Table 1.
Study | Patient | Average age (yr) | M:F | Pathology | Average duration of symptoms | Intervention/control | Methodology | Outcome measure | Site of injection | Injection/interval | Injection technique | Injection volume (mL) | Cointervention | Adverse effect |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Barreto et al. (2019) [14] | PRP, 26; | 53.3 | 36:66 | Rotator cuff impingement | NR | PRP | 6 Months, single centre, randomized, controlled, parallel group, double-blind clinical trial | UCLA, CMS, DASH (function) | Sub-acromial bursa | 1/NA | Landmark guided | 3 | No mention | No complication (only injection-related pain) |
corticosteroid, 25 | Corticosteroid | |||||||||||||
Cai et al. (2019) [15] | PRP, 50; | 40.6 | 99:85 | Partial-thickness tears (<1 cm) | 13.76 wk | PRP | 12 Months, multi-centres, randomized, controlled, double blind, clinical trial | Constant score, ASES (function), VAS (pain) | Sub-acromial bursa | 4/1 wk | USG-guided | 4 | No mention | Intolerance to PRP (n=2) |
normal saline, 50; | 39.9 | NS | ||||||||||||
SH, 50; | 38.9 | SH | ||||||||||||
SH+PRP, 50 | 39.6 | SH+PRP | ||||||||||||
Ilhanli et al. (2015) [16] | PRP, 30; | 59.2 | 45:17 | Partial thickness tear | 7.24 mo (mean duration) | PRP | 12 Months, single centre, randomized, controlled, parallel group, single blind, clinical trial | VAS (pain), ROM, DASH (function), Beck depression inventory | Intra-articular | 3/1 wk | NR | 6 | Home exercise program without PT | No complications |
PT, 32 | 59.7 | PT | ||||||||||||
Kesikburun et al. (2013) [17] | PRP, 20; | 45.5 51.4 |
13:27 | Partial thickness tear or tendinosis | >3 mo (IC) | PRP | 12 Months, single centre, Randomized, placebo controlled, double blind, clinical trial | WORC (QOL), SPADI (function), VAS (pain), passive ROM | Sub-acromial Space | 1/NA | USG-guided | 5 | Exercise program (supervised by PT), then home program | No complications (only injection-related pain) |
placebo, 20 | Placebo (NS) injection | |||||||||||||
Kothari (2017) [18] | PRP, 62; | 51.9 52.7 | 86:94 | Adhesive capsulitis | 4.67 mo (mean duration) | PRP | 12 Weeks, single centre, randomized, controlled, parallel group, clinical trial | ROM, VAS (pain), QuickDASH (function) | Intra-articular injection | 1/NA | Landmark guided | 2 | Home exercises | No complications |
corticosteroid, 60; | 51.2 | CorticosteroidUST (programmed-PT) | ||||||||||||
UST (PT), 58 | ||||||||||||||
Nejati et al. (2017) [19] | PRP, 22; | 52.5 53.9 | 15:27 | Sub-acromial impingement syndrome | >3 mo (IC) | PRP | 6 Months, single centre, randomized controlled, parallel group, single blind, clinical trial | VAS (pain), ROM, strength, DASH (function), WORC (QOL) | Into the tear and sub-acromial bursa | 1/NA | USG-guided | 4 Total | No exercise program | No mention |
exercise, 20 | Exercise | |||||||||||||
Pasin et al. (2019) [20] | PRP, 30; | 49.4 47.7 | 37:53 | Sub-acromial Impingement syndrome | >3 mo (IC) | PRP | 8 Weeks, single centre, randomized controlled, parallel group, single blind, clinical Trial | VAS (pain), SDQ (function), Quick DASH (function), UCLA SRS), SF-36 (QoL) | Sub-acromial bursa injection | 1/NA | NR | 4 | Exercise program (supervised by PT) | No mention |
corticosteroid, 30; PT, 30 | 49.9 | CorticosteroidPT | ||||||||||||
Rha et al. (2013) [21] | PRP, 20; | 52.2 | 17:22 | Partial thickness tear (<1 cm) or tendinosis | 9.4 mo (mean duration) | PRP | 6 Months, single centre, randomized controlled, double blind, clinical trial | SPADI (function), passive ROM of shoulder, physician global rating scale | Into tear | 2/4 wk | USG-guided | 3 | Self-exercise rehabilitation program | No complications |
dry-needling, 19 | 53.9 | Dry-needle | ||||||||||||
Sari and Eroglu (2020) [22] | PRP, 30; | 52.1 | 43:77 | Rotator cuff lesions | 4.87 mo (mean duration) | PRP Prolotherapy Corticosteroid Lidocaine | 24 Weeks, single centre, randomized controlled, parallel group, triple blind, clinical trial | VAS (pain), ASES (function), WORC (QOL) | Sub-acromial bursa | 1/NA | USG-guided | 5 | Home exercises | No mention |
corticosteroid, 30; | ||||||||||||||
prolotherapy, 30; | ||||||||||||||
lidocaine (placebo), 30 | ||||||||||||||
Schwitzguebel et al. (2019) [23] | PRP, 41; | 48.2 | 43:35 | Interstitial supraspinatus tear | ≥6 mo (IC) | PRP | 12 Months, single centre, randomized controlled, clinical trial | Lesion-volume, VAS (pain), SANE, CMS, ASES (function) | Into tear | 2/1 mo | USG-guided | 2 | Daily activities and light sports allowed (no PT) | At 19.5 months, PRP group reported (pain >48 hr/frozen shoulder/extension of lesion) 54% compared to 26% in saline group |
saline, 39 | 47.6 | Saline injection | ||||||||||||
Shams et al. (2016) [24] | PRP, 20; | 52 | 21:19 | Partial-thickness tear | >3 mo (IC) | PRP | 6 Months, multi-centre, randomized controlled, clinical trial | ASES (function), CMS, Simple Shoulder Test, VAS (pain) | Sub-acromial injection | 1/NA | Landmark-guided | 2–2.5 | Home exercises without PT | No mention |
corticosteroid, 20 | 50 | Corticosteroid | ||||||||||||
Wongworawat (2013) [25] | PRP, 7 | 59.3 | 8:4 | Rotator cuff lesions | >4 wk (IC) | PRP | 12 Weeks, single centre, randomized controlled, clinical trial | ASES | Sub-acromial space | 1/NA | Landmark-guided | 5 | Not reported | No complications |
corticosteroid, 5 | 59.2 | Corticosteroid | ||||||||||||
Ibrahim et al. (2019) [26] | PRP, 15; | 46.8 | 13:17 | Rotator Cuff tendinopathy | 1.62 mo (mean duration) | PRP | 8 Weeks, single centre, randomized controlled, clinical trial | SDQ | Sub-acromial space | 1/NA | USG-guided | 2 | Home exercises | No complications |
corticosteroid, 15 | 41.5 | Corticosteroid | ||||||||||||
Šmíd et al. (2018) [27] | PRP, 25; | 48.7 | 31:19 | shoulder impingement syndrome | >4 wk | PRP | 6 Months, single centre, randomized controlled, parallel group, clinical trial | ASES (function), VAS (pain intensity score) | Sub-acromial space | 3/1 wk | USG-guided | 3 | Home exercises | No complications |
corticosteroid, 25 | 50.1 | Corticosteroid | ||||||||||||
Upadhyay et al. (2020) [28] | PRP, 60; | 47.6 46.4 | 50:70 | Adhesive capsulitis | >1 mo (IC) | PRP Corticosteroid | 6 Months, single centre, randomized controlled, single blind, parallel group, clinical trial | SPADI (function) | Intra-articular injection | 1/NA | Fluoroscope-guided | 2 | Home exercises | No complications (only injection related pain) |
Corticosteroid, 60 | ||||||||||||||
Wesner et al. (2016) [11] | PRP, 7; | 49.4 | 6:3 | Degenerative Tendinopathies | 62.2 mo (mean duration) | PRP | 6 Months, single centre, randomized, controlled, clinical trial | VAS (pain), DASH, WORC (QoL) | Into degenerative area of tendon/tear | 1/NA | USG-guided | 4 | Home exercises | No mention |
Placebo, 2 | 49.5 | Saline | ||||||||||||
Jeyaraman et al. (2018) [29] | PRP, 46; | 51.8 57.5 | 61:30 | Adhesive capsulitis | >1 mo (IC) | PRP | 12 Months, single centre, randomized controlled, parallel group, clinical trial | VAS (pain), DASH (function) | Intra-articular injection | 1/NA | Fluoroscope-guided | 3 mL PRP | Home exercises | At 1 month: with PRP, 17 reported pain and 7 swelling; with hydro-dissection, 23 reported pains |
hydro-dissection, 45 | Hydro-dissection |
PRP: platelet-rich plasma, NR: not reported, UCLA: University of California Los Angeles, CMS: Constant-Murley score, DASH: Disabilities of the Arm, Shoulder and Hand, NA: not available, SH: sodium hyaluronate, NS: normal saline, ASES: American Shoulder and Elbow Surgeons score, VAS: visual analog scale, USG: ultrasonography, PT: physical therapy, ROM: range of motion, IC: inclusion criteria, WORC: Western Ontario Rotator Cuff Index, QoL: quality of life, SPADI: Shoulder Pain and Disability Index, UST: ultrasonic therapy, QuickDASH: Shortened DASH, SDQ: shoulder disability questionnaire, SRS: shoulder rating scale, SF-36: 36-item short form survey, SANE: Single Assessment Numeric Evaluation.