 April 2016 Volume 2016:12 Pages 931—939

DOI https://doi.org/10.2147/NDT.S100908

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3

Editor who approved publication: Dr Roger Pinder


Monica Zolezzi

Clinical Pharmacy and Practice, College of Pharmacy, Qatar University, Doha, Qatar

Abstract: Electroconvulsive therapy (ECT) has demonstrated to be highly effective and safe, even life saving for many psychiatric disorders such as major depression, bipolar disorder and schizophrenia. Most patients who require ECT are also on concurrent pharmacotherapy. As such, the objective of this article is to provide a review of the most recent literature focusing on the medications used during an ECT procedure and on the effects of concurrent psychiatric and non-psychiatric medications on the effectiveness and safety of ECT. The review also attempts to summarize the recommendations derived from existing documents to guide pharmacotherapy decisions for patients undergoing ECT. For this purpose, using electronic databases, an extensive search of the current literature was made using ECT and medications or drug classes as keywords.

Keywords: ECT, medications, drug interactions

Introduction

Several evidence-based documents on the use of electroconvulsive therapy (ECT) indicate that it is a safe and effective treatment for a variety of psychiatric disorders.13 Although major depression refractory to antidepressant medications is the primary indication for ECT, there is also significant evidence to support its use in other psychiatric disorders such as catatonia, psychotic depression, mania, bipolar disorder and schizophrenia.13

The goal of ECT is to produce a controlled and monitored seizure lasting from 30 to 90 seconds in duration to be considered therapeutic.1,46 Although the exact mechanism of ECT is unknown, the induced seizure affects nearly every neurotransmitter system, including β-adrenergic, serotonin, muscarinic, cholinergic, and dopaminergic systems.6,7 Brain-derived neurotrophic factor may also play a role in the efficacy of ECT.8 There are no absolute contraindications to ECT; nevertheless, ECT can induce side effects and may be physically risky for certain individuals. As such, all patients must be assessed prior to ECT for the presence of conditions such as cardiovascular disease, space-occupying intracranial lesion with the evidence of elevated intracranial pressure, recent cerebral hemorrhage or stroke, bleeding or otherwise unstable vascular aneurysm, and severe pulmonary disease, as all of these can be associated with increased risk of complications from the general anesthesia and induction of seizure activity.1 ECT is considered safe with a mortality of ~1/10,000 patients or 1/80,000 treatments.6 Most patients report some adverse cognitive effects during and after a course of ECT, such as postictal confusion state (the result of both anesthesia and the seizure), anterograde amnesia (decreased ability to retain newly acquired information), and retrograde amnesia (forgetting recent memories).9 However, objective tests indicate that cognitive abnormalities caused by ECT are generally short lived. Acute confusional states typically resolve 10 to 30 minutes after the procedure, whereas anterograde amnesia resolves within 2 weeks after completing the course. Retrograde amnesia recovers more slowly than anterograde amnesia.10 Permanent memory loss is rare but can occur.9,11 Other adverse effects include myalgias, headache, nausea, drowsiness, and musculoskeletal weakness.1,47

Several parameters have the potential to influence the induction of a well-organized seizure, which is critical for ECT efficacy, such as electric stimuli, seizure threshold, and medications, including those used during the ECT procedure itself, as well as those regularly used to treat the individual’s concomitant psychiatric or medical conditions.12 As such, assessing all concurrent medications and monitoring for the potential effects of these medications before, during, and after the ECT procedure are recommended.13,6,7 This article aims to review all the different classes of medications that may be used in patients undergoing ECT and their influence on ECT outcomes. Most of the available guidelines describing medications used in ECT are a decade old, and thus, an update on this topic is warranted.

A review of the literature was undertaken using Medline (OvidSP), PubMed Central, and Google Scholar using the keywords “electroconvulsive therapy”, “drug(s)”, “medication(s)”, and “drug/medication interactions”. Only studies with human subjects, reports written in the English language and published after January 1, 2000, were included. Additional references were identified from the bibliographies of published review articles regardless of the date of publication and from ECT guidelines.13 In addition, using the same electronic databases, separate searches were undertaken using ECT and various drugs or drug classes as keywords.

The findings have been summarized as 1) medications that are used during the ECT procedure and 2) interactions between regularly prescribed medications and medications used during the ECT procedure itself. Management strategies for these medication interactions have also been extracted from the retrieved articles whenever available to help clinicians in making decisions about which medications to taper or stop before the procedure, which medications can safely be given just before the procedure, and which can be continued during the course of ECT (or held until after each treatment).

Medications during the ECT procedure

Table 1 lists common medications that patients may receive during an ECT procedure. These include anesthetic induction agents, anticholinergic agents, muscle relaxants, antihypertensives, and narcotics.

Table 1 Medications during the ECT procedure
Abbreviation: ECT, electroconvulsive therapy.

Anesthetic agents and muscle relaxants are used to induce a state of insensibility and to decrease the likelihood of bone and soft tissue injury.1 Due to the brief nature of ECT, an ideal anesthetic agent should rapidly induce hypnosis and allow for rapid emergence from anesthesia without significantly shortening seizure activity or causing hemodynamic instability.13,14 Among the barbiturates, methohexital and thiopental, which have minimal anticonvulsant properties compared with other barbiturates, were considered as gold standard as ECT anesthetic induction agents, but due to recent worldwide shortages of these agents, other drugs such as propofol, etomidate and ketamine have become more widely used.1521

The advantages of propofol over methohexital include a quicker and smoother emergence from anesthesia and a somewhat more favorable hemodynamic profile.1417 Disadvantages are its much greater anticonvulsant effect and higher cost. Etomidate is an alternative particularly in patients who have seizures of short duration or hard to elicit.14,17,20 Ketamine has shown to be slightly proconvulsant and has intrinsic antidepressant properties. Disadvantages include hypertension and occasional transient dissociative symptoms on wake up.17,19,21 A recent systematic review concluded that robust evidence to recommend a particular induction agent for ECT is lacking and indicated that anesthetic agents should be chosen on the basis of adverse effect profile, emergence, and how these medications affect seizure duration.18 Opioids, such as remifentanil and alfentanil, combined with anesthetic agents have been used to increase the seizure duration by an induction agent dose-sparing effect.17,2224 Caffeine, in the form of caffeine sodium benzoate intravenous injection 250–1,000 mg, and other methylxanthines have also been administered prior to ECT to increase the seizure duration but do not appear to reduce seizure threshold.24 However, because the potential cardiac and other complications of caffeine use are known, this augmenting strategy is not generally recommended, especially in the elderly.24,25 Muscle relaxation during the application of the stimulus, as well as for the duration of the motor portion of the seizure, prevents musculoskeletal injury; this is especially important if the patient has osteoporosis or a history of spinal injury.1,6,7 Because of the short duration of ECT, succinylcholine (also known as suxamethonium) is the drug of choice for neuromuscular blockade.1,17,26 Succinylcholine is a depolarizing neuromuscular blocker with an ultrashort duration of action, slightly less than that of the anesthetic agent. The duration of muscle paralysis is, thus, very brief, and spontaneous respirations return shortly after the seizure ends. In patients in whom its use is contraindicated, rocuronium or other nondepolarizing agents are alternatives.1,26

During ECT, significant changes in autonomic function can occur. Initially a parasympathetic surge can result in significant bradycardia, hypotension, and, in some cases, brief asystole.1,6 Patients already on β-blockers may be at risk of bradycardia if stimulation is given but a seizure is not induced.4,7 To counteract the parasympathetic effect, anticholinergic medications (eg, glycopyrrolate and atropine) may be given, although this is not routinely required. Glycopyrrolate is preferred over atropine since it does not cross the blood–brain barrier, which reduces unwanted cognitive effects after ECT.6

Following stimulus termination, the resulting seizure is accompanied by a profound sympathetic surge, typically associated with tachycardia and hypertension.1,27 Deleterious sympathetic effects may be controlled with β-blockers either pre- (atenolol) or intraprocedurally (labetalol and esmolol).13,17 There is controversy, however, regarding whether labetalol and esmolol reduce seizure duration.28 Sublingual nifedipine and intravenous nicardipine have been used (although tachycardia can occur), as has diltiazem, although it also may reduce seizure duration.27 Preoperative α-2 agonists, such as dexmedetomidine, also blunt the hyperdynamic response as does glyceryl trinitrate, which should be considered in patients at high risk of myocardial ischemia.17,27,28

Interactions between regularly prescribed medications and ECT

The majority of patients requiring ECT are likely to be receiving concurrent regularly prescribed medications for treating psychiatric, medical, and comorbid conditions. Therefore, not surprisingly, drug interactions can occur between psychotropic agents, drugs prescribed for chronic medical conditions, anesthesia-inducing agents, and other medications used for the ECT procedure itself. These drug interactions can be classified into the following categories: 1) interactions with medications used during the ECT procedure, 2) interactions that affect the efficacy of ECT (ie, suppressing seizure activity), and 3) interactions that can increase the risks associated with ECT (eg, increase risk of complications, such as prolonged seizures and cardiotoxicity).

In general, medications that raise seizure threshold or impede seizure propagation (interfere with induction or spread of a robust seizure) should be avoided if possible, or the dose decreased (eg, anticonvulsants and benzodiazepines). Cardiac medications, antihypertensives, and antigastric medications can typically be continued. Table 2 provides a summary of the most often reported drug interactions based on the major classes of commonly used medications by patients undergoing ECT. For each specific drug interaction, the possible undesired effect and how it can be managed are also included for easy reference. There are no studies exploring the effects of herbal medicines on ECT; however, several direct and indirect mechanisms whereby such use may impact the ECT procedure are also summarized in Table 2.


Table 2 Drug interactions reported in patients undergoing ECT
Abbreviations: BZD, benzodiazepine; CBZ, carbamazepine; ECT, electroconvulsive therapy; FGA, first-generation antipsychotics; LTG, lamotrigine; MAOI, monoamine oxidase inhibitor; SGA, second-generation antipsychotics; SNRIs, serotonin norepinephrine reuptake inhibitors; SSRIs, serotonin reuptake inhibitors; TCA, tricyclic antidepressant; VPA, valporic acid; CNS, Central Nervous System; GERD, Gastroesophageal Reflux Disease; INR, International Normalization Ratio; COMT, Catecholl-O-Amine Transferase; GABA, Gamma Amino-Butiric Acid.

Conclusion

Despite the vast potential for drug interactions in patients receiving ECT, available evidence on those interactions that are clinically significant is scarce, and it is almost exclusively retrospective in nature, or derived from case reports or case series. A summary of the existing evidence as presented in this article can inform clinicians on the potential and documented consequences of these interactions, and assist them weighing the risks and benefits before making decisions on the concurrent use of medications in patients receiving ECT.

Disclosure

The author reports no conflicts of interest in this work.


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