| Literature DB >> 33630476 |
Hany Zayed1, Mustafa Musajee1, Narayanan Thulasidasan1, Mohamed Sayed1, Federica Francia1, Meryl Green1, Martin Arissol2, Alpa Lakhani2, Lukla Biasi1, Sanjay Patel1.
Abstract
OBJECTIVE: Examine the impact of COVID-19 pandemic on the outcomes in patients with CLTI or DFI.Entities:
Mesh:
Year: 2020 PMID: 33630476 PMCID: PMC9132240 DOI: 10.1097/SLA.0000000000004677
Source DB: PubMed Journal: Ann Surg ISSN: 0003-4932 Impact factor: 13.787
Patient Demographics and Medication
| Period 1 (N = 139) | Period 2 (N = 95) |
| |
| Age (mean (SD) (yrs) | 70 (±11) | 67 (±12) | 0.10† |
| Sex (M:F) | 102:37 | 64:31 | 0.38∗ |
| IHD n (%) | 46 (33) | 31 (32) | 0.52∗ |
| Stoke/TIA n (%) | 18 (13) | 8 (8) | 0.12∗ |
| DM n (%) | 84 (60) | 57 (60) | 0.52∗ |
| Smoker n (%) | 112 (81) | 57 (60) | 0.02∗ |
| Hypertension n (%) | 104 (75) | 82 (86) | 0.034∗ |
| Hypercholesterolaemia n (%) | 72 (52) | 63 (64) | 0.06∗ |
| eGFR (mean (SD) (ml/min/1.73 m2) | 75 (±36) | 74 (±50) | 0.90† |
| Renal replacement therapy | 4 (3) | 8 (8) | 0.072∗ |
| Preoperative anticoagulation | |||
| Warfarin | 8 (6) | 6 (6) | |
| Direct oral anticoagulant (DOAC) | 11 (8) | 16 (17) | 0.09∗ |
| Low molecular weight heparin | 5 (4) | 7 (7) | |
| Preoperative antiplatelets | |||
| Aspirin | 63 (45) | 33 (35) | |
| Clopidogrel | 18 (13) | 12 (13) | 0.001∗ |
| Dual antiplatelets | 8 (6) | 15 (16) | |
| Postoperative anticoagulation | |||
| Warfarin | 9 (6) | 9 (6) | |
| Direct oral anticoagulant (DOAC) | 15 (11) | 18 (19) | 0.001∗ |
| Low molecular weight heparin | 6 (4) | 16 (17) | |
| Postoperative antiplatelets | |||
| Aspirin | 29 (21) | 31 (33) | |
| Clopidogrel | 41 (29) | 19 (20) | 0.001∗ |
| Dual antiplatelets | 59 (42) | 26 (27) | |
Chi-Square.
Unpaired t-test.
DM indicates diabetes mellitus; eGFR, estimated glomerular filtration rate; IHD, ischaemic heart disease; TASC, Transatlantic Inter-Society Consensus; TIA, transient ischaemic attack.
Presentation
| Period 1 (N = 139) | Period 2 (N = 95) |
| |
| Clinical presentation n (%) | |||
| Critical limb ischemia | 76 (55) | 47 (49) | |
| Neuro-ischemic infection/tissue loss | 37 (27) | 26 (27) | 0.26∗ |
| Diabetic foot infection/tissue loss | 17 (12) | 16 (17) | |
| Acute limb ischaemia | 8 (6) | 4 (4) | |
| Aneurysmal disease | 1 (1) | 2 (2) | |
| Rutherford classification n (%) | N=113 | N=73 | |
| 4 | 30 (27) | 28 (38) | |
| 5 | 41 (36) | 24 (32) | 0.25∗ |
| 6 | 46 (40) | 21 (29) | |
| Level of critical lesion (s) n (%) | |||
| Iliac | 13 (12) | 6 (8) | |
| Femoro-popliteal | 31 (28) | 17 (23) | 0.19∗ |
| Infra-popliteal | 26 (23) | 14 (19) | |
| Multi-level | 43 (38) | 36 (49) | |
| Overall GLASS classification n (%) | |||
| I | 22 (19) | 19 (26) | |
| II | 11 (10) | 9 (12) | 0.38∗ |
| III | 80 (71) | 45 (62) | 0.014‡ |
| WCC on admission - mean (±SD) | 9.5 (±3.9) | 11 (±4.5) | |
| CRP on admission - median (range) | 44 (1–354) | 73 (1–321) | 0.004† |
Chi-square.
Man-Whitney U test.
Unpaired t-test.
Procedural Details
| Period 1 (N = 139) | Period 2 (N = 95) |
| |
| Surgical revascularisation | |||
| Bypass | 18 (13) | 14 (14) | |
| Embolectomy | 3 (2) | 2 (2) | 0.66∗ |
| Endovascular revascularisation | |||
| Percutaneous PTA+/_stent | 72 (52) | 42 (44) | |
| Arterial lysis | 5 (4) | 2 (2) | 0.45∗ |
| Hybrid revascularisation (CFA endarterectomy + PTA+/_stent) | 17 (12) | 14 (14) | 0.58∗ |
| Primary major amputation | 10 (7) | 5 (5) | 0.62∗ |
| Primary minor amputation/debridement | 14 (10) | 16 (17) | 0.09∗ |
| Median time from revascularisation to amputation (Range) | 13 (1–84) days | 13 (1–90) days | NS |
Chi-Square.
FIGURE 1Amputation free survival by Kaplan Meier analysis. Log rank test.
FIGURE 2A, Primary patency. B, Freedom from (major adverse limb event) MALE - by Kaplan Meier analysis. Log Rank test.
Multivariate Cox Regression Analysis Showing Factors Affecting Primary Patency and Freedom From MALE
| Predictors of Outcome | Hazard Ratio (95% CI) |
| |
| Primary patency | WCC on admission | 0.83 (0.81–0.98) | 0.018 |
| Presentation period | 0.19 (0.06–0.56) | 0.003 | |
| f-MALE | eGFR | 1.01 (1.0–1.014) | 0.038 |
| Presentation period | .41 (0.21–0.79) | 0.009 | |
| Postprocedural DAPT | 0.44 (0.27–0.74) | 0.002 |
Thirty Day Morbidity (I-IV) and Mortality (V) Stratified Using the Clavien-Dindo Classification
| Complication Grade | Period 1 N = 139 (%) | Period 2 N = 95 (%) |
|
| I | 7 (5) | 5 (5) | 0.08 |
| II | 10 (7) | 4 (4) | |
| III | 9 (6) | 4 (4) | 0.07 |
| IV | 8 (6) | 3 (3) | |
| V | 3 (2) | 2 (2) | 0.91 |
Chi square based on minor- Grade I and II or major - Grade III and IV complications.