Early post-marketing phase vigilance (EPPV) of paliperidone palmitate (PAL-P) revealed a mortality of at least 32 (0.29%) out of approximately 11,000 patients with schizophrenia administered PAL-P between November 2013 and May 2014 (average administration period of four months). Since then, many psychiatrists may have become distrustful of PAL-P, as well as of other long-acting injectable antipsychotics (LAI). This study reviewed the mortality data observed in several premarketing clinical trials of antipsychotics, including PAL-P, post-mar- keting surveillances (PMS) of antipsychotics conducted in Japan, and several large-scale cohort studies performed in developed countries, and re-evaluated the mortality risk of PAL-P. The results of the literature review were as follows: 1) the mortality of the patients on LAI in clinical trials was 3.56-7.95/1,000 person-years. This number was not higher than that of those on oral antipsychotics (5.00-8.55/1,000 person-years) ; 2) the mortality of those on PAL-P in clinical trials (3.56/1,000 person-years) was not higher than that on the other LAIs (6.34-7.95/ 1,000 person-years); 3) the mortality of those on PAL-P observed in the EPPV (equivalent to 0.22% per three months) was similar to the three-month mortality observed in the PMSs of risperidone LAI, oral paliperidone, or oral blonanserin (0.19-0.31%); and 4) based on data of the cohort studies, the four-month mortality of those with schizophrenia was estimated at 0.35-0.68%. Therefore, the mortality observed in the EPPV of PAL-P did not seem to be of clinical significance, even allowing for the possibility of underestimating the mortality in the EPPV.
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Circ Res
January 2025
Key Laboratory of Drug Targets and Translational Medicine for Cardio-cerebrovascular Diseases, Key Laboratory of Targeted Intervention of Cardiovascular Disease, Collaborative Innovation Center for Cardiovascular Disease Translational Medicine, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Gusu School, Nanjing Medical University, Jiangsu, China (X.T., X.L., X.S., Y. Zhang, Y. Zu, Q.F., L.H., S.S., F.C., L.X., Y.J.).
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Division of Biostatistics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Clinical trials (CTs) often suffer from small sample sizes due to limited budgets and patient enrollment challenges. Using historical data for the CT data analysis may boost statistical power and reduce the required sample size. Existing methods on borrowing information from historical data with right-censored outcomes did not consider matching between historical data and CT data to reduce the heterogeneity.
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Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.
A recent study design for clinical trials with small sample sizes is the small n, sequential, multiple assignment, randomized trial (snSMART). An snSMART design has been previously proposed to compare the efficacy of two dose levels versus placebo. In such a trial, participants are initially randomized to receive either low dose, high dose or placebo in stage 1.
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Department of Anaesthesiology, Pharmacology and Therapeutics, Faculty of Medicine, University of British Columbia, Vancouver.
In older adults with type 2 diabetes (T2DM), tight glycaemic control (HbA1c 7%) can result in more harm than benefit, especially when using insulin or sulfonylureas. Older adults are at higher risk for adverse drug events, especially hypoglycaemia, which may cause falls, confusion and hospitalisations. This Therapeutic Letter evaluates the risks of tight glycaemic control in older adults with T2DM, focusing on deprescribing diabetes medications in those over 65, especially those with multimorbidity and polypharmacy.
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Third Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, China.
Cholangiocarcinoma is the second most common primary liver cancer, and its global incidence has increased in recent years. Radical surgical resection and systemic chemotherapy have traditionally been the standard treatment options. However, the complexity of cholangiocarcinoma subtypes often presents a challenge for early diagnosis.
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