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. Author manuscript; available in PMC: 2020 Oct 26.
Published in final edited form as: Lancet. 2019 Oct 23;394(10208):1560–1579. doi: 10.1016/S0140-6736(19)32229-9

Table 2:

Existing evidence for impacts* of opioid agonist treatment with methadone or buprenorphine

Effect Level of evidence Sources
OAT vs. no treatment in the community
Opioid use RR 0.48 (0.41, 0.55) SYNTH A 106
Injecting frequency SMD −0.59 (−0.91, −0.26) SYNTH A 106
Injecting risk (sharing needles/syringes) RR 0.53 (0.4, 0.7) SYNTH A 106
HIV linkage to care and treatment HR 1.87 (1.50, 2.33) C 109
HIV treatment adherence OR 2.14 (1.41, 3.26) C 109
HIV treatment attrition/discontinuation OR 0.77 (0.63, 0.95) C 109
HIV viral suppression OR 1.45 (1.21, 1.73) C 109
HIV incidence RR 0.46 (0.32, 0.67) C 107
HCV testing OR 1.73 (1.19, 2.51) C 169
HCV linkage to care and treatment OR 1.40 (0.90, 2.17) C 169
HCV treatment sustained virological response × OR 0.75 (0.45, 1.25) C 169
HCV incidence RR 0.50 (0.40, 0.63) C 108
Skin and soft tissue infections ? NE D 86
Mental health problems SMD 0.49 (0.35, 0.63) C 170
Quality of life (social – WHOQOL-BREF) SMD 0.29 (0.16, 0.42) C 170
Criminal activity SMD −0.57 (−1.00, −0.13) 110
Contact with the criminal justice system × RR 0.75 (0.46, 1.23) C 171
Overdose mortality RaRa 0.25 (0.18, 0.36) SYNTH C 111
Suicide mortality RaRa 0.48 (0.39, 0.59) E 112
Other injury mortality RaRa 0.40 (0.34, 0.46) E 112
All-cause mortality RaRa 0.33 (0.28, 0.39) SYNTH C 111
OAT vs. no treatment in prison
Unsanctioned opioid use NE B 172
Injecting frequency NE B 172
Injecting risk behaviour NE B 172
HIV incidence ? NE B 172
HCV incidence ? NE B 172
Prison infractions NE E 172
Criminal activity (post-release) ? NE B 172
Reincarceration ? NE C 172
OAT engagement (post-release) NE B 173,174
HIV treatment adherence (post-release) NR
HIV viral suppression (post-release) NR
Overdose/suicide/injury mortality (in prison) aHR 0.13 (0.05, 0.35) E 175
All-cause mortality (in prison) aHR 0.26 (0.13, 0.50) E 175
All-cause mortality (4 weeks post-release) aHR 0.25 (0.14, 0.45) E 114,115
Buprenorphine vs. methadone (ref)
Retention in treatment RR 0.83 (0.72, 0.95) A 117
Mortality during induction (4 weeks) RaRa 0.28 (0.08, 0.95) SYNTH C 111,118
Mortality remainder in treatment ND RaRa 0.68 (0.44, 1.04) SYNTH C 111,118
Mortality following cessation (4 weeks) ND RaRa 0.62 (0.16, 2.42) SYNTH C 111,118
Neonatal outcomes…
   …Head circumference  RCT WMD 0.91cm (0.14 1.66) B 119
   …Low birth weight RCT WMD 324g (32, 617) B 119
   …Preterm birth RR 0.40 (0.18, 0.91) B 119

For details of the search strategies used please see Appendix J.

*

Please note that the comparator groups used vary across outcomes; they can include a placebo or active control or an out-of-treatment comparator.

SYNTH – we pooled estimates for this review. NR – no quantification located. NE – no quantitative synthesis reported. ND – no difference between methadone and buprenorphine detected. RR – relative risk. RaRa – rate ratio. RCT – randomised controlled trial. WMD – weighted mean difference. SMD – standardised mean difference. HR – hazard ratio. OR – odds ratio.

Presence or absence of effect

×

OAT does not appear to have a significant effect upon the outcome

This outcome may be increased by OAT

This outcome is decreased by OAT

?

Unclear if OAT has an impact on this outcome

Level of evidence

A

Consistent conclusions across meta-analyses, high quality systematic reviews, or multiple RCTs

B

Evidence from one or two randomised controlled trials only

C

High quality systematic reviews of cohort, case-control or cross-sectional studies

D

Systematic reviews with inconsistent conclusions from authors; OR multiple consistent ecological studies

E

Cross-sectional association, case series suggesting outcome, single cohort study