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1.
J Opioid Manag ; 20(3): 233-241, 2024.
Article in English | MEDLINE | ID: mdl-39017615

ABSTRACT

OBJECTIVE: This study aimed to determine whether there is a difference in pain scores and opioid consumption after elective surgery in patients maintained on methadone or buprenorphine for opioid use disorder (OUD). Additionally, we investigated the impact of continuing or discontinuing methadone or buprenorphine on post-operative pain outcomes. DESIGN: A single-center retrospective cohort study. SETTING: Tertiary care medical center. PATIENTS AND PARTICIPANTS: Adults aged 18 years or older with OUD maintained on buprenorphine or methadone who underwent elective surgery between January 1, 2017, and January 1, 2021. INTERVENTIONS: Patients were identified through electronic medical records, and demographic and clinical data were collected. MAIN OUTCOME MEASURES: The primary outcome was opioid consumption at 24 hours post-operatively, measured in milligram morphine equivalents. The secondary outcome was opioid consumption and pain scores up to 72 hours post-operatively, assessed using a numeric rating scale. RESULTS: This study included 366 patients (64 percent on buprenorphine and 36 percent on methadone). Opioid utilization significantly increased when buprenorphine was not administered post-operatively. Both groups exhibited comparable total opioid consumption during the post-operative period. In the buprenorphine cohort, pain scores differed significantly based on the receipt of medications for OUD post-operatively. CONCLUSIONS: This study reinforces existing evidence supporting the continuation of medications for opioid use disorder, specifically buprenorphine and methadone, during the perioperative period. Dissemination of guideline recommendations is essential to ensure optimal post-operative pain management for this patient population.


Subject(s)
Analgesics, Opioid , Buprenorphine , Methadone , Opiate Substitution Treatment , Opioid-Related Disorders , Pain, Postoperative , Humans , Buprenorphine/therapeutic use , Buprenorphine/administration & dosage , Pain, Postoperative/drug therapy , Pain, Postoperative/diagnosis , Methadone/therapeutic use , Methadone/administration & dosage , Male , Opioid-Related Disorders/prevention & control , Female , Retrospective Studies , Middle Aged , Analgesics, Opioid/therapeutic use , Adult , Pain Management/methods , Pain Measurement , Aged , Elective Surgical Procedures
2.
J Parkinsons Dis ; 10(3): 1123-1132, 2020.
Article in English | MEDLINE | ID: mdl-32310186

ABSTRACT

BACKGROUND: Both genetic and environmental factors contribute to Parkinson's disease (PD) risk. OBJECTIVE: We investigated the potential association of several relevant variables with PD age at onset (AAO), focusing on LRRK2 p.G2019S and GBA p.N370S mutations. METHODS: Ashkenazi Jewish (AJ) PD patients, screened for LRRK2 and GBA mutations, underwent an interview regarding exposure to the following environmental and lifestyle factors: cigarette smoking, consumption of coffee, tea and alcohol, head injury and rural living. Multivariate linear regression (adjusted for sex) was used to examine the association with AAO, and models included LRRK2 p.G2019S and GBA p.N370S mutation status (carrier/non-carriers), single environmental variable and their interactions terms, as independent variables. RESULTS: 225 Israeli AJ PD patients were enrolled: 65 LRRK2 p.G2019S mutation carriers, 60 GBA p.N370S carriers and 100 non-carries of these mutations. In the dichotomized exposure/non-exposure analyses, positive LRRK2 p.G2019S status was associated with younger AAO in all models, at nominal or near significant levels (p = 0.033-0.082). Smoking was associated with older AAO (p = 0.032), and the interaction between GBA p.N370S and history of head injury was associated with younger AAO (p = 0.049), both at nominal significance. There was no indication of a consistent main effect for GBA p.N370S status or significant LRRK2 p.G2019S-environmental factor interaction. In the dose-dependent analyses, increased coffee and tea consumption levels were associated with older AAO (p = 0.001 and p = 0.002, respectively). CONCLUSIONS: Our results suggest that genetic and environmental factors may affect AAO in PD patients, but validation in additional samples is required.


Subject(s)
Gene-Environment Interaction , Glucosylceramidase/genetics , Jews , Leucine-Rich Repeat Serine-Threonine Protein Kinase-2/genetics , Parkinson Disease , Adult , Age of Onset , Aged , Coffee , Drinking Behavior/physiology , Female , Heterozygote , Humans , Israel/ethnology , Jews/genetics , Jews/statistics & numerical data , Male , Middle Aged , Parkinson Disease/ethnology , Parkinson Disease/etiology , Parkinson Disease/genetics , Tea
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