Anderson 2001
Methods | Computer‐generated random assignment Non blinded assessment Mean follow‐up: 35.4 months Loss to follow‐up: 2 HT (these were excluded from the analysis) Graft re‐ruptures: not reported | |
Participants | USA Study recruitment period: 1991 to 1993 70 participants with acute (< 12 weeks) or chronic (> 12 weeks) ACL deficiency PT: n = 35, mean 23.6 years (14 to 44 years), 23 males / 12 females HT: n = 35, mean 20.1 years (14 to 38 years), 23 males / 12 females | |
Interventions | Arthroscopically‐assisted ACL reconstruction with: 1. Patellar tendon (single incision; proximal fixation ‐ interference screw (7 x 25 mm); tibial fixation ‐ barbed staples) versus 2. Hamstring tendon: semitendinosus/gracilis tendons (2 strands; single incision; proximal fixation ‐ barbed staples; tibial fixation ‐ non‐absorbable sutures) | |
Outcomes | Mean 35 months follow‐up for: Static stability with KT‐1000; range of motion; pivot shift; IKDC; return to sport/activity; strength with Cybex II (60 & 180 deg/s); patellofemoral crepitus | |
Notes | A third intervention group involving HT with extra‐articular procedure (semitendinosus/gracilis tendons with a Losee extra‐articular iliotibial band tenodesis) in 35 patients is not included in this review. Additional methodological information received from Anderson comprised a description of the sample size calculation, patient recruitment / inclusion / exclusion numbers, and the number or re‐ruptures and revisions. Individual patient data were unavailable. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer generated. |
Allocation concealment (selection bias) | Unclear risk | No information |
Blinding (performance bias and detection bias) All outcomes | High risk | |
Incomplete outcome data (attrition bias) All outcomes | Low risk | |
Selective reporting (reporting bias) | High risk | Did not report re‐ruptures, contralateral ruptures or withdrawals. |
Other bias | Low risk |