Low risk of seizures with slow flumazenil infusion and routine anticonvulsant prophylaxis for high-dose benzodiazepine dependence

2017 ◽  
Vol 31 (10) ◽  
pp. 1369-1373 ◽  
Author(s):  
Stefano Tamburin ◽  
Marco Faccini ◽  
Rebecca Casari ◽  
Angela Federico ◽  
Laura Morbioli ◽  
...  

High-dose benzodiazepine (BZD) dependence represents an emerging and under-reported addiction phenomenon and is associated with reduced quality of life. To date there are no guidelines for the treatment of high-dose BZD withdrawal. Low-dose slow flumazenil infusion was reported to be effective for high-dose BZD detoxification, but there is concern about the risk of convulsions during this treatment. We evaluated the occurrence of seizures in 450 consecutive high-dose BZD dependence patients admitted to our unit from April 2012 to April 2016 for detoxification with low-dose slow subcutaneous infusion of flumazenil associated with routine anticonvulsant prophylaxis. In our sample, 22 patients (4.9%) reported history of convulsions when previously attempting BZD withdrawal. Only four patients (0.9%) had seizures during ( n = 2) or immediately after ( n = 2) flumazenil infusion. The two patients with seizures during flumazenil infusion were poly-drug misusers. The most common antiepileptic drugs (AEDs) used for anticonvulsant prophylaxis were either valproate 1000 mg or levetiracetam 1000 mg. Our data indicate that, when routinely associated with AEDs prophylaxis, low-dose slow subcutaneous flumazenil infusion represents a safe procedure, with low risk of seizure occurrence.

2020 ◽  
Author(s):  
Tsai-Ju Chien ◽  
Yi-Shuo Huang ◽  
Chun-Yu Kuo ◽  
Yu-Ching Cho ◽  
Hsin-Yu Chen ◽  
...  

Abstract Background The study examined whether the acupuncture dose (number of acupoints stimulated) impacted the efficacy of acupuncture on dysmenorrhea and the relationship with autonomic nervous system regulation.Methods This three-arm randomized controlled study included a high-dose acupuncture (12 acupoints, N = 23), low-dose acupuncture (6 acupoints, N = 30) and control (N = 30) arm. The treatment course was three months. We set heart rate variation (HRV) and analgesics dependence as the primary outcome measurements; Visual Analog Scale (VAS) score, Verbal Multidimensional Scoring System (VMSS) and the 12-Item Short Form Health Survey (SF-12) quality of life questionnaires were set as secondary outcomes. SPSS version 24 was used for data analysis.Results Low-dose acupuncture was superior to high-dose in analgesics dependence (p value: low/high/control: p = 0.043/p = 0.056/p = 0.376); symptom relief (VMSS: low/high/control: p < 0.001/p = 0.007/p = 0.109); and physical quality of life (low/high/control: p < 0.001/p = 0.01/p = 0.007). The groups did not differ in HRV parameters (p > 0.05). In intergroup analysis, more significant changes were noted in the high-dose than in the low-dose group. The scattered nature of the significant changes implies that acupuncture may have a short-term effect on HRV parameters which does not correlate with the acupuncture dose.Conclusions Acupuncture can effectively treat dysmenorrheal pain, improve symptoms and reduce analgesic dependence, but the effect does not correlate with the number of acupoints stimulated. The acupuncture has short-term effect on HRV; yet whether its efficacy on dysmenorrhea is directly related to adjusting the autonomic nervous system may need more large-scale study. It is a safe and effective alternative therapy for dysmenorrhea.Trial: The Efficacy of Different Doses of Acupuncture in Dysmenorrhea, NCT03881319 at ClinicalTrials.gov,


2021 ◽  
Vol 14 (11) ◽  
pp. e243773
Author(s):  
Leonard Timoney ◽  
Christopher B Bunker

A 53-year-old woman presented with a 25-year history of acne excoriée and prurigo excoriée. Her symptoms began in 1988 coinciding with her husband’s death from a brain tumour when she was 27. The pruritus affected her quality of life and disturbed her sleep. She had scarring on her face and body resulting from persistent scratching. The pruritus proved refractory to treatment despite a multi-modal treatment approach including multiple topicals, phototherapy and systemic agents such as isotretinoin, antibiotics, anxiolytic agents and neuromodulators. She was extremely frustrated that various treatments had been ineffective at controlling the itch-scratch cycle. She was commenced on low dose naltrexone (LDN), 3 mg nocte, and she became itch free within a few weeks. She reports that the LDN has had a beneficial impact on her quality of life.


2021 ◽  
Vol 13 (3) ◽  
pp. 306-310
Author(s):  
Article Editorial

On June 26, 2021, a meeting of the experts of the Russian League Against Epilepsy (RLAE) was held, dedicated to the effectiveness, safety and assessing the results of drug therapy in patients with epilepsy. Having considered the history of the issue and guided by domestic and foreign experience, the participants discussed the problems associated with the use of various antiepileptic drugs for different forms of epilepsy in patients of different sex and age. Special attention was paid to psychiatric comorbidity in patients with epilepsy, increasing their compliance with treatment and quality of life. The article presents the Resolution of RLAE experts meeting adopted as a result of the discussion.


1989 ◽  
Vol 7 (10) ◽  
pp. 1407-1418 ◽  
Author(s):  
M A Poon ◽  
M J O'Connell ◽  
C G Moertel ◽  
H S Wieand ◽  
S A Cullinan ◽  
...  

The purpose of this study was to evaluate the effectiveness of several new approaches designed to enhance the activity of fluorouracil (5-FU) in the management of advanced colorectal cancer. A total of 429 patients were randomized to one of the following regimens: single-agent 5-FU, given by standard 5-day, intensive-course intravenous bolus technique; 5-FU plus high-dose folinic acid (leucovorin) or 5-FU plus low-dose leucovorin; 5-FU plus high-dose methotrexate (MTX) with oral leucovorin rescue; 5-FU plus low-dose MTX; and 5-FU plus cisplatin (CDDP). The median survival for patients receiving 5-FU alone was 7.7 months. The high- and low-dose leucovorin plus 5-FU regimens had median survivals of 12.2 and 12.0 months, respectively, and offered a significant survival advantage over 5-FU alone with one-sided P values of .037 and .050, respectively (P = .051 for each treatment after correction for prognostic variables). The only other regimen possibly associated with improved survival was high-dose MTX plus 5-FU, with a median survival of 10.5 months (P = .21, P = .076 corrected). In addition, both high- and low-dose leucovorin plus 5-FU regimens were associated with significantly improved tumor response rates (P = .04 and .001) and significantly improved interval-to-tumor-progression rates (P = .015 and .007) when compared with 5-FU alone. Only the low-dose leucovorin plus 5-FU regimen was associated with significant (P less than .05) superiority in each of the following parameters of quality of life: performance status, weight gain, and symptomatic relief. The overall most therapeutically favorable regimen in this trial was 5-FU given with low-dose leucovorin; fortuitously, this regimen is associated with very low drug cost. Whereas this is the first study to demonstrate both improved palliation and survival for any regimen compared with 5-FU given by rapid intravenous (IV) injection for 5 consecutive days at a dose of 500 mg/m2/d in patients with advanced colorectal cancer, the magnitude of the gain is still relatively small. Our low-dose leucovorin plus 5-FU regimen is currently being studied in a national trial with the hope that this increased advanced disease activity may produce more substantive gains in the surgical adjuvant setting.


2011 ◽  
Vol 29 ◽  
pp. e170
Author(s):  
M. Zdravkovic ◽  
M. Krotin ◽  
M. Ristic ◽  
J. Perunicic ◽  
N. Milic ◽  
...  

2019 ◽  
Vol 4 (22;4) ◽  
pp. 401-411
Author(s):  
Yohei Denawa

Background: Chronic non-cancer pain (CNCP) is a major health concern. Opioids may be a useful treatment option, but their use still remains controversial given the significant risks and epidemic of opioid addiction and abuse. There is limited data on whether opioid therapy is an effective treatment option for chronic non-cancer pain. Objective: To assess both physical and emotional dimensions of health for patients on opioid therapy for CNCP by reviewing the 36-Item Short Form Health Survey (SF-36) . Study Design: This study was a retrospective cohort review. Setting: Outpatient pain clinic Methods: We recruited 182 patients at the West Penn Pain Institute outpatient pain clinic: 94 patients were recruited for the low-dose opioid group (5-30 morphine milligram equivalents [MME]) while 88 patients were recruited for the high-dose opioid group (> 90 MME). Each patient filled out the SF-36 survey used to assess both the physical and emotional dimensions of their health. We also analyzed patients’ employment status, reasons for unemployment, pain diagnosis, side effects, and compliance issues through the electronic medical record (EMR). Results: Mean scores on General Health Perceptions for the low-dose and high-dose opioid groups were 50.3 ± 21.6 and 44.4 ± 21.9, respectively (P = .07). Though not reaching statistical significance, highdose patients had lower item scores, indicating a perception of poorer health. There were no significant differences between the low-dose and high-dose opioid treatment groups on any of the mean scores from the 8 domains of the SF-36. There was a statistically significant association between opioid treatment group and working status, noncompliance, and the self-reported number of side effects. Patients treated with high-dose opioids had significantly higher rates of unemployment (85%) than did low-dose opioid patients (66%) (χ2 [1] = 8.48, P =.004; odds ratio [OR] = 2.89 [95% confidence interval (CI), 1.39-6.01]). Unemployed patients in the highdose treatment group were more likely to list disability as unemployment while retirement was the most common response in the low-dose treatment group. Patients treated with high-dose opioids had significantly higher rates of self-reported side effects (46%) than did low-dose opioid patients (21%) (χ2 [1] = 12.02, P =.001; OR = 3.08 [95% CI, 1.61-5.89]). Patients treated with high-dose opioids had significantly higher rates of noncompliance (49%) than did low-dose opioid patients (33%) (χ2 [1] = 4.75, P =.029; OR = 1.94 [95% CI, 1.07-3.54]). Thus, the odds of a high-dose opioid patient being unemployed were 2.89 times greater than the odds for a low-dose opioid patient; the odds of a high-dose opioid patient self-reporting side-effects were 3.08 times greater than the odds for a low-dose opioid patient; and the odds of a high-dose opioid patient being noncompliant with their medications were 1.94 times greater than the odds for a low-dose opioid patient. Limitations: The observation al design prohibits drawing causal relationships, and entry criteria was restricted. Conclusions: These data suggest that patients receiving low-dose and high-dose opioid treatment do not have significantly different quality-of-life outcomes. Future studies that incorporate longitudinal data are necessary to examine the temporal relationship between quality of life and opioid therapy. Key words: Chronic pain, chronic non-cancer pain, opioids, pain, quality of life, side effects, noncompliance, unemployment


2017 ◽  
Vol 10 (2) ◽  
pp. 201-214
Author(s):  
Martina Estevam Brom Vieira ◽  
Cibelle Kayenne Martins Roberto Formiga ◽  
Maria Beatriz Martins Linhares

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