Background: Anterior cruciate ligament is most common ligament that gets injured in knee joint. Rupture of Anterior cruciate ligament leads to knee instability, recurrent giving-way episodes, and impaired functional performance which significantly affects the quality of life. When conservative management fails, anterior cruciate ligament reconstruction using central quadriceps tendon as primary graft has emerged as a reliable surgical technique to restore knee stability, function, and return to activity, owing to its favorable biomechanical strength and low donor-site morbidity.
Purpose: To evaluate functional outcomes of central quadricep tendon autograft technique for anterior cruciate ligament reconstruction
Method : A prospective study was conducted over a period of approximately 18 months. A total of 15 patients aged between 18 and 45 years with anterior cruciate ligament rupture, fulfilling the selection criteria, were included in the study. All patients were admitted to the Department of Orthopaedics at a tertiary health care hospital in Surat and underwent anterior cruciate ligament reconstruction using a central quadriceps tendon autograft technique.
Conclusion: The central quadriceps tendon autograft provides a thicker and stronger graft, improving graft strength and resistance to failure in ACL reconstruction. Smaller hamstring grafts, particularly those around 7 mm in diameter, have been associated with higher failure rates. This approach eliminates the need for additional graft harvesting or allografts while maintaining adequate graft strength.
Results : The study demonstrates that anterior cruciate ligament reconstruction using a central quadriceps tendon autograft provides significant functional improvement, high rates of return to sport, and a low incidence of graft-related complications at mid-term follow-up.
A statistically significant improvement in postoperative functional outcome scores (p < 0.001) indicates effective restoration of knee stability and function. The majority of patients were able to return to their pre-injury level of sporting activity without residual instability or giving-way symptoms, highlighting the reliability of the quadriceps tendon as a load-bearing graft in high-demand individuals such as athletes.
The low graft failure rate observed in this study is consistent with previously published literature, which reports comparable or lower failure rates for quadriceps tendon autografts when compared with hamstring tendon. The larger cross-sectional area and superior tensile strength of the quadriceps tendon may contribute to enhanced graft durability and resistance to elongation.
Donor-site morbidity was minimal, with fewer complaints of anterior knee pain or kneeling discomfort compared to hamstring grafts. Preservation of hamstring integrity avoided postoperative hamstring weakness, which is commonly reported with hamstring autograft techniques. Although mild quadriceps weakness was noted in the early postoperative period, this improved with structured rehabilitation and did not adversely affect long-term functional outcomes.
The versatility of the central quadriceps tendon autograft, allowing both all–soft tissue and bone-plug configurations, provides surgeons with flexibility in fixation methods and graft sizing. This is particularly advantageous in athletic patients and revision cases where larger graft diameter is desirable.
To assess the clinical and functional outcomes, rate of return to sports, and graft-related complications following anterior cruciate ligament reconstruction using a central quadriceps tendon autograft.
Study design and setting, patients, preoperative assessment, surgical technique, postoperative rehabilitation, outcome measures, and statistical analysis are described.
This was a prospective observational study done over a period of 18 months from January 2024 to July 2025 conducted in the Department of Orthopaedics at Tertiary Care Hospital, Surat.
All the patients who had ACL tear and admitted in Department of Orthopaedics at Tertiary Care Hospital, Surat, Gujarat, during the mentioned study period and fulfilling the selection criteria mentioned below were recruited for the study.
Study Duration: 18 months
Inclusion criteria
Confirmed ACL Tear
Age Range
Functional Instability
Activity Level
Suitable Quadriceps Tendon
Primary or Revision ACL Reconstruction
Patient Consent
Time from Injury
General Health Criteria
Willingness for Postoperative Rehabilitation
Exclusion criteria
Skeletally Immature Patients
Open growth plates (physis) that could be damaged during graft harvesting or tunnel drilling.
Previous Quadriceps Tendon Injury or Surgery
History of quadriceps tendon rupture, tear, or prior harvesting for surgery.
Scarring or tendon weakness that would compromise graft quality.
Severe Osteoarthritis or Knee Degeneration
Advanced cartilage loss (Kellgren-Lawrence grade III–IV) or degenerative changes that impair functional outcome after ACL reconstruction.
Multi-Ligament Knee Injuries
Concomitant PCL, MCL, LCL, or posterolateral corner injuries requiring complex reconstruction unless staged or part of combined reconstruction protocol.
Chronic Infection or Active Inflammatory Joint Disease
Septic arthritis or chronic osteomyelitis.
Rheumatoid arthritis or other inflammatory arthropathies affecting tendon healing.
Systemic Health Issues Affecting Healing
Uncontrolled diabetes mellitus, immunosuppression, or vascular insufficiency.
Coagulopathy or bleeding disorders that increase surgical risk.
Inadequate Quadriceps Tendon Size
Tendon thickness <7 mm or insufficient length for graft preparation.
Poor tissue quality observed intraoperatively.
Neuromuscular Disorders
Conditions affecting quadriceps function or knee stability (e.g., polio, stroke, neuropathies).
Previous Knee Surgery Limiting Graft Harvest
Patellar fracture or previous ACL reconstruction that compromises extensor mechanism or quadriceps tendon.
Non-Compliance or Inability to Participate in Rehabilitation
Patients unwilling or unable to follow postoperative physiotherapy protocol.
Lifestyle or occupational limitations preventing proper recovery.
Pregnancy
Elective surgery is usually postponed due to anesthesia and postoperative rehabilitation considerations.
Knee Society Score (KSS): Combines a Knee Score (pain, ROM, stability, alignment) and a Function Score (walking, stairs) for total 100 points each, widely used for arthroplasty outcomes.
The patient is positioned supine on a radiolucent operating table in hanging leg position under spinal or general anesthesia. A lateral post is placed at the level of the proximal thigh used to maintain knee in flexion and valgus position whenever required . A pneumatic tourniquet is applied to the proximal thigh but inflated only after limb exsanguination. The limb is prepared and draped in standard sterile fashion.
Fig.1- Hanging Leg position
Harvesting the central quadriceps tendon autograft
Graft Harvest
A double-bladed knife or scalpel is used to harvest the central third of the tendon. The graft is dissected proximally to obtain a length of approximately 7–9 cm.
The graft may be harvested as:
Hemostasis is achieved, and the donor site is irrigated.
Fig.2- Graft Preparation
The common femoral tunnel preparation
The femoral tunnel is prepared using an anatomic anteromedial portal technique. The knee is flexed to 120–130° to prevent posterior wall blowout and allow accurate tunnel placement. After debridement of ACL remnants, the native femoral ACL footprint is identified using landmarks such as the resident’s ridge and posterior cartilage margin.
A guide pin is placed at the center of the femoral footprint through the anteromedial portal, ensuring adequate posterior wall preservation. A cannulated reamer matching the graft diameter (usually 8–10 mm) is used to drill the femoral tunnel to a depth of 25–30 mm under direct arthroscopic visualization. Tunnel integrity and position are confirmed, and a shuttle suture is passed for graft passage.
The tibial tunnel for ACL
With the knee flexed to 90°, residual ACL fibers are debrided to expose the native tibial footprint, located anterior to the tibial spine, medial to the anterior horn of the lateral meniscus, and posterior to the intermeniscal ligament. A tibial aiming guide set at 55–60° is positioned at the center of the footprint. A guide wire is passed and confirmed arthroscopically to avoid roof impingement. Over the guide wire, a cannulated reamer matching the graft diameter (8–10 mm) is used to create the tibial tunnel. Tunnel position and smoothness are confirmed, and a shuttle suture is passed for graft passage.
Fig.3- Intra-operative photo
Graft preparation
The harvested central quadriceps tendon graft is cleared of excess soft tissue and measured for length and diameter. The graft length is usually 7–9 cm, with a diameter of 8–10 mm. Both ends of the graft are secured using Krackow or whip-stitch sutures with high-strength non-absorbable sutures. The prepared graft is kept moist in saline until implantation.
Graft fixation
The graft is passed through the tibial tunnel into the femoral tunnel.
Femoral fixation is achieved using a suspensory fixation device or interference screw, depending on graft type.
Tibial fixation is performed using an interference screw with the knee held in 20–30° of flexion under appropriate graft tension. The knee is cycled to remove graft creep before final fixation, and stability is reassessed.
Fig.4- Clinical photo
Closure
After completion of graft fixation and confirmation of knee stability, meticulous hemostasis is achieved at the quadriceps tendon harvest site. The quadriceps tendon defect is closed using interrupted absorbable sutures, ensuring approximation without excessive tension. The paratenon is carefully repaired in a continuous or interrupted manner to restore the tendon gliding surface and minimize postoperative adhesions and anterior knee pain.
Subcutaneous tissues are closed with absorbable sutures, followed by skin closure using interrupted or subcuticular sutures as per surgeon preference. Arthroscopic portal sites are closed with absorbable sutures after thorough joint lavage and evacuation of fluid. A sterile dressing is applied over all incisions, and a compression bandage is placed to reduce postoperative swelling. A knee brace may be applied depending on the rehabilitation protocol.
REHABILITATION PROTOCOL
|
Phase |
Time Frame |
Goals |
Weight Bearing |
ROM Goals |
Exercises / Activities |
|
Phase I: Immediate Post-Op |
0–2 weeks |
Reduce pain & swelling, protect graft, activate quadriceps |
WBAT* with crutches |
0–90° |
Ankle pumps, quad sets, straight leg raises, heel slides, patellar mobilization |
|
Phase II: Early Rehab |
2–6 weeks |
Restore ROM, improve gait, build strength |
Full WB (wean crutches) |
0–120°+ |
Closed-chain exercises, mini-squats, leg press (light), stationary bike |
|
Phase III: Strengthening |
6–12 weeks |
Increase strength & endurance, neuromuscular control |
Full |
Full ROM |
Lunges, step-ups, hamstring curls, balance training, core strengthening |
|
Phase IV: Advanced Strength |
3–5 months |
Improve power, agility, dynamic stability |
Full |
Full |
Plyometrics, lateral movements, agility drills, single-leg strengthening |
|
Phase V: Return to Sport Prep |
5–9 months |
Sport-specific training, injury prevention |
Full |
Full |
Running progression, cutting drills, jumping/landing mechanics |
|
Phase VI: Return to Sport |
9–12 months |
Safe return to competition |
Full |
Full |
Full practice participation after functional testing clearance |
CASE-1
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Fig.14
Fig.15