Abstract:Given the low or very low quality of the evidence for the reported outcomes, and the small number of trials identified with a limited number of participants for each comparison, it is not possible to draw firm conclusions regarding pharmacological interventions to facilitate benzodiazepine discontinuation in chronic benzodiazepine users. Due to poor reporting, adverse events could not be reliably assessed across trials. More randomised controlled trials are required with less risk of systematic errors ('bias')… Show more
“…Add‐on medications to facilitate benzodiazepine discontinuation have been extensively investigated. In a recent Cochrane Review covering the topic, the following results were emphasized: several different pharmacological interventions had been investigated but mostly in underpowered studies of low scientific quality. Most results were based on single small‐sized randomized trials with a high risk of type II error.…”
Schizophrenia is a severe mental disorder characterized by a heterogeneous symptom profile which comprises a clinical platform for widespread use of polypharmacy even though antipsychotic monotherapy is the recommended treatment regimen. This narrative review provides a summary of the current gap between evidence and practice for use of antipsychotic combination therapy in patients with schizophrenia. Antipsychotic polypharmacy is frequently prescribed instead of following international consensus of clozapine monotherapy in treatment‐resistant patients. Antipsychotic‐benzodiazepine combination therapy clearly has a role in the treatment of acute agitation whereas there is no evidence to support an effect on core schizophrenia symptoms when chronically prescribed. Antidepressants are typically added to antipsychotic treatment in case of persistent negative symptoms. Available evidence suggests that antidepressants may improve negative symptom control in schizophrenia. Combining an antipsychotic with an antiepileptic is not supported by any firm evidence, but individual mood stabilizers have come out positively in single trials. Generally, the evidence base for polypharmacy in schizophrenia maintenance treatment is sparse but may be warranted in certain clinical situations. Therapeutic benefits and side effects should be carefully monitored and considered to ensure a beneficial risk‐benefit ratio if prescribing polypharmacy for specific clinical indications.
“…Add‐on medications to facilitate benzodiazepine discontinuation have been extensively investigated. In a recent Cochrane Review covering the topic, the following results were emphasized: several different pharmacological interventions had been investigated but mostly in underpowered studies of low scientific quality. Most results were based on single small‐sized randomized trials with a high risk of type II error.…”
Schizophrenia is a severe mental disorder characterized by a heterogeneous symptom profile which comprises a clinical platform for widespread use of polypharmacy even though antipsychotic monotherapy is the recommended treatment regimen. This narrative review provides a summary of the current gap between evidence and practice for use of antipsychotic combination therapy in patients with schizophrenia. Antipsychotic polypharmacy is frequently prescribed instead of following international consensus of clozapine monotherapy in treatment‐resistant patients. Antipsychotic‐benzodiazepine combination therapy clearly has a role in the treatment of acute agitation whereas there is no evidence to support an effect on core schizophrenia symptoms when chronically prescribed. Antidepressants are typically added to antipsychotic treatment in case of persistent negative symptoms. Available evidence suggests that antidepressants may improve negative symptom control in schizophrenia. Combining an antipsychotic with an antiepileptic is not supported by any firm evidence, but individual mood stabilizers have come out positively in single trials. Generally, the evidence base for polypharmacy in schizophrenia maintenance treatment is sparse but may be warranted in certain clinical situations. Therapeutic benefits and side effects should be carefully monitored and considered to ensure a beneficial risk‐benefit ratio if prescribing polypharmacy for specific clinical indications.
“…Priorities for further research include adequately powered, high-quality, randomized controlled trials comparing pharmacological interventions to facilitate BZD discontinuation in chronic BZD users. Th ese trials need to be conducted with minimal bias, be independent of industry involvement, and include adverse effects, along with patient-centered and long-term clinical outcomes (Baandrup et al, 2018). Randomized controlled trials in participants newly prescribed BZDs need to take the "new user" eff ect into consideration and outline clearly in the patient information sheet what to expect and what routine tasks to avoid (Díaz-Gutiérrez et al, 2017).…”
Section: Recommendations For the Management Of Falls Preventionmentioning
“…However, there is a paucity of evidence for effective interventions to support withdrawal, and a recent review failed to identify evidence of sufficient quality to support any pharmacological interventions. 18 Psychosocial interventions may be more promising: cognitive behavioural therapy plus tapering is effective in the short term, and relaxation techniques and individualised GP letters to patients can facilitate withdrawal. 3 However, better evidence is urgently required for both drug and non-drug options.…”
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