Table 2.
Author, year | Study design | Location | Extended method continuation | Loss to follow‐up | Implant type | Duration | Pregnancy outcomes and assessment | Strengths | Weaknesses | Quality |
---|---|---|---|---|---|---|---|---|---|---|
McNicholas et al. 201715 | Noncomparative cohort | USA | n=223 completing 3rd year | 5% at 24 mo | 1 rod ENG | Up to 2 y extended use | Year 4: Zero pregnancies per 100 woman years | Assessment of ancillary methods of contraception (barrier methods etc.) and comorbidities that may affect fertility (BMI, age) | Small sample size completing each additional year | II‐3, Fair |
n=102 completing 4th year | Year 5: Zero pregnancies per 100 woman years | Detailed description of study population provided | Self‐selected cohort extending duration | |||||||
Assessment: Self‐report (with validation through medical record review where possible) | Study results generalizable with diverse demographics of study population | Pregnancy assessment – validation only where possible | ||||||||
Ali et al. 201620 | Noncomparative cohort analysis from RCT | Brazil, Chile, Dominican Republic, Hungary, Thailand, Turkey, Zimbabwe | n=311 completing 4th year | 2% | 1 rod ENG | Up to 2 y extended use | Year 4: Zero pregnancies per 100 woman years | Detailed description of study population provided | Small sample size completing each additional year | II‐3, Fair |
n=204 completing 5th year | Year 5: Zero pregnancies per 100 woman years | Study results generalizable with multiple study sites | High implant discontinuation rate over extended duration (48%) | |||||||
Assessment: Urine pregnancy testing if suspicion of pregnancy | Pregnancy assessment well defined | |||||||||
Low loss to follow‐up | ||||||||||
Yao and Du, 200321 | Nonrandomized, comparative, prospective observational | Not discussed | n=51 completing the 4th year | 0% | 1 rod ENG | Up to 1 y extended use | Zero pregnancies | Unable to assess generalizability | Small sample size completing each additional year | II‐3, Poor |
Assessment: No information | No assessment for potential confounders | |||||||||
Self‐selected cohort extending duration | ||||||||||
No comparison group | ||||||||||
Sivin et al. 200116 | Multicenter, pharmacokinetic trial | USA | n=43 completing 6th year | No information | 2 rod LNG | Up to 2 y extended use | 2 pregnancies in the 5th year and 3 in the 7th year | Multiple study sites | Small sample size completing each additional year | II‐3, Poor |
non‐USA | n=39 completing 7th year | Assessment: No information | Self‐selected cohort extending duration | |||||||
No comparison group | ||||||||||
Zheng et al. 199922 | Noncomparative, multicenter prospective observational | China | n=151 completing 4th year | 1% | 1 rod ENG | Up to 1 y extended use | Zero pregnancies | Assessment of appropriate confounders including: age (age at enrollment was <35 y old) | Small sample size completing each additional year | II‐3, Poor |
Assessment: Urine pregnancy testing if suspicion of pregnancy | Pregnancy assessment well defined | Self‐selected cohort extending duration | ||||||||
No comparison group | ||||||||||
Lack of generalizability secondary to limited demographic data and all study sites within one country | ||||||||||
Kiriwat et al. 199823 | Noncomparative cohort | Thailand | n=47 completing 4th year | 8% | 1 rod ENG | Up to 1 y extended use | Zero pregnancies | Pregnancy assessment well defined | Small sample size completing each additional year | II‐3, Poor |
Assessment: Urine pregnancy testing if suspicion of pregnancy | No assessment for potential confounders | |||||||||
Self‐selected cohort extending duration | ||||||||||
No comparison group | ||||||||||
Lack of generalizability secondary to limited demographic data |
Abbreviations: ENG, Etonogestrel; LNG, Levonorgestrel.