PurposeTo perform a meta‐analysis of RCTs evaluating donor site morbidity after bone–patellar tendon–bone (BTB), hamstring tendon (HT) and quadriceps tendon (QT) autograft harvest for anterior cruciate ligament reconstruction (ACLR).
MethodsPubMed, OVID/Medline and Cochrane databases were queried in July 2022. All level one articles reporting the frequency of specific donor‐site morbidity were included. Frequentist model network meta‐analyses with P‐scores were conducted to compare the prevalence of donor‐site morbidity, complications, all‐cause reoperations and revision ACLR among the three treatment groups.
ResultsTwenty‐one RCTs comprising the outcomes of 1726 patients were included. The overall pooled rate of donor‐site morbidity (defined as anterior knee pain, difficulty/impossibility kneeling, or combination) was 47.3% (range, 3.8–86.7%). A 69% (95% confidence interval [95% CI]: 0.18–0.56) and 88% (95% CI: 0.04–0.33) lower odds of incurring donor‐site morbidity was observed with HT and QT autografts, respectively (p < 0.0001, both), when compared to BTB autograft. QT autograft was associated with a non‐statistically significant reduction in donor‐site morbidity compared with HT autograft (OR: 0.37, 95% CI: 0.14–1.03, n.s.). Treatment rankings (ordered from best‐to‐worst autograft choice with respect to donor‐site morbidity) were as follows: (1) QT (P‐score = 0.99), (2) HT (P‐score = 0.51) and (3) BTB (P‐score = 0.00). No statistically significant associations were observed between autograft and complications (n.s.), reoperations (n.s.) or revision ACLR (n.s.).
ConclusionACLR using HT and QT autograft tissue was associated with a significant reduction in donor‐site morbidity compared to BTB autograft. Autograft selection was not associated with complications, all‐cause reoperations, or revision ACLR. Based on the current data, there is sufficient evidence to recommend that autograft selection should be personalized through considering differential rates of donor‐site morbidity in the context of patient expectations and activity level without concern for a clinically important change in the rate of adverse events.
Level of evidenceLevel I.