| Literature DB >> 32990034 |
Barry Ting Sheen Kweh1,2, Hui Qing Lee1,2, Terence Tan1,2, Joost Rutges3, Travis Marion4, Kim Siong Tew5, Vikram Bhalla5, Shyaman Menon5, Fetullah Cumhur Oner6, Charles Fisher7, Jin Wee Tee1,2.
Abstract
STUDYEntities:
Keywords: braces; orthotic devices; osteoporotic fractures; spinal fractures
Year: 2020 PMID: 32990034 PMCID: PMC8258809 DOI: 10.1177/2192568220948036
Source DB: PubMed Journal: Global Spine J ISSN: 2192-5682
Figure 1.Search strategy flow diagram in accordance with the Preferred Reporting Itemsfor Systematic Reviews and Meta-Analyses (PRISMA) protocol.
Complete List of 28 Full-Text Articles Assessed and Reason for Exclusion.
| Reason for exclusion | Type of orthosis | ||||
|---|---|---|---|---|---|
| Rigid | Semirigid | Flexible or elastic | Mixed orthoses | ||
| Thoracolumbosacral orthosis (TLSO): | Thoracolumbar orthosis (TLO): | Thoracolumbar Backpack (TLO): Spinomed | Garment: | ||
| Age group | Murata et al, 201 2
| Shariatzadeh et al, 201 6
| Jacobs et al, 201 9
| Vogt et al, 200 8
| Dionyssiotis et al, 201 5
|
| Non–osteoporotic vertebral fractures | Urquuhart et al, 201 6
| Alin et al, 201 9
| Stadhouder et al, 200 9
| Chiba et al, 201 1
| |
| Review article | Ameis et al, 201 8
| Karimi et al, 201 5
| |||
Study Design and Patient Demographics of the 4 Randomized Controlled Trials (RCTs) and 3 Prospective Cohort Studies Which Were Included.
| Study | Study design | Indication for orthosis | Participant source | Sample size | Female gender (%) | Mean age intervention group (range), years | Average age comparison group (range), years |
|---|---|---|---|---|---|---|---|
| Kato et al, 201 9
| RCT | Osteoporotic females with acute single-level vertebral compression fracture | Hospital | 284 | 100 | 76.0 (70.8-81.2) | 75.5 (70.1-80.9) |
| Abe et al, 201 8
| Prospective cohort | Osteoporotic patients with single-level vertebral fracture | Hospital | 154 | 85.7 | 81.2 (60-98) | |
| Meccarielloet al, 201 7
| Prospective cohort study | Osteoporotic patients with acute single-level vertebral compression fracture | Hospital | 140 | 71.4 | 81.9 (65-90) | 82.8 (65-93) |
| Hoshino et al, 201 3
| Prospective cohort | Osteoporotic patients with acute vertebral fracture | Hospital | 362 | 83.7 | 76.2 (NR) | 77.0 (NR) |
| Pfeifer et al, 201 1
| RCT | Osteoporotic women with vertebral fracture | Community | 108 | 100 | Group 1 (Spinomed): 72.8 (65.7-79.9) | 69.7 (60.8-78.6) |
| Liaw et al, 200 9
| Cross RCT | Osteoporotic patients with vertebral compression fracture | Hospital | 47 | 78.7 | 68.2 (59.6-76.8) | |
| Pfeifer et al, 200 4
| RCT | Osteoporotic women with subacute vertebral fracture | Community | 62 | 100 | 72.8 (65.7-79.9) | 72.3 (65.6-79.0) |
Abbreviations: RCT, randomized controlled trial; NR, not reported.
Intervention Characteristics of Included Studies.
| Study | Intervention group | No. of participants: intervention | Comparison group | No. of participants: comparison | Phase of fracture | Level of fracture | Duration of orthosis use | Follow-up |
|---|---|---|---|---|---|---|---|---|
| Kato et al, 201 9
| Rigid TLSO | 141 | Soft TLSO | 143 | Acute | T10-L2 | 12 weeks | 4, 8, 12, 24, and 48 weeks |
| Abe et al, 201 8
| Rigid TLO (Jewett brace) proceeding 2 weeks of bed rest | 154 | Nil | Not applicable | Acute | T4-L5 | 12-24 weeks | 6-8, and 24 weeks |
| Meccariello et al, 201 7
| Three-point orthosis (3PO) | 72 | TLO Backpack (Spinomed) | 68 | Acute | T6-L3 | 10 weeks | 1, 3, and 6 months |
| Hoshino et al, 201 3
| Brace | 327 | No brace | 35 | Acute | T5-L5 | 4.1 months (2.2-6.0) | 6 months |
| Pfeifer et al, 201 1
| Group 1: Spinomed orthosis | Group 1: 36 | No brace | 36 | Subacute | NR | 6 months | 6 months |
| Liawet al, 200 9
| Rigid TLSO (Knight-Taylor orthosis) | 47 | No brace | 47 | NR | NR | Immediate | Immediate |
| Pfeifer et al, 200 4
| Spinomed orthosis | 31 | No brace | 31 | Subacute | NR | 6 months | 6 months |
Abbreviations: TLSO, thoracolumbosacral orthosis; TLO, thoracolumbar orthosis; NR, not reported.
Figure 2.Risk of bias as assessed by the Risk of Bias of Randomized Controlled Trials (RoB 2) tool based on the Cochrane Handbook for Systematic Reviews of Interventions.
Figure 3.Risk of bias as assessed by the Risk Of Bias In Non-Randomized Studies of Interventions (ROBINS-I) tool as recommended by the Cochrane Handbook for Systematic Reviews of Intervention.
Primary and Secondary Outcomes of Included Studies.
| Study | Outcomes | Conclusion |
|---|---|---|
| Kato et al, 201 9
| Primary outcome: | Primary outcome: |
| Abe et al, 201 8
| Primary outcome: | Primary outcome: |
| Meccariello et al, 201 7
| Primary outcomes—functional recovery: | Primary outcomes (statistically significant) |
| Hoshino et al, 201 3
| Primary outcomes: | Primary outcomes: |
| Pfeifer et al, 201 1
| Primary outcomes: | Primary outcomes: Favoring group 1 (Spinomed) and group 2 (Spinomed active) group: |
| Liaw et al, 200 9
| Primary outcomes (assessed by computerized dynamic posturography): | Primary outcomes: |
| Pfeifer et al, 200 4
| Primary outcomes: | Primary outcomes. All in favor of Spinomed orthosis group: |