Anterior cruciate ligament (ACL) injury is one of the most common knee injuries in sports such as soccer, handball, basketball, and rugby.1 Approximately 175,000 ACL reconstruction (ACLR) surgeries are performed in the United States each year to restore knee stability and function. Despite undergoing surgical reconstruction and rehabilitation, a high noncontact ACL reinjury rate of 25.4% (either the reconstructed side or the contralateral side) has been reported in athletes who returned to high risk (Level I or 2) sports, and the ACL injury risk after ACLR is 15 times that of the healthy population.2
Landing in athletic maneuvers such as hopping and drop jumping has been shown to have one of the highest risks for ACL injury.3,4 Landing tasks have been widely used for biomechanics analysis after ACL injury and reconstruction. Previous systematic reviews have summarized that altered biomechanics, such as decreased peak knee-flexion and knee-extension moments, are commonly observed in patients after ACLR when compared with healthy people during landing.5,6 Aberrant biomechanical patterns may persist subsequent to patients returning to sport after ACLR, and this may explain the high rate of a second ACL injury.7,8
To prevent ACL reinjury, the knee joint must be stabilized and protected by the passive restraint (ligaments) and the active restraint (muscles). However, deficits in muscle strength, muscle activity, and motor control can be found after ACLR.9–11 Despite the recovery of normal strength symmetry, deficits in neuromuscular control can still be observed.8,12 Neuromuscular control is defined as “an unconscious activation of dynamic restraints, occurring in preparation for and in response to joint motion and loading, for the purpose of maintaining and restoring functional joint stability.”13 Adequate neuromuscular control helps to accommodate muscle contractions and attenuate forces when there are impact forces on the knee.14 Neuromuscular control can be evaluated by the pattern of muscle activity during movements, which consists of amplitude, timing, and frequency assessed by electromyography (EMG). Earlier onset of muscle activity prior to landing increases the stiffness of the joints, which allows the muscles to have enough time to generate force, providing less impact force on the knee during landing.15,16 A case study suggests that delayed muscle activity onset may be associated with ACL injury.17 Individuals who did not experience a secondary ACL reinjury used greater levels of hamstring activity prior to landing.18 It has been reported that greater quadriceps and gluteus activity, with less hamstring and gastrocnemius activity, are correlated with smaller knee-flexion angles. This may predispose an individual to increased impact forces during landing.19 Coactivation of knee musculature during dynamic activity is identified as an attempt to stabilize the joint and to reduce forces on the knee.20
A previous systematic review was conducted to evaluate the changes in muscle activity such as walking and running in patients with ACLR.21 However, the activity pattern in patients with ACLR during landing has not been systematically reviewed. Some researchers have found decreased quadriceps activity and greater hamstring activity during landing when compared with healthy controls, whereas other researchers have not reported similar findings.22,23 These neuromuscular alterations may be associated with biomechanical deficits, which contribute to ACL reinjury. Given that muscle activity is a modifiable factor that can be improved through neuromuscular exercises,24,25 it is essential to understand the muscular strategy adopted by patients with ACLR during landing tasks, as rehabilitation can modify this outcome. The aim of this review was to evaluate the changes in neuromuscular activity of the lower-extremities during landing tasks in patients with ACLR assessed by EMG.
Methods
The method of this systematic review was chosen according to preferred reporting items for systematic reviews and meta-analysis.26 The protocol was prospectively registered on the PROSPERO International register for systematic reviews (http://www.crd.york.ac.uk/PROSPERO) (CRD42018095560).
Searching Strategy
An electronic database search was performed of PubMed, Ovid, Scopus, and Web of Science from the inception of the databases until July 2019. A combination of the following keywords and their variations were used: (anterior cruciate ligament OR ACL) AND (electromyography OR EMG) AND (landing OR land). The search was complemented by reviewing the reference lists of papers selected from the original database search. All articles were screened by 2 reviewers independently (X.H. and O.Y.L.). Any disagreement was discussed, and unresolved items were passed to a third reviewer (H.T.L.) for consensus. The search results were imported into reference manager software (Endnote X5; Thomson, New York, NY) to avoid the duplication of records.
Selection Criteria
After removing the duplicates, all the titles and abstracts were reviewed to determine their possible eligibility for inclusion. The inclusion criteria were as follows: (1) patients with ACLR were recruited; (2) at least 1 landing task under nonfatigue condition was performed, including drop landing, jump landing, and hop landing; (3) muscular activity amplitude, timing (onset/duration), or frequency of lower limb prior to or during landing assessed by EMG was reported; and (4) healthy subjects or the contralateral uninvolved limbs were included as a control group. Non-English language publications, review articles, comments, editorials, letters, animal studies, and cadaveric studies were excluded. Studies in which subjects landed with any external support, such as a knee brace, were also excluded. No limitations were placed on the year of publication, age, gender, type of graft, or time since surgery.
Quality Assessment
The methodological quality of the included studies was rated using the modified version of the Downs and Black checklist, which only includes criteria that are relevant to assessing potential sources of bias. The modified Downs and Black checklist is a valid and reliable instrument used for assessing both randomized and nonrandomized investigations.27 With a maximum score of 15, a total score of ≥12 indicates high methodological quality, a score of 10 or 11 indicates moderate quality, and a score ≤9 indicates low quality.28 Two reviewers (X.H. and O.Y.L.) independently reviewed and scored each article based on the criteria (see the Supplemental Material A). Any disagreement was discussed, and unresolved items were passed to a third reviewer (H.T.L.) for consensus. The intraclass correlation coefficient was calculated using SPSS for Windows (version 24; SPSS Inc, Chicago, IL) to measure the interrater agreement between the 2 reviewers.
Data Extraction and Statistical Analysis
The relevant data were extracted from all included studies: (1) general information (author and year of publication), (2) subjects’ characteristics (age, gender, and activity level), (3) time since surgery, (4) graft type, (5) functional status/sport involvement, (6) task(s) performed, (7) muscle(s) tested, and (8) control group (contralateral side/healthy controls). The EMG results used for the medial hamstrings were gathered either from the semitendinosus muscle or the semimembranosus muscle, given their similar function and the high degree of cross talk in their surface EMG signals.29 Data regarding the muscle activity pattern (onset/time to peak/amplitude/cocontraction) and corresponding phase, normalization method, and main findings were also extracted. The data were analyzed by limb using 2 comparisons: (1) the ACLR limb compared with the contralateral uninjured limb and (2) the ACLR limb compared with a healthy matched control limb. In addition, the type of landing task (single-leg or double-leg landing) was also used to stratify the data.
Statistical Analysis
The results were not precisely reported by the authors. To calculate the effect size and 95% confidence interval (CI), the sample size and mean (SD) of the parameters are needed. When the comprehensive data were not provided, we contacted the corresponding author via email to request the data. The effect sizes were calculated for the involved limbs in comparison with the healthy control/contralateral limbs using the following formula: Cohen d = mean (injured side) − mean (control)/SD (pooled). Based on Cohen suggestion, the effect size of ≤0.4 represents a small effect, >0.5–8 a moderate effect, and ≥0.8 is considered a large effect.30
Results
Literature Search
A total of 326 studies were identified using the search strategy (Figure 1). After removing all duplicates, 209 studies were evaluated by title and abstract. The full texts of 35 studies were retrieved, with 21 studies meeting the selection criteria. Only 5 of these studies provided separate data for cohorts within the ACLR groups. Coats-Thomas et al31 and Nyland et al22 reported individual data for males and females, Nyland et al32 reported data by sport participation or capacity, and Bryant et al33 and Rocchi et al34 separated data by graft type.
—The flowchart and the results from the search strategy. ACLR indicates anterior cruciate ligament reconstruction.
Citation: Journal of Sport Rehabilitation 29, 8; 10.1123/jsr.2019-0393
Methodological Quality
The methodological quality scores ranged from 10 to 14 (of 15), with an average score of 11.43 (see Supplementary Table A [available online]). Among the included studies, 6 (28.6%) were classified as high quality,22,32–36 whereas 15 (71.4%) were considered to be moderate quality.16,18,23,31,37–47 All these studies scored positively on Items 1 (clear aim), 2 (outcome described), 3 (subjects described), 5 (distribution of confounding factors described), 6 (main finding clearly described), 7 (estimate of random variability), 18 (appropriate statistics), 20 (clearly described method), and 21 (subjects recruited from the same population), and negatively on item 11 (subjects asked represent population). Only 4 studies reported results with adjustment for confounding factors.22,33,34,35 The intraclass correlation coefficient of rating was .855 (95% CI, .652 to .940) between 2 reviewers.
Subjects’ Characteristics
A total of 398 subjects (208 males and 190 females, with mean age ranging from 16.0 to 29.4 years) were derived from the 21 studies. The reported time post ACLR ranged from 6 months to 6 years. Twenty studies reported the graft type used for ACLR. Three studies used bone patellar tendon-bone grafts,16,18,46 3 studies used semitendinosus–gracilis tendon grafts,23,36,37 and 2 studies used allograft.22,32 The remaining studies used a mixture of bone-patellar tendon-bone grafts, semitendinosus tendon grafts, semitendinosus–gracilis tendon grafts, or allograft. Eighteen studies reported the preinjury activity level of the ACLR subjects. Briem et al37 included 27 professional athletes from top leagues in football, handball, and basketball, and Jordan et al40 included 11 elite ski racers. The remaining studies included recreational sport players. From 14 studies, 308 subjects returned to sport/were cleared for sport return.18,22,32,34,36,37,39–42,44–47 Only 3 studies22,32,34 reported the criteria for a return to sports, which included passive knee stability, more than 85% symmetry in isokinetic/isometric quadriceps and hamstring muscle strength, and single-leg hop/jump performance. The study characteristics are presented in Table 1.
Study Characteristics of the Included Studies
Author (year) | ACLR subjects | Graft | Time post-ACLR | Functional status/sports involvement | Task | Muscles | Control group |
---|---|---|---|---|---|---|---|
Briem (2016)37 | n = 18, females Age: 21.5 (2.7) y top leagues in football, handball, and basketball | STG | 1–6 y | All returned to competition | Single-leg crossover hop test | MH and LH | n = 18, healthy controls |
Bryant (2009)33 | n = 27, males Age: BPTB graft: 30.9 (7.3) y STG graft: 22.9 (3.8) y Activity level: not reported | BPTB (n = 14), STG (n = 13) | BPTB: 15.1 (5.0) mo, STG: 14.2 (4.5) mo | 1. All regained full ROM 2. Overall knee functional score: BPTB: 81.1 (16.1) STG: 87.5 (11.8) | Single-leg maximal, countermovement hop for distance | VL, VM, MH, and LH | n = 22, healthy controls |
Coats‐Thomas (2013)31 | n = 10, 4 males and 6 females Age: male 29.3 (6.1) y; female 24.7 (6.7) y Activity level: Tegner score ≥ 5 | BPTB (n = 7), ST (n = 3) | >5 y | Not reported | Double-leg jump-cut maneuver | RF, VM, MH, LH MG, and LG | n = 10, healthy controls |
Dashti Rostami (2018)38 | n = 12, males Age: 23.83 (5.49) y Activity level: I and II sports | BPTB (n = 4), STG (n = 6), and allograft (n = 2) | 23.75 (6.30) mo | Not reported | Single-leg vertical drop landing (30-cm box) | VL, VM, LH, MH, LG, and MG | n = 12, healthy controls |
Dashti Rostami (2019)39 | n = 12, males Age: 22.5 (4.1) y Activity level: recreationally active | BPTB (n = 4), STG (n = 6), and allograft (n = 2) | 23.75 (6.3) mo | All allowed to return to sport activities | Single-leg vertical drop landing (30 cm) | GMed, and AL | n = 12, healthy controls |
Gokeler et al (2010)16 | n = 9, 6 males and 3 females Age: 28.4 (9.7) y Activity level: levels I–II sports | BPTB | 27 (1.5) wk | IKDC: 81 (7.1) | Single-leg hop | GMax, MH, LH, VM, VL, RF, MG, LG, and SO | n = 11, healthy controls |
Jordan et al (2017)40 | n = 11, 6 males and 5 females Age: male 26.5 (5.8) y; female 23.6 (1.8) y Activity level: elite ski racers | STG (n = 7), ST (n = 1), and allograft (n = 3) | 3.0 (2.8) y | All were cleared to compete | Double-leg squat jump | VM, VL, MH, and LH | n = 11, healthy controls |
Lessi and Serrão (2017)41 | n = 20, 13 males and 7 females Age: 25.1 (4.2) y Activity level: recreational (≥3 times/wk) | BPTB (n = 7) and ST (n = 13) | 23.75 (6.30) mo | All were cleared to return to sport | Single-leg drop vertical jump (31-cm box) | VL, LH, GMed, and GMax | n = 20, healthy controls |
Lessi et al (2018)42 | n = 14, 7 males and 7 females Age: male 23.90 (2.80) y; female 24.7 (5.3) y Activity level: recreational (3.1–5.7 h/wk) | BPTB (n = 5) and ST (n = 9) | Male: 21.1 (6.8) mo Female: 24.2 (9.5) mo | All returned to sport | Single-leg drop vertical jump (31-cm box) | VL, LH, GMed, and GMax | Contralateral side |
Lepley et al (2013)35 | n = 12, 7 males and 5 females Age: 22.08 (4.7) y Activity level: not reported | BPTB (n = 7) and STG (n = 5) | 248 (54.6) d (7–10 mo) | Not reported | Single-leg landing after double-leg jump (17 cm) | VL and LH | n = 13, healthy controls |
Mielińska et al (2015)43 | n = 6, males Age: 26.2 (2.3) y Activity level: not reported | Not reported | 8 mo | Not reported | Double-leg Jumping down from 0.1-, 0.2-, and 0.3-m step heights | MH, MG, LG, and VM | n = 22, healthy controls |
Nyland et al (2010)22 | n = 70, 35 males and 35 females Age: not reported Activity level: 12.9% highly competitive, 31.4% frequently sporting, 35.7% sporting sometimes, and 20% nonsporting | Allograft | Male: 5.6 (3.2) y Female: 5.1 (2.6) y | All were cleared to return to sport IKDC: male 84.9 (15.3); female 81.4 (13.5) | Single-leg countermovement jump | GMax, VM, MH, and MG | Contralateral side |
Nyland et al (2014)32 | n = 65 32 males and 33 females Age: Group 1: 26.5 (95% CI, 21.9 to 31.8) y Group 2: 29.3 (95% CI, 24.1 to 34.4) y Group 3: 33.6 (95% CI, 26.4 to 39.1) y Activity capacity: Group 1: very capable (n = 20) Group 2: capable (n = 23) Group 3: not capable (n = 22) | Allograft | Post-op: Group 1: 4.6 (95% CI, 2.8 to 6.2) y Group 2: 5.4 (95% CI, 4.2 to 6.6) y Group 3:5.2 (95% CI, 3.8 to 6.5) y | All were cleared to return to sport IKDC: Group 1: 91 (95% CI, 84.1 to 94.6) Group 2: 87.2 (95% CI, 82.1 to 92.4) Group 3: 76.8 (95% CI, 67.4 to 80.3) | Single-leg hop | GMax, VM, MH, and MG | Contralateral side |
Ortiz et al (2008)44 | n = 14, females Age: 25.4 (3.1) y Activity level: recreational | BPTB (n = 9), STG (n = 3), and allograft (n = 2) | 7.2 (4.2) y | All engaged in recreational fitness activities, such as jogging, running, and weight lifting | 1. Single-leg 40-cm drop jump 2. Single-leg 20-cm up–down hop | GMax, Qua, LH, and MH | n = 15, healthy controls |
Ortiz et al (2011)45 | n = 14, females Age: 25.4 (3.1) y Activity level: recreational | BPTB (n = 9), STG (n = 3), and allograft (n = 2) | 7.2 (4.2) y | All engaged in recreational fitness activities, such as jogging, running, and weight lifting | 1. Crossover hopping 2. Sidehopping | GMed, Qua, LH, and MH | n = 15, healthy controls |
Oritiz et al (2014)36 | n = 14, females Age: 28.5 (4.59) y Activity level: volleyball, basketball, and soccer at the college or intramural level | STG | 1–5 y | All allowed to return to preinjury activity | 1. Single-leg drop jump (40-cm box) 2. Double-leg drop jump (60-cm box) | VM, VL, RF, MH, and LH | n = 16, healthy controls |
Palmieri-Smith et al (2019)18 | n = 14, 10 males and 4 females Age:ACL-1: 17.14 (2.7) y ACL-2: 16.0 (1.1) y Activity level: Tegner score ACL-1: 6.29 (1.89) ACL-2: 6.14 (2.96) | BPTB | ACL-1: 230.71 (50.5) d ACL-2: 189.71 (10.7) d | All returned to unrestricted sport activities | Single-leg hop | VL, BF, and LG | n = 7, healthy controls |
Rocchi et al (2018)34 | n = 26, males Age: BPTB: 21 (3) y STG: 21 (5) y Activity level: Tegner score 7–9 | BPTB (n = 15) and STG (n = 11) | 6.0 (1.2) mo | All returned to unrestricted sport activities | Single-leg drop landing (20 cm) and hop landing | VM, RF, VL, BF, and ST | n = 15, healthy controls |
Swanik et al (1999)46 | n = 6, female Age: 29.4 (10.4) y Activity level: Tegner: 6.8 (1) | BPTB | 6–30 mo | All attempted to return to previous level of activity | Single-leg jump landing (20.3 cm) | VM, VL, MH, and LH | n = 6, healthy controls |
Tsai et al (2012)47 | n = 10, females Age: 25.3 (2.4) y Activity level: recreational | Allograft and BPTB | 1–5 y | All returned to unrestricted sport activities | Single-leg drop landing | VL, VM, RF, MH, LH, MG, and LG | n = 10, healthy controls |
Vairo et al (2008)23 | n = 14, 5 males and 9 females Age: 22.5 (4.1) y Activity level: moderate activity with minimum frequency of 3 d/wk, 30-min duration | STG | 21.4 (10.7) mo | Not reported | Single-leg vertical drop (30 cm) | VM, VL, MH, LH, and MG | n = 11, healthy controls |
Abbreviations: ACLR, anterior cruciate ligament reconstruction; AL, adductor longus; BF, biceps femoris; BPTB, bone patellar tendon bone graft; GMax, gluteus maximus; GMed, gluteus medius; IKDC, International Knee Documentation Committee score; LG, lateral gastrocnemius; LH, lateral hamstring; MG, medial gastrocnemius; MH, medial hamstring; Qua, quadriceps; RF, rectus femoris; ROM, range of motion; SO, soleus; ST, semitendinosus tendon graft; STG, semitendinosus-gracilis tendon graft; VL, vastus lateralis; VM, vastus medialis.
Primary Outcome
Of the included studies, various muscle activity patterns were assessed, including (1) muscle activity onset of the quadriceps,16,33,34,38 hamstrings,16,33,34,38 gluteus maximus,16 gastrocnemius,16,38 and soleus16; (2) time to peak muscle activity of the quadriceps,31,33,36 hamstrings,31,33,36 and gastrocnemius31; (3) preparatory activity amplitude of the quadriceps,18,23,40 hamstrings,18,23,40 gastrocnemius,18,23 gluteus medius,39 and adductor longus39; (4) reactive activity amplitude of the quadriceps,18,22,23,33–36,38,40–47 hamstrings,18,22,23,33–38,40–45,47 gastrocnemius,18,22,23,32,38,43,47 gluteus maximus,22,32,41,42,44,45 gluteus medius,39,41 and adductor longus39; and (5) the quadriceps and hamstring cocontraction ratio.23,31,35,36,44,47 Regarding the tasks performed, 7 studies investigated the single-leg hop tasks16,18,32,33,34,37,45 and 10 studies involved the single-leg drop landing tasks (height ranges from 20 to 40 cm).23,34,36,38,39,41–44,47 Five studies used single-leg or double-leg jump landing tasks.22,31,35,40,46 For the normalization procedure, 8 studies used maximum isometric voluntary contraction,22,23,32,34,37–40 8 studies normalized the amplitude to peak amplitude during a dynamic task,18,35,36,41,42,44,45,47 and 2 studies reported the area under the EMG curve.31 Only one study normalized the amplitude to free standing.43 Details of the method are summarized in Supplementary Tables B1–B6 (available online).
Secondary Outcomes
In addition to the muscle activity measurements, other outcome measures were considered. Some studies implemented patient-reported outcomes, including the Cincinnati,33 International Knee Documentation Committee,16,22,32 and Knee injury and Osteoarthritis Outcome Score (KOOS)37 scores. Knee biomechanics were measured in 13 studies,22,23,31–34,36,41–45,47 including kinetic and kinematic variables, such as joint angles, ground reaction forces, tibial acceleration, and body mass center. In addition, functional assessments such as isokinetic muscle strength and hop/jump performance were reported in 6 studies.16,18,23,32,37,40
Main Findings
Of the 21 studies, 16 studies reported an altered muscle activity pattern during landing tasks when compared with either the healthy controls or the contralateral side.16,18,22,23,31,32,34–40,43,44,47 Among them, 8 studies involved patients who returned to sport/were cleared for sport return,18,22,32,34,37,39,40,47 and 8 studies also reported altered kinematics/kinetics during landing.16,22,23,34,36,43,44,47 According to 6 studies,22,23,32,34,37,40 patients with ACLR demonstrated altered muscle activity patterns, even though muscle strength or functional performance had been restored (achieve more than 85% symmetry or no difference between groups).
Muscle activity onset: Four studies compared the muscle activity onset during single-leg landing between the ACLR-involved limb and healthy controls (Supplementary Table B1 [available online]). Rocchi et al34 found significant earlier onset of quadriceps and hamstring activity in the ACLR-involved limb when compared with healthy controls, and the effect size is large in both quadriceps (d = 1.51; 95% CI, 0.77 to 2.19; P < .05) and hamstrings (d = 1.46; 95% CI, 0.72 to 2.13; P < .05). Two studies found a trend of earlier onset of quadriceps activity in the ACLR-involved limb when compared with healthy controls; however, the effect sizes were small to moderate (d = 0.22–0.75, P > .05).33,38 Three studies exhibited a trend toward earlier onset in the hamstrings in the ACLR-involved limb when compared with healthy controls, with small to large effect sizes (d = 0.01–1.13, P >.05).16,33,38 Only one study by Gokeler et al16 compared the involved limb with the contralateral side for patients with ACLR. They reported an earlier onset of the quadriceps, hamstrings, gluteus maximus, gastrocnemius, and soleus, with effect sizes ranging from moderate to large (d = 0.64–2.53, P < .05).
Time to peak muscle activity: Two studies reported the time to peak muscle activity during landing (Supplementary Table B2 [available online]). When comparing the ACLR-involved limb and healthy controls during double-leg landing, Coats-Thomas et al31 found delayed time to peak activity in the quadriceps (d = 0.48–1.48, P < .05) and hamstrings (d = 0.39–1.94, P < .05); however, Ortiz et al36 reported no difference in both the quadriceps (P = .74) and hamstring (P = .91) activity. When comparing the ACLR-involved limb and healthy controls during single-leg landing, Ortiz et al36 found significantly earlier time to peak activity in the quadriceps (P = .01) and hamstrings (P = .01), whereas Bryant et al33 found no difference between them (P > .05).
Preparatory muscle activity amplitude: Four studies assessed the preparatory muscle activity amplitude prior to landing (Supplementary Table B3 [available online]). Jordan et al40 showed that the ACLR-involved limbs land with increased hamstring activity prior to double-leg landing when compared with healthy controls, and the effect size is large (d = 1.19; 95% CI, 0.27 to 2.11; P < .01). In addition, they also found significantly decreased quadriceps activity in ACLR-involved limbs when compared with the contralateral side, with a moderate effect size (d = −0.71; 95% CI, −1.58 to 0.15; P < .01). Contrary to their findings, Vairo et al23 found no difference in the quadriceps and hamstrings, either between group or between limb (P > .05); but they did find decreased medial gastrocnemius activity in the ACLR-involved limb when compared with their contralateral side prior to single-leg landing, and the effect size was large (d = −0.92; 95% CI, −1.70 to −0.15; P = .01). Palmieri-Smith et al18 also found no significant difference in quadriceps, hamstring, and gastrocnemius activity prior to single-leg landing (P > .05). Dashti Rostami et al39 also reported no significant difference in gluteus medius (P = .77) and adductor longus activity (P = .54) between the ACLR-involved limb and healthy controls during single-leg landing.
Reactive muscle activity amplitude: Eleven studies compared the reactive muscle activity amplitude in the quadriceps between the ACLR-involved limbs and healthy controls during single-leg landing, and 6 studies found no significant difference (P >.05).34,38,41,45–47 Contrary to their findings, 3 studies reported an increase in quadriceps activity of the ACLR-involved limbs when compared with the healthy controls during single-leg landing.23,36,44 However, the effect size was calculated for only one study, which exhibited a large effect size in the vastus medialis (d = 0.86; 95% CI, 0.08 to 1.64; P = .01) and vastus lateralis (d = 0.97; 95% CI, 0.16 to 1.73; P = .01).23 The other 2 studies found a decrease in vastus lateralis activity of the ACLR-involved limbs when compared with the healthy controls during single-leg landing with a large effect size (d = −2.00 to −1.29, P < .05).18,35 Three studies reported the reactive muscle activity amplitude in quadriceps activity between the ACLR-involved limbs and healthy controls during double-leg landing.36,40,43 Ortiz et al36 found a significant decrease (d = 0.22, P = .01) in the quadriceps activity of the ACLR-involved limbs when compared with the healthy controls during double-leg landing, whereas others found no significant difference.40,43
Eleven studies compared the reactive muscle activity amplitude in the hamstrings between the ACLR-involved limbs and healthy controls during single-leg landing, and 8 studies found no significant difference (P > .05).18,34–36,38,41,44,45 Contrary to their findings, 2 studies found an increase in hamstring activity of the ACLR-involved limbs when compared with healthy controls during single-leg landing, and the effect size was moderate to large (d = 0.76; 95% CI, −0.01 to 1.53; P = .02 and d = 1.12; 95% CI, 0.16 to 2.08; P = .02).23,47 Three studies reported the reactive muscle activity amplitude in hamstring activity between the ACLR-involved limbs and healthy controls during double-leg landing.36,40,43 Ortiz et al36 demonstrated a decrease in hamstring activity of the ACLR-involved limbs when compared with healthy controls during double-leg landing (d = 0.18, P = .02), but similar findings were not reported in the other 2 studies.40,43
Three studies compared the reactive muscle activity amplitude in the gluteus maximus between the ACLR-involved limbs and healthy controls during single-leg landing.41,44,45 Ortiz et al44 found significantly increased activity in the gluteus maximus of the ACLR-involved limb when compared with the healthy controls during single-leg landing (d = 0.29, P = .003), whereas others found no significant difference (P > .05).41,45 Only one study by Dashti Rostami et al39 assessed the activity of the gluteus medius and adductor longus during single-leg landing and found a significant decrease in the activity of the gluteus medius, with a moderate effect size (d = −0.75; 95% CI, −1.55 to 0.10; P = .02), and no significant difference in adductor longus activity (P = .11) when compared with the healthy controls. Three studies compared the reactive muscle activity amplitude in the gastrocnemius between the ACLR-involved limbs and healthy controls during single-leg landing.23,38,47 Dashti Rostami et al38 reported a significant decrease in the gastrocnemius activity of the ACLR-involved limbs when compared with the healthy controls during single-leg landing, whereas others found no significant difference (P > .05).23,47 Only one study by Mielińska et al43 reported the gastrocnemius activity during double-leg landing and found that it was increased when compared with the healthy controls (P = .01).
Six studies compared the reactive muscle activity amplitude in both the quadriceps and hamstrings between the ACLR-involved limbs and contralateral sides during single-leg landing, and no difference was found (P > .05).22,23,32,40–42 Four studies compared the reactive muscle activity amplitude in the gluteus maximus between the ACLR-involved limbs and contralateral sides during single-leg landing,22,32,41,42 of which, 2 studies found increased activity in the gluteus maximus of the ACL-involved limb when compared with the contralateral sides,22,32 and the effect size ranged from moderate to large (d = 0.54–0.85, P < .05). However, the other 2 studies reported no difference in activity of the gluteus maximus of the ACL-involved limb when compared with the contralateral side (P > .05).41,42 Three studies compared the gastrocnemius activity between the ACLR-involved limbs and contralateral side during single-leg landing and reported contradictory findings.22,23,32 Nyland et al22 found increased activity in the medial gastrocnemius (d = 0.60; 95% CI, 0.12 to 1.08; P <.001) in male patients when compared with the contralateral side, whereas Vairo et al23 found a significant decrease (d = −0.79; 95% CI, −1.56 to −0.01; P = .01). Nyland et al32 found no difference in activity of the medial gastrocnemius of the ACLR-involved limbs when compared with the contralateral sides (P > .05; Supplementary Table B4 [available online]).
Quadriceps and hamstring cocontraction: Cocontraction of the quadriceps and hamstrings represents synchronized activation of agonist and antagonist muscles. Two studies compared the quadriceps and hamstring cocontraction ratio between ACLR-involved limbs and healthy controls prior to landing and reported contrary findings.23,31 Vairo et al23 reported an increased cocontraction using the more activated muscle as a divisor (d = 0.70; 95% CI, −0.14 to 1.49; P = .03) during single-leg landing; however, Coat-Thomas et al31 found no significant difference in the Q/H ratio during double-leg landing when compared with the healthy controls (P > .34; Supplementary Table B5 [available online]).
Five studies compared the quadriceps and hamstring cocontraction ratio between ACLR-involved limbs and healthy controls during single-leg landing,23,35,36,44,47 of which, 2 studies used similar ratio equations (more activated muscle used as a divisor), and they demonstrated significantly increased quadriceps and hamstring cocontraction of ACLR-involved limbs when compared with the healthy controls (d = 0.25–0.74, P < .05).23,44 However, Lepley et al35 reported no significant difference (P = .45), and Ortiz et al36 found a decreased quadriceps and hamstring cocontraction of the ACLR-involved limbs when compared with healthy controls using the same equation (P = .02). Tsai et al47 reported an increased cocontraction ratio of the ACLR-involved limbs when compared with the healthy controls with the equation of H+G/Q (d = 1.26; 95% CI, 0.26 to 2.16; P = .004). Two studies compared the quadriceps and hamstring cocontraction ratio between ACLR-involved limbs and healthy controls during double-leg landing and generated contrary findings.31,36 Coats-Thomas et al31 reported greater Q/H cocontraction (P = .06), whereas Ortiz et al36 found no significant difference using the equation of EMG amplitude of the less activated muscle (EMGS)/EMG amplitude of the more activated muscle (EMGL) (P = .22). Only one study by Vairo et al23 compared the quadriceps and hamstring cocontraction ratio between the ACLR-involved limbs and the contralateral sides during single-leg landing, but no difference was found (P = .26; Supplementary Table B6 [available online]).
Discussion
In this review, we systematically evaluated the muscle activation patterns of ACLR limbs during landing tasks when compared with the contralateral side or healthy group. Over 70% of the included studies found altered muscle activity patterns during landing tasks in patients more than 6 months after ACLR, even though they were considered to be capable of returning to sport. It is not surprising that an ACLR limb adopts a different muscle strategy during landing, which is in agreement with the aberrant biomechanical patterns that persist in patients returning to sport after ACLR.6,7 However, the evidence for the alteration in some specific muscle activity patterns is controversial due to the great heterogeneity.
The results show that patients after ACLR tend to activate the quadriceps and hamstring muscles of the involved limb earlier than healthy people or the contralateral side. This indicates that patients with ACLR, unconsciously or consciously, increase the pretension of the lower limb muscles before landing.48 This may serve as a compensatory strategy to resist a given load during landing. Rocchi et al34 and Gokeler et al16 found significant earlier onset time of the quadriceps and hamstrings during single-leg hopping, whereas Dashti Rostami38 and Bryant et al33 found a trend toward earlier muscle onset during drop landing or countermovement hop landing, though the findings were not significant. The different results could be mainly due to the variations in the time since surgery. The average time since surgery reported by Rocchi et al34 and Gokeler et al16 was around 6 months, whereas that reported by Dashti Rostami et al38 and Bryant et al33 was more than 12 months. Neuromuscular function may be recovered for those who are rehabilitated well, which explains the nonsignificant results. In addition, the onset determination and landing tasks involved are different among these studies, which may contribute to different results. Even for similar tasks, some degree of variability can be found between studies regarding its implementation.
It appears that patients with ACLR adopt similar reactive activity patterns of the quadriceps and hamstrings during landing tasks when compared with healthy controls or the contralateral side.34,38,40,41,43,45 The “quadriceps–avoidance” pattern has been observed during gait and hop landing in ACLD subjects. ACLD subjects alter their gait or landing strategy with decreased quadriceps activation to minimize anterior translation.21,49,50 However, this review does not support the existence of this pattern. Of the 14 studies that reported the reactive quadriceps activity amplitude during single-leg landing, only 2 studies found a significant decrease in vastus lateralis activity.18,35 The majority of the included studies found no significant difference in quadriceps and hamstring reactive muscle activity amplitude. These results were also different from previous studies, which reported greater hamstring activity in ACL-deficient patients.21,51 It should be noted that the majority of the patients included in this review were all rehabilitated and capable of return to play, with the time post ACLR ranging from 6 months to 6 years. Therefore, the reactive activation capacity of the quadriceps and hamstrings may be restored. The results for alterations in the gluteus maximus and gastrocnemius are inconsistent, when taking the variations in gender, graft type, phase determination, and normalization method into consideration. It is likely that the findings are biased by the fact that the authors did not consider the patients’ previous experience of landing maneuvers and the variations in instructions, as well as the post-op rehabilitation protocols.52,53
Patients with ACLR tend to use increased quadriceps and hamstring cocontraction during single-leg landing when compared with healthy people. This indicates the potential capacity of the quadriceps and hamstring muscles to act collectively in stabilizing the knee joint. During landing, while the quadriceps muscles contracting is an attempt to control knee flexion through eccentric contraction, cocontraction of the hamstrings is essential to prevent excessive ACL loading due to the anterior shear force produced by the quadriceps.54,55 It may be that patients have adapted based on their negative experiences, such as a knee giving way episode before surgery, or modified their motor programming by increasing the cocontraction of the knee muscles to “tense up” in an attempt to increase dynamic knee stability.20,56 However, we can only find trending results due to the great heterogeneity in the methodologies. There is no standardized equation for the quadriceps and hamstring cocontraction ratio. The equations EMGS/EMGL × (EMGS + EMGL) or EMGS/EMGL were used in 4 studies to provide an estimate of the relative level of cocontraction, where EMGS is the level of activity in the less active muscle and EMGL is the level of activity in the more active muscle.23,35,36,44 Two other studies used either quadriceps or hamstrings as the divider.31,47 In addition, the EMG amplitude normalization procedure, muscles selected, and landing phase used for the calculation of the cocontraction ratios were different in all these studies, which also influenced the results.57
The results regarding time to peak muscle activity, preparatory muscle activity amplitude, and quadriceps and hamstring cocontraction ratio prior to landing are inconclusive, as they are based on limited studies. A recent study indicated that the timing of noncontact ACL injury ranges from 17 to 50 ms after initial ground contact. Therefore, preparatory muscle activity is important for ACL injury prevention because it is too slow (>100 ms) for afferent mechanosensory feedback loops from the knee to stabilize the joint.58–61 Proper muscle timing allows muscle forces to be generated at the appropriate time to be successful in regard to the task at hand.15 In addition to the quadriceps and hamstring muscles, the gluteal muscles also play an important role in lower limb movement control.62 However, there is limited evidence regarding the gluteus medius, which is associated with dynamic knee valgus.63,64 Therefore, more research is required to provide a definite conclusion about the alterations in these muscle activity patterns after ACLR.
There are some limitations in this systematic review that need to be considered. (1) Only English publications were included. (2) It should be stated that the majority of the studies did not adjust for some potentially confounding variables, such as gender, age, graft type, activity level, or functional status within the recruited population, which may influence our findings. Comparisons between sexes can be made, as greater quadriceps activation and lower hamstring activation have been found and linked to other factors that increase the risk of biomechanical injury in women.65,66 It has been demonstrated that the surgical technique can influence postinjury muscle recovery, potentially leading to impairments of neuromuscular control and functional performance.67,68 In this review, only 2 studies adjusted the results by graft type. Thus, future investigations are required to assess the role of different graft types on muscle activation pattern during landing tasks, and the ACLR group can be further classified according to the graft used. (3) The ACLR subjects also had a high variation in time since surgery, ranging from 6 months to 6 years, and the rehabilitation protocol was not specified. The large discrepancy in the participants’ post-ACLR status in the selected studies may represent a critical source of variability. (4) Regarding the assessment methods, full protocol descriptions associated with the correct use of the surface EMG techniques, cross talk testing, or skin preparation were missing in the majority of these studies. Moreover, the normalization procedure for activation level and phase determination varied between the studies. In this review, the included studies investigated different landing tasks, like drop jump, vertical jump, or hop landing. Because of the heterogeneity in the methodologies and the absence of a gold standard execution protocol as mentioned above, caution is warranted regarding the interpretation of the results. (5) Some studies regarded the quadriceps and hamstring muscles as an entirety, but the fact is that the lateral and medial components of the muscle groups play different roles in knee stability. Increased dominance of the lateral quadriceps relative to the medial hamstrings is associated with knee valgus, which increases the risk of an ACL injury.46,51,69 Therefore, different components of these muscles should be taken into consideration.
Conclusion
This review suggests that patients with ACLR display altered muscle activity patterns during landing tasks, even though they are considered to be capable of returning to sport. Nevertheless, a firm conclusion could not be drawn due to the great heterogeneity in the subject selection and study methods. As proper recovery of neuromuscular activity after ACLR is important to regain appropriate mechanical function of the knee joint, future research is needed to understand the neuromuscular alterations depending on gender, graft type, and functional status and to investigate whether differential muscle activity patterns are associated with increased ACL reinjury risk. Specific modes of training, such as postural balance exercises, verbal instructions for soft landing, and plyometric jump and landing exercises, have been reported to be effective in improving neuromuscular activity patterns with increased hamstring activity and quadriceps to hamstring cocontraction during landing in healthy athletes.70,71 However, whether the altered neuromuscular activity during landing can be modified as a result of rehabilitation after ACLR warrants further investigation.
References
- 1.↑
Beynnon BD, Johnson RJ, Abate JA, Fleming BC, Nichols CE. Treatment of anterior cruciate ligament injuries, part 2. Am J Sports Med. 2005;33(11):1751–1767. PubMed ID: 16230470 doi:10.1177/0363546505279922
- 2.↑
Paterno MV, Rauh MJ, Schmitt LC, Ford KR, Hewett TE. Incidence of contralateral and ipsilateral Anterior Cruciate Ligament (ACL) injury after primary ACL reconstruction and return to sport. Clin J Sport Med. 2012;22(2):116–121. PubMed ID: 22343967 doi:10.1097/JSM.0b013e318246ef9e
- 3.↑
Pappas E, Hagins M, Sheikhzadeh A, Nordin M, Rose D. Biomechanical differences between unilateral and bilateral landings from a jump: gender differences. Clin J Sport Med. 2007;17(4):263–268. PubMed ID: 17620779 doi:10.1097/JSM.0b013e31811f415b
- 4.↑
Yeow CH, Lee PVS, Goh JCH. An investigation of lower extremity energy dissipation strategies during single-leg and double-leg landing based on sagittal and frontal plane biomechanics. Hum Mov Sci. 2011;30(3):624–635. PubMed ID: 21411162 doi:10.1016/j.humov.2010.11.010
- 5.↑
Lepley AS, Kuenze CM. Hip and knee kinematics and kinetics during landing tasks after anterior cruciate ligament reconstruction: a systematic review and meta-analysis. J Athl Train. 2018;53(2):144–159. PubMed ID: 29350551 doi:10.4085/1062-6050-334-16
- 6.↑
Johnston PT, McClelland JA, Webster KE. Lower limb biomechanics during single-leg landings following anterior cruciate ligament reconstruction: a systematic review and meta-analysis. Sports Med. 2018;48(9):2103–2126. PubMed ID: 29949109 doi:10.1007/s40279-018-0942-0
- 7.↑
Luc B, Gribble PA, Pietrosimone BG. Osteoarthritis prevalence following anterior cruciate ligament reconstruction: a systematic review and numbers-needed-to-treat analysis. J Athl Train. 2014;49(6):806–819. PubMed ID: 25232663 doi:10.4085/1062-6050-49.3.35
- 8.↑
Di Stasi SL, Logerstedt D, Gardinier ES, Snyder-Mackler L. Gait patterns differ between ACL-reconstructed athletes who pass return-to-sport criteria and those who fail. Am J Sports Med. 2013;41(6):1310–1318. PubMed ID: 23562809 doi:10.1177/0363546513482718
- 9.↑
Lafortune MA, Lake MJ, Hennig EM. Differential shock transmission response of the human body to impact severity and lower limb posture. J Biomech. 1996;29(12):1531–1537. PubMed ID: 8945651 doi:10.1016/S0021-9290(96)80004-2
- 10.
Mattacola CG, Perrin DH, Gansneder BM, Gieck JH, Saliba EN, McCue FC III. Strength, functional outcome, and postural stability after anterior cruciate ligament reconstruction. J Athl Train. 2002;37(3):262. PubMed ID: 12937583
- 11.↑
Ardern CL, Webster KE, Taylor NF, Feller JA. Return to sport following anterior cruciate ligament reconstruction surgery: a systematic review and meta-analysis of the state of play. Br J Sports Med. 2011;45(7):596–606. PubMed ID: 21398310 doi:10.1136/bjsm.2010.076364
- 12.↑
Hartigan E, Axe MJ, Snyder-Mackler L. Perturbation training prior to ACL reconstruction improves gait asymmetries in non‐copers. J Orthop Res. 2009;27(6):724–729. PubMed ID: 19023893 doi:10.1002/jor.20754
- 13.↑
Riemann BL, Lephart SM. The sensorimotor system, part I: the physiologic basis of functional joint stability. J Athl Train. 2002;37(1):71. PubMed ID: 16558670
- 14.↑
Lephart SM, Ferris CM, Riemann BL, Myers JB, Fu FH. Gender differences in strength and lower extremity kinematics during landing. Clin Orthop Relat Res. 2002;401:162–169. doi:10.1097/00003086-200208000-00019
- 15.↑
Solomonow M, Krogsgaard M. Sensorimotor control of knee stability: a review. Scand J Med Sci Sports. 2001;11(2):64–80. PubMed ID: 11252464 doi:10.1034/j.1600-0838.2001.011002064.x
- 16.↑
Gokeler A, Hof AL, Arnold MP, Dijkstra PU, Postema K, Otten E. Abnormal landing strategies after ACL reconstruction. Scand J Med Sci Sports. 2010;20(1):e1–e19. doi:10.1111/j.1600-0838.2008.00873.x
- 17.↑
Saunders N, McLean SG, Fox AS, Otago L. Neuromuscular dysfunction that may predict ACL injury risk: a case report. Knee. 2014;21(3):789–792. PubMed ID: 24529986 doi:10.1016/j.knee.2014.01.005
- 18.↑
Palmieri-Smith R, Strickland M, Lepley LK. Hamstring muscle activity after primary anterior cruciate ligament reconstruction—a protective mechanism in those who do not sustain a secondary injury? A preliminary study. Sports Health. 2019;11(4):316–323. PubMed ID: 31194624 doi:10.1177/1941738119852630
- 19.↑
Walsh M, Boling MC, McGrath M, Blackburn JT, Padua DA. Lower extremity muscle activation and knee flexion during a jump-landing task. J Athl Train. 2012;47(4):406–413. PubMed ID: 22889656 doi:10.4085/1062-6050-47.4.17
- 20.↑
Olmstead TG, Wevers HW, Bryant JT, Gouw GJ. Effect of muscular activity on valgus/varus laxity and stiffness of the knee. J Biomech. 1986;19(8):565–577. doi:10.1016/0021-9290(86)90162-4
- 21.↑
Shanbehzadeh S, Bandpei MAM, Ehsani F. Knee muscle activity during gait in patients with anterior cruciate ligament injury: a systematic review of electromyographic studies. Knee Surg Sports Traumatol Arthrosc. 2017;25(5):1432–1442. PubMed ID: 26704804 doi:10.1007/s00167-015-3925-9
- 22.↑
Nyland J, Klein S, Caborn DNM. Lower extremity compensatory neuromuscular and biomechanical adaptations 2 to 11 years after anterior cruciate ligament reconstruction. Arthroscopy. 2010;26(9):1212–1225. PubMed ID: 20810079 doi:10.1016/j.arthro.2010.01.003
- 23.↑
Vairo G, Myers J, Sell T, Fu F, Harner C, Lephart S. Neuromuscular and biomechanical landing performance subsequent to ipsilateral semitendinosus and gracilis autograft anterior cruciate ligament reconstruction. Knee Surg Sports Traumatol Arthrosc. 2008;16(1):2–14. PubMed ID: 17973098 doi:10.1007/s00167-007-0427-4
- 24.↑
Hewett TE, Di Stasi SL, Myer GD. Current concepts for injury prevention in athletes after anterior cruciate ligament reconstruction. Am J Sports Med. 2013;41(1):216–224. PubMed ID: 23041233 doi:10.1177/0363546512459638
- 25.↑
Di Stasi S, Myer GD, Hewett TE. Neuromuscular training to target deficits associated with second anterior cruciate ligament injury. J Orthop Sports Phys Ther. 2013;43(11):777–792. PubMed ID: 24175599 doi:10.2519/jospt.2013.4693
- 26.↑
Moher D, Liberati A, Tetzlaff J, Altman DG, Prisma Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097. PubMed ID: 19621072 doi:10.1371/journal.pmed.1000097
- 27.↑
Downs SH, Black N. The feasibility of creating a checklist for the assessment of the methodological quality both of randomised and non-randomised studies of health care interventions. J Epidemiol Community Health. 1998;52(6):377–384. PubMed ID: 9764259 doi:10.1136/jech.52.6.377
- 28.↑
Munn J, Sullivan SJ, Schneiders AG. Evidence of sensorimotor deficits in functional ankle instability: a systematic review with meta-analysis. J Sci Med Sport. 2010;13(1):2–12. PubMed ID: 19442581 doi:10.1016/j.jsams.2009.03.004
- 29.↑
Clarys JP, Scafoglieri A, Tresignie J, Reilly T, Van Roy P. Critical appraisal and hazards of surface electromyography data acquisition in sport and exercise. Asian J Sports Med. 2010;1(2):69.
- 30.↑
Cohen J, Cohen P, West SG, Aiken LS. Applied Multiple Regression/Correlation Analysis for the Behavioral Sciences. Mahwah, NJ: Routledge; 2013.
- 31.↑
Coats-Thomas MS, Miranda DL, Badger GJ, Fleming BC. Effects of ACL reconstruction surgery on muscle activity of the lower limb during a jump-cut maneuver in males and females. J Orthop Res. 2013;31(12):1890–1896. doi:10.1002/jor.22470
- 32.↑
Nyland J, Wera J, Klein S, Caborn DNM. Lower extremity neuromuscular compensations during instrumented single leg hop testing 2–10 years following ACL reconstruction. Knee. 2014;21(6):1191–1197. PubMed ID: 25245550 doi:10.1016/j.knee.2014.07.017
- 33.↑
Bryant AL, Newton RU, Steele J. Successful feed-forward strategies following ACL injury and reconstruction. J Electromyogr Kinesiol. 2008;19(5):988–997. PubMed ID: 18656383 doi:10.1016/j.jelekin.2008.06.001
- 34.↑
Rocchi JE, Labanca L, Laudani L, Minganti C, Mariani PP, Macaluso A. Timing of muscle activation is altered during single-leg landing tasks after anterior cruciate ligament reconstruction at the time of return to sport [published online ahead of print October 29, 2018]. Clin J Sport Med. doi:10.1097/JSM.0000000000000659
- 35.↑
Lepley LK, Thomas AC, McLean SG, Palmieri-Smith RM. Fatigue’s lack of effect on thigh-muscle activity in anterior cruciate ligament-reconstructed patients during a dynamic-landing task. J Sport Rehabil. 2013;22(2):83–92. PubMed ID: 23069653 doi:10.1123/jsr.22.2.83
- 36.↑
Ortiz A, Capo-Lugo CE, Venegas-Rios HL. Biomechanical deficiencies in women with semitendinosus-gracilis anterior cruciate ligament reconstruction during drop jumps. PM R. 2014;6(12):1097–1106. doi:10.1016/j.pmrj.2014.07.003
- 37.↑
Briem K, Ragnarsdóttir A, Árnason S, Sveinsson T. Altered medial versus lateral hamstring muscle activity during hop testing in female athletes 1–6 years after anterior cruciate ligament reconstruction. Knee Surg Sports Traumatol Arthrosc. 2016;24(1):12–17. PubMed ID: 25246177 doi:10.1007/s00167-014-3333-6
- 38.↑
Dashti Rostami K, Alizadeh M, Minoonejad H, Yazdi H, Thomas A. Effect of fatigue on electromyographic activity patterns of the knee joint muscles in anterior cruciate ligament reconstructed and deficient patients during landing task. J Funct Morphol Kinesiol. 2018;3(2):22. doi:10.3390/jfmk3020022
- 39.↑
Dashti Rostami K, Naderi A, Thomas A. Hip abductor and adductor muscles activity patterns during landing after anterior cruciate ligament injury. J Sport Rehabil. 2019;28(8):871–876.
- 40.↑
Jordan MJ, Aagaard P, Herzog W. Asymmetry and thigh muscle coactivity in fatigued anterior cruciate ligament–reconstructed elite skiers. Med Sci Sports Exerc. 2017;49(1):11–20. PubMed ID: 27532454 doi:10.1249/MSS.0000000000001076
- 41.↑
Lessi G, Serrão F. Effects of fatigue on lower limb, pelvis and trunk kinematics and lower limb muscle activity during single-leg landing after anterior cruciate ligament reconstruction. Knee Surg Sports Traumatol Arthrosc. 2017;25(8):2550–2558. PubMed ID: 26298713 doi:10.1007/s00167-015-3762-x
- 42.↑
Lessi GC, Silva RS, Serrão FV. Comparison of the effects of fatigue on kinematics and muscle activation between men and women after anterior cruciate ligament reconstruction. Phys Ther Sport. 2018;31:29–34. PubMed ID: 29524910 doi:10.1016/j.ptsp.2018.01.009
- 43.↑
Melińska A, Czamara A, Szuba Ł, Będziński R. Biomechanical characteristics of the jump down of healthy subjects and patients with knee injuries. Acta Bioeng Biomech. 2015;17(2):111.
- 44.↑
Ortiz A, Olson S, Libby CL, et al. Landing mechanics between noninjured women and women with anterior cruciate ligament reconstruction during 2 jump tasks. Am J Sports Med. 2008;36(1):149–157. PubMed ID: 17940142 doi:10.1177/0363546507307758
- 45.↑
Ortiz A, Olson S, Trudelle-Jackson E, Rosario M, Venegas HL. Landing mechanics during side hopping and crossover hopping maneuvers in noninjured women and women with anterior cruciate ligament reconstruction. PM R. 2011;3(1):13–20. PubMed ID: 21257128 doi:10.1016/j.pmrj.2010.10.018
- 46.↑
Swanik CB, Lephart SM, Giraldo JL, DeMont RG, Fu FH. Reactive muscle firing of anterior cruciate ligament-injured females during functional activities. J Athl Train. 1999;34(2):121. PubMed ID: 16558554
- 47.↑
Tsai L, McLean S, Colletti PM, Powers CM. Greater muscle co-contraction results in increased tibiofemoral compressive forces in females who have undergone anterior cruciate ligament reconstruction. J Orthop Res. 2012;30(12):2007–2014. PubMed ID: 22730173 doi:10.1002/jor.22176
- 48.↑
Dyhre-Poulsen P, Simonsen EB, Voigt M. Dynamic control of muscle stiffness and H reflex modulation during hopping and jumping in man. J Physiol. 1991;437(1):287–304. doi:10.1113/jphysiol.1991.sp018596
- 49.↑
Gauffin H, Tropp H. Altered movement and muscular-activation patterns during the one-legged jump in patients with an old anterior cruciate ligament rupture. Am J Sports Med. 1992;20(2):182–192. PubMed ID: 1558247 doi:10.1177/036354659202000215
- 50.↑
Berchuck M, Andriacchi TP, Bach BR, Reider B. Gait adaptations by patients who have a deficient anterior cruciate ligament. J Bone Joint Surg. 72, 1990:871–877. doi:10.2106/00004623-199072060-00012.
- 51.↑
Boerboom AL, Hof AL, Halbertsma JP, et al. Atypical hamstrings electromyographic activity as a compensatory mechanism in anterior cruciate ligament deficiency. Knee Surg Sports Traumatol Arthrosc. 2001;9(4):211–216. PubMed ID: 11522076 doi:10.1007/s001670100196
- 52.↑
Theisen D, Rada I, Brau A, Gette P, Seil R. Muscle activity onset prior to landing in patients after anterior cruciate ligament injury: a systematic review and meta-analysis. PLoS One. 2016;11(5):e0155277. PubMed ID: 27166929 doi:10.1371/journal.pone.0155277
- 53.↑
Yabroudi MA, Irrgang JJ. Rehabilitation and return to play after anatomic anterior cruciate ligament reconstruction. Clin Sports Med. 2013;32(1):165–175. PubMed ID: 23177470 doi:10.1016/j.csm.2012.08.016
- 54.↑
Berns GS, Hull ML, Patterson HA. Strain in the anteromedial bundle of the anterior cruciate ligament under combination loading. J Orthop Res. 1992;10(2):167–176. PubMed ID: 1740734 doi:10.1002/jor.1100100203
- 55.↑
Markolf KL, Burchfield DM, Shapiro MM, Shepard MF, Finerman GA, Slauterbeck JL. Combined knee loading states that generate high anterior cruciate ligament forces. J Orthop Res. 1995;13(6):930–935. PubMed ID: 8544031 doi:10.1002/jor.1100130618
- 56.↑
Engelhardt M, Freiwald J, Reuter I, Mortier J, Huth D. Neuromuscular alterations after trauma and surgery of the knee joint—implicatione for sports capability. Arthroskopie. 2000;13(6):302–306. doi:10.1007/s001420050179
- 57.↑
Ervilha UF, Graven-Nielsen T, Duarte M. A simple test of muscle coactivation estimation using electromyography. Braz J Med Biol Res. 2012;45(10):977–981. PubMed ID: 22641413 doi:10.1590/S0100-879X2012007500092
- 58.↑
Wikstrom EA, Tillman MD, Chmielewski TL, Borsa PA. Measurement and evaluation of dynamic joint stability of the knee and ankle after injury. Sports Med. 2006;36(5):393–410. PubMed ID: 16646628 doi:10.2165/00007256-200636050-00003
- 59.
Krosshaug T, Nakamae A, Boden BP, et al. Mechanisms of anterior cruciate ligament injury in basketball: video analysis of 39 cases. Am J Sports Med. 2007;35(3):359–367. PubMed ID: 17092928 doi:10.1177/0363546506293899
- 60.
Dyhre-Poulsen P, Krogsgaard MR. Muscular reflexes elicited by electrical stimulation of the anterior cruciate ligament in humans. J Appl Physiol. 2000;89(6):2191–2195. PubMed ID: 11090567 doi:10.1152/jappl.2000.89.6.2191
- 61.↑
Hewett TE, Zazulak BT, Myer GD, Ford KR. A review of electromyographic activation levels, timing differences, and increased anterior cruciate ligament injury incidence in female athletes. Br J Sports Med. 2005;39(6):347–350. PubMed ID: 15911605 doi:10.1136/bjsm.2005.018572
- 62.↑
Khayambashi K, Ghoddosi N, Straub RK, Powers CM. Hip muscle strength predicts noncontact anterior cruciate ligament injury in male and female athletes: a prospective study. Am J Sports Med. 2016;44(2):355–361. PubMed ID: 26646514 doi:10.1177/0363546515616237
- 63.↑
Rowe J, Shafer L, Kelley K, et al. Hip strength and knee pain in females. N Am J Sports Phys Ther. 2007;2(3):164. PubMed ID: 21522212
- 64.↑
An K. Muscle force and its role in joint dynamic stability. Clin Orthop Relat Res. 2002;403:S37–S42. doi:10.1097/00003086-200210001-00005
- 65.↑
Malinzak RA, Colby SM, Kirkendall DT, Yu B, Garrett WE. A comparison of knee joint motion patterns between men and women in selected athletic tasks. Clin Biomech. 2001;16(5):438–445. doi:10.1016/S0268-0033(01)00019-5
- 66.↑
Landry SC, McKean KA, Hubley-Kozey CL, Stanish WD, Deluzio KJ. Neuromuscular and lower limb biomechanical differences exist between male and female elite adolescent soccer players during an unanticipated side-cut maneuver. Am J Sports Med. 2007;35(11):1888–1900. PubMed ID: 17921416 doi:10.1177/0363546507300823
- 67.↑
Kasović M, Mejovšek M, Matković B, Janković S, Tudor A. Electromyographic analysis of the knee using fixed-activation threshold after anterior cruciate ligament reconstruction. Int Orthop. 2011;35(5):681–687. doi:10.1007/s00264-010-1050-4
- 68.↑
Mohammadi F, Salavati M, Akhbari B, Mazaheri M, Mohsen Mir S, Etemadi Y. Comparison of functional outcome measures after ACL reconstruction in competitive soccer players: a randomized trial. J Bone Joint Surg. 2013;95(14):1271–1277. PubMed ID: 23864175 doi:10.2106/JBJS.L.00724
- 69.↑
Zebis MK, Andersen LL, Bencke J, Kjær M, Aagaard P. Identification of athletes at future risk of anterior cruciate ligament ruptures by neuromuscular screening. Am J Sports Med. 2009;37(10):1967–1973. PubMed ID: 19574475 doi:10.1177/0363546509335000
- 70.↑
Nagano Y, Ida H, Akai M, Fukubayashi T. Effects of jump and balance training on knee kinematics and electromyography of female basketball athletes during a single limb drop landing: pre–post intervention study. Sports Med Arthrosc Rehabil Ther Technol. 2011;3(1):14. doi:10.1186/1758-2555-3-14
- 71.↑
Letafatkar A, Rajabi R, Tekamejani EE, Minoonejad H. Effects of perturbation training on knee flexion angle and quadriceps to hamstring cocontraction of female athletes with quadriceps dominance deficit: pre–post intervention study. Knee. 2015;22(3):230–236. PubMed ID: 25709088 doi:10.1016/j.knee.2015.02.001