Estimating Risk of Antidepressant Withdrawal from a Review of Published Data

• Published in: CNS drugs 2023-02, Vol.37 (2), p.143-157
• Main Authors: Horowitz, Mark Abie, Framer, Adele, Hengartner, Michael P., Sørensen, Anders, Taylor, David
• Format: Article
• Language: English
• Subjects: Adaptation; Addictions; Antidepressants; Antidepressive Agents - adverse effects; Brain research; Caffeine; Drug abuse; Drug dosages; Drug withdrawal; Homeostasis; Humans; Laboratories; Medicine; Medicine & Public Health; Mental disorders; Nervous system; Neurobiology; Neurology; Neurosciences; Norepinephrine; Paroxetine; Patients; Pharmacology; Pharmacotherapy; Physiology; Psychiatry; Psychopharmacology; Review; Review Article; Selective Serotonin Reuptake Inhibitors; Serotonin; Serotonin uptake inhibitors; Withdrawal
• ISSN: 1172-7047; 1179-1934
• DOI: 10.1007/s40263-022-00960-y

Adaptation of the brain to the presence of a drug predicts withdrawal on cessation. The outcome of adaptation is often referred to as ‘physical dependence’ in pharmacology, as distinct from addiction, although these terms have unfortunately become conflated in some diagnostic guides. Physical dependence to antidepressants may occur in some patients, consistent with the fact that some patients experience withdrawal effects from these medications. It is thought that longer duration of use, higher dose and specific antidepressants affect the risk of antidepressant withdrawal effects as they might cause greater adaptation of the brain. We searched PubMed for relevant systematic reviews and other relevant analyses to summarise existing data on determinants of antidepressant withdrawal incidence, severity and duration. Overall, data were limited. From survey data, increased duration of use was associated with an increased incidence and severity of withdrawal effects, consistent with some evidence from data provided by drug manufacturers. Duration of use may be related to duration of withdrawal effects but data are heterogenous and sparse. Serotonin and noradrenaline reuptake inhibitors and paroxetine are associated with higher risks than other antidepressants, though data for some antidepressants are lacking. Higher doses of antidepressant has some weak association with an increased risk of withdrawal, with some ceiling effects, perhaps reflecting receptor occupancy relationships. Past experience of withdrawal effects is known to predict future risk. Based on these data, we outline a preliminary rubric for determining the risk of withdrawal symptoms for a particular patient, which may have relevance for determining tapering rates. Given the limited scope of the current research, future research should aim to clarify prediction of antidepressant withdrawal risk, especially by examining the risk of withdrawal in long-term users of medication, as well as the severity and duration of effects, to improve the preliminary tool for predictive purposes. Further research into the precise adaptations in long-term antidepressant use may improve the ability to predict withdrawal effects for a particular patient.