INSERM, IRD, SESSTIM, Sciences Économiques & Sociales de La Santé & Traitement de L'information Médicale, Aix-Marseille Univ, Marseille, France.
ORS PACA, Observatoire Régional de La Santé Provence-Alpes-Côte D'Azur, Marseille, France.
Harm Reduct J. 2021 Jan 19;18(1):11. doi: 10.1186/s12954-021-00460-0.
Some people do not benefit from oral administration of opioid agonist treatment, and an intravenous (IV) formulation may be more suitable. Our objective was to evaluate the willingness of people who regularly inject sublingual buprenorphine to receive IV buprenorphine as a prescribed treatment, and to examine related correlates.
We performed a secondary analysis of data from the cross-sectional study PrebupIV, conducted in France in 2015 among 557 people who inject opioids. The study comprised questionnaires completed either face to face or online and community-based workshops. We only included participants who reported buprenorphine as their main injected drug (n = 209). Willingness to receive IV buprenorphine treatment was measured on a scale from 0 to 10. Ordinal logistic regression identified correlates of willingness. Artworks and testimonies from participants in the workshops were also used to illustrate correlates of willingness.
Among the 209 participants, the mean score (SD) for willingness to receive IV buprenorphine was 8.0 (2.8). Multivariate analysis showed that participants who reported using non-prescribed buprenorphine (AOR = 4.82, p = 0.019), a higher daily dosage of buprenorphine (AOR (for 1 mg) = 1.05, p = 0.043), and a higher number of complications due to injection (AOR = 2.28, p = 0.037), were more willing to receive IV buprenorphine treatment.
Willingness to initiate IV buprenorphine treatment was high among people who regularly inject sublingual buprenorphine. A prescribed IV formulation could attract and retain more people into care and reduce harms associated with the injection of buprenorphine tablets.
有些人不能从口服阿片类激动剂治疗中获益,而静脉(IV)制剂可能更合适。我们的目的是评估经常舌下注射丁丙诺啡的人接受处方 IV 丁丙诺啡治疗的意愿,并探讨相关的影响因素。
我们对 2015 年在法国进行的横断面研究 PrebupIV 的数据进行了二次分析,该研究纳入了 557 名注射阿片类药物的人群。该研究包括面对面或在线完成的问卷和基于社区的研讨会。我们仅纳入报告丁丙诺啡为主要注射药物的参与者(n=209)。对接受 IV 丁丙诺啡治疗的意愿进行了 0-10 分的评分。有序逻辑回归确定了意愿的相关因素。还使用了参与者在研讨会上的艺术作品和证词来说明意愿的相关因素。
在 209 名参与者中,接受 IV 丁丙诺啡治疗的意愿平均得分为 8.0(2.8)。多变量分析显示,报告使用非处方丁丙诺啡(AOR=4.82,p=0.019)、丁丙诺啡日剂量更高(AOR(每 1mg)=1.05,p=0.043)和因注射而导致的并发症更多(AOR=2.28,p=0.037)的参与者更愿意接受 IV 丁丙诺啡治疗。
经常舌下注射丁丙诺啡的人愿意开始接受 IV 丁丙诺啡治疗。处方 IV 制剂可以吸引和留住更多的人接受治疗,并减少与丁丙诺啡片剂注射相关的危害。