| Literature DB >> 28670345 |
Benedictine Y C Khor1, Pamela Price2.
Abstract
BACKGROUND: Ischaemic ulcerations have been reported to persist and/or deteriorate despite technically successful revascularisations; a higher incidence of which affects patients with diabetes and critical limb ischaemia. In the context of wound healing, it is unclear if applications of the angiosome concept in 'direct revascularisation' (DR) would be able to aid the healing of chronic foot ulcerations better than the current 'best vessel' or 'indirect revascularisation' (IR) strategy in patients with co-morbid diabetes and critical limb ischaemia.Entities:
Keywords: Angiosome; Critical limb ischaemia; Diabetic foot; Peripheral vascular disease; Revascularisation; Wound healing
Mesh:
Year: 2017 PMID: 28670345 PMCID: PMC5490238 DOI: 10.1186/s13047-017-0206-5
Source DB: PubMed Journal: J Foot Ankle Res ISSN: 1757-1146 Impact factor: 2.303
Fig. 1The Angiosome Concept
Comparison of PAD Characteristics [1, 23, 76–79]
| Patients with Diabetes | Patients without Diabetes | |
|---|---|---|
| Age of onset | Younger | Older |
| Disease progression | Aggressive | Gradual |
| Anatomical localisation | • Mainly distal | • Mainly proximal |
| Type of atherosclerotic lesions | • Stenosis | • Stenosis |
| Calcification | Commonly present | Absent |
| Collateral network | Poor | Unaffected |
Literature Search Strategy
| Search terms | S1–“critical limb isch?emia” OR “isch?emi*” |
| Databases searched | EBSCOhost (AMED, CINAHL), The Cochrane Library, ProQuest (ProQuest Health & Medicine Complete, ProQuest Nursing & Allied Health Source), PubMed, ScienceDirect, TRIP database |
| Part of journals searched | Title and Abstract |
| Years of search | No limits set |
| Language | No limits set |
Inclusion and Exclusion Criteria
| Inclusion Criteria | Exclusion Criteria | |
|---|---|---|
| Study design | • Full-text available in English | • Non-English |
| Population (P) | • Human | • Cadaver or animal |
| Intervention (I), Comparison (C) | • Arterial revascularisations | • Non-arterial revascularisations |
| Outcome (O) | • Studies which utilised wound healing as an outcome measure | • Studies where wound healing was not utilised as an outcome measure |
Fig. 2PRISMA Flow Diagram (adapted from [80])
Key Characteristics of Included Studies
| Fossaceca et al., 2013 [ | Söderström et al., 2013 [ | Acín et al., 2014 [ | Lejay et al., 2014 [ | Jeon et al., 2016 [ | |
|---|---|---|---|---|---|
| Participants | Italy, single-centre | Finland, single-centre | Spain, single-centre | France, single-centre | South Korea, unspecified number of centres |
| Diagnostic criterion for diabetes | Diagnostic criterion unstated in-text, however the following information was tabulated: | • On hyperglycaemia reducing diet | • Baseline blood glucose levels >120 g/dL, or | — | Diagnostic criterion unstated, however the following information was provided: |
| Intervention | Angioplasty: PTA | Angioplasty: PTA | Stents used selectively | Bypass | Angioplasty: PTA |
| Guiding principle for interventions | Angiosome concept | Best vessel strategy | Best vessel strategy | Angiosome concept | Angiosome concept |
| Pre-revascularisation care | |||||
| - Wound care | • Debridement of necrotic tissue | Local wound care tailored to lesion characteristics. | • Early debridement, abscess drainage, minor amputations, and wet dressings. | — | • Unstated. |
| - Medications | • Prophylaxis broad-spectrum antibiotic therapy | • Aspirin (100 mg/day), if not contraindicated. | • Broad-spectrum antibiotic therapy for severe infections in accordance with a general protocol. | — | • Dual anti-platelet therapy at least 72 h before the procedure. (Aspirin 100 mg/day, Clopidogrel 75 mg/day) |
| Post-revascularisation care | |||||
| - Medications | • Dual anti-platelet therapy maintained (Aspirin 100 mg/day and Clopidogrel 75 mg/day) for 6 weeks, then Aspirin alone indefinitely. | • Lifelong Aspirin therapy, accompanied by Clopidogrel (75 mg/day) for 3 months after PTA | — | — | • Dual anti-platelet therapy maintained (Aspirin 100 mg/day and Clopidogrel 75 mg/day) once daily for at least 3 months if there were no contraindications to either drug. |
| Outcome measures | |||||
| - Wound healing |
|
|
|
|
|
| partial/complete | at 12 months | at 12 months | at 3, 6, 12 months | at 12 months | |
| - Limb salvage |
|
|
|
|
|
| at 1, 6, 12 months | at 12 months | at 24 months | at 12 months | at 12, 24 months | |
| - Additional measures | Amputation (minor and major), Average TcPO2, Mortality, PTA retreatment, Restenosis, Technical success | AFS, AFS with healed ulcer, Median time to ulcer healing, Survival, Vascular Re-intervention | AFS, Major amputation at 30 days, MACE, MALE, Freedom from MALE + POD, Freedom from RAS, Freedom from RAO, Overall survival at 24 months | Median Ulcer Healing Time, Primary Patency, Survival, TcPO2 | Amputation, Angiosome Score, Major and minor complications, Mortality, PTA reintervention, Technical Success, Wound Healing Time |
| Wound classification | — | UTWCS | — | UTWCS | Wagner |
| Presence of infection accounted for | — |
| Graded according to CDC/NHSN surveillance definition [ |
| — |
| Follow-up (months) | • Protocol: 1, 6, 12 | • Protocol: 1 month, and at 1–3 months thereafter depending on clinical condition of the foot | • Protocol: 1, 3 and every 6 months thereafter. | • Protocol: 1, 3, and every 6 months thereafter. | • Protocol: 12, 24 |
| Main findings: wound healing rate | No statistically significant difference found in therapeutic efficacy. ( | • DR had a highly statistically significant improvement in wound healing rates at 12 months ( | • DR had a highly statistically significant improvement in wound healing rates as compared to IR ‘without collaterals’ group at 12 months ( | • DR had a statistically significant improvement in wound healing rates as compared to IR at 3, 6 and 12 months ( | • DR had a statistically significant improvement in wound healing rates as compared to IR at 12 months ( |
| Strengths of study | • TASC-II diagnostic criteriona for CLI satisfied | • TASC-II diagnostic criteriona for CLI satisfied | • TASC-II diagnostic criteriona for CLI satisfied | • TASC-II diagnostic criteriona for CLI satisfied | • TASC-II diagnostic criteriona for CLI satisfied |
| Limitations of study | • Non-consecutive sample | • No data on subjects’ duration of diabetes | • No data on subjects’ duration of diabetes | • No data on diagnostic criteria for diabetes | • Drop-outs unaccounted |
| NOS scores | 6/9 | 8/9 | 5/9 | 7/9 | 5/9 |
A tabulated summary of the key characteristics of included studies to allow easy visualisation and comparison across studies
Abbreviations: AFS Amputation-Free Survival, ABPI Ankle-Brachial Pressure Index, BTK Below-the-knee, CDC Centre for Disease Control and Prevention, CLI Critical Limb Ischaemia, CI Confidence Intervals, DR Direct Revascularisations, DUS Duplex Ultrasound, ESRD End-Stage Renal Disease, HbA1c Glycated haemoglobin, HR Hazard Ratio, IR Indirect Revascularisations, MACE Major adverse cardiovascular event, MALE Major adverse limb event, NHSN National Healthcare Safety Network, NOS Newcastle-Ottawa Scale, TcPO Transcutaneous oximetry, PTA Percutaneous Transluminal Angioplasty, PAD Peripheral Arterial Disease, POD Pre-operative Death, RAO Reintervention or amputation, RAS Reintervention, Amputation or Stenosis, SPP Skin Perfusion Pressure, UTWCS University of Texas Wound Classification System
Key: —, no data provided
aAdditional details: TASC-II diagnostic criterion [1] is for the clinical diagnosis of CLI to be confirmed with objective quantifications of haemodynamic compromise, following the presence of symptoms for more than 2 weeks. The term CLI implies chronicity and is to be distinguished from acute limb ischemia
Baseline Population Characteristics between DR and IR groups
| No. of patients | No. of limbs | Age | Male/Female | Ethnicity | HTN | DLP | History of smoking | ESRD/on dialysis | CAD | CVD | |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Fossaceca et al., 2013 [ | |||||||||||
| DR | 201 | - | 75.5 ± 9.5 | 136 M/65 F | - | 124 (62%) | - | - | 15 (7%) | 65 (32%) | - |
| IR | |||||||||||
|
| NA | - | - | - | - | - | - | - | - | - | - |
| Söderström et al., 2013 [ | |||||||||||
| DR | 226 | 121 | 68.4 ± 11.9 | 89 M/32 F | - | 89 (74%) | 78 (65%) | 24 (18%) | 26 (22%) | 69 (57%) | 29 (24%) |
| IR | 129 | 73.8 ± 11.1 | 71 M/58 F | - | 102 (79%) | 84 (65%) | 20 (24%) | 13 (10%) | 90 (70%) | 24 (19%) | |
|
| NA | NA | 0.001 | 0.002 | - | NS | NS | NS | 0.012 | 0.044 | NS |
| DR: propensity score matched pairs | - | 84 | 71.7 ± 11.0 | 59 M/25 F | - | 63 (75%) | 50 (60%) | 18 (25%) | 14 (17%) | 53 (63%) | 20 (24%) |
| IR: propensity score matched pairs | 84 | 70.3 ± 10.9 | 58 M/26 F | - | 63 (75%) | 60 (71%) | 15 (20%) | 12 (14%) | 55 (66%) | 17 (20%) | |
|
| NA | NA | NS | NS | - | NS | NS | NS | NS | NS | NS |
| Acín et al., 2014 [ | |||||||||||
| DR | 46 | - | 72 (63–78) | 30 M/16 F | - | 31 (67%) | 13 (28%) | 36 (78%) | Excluded | 17 (37%) | 9 (20%) |
| IR ‘through collaterals’ | 22 | - | 72 (68–75) | 11 M/11 F | - | 18 (82%) | 9 (41%) | 15 (68%) | Excluded | 5 (23%) | 6 (27%) |
| IR ‘without collaterals’ | 17 | - | 69 (63–77) | 9 M/8 F | - | 14 (82%) | 4 (24%) | 11 (65%) | Excluded | 4 (24%) | 3 (17%) |
|
| NA | - | NS | NS | - | NS | NS | NS | NS | NS | NS |
|
| NA | - | NS | NS | - | NS | NS | NS | NS | NS | NS |
| Lejay et al., 2014 [ | |||||||||||
| DR | 36 | - | 68 ± 10 | 25 M/11 F | - | 34 (95%) | 19 (53%) | 25 (69%) | 19 (53%) | 19 (53%) | 4 (11%) |
| IR | 22 | - | 71 ± 10 | 15 M/7 F | - | 21 (96%) | 12 (55%) | 16 (73%) | 12 (55%) | 12 (55%) | 2 (9%) |
|
| NA | - | NS | NS | - | NS | NS | NS | NS | NS | NS |
| Jeon et al., 2016 [ | |||||||||||
| DR | 70 | 63 | 69.6 ± 10 | 51 M/19 F | - | 63 (90%) | - | - | 24 (34%) | 31 (44%) | - |
| IR | 19 | ||||||||||
|
| NA | NA | - | - | - | - | - | - | - | - | - |
A detailed breakdown of baseline population characteristics as derived from primary studies
Abbreviations: CAD Coronary Artery Disease, CVD Cerebrovascular Disease, ESRD End-Stage Renal Disease, DLP Dyslipidaemia, HTN Hypertension, NA Not applicable, NS Not significant; where p ≥ 0.05
Key: —, no data provided
Fig. 3Multidisciplinary Approach for global patient management [82–84]