| Literature DB >> 35092566 |
Shaojun Jiang1, Meina Lv1, Zhiwei Zeng1, Zongwei Fang1, Mingrong Chen1, Jiafen Qian1, Tingting Wu1, Wenjun Chen1, Jinhua Zhang2.
Abstract
This study aimed to explore the effectiveness, and safety of internet-based warfarin management during the pandemic. In this single-center retrospective cohort study, we compared the safety and efficacy of online warfarin management using a smartphone app (the Alfalfa app) versus conventional outpatient clinic management from January 1, 2020 to March 31, 2020. Patients in the online management group used the Alfalfa app to communicate coagulation test results and other relevant information to a doctor or clinical pharmacist, who then responded with the dose adjustment plan and the date of the next blood test. The outcomes examined were the time in therapeutic range (TTR), incidence of clinical events (i.e., bleeding events, thrombotic events, warfarin-related emergency department visits, and warfarin-related hospital admissions), and the distribution of international normalized ratio (INR) values. Data from 117 patients were analyzed in this study. TTR was significantly higher in the online group than in the offline group (61.0% vs. 39.6%, P < 0.01). Incidence of major bleeding events, thrombotic events, and warfarin-related hospital admissions were comparable between the online and offline groups. However, minor bleeds (5.3% vs. 28.3%, P < 0.01) and warfarin-related emergency department visits (1.8% vs. 23.3%, P = 0.02) were significantly fewer in the online group than in the offline group. The proportion of INR values in the therapeutic range (53.8% vs. 40.1%, P < 0.01) was significantly higher in the online group. Warfarin management using the Alfalfa app appears to be a safe and effective method for warfarin management when patients cannot physically visit hospitals for follow-up.Entities:
Keywords: COVID-19; Healthcare delivery; Remote consultation; Telemedicine; Warfarin
Mesh:
Substances:
Year: 2022 PMID: 35092566 PMCID: PMC8799972 DOI: 10.1007/s11239-021-02630-0
Source DB: PubMed Journal: J Thromb Thrombolysis ISSN: 0929-5305 Impact factor: 2.300
Fig. 1Screenshots of Alfalfa app. A Report Interfacem B home page of patient terminal, C doctor’s reply, D patient education, E home page of doctor terminal, F medical strategy development, G checking patient’s report records
Characteristics of the study population
| Characteristics | Total (n = 117) | Offline group (n = 60) | Online group (n = 57) | P |
|---|---|---|---|---|
| Demographic characteristic | ||||
| Age (year) | 50.4 ± 13.1 | 52.7 ± 12.8 | 48.1 ± 13.1 | 0.06 |
| Male (%) | 55 (47.0) | 29 (48.3) | 26 (45.6) | 0.79 |
| Height (cm) | 161.5 ± 18.1 | 159.1 ± 22.7 | 164.4 ± 9.4 | 0.77 |
| Weight (kg) | 59.4 ± 9.78 | 58.4 ± 8.9 | 60.6 ± 10.8 | 0.24 |
| Smoking (%) | 75 (64.1) | 37 (61.7) | 38 (66.7) | 0.57 |
| Alcohol (%) | 30 (25.6) | 16 (26.7) | 14 (24.6) | 0.79 |
| Duration of anticoagulation at baseline (days) | 53.9 ± 17.8 | 54.2 ± 15.0 | 53.7 ± 20.5 | 0.89 |
| Mean warfarin dose (mg/d) | 3.81 ± 0.56 | 3.87 ± 0.53 | 3.73 ± 0.59 | 0.18 |
| Comorbidity n (%) | ||||
| Hypertension | 22 (18.8) | 14 (23.3) | 8 (14.0) | 0.20 |
| Diabetes | 2 (1.7) | 1 (1.7) | 1 (1.7) | > 0.99 |
| Gout or hyperuricemia | 6 (5.1) | 3 (5.0) | 3 (5.3) | 0.95 |
| Previous major thrombosis | 6 (5.1) | 3 (5.0) | 3 (5.3) | 0.95 |
| Previous major bleeding | 1 (0.8) | 0 (0.0) | 1 (1.8) | 0.49 |
| Indication n (%) | ||||
| Single valve replacement or valvuloplasty | 87 (74.4) | 41 (68.3) | 46 (80.6) | 0.13 |
| Double valves replacement or valvuloplasty | 23 (19.7) | 15 (25.0) | 8 (14.0) | 0.14 |
| Triple valves replacement or valvuloplasty | 5 (4.3) | 4 (6.7) | 1 (1.8) | 0.37 |
| NVAF | 1 (0.8) | 0 (0.0) | 1 (1.8) | 0.49 |
| VTE or PE | 1 (0.8) | 0 (0.0) | 1 (1.8) | 0.49 |
NVAF nonvalvular atrial fibrillation, VTE venous thromboembolism, PE pulmonary embolism
Study outcomes
| Outcomes | Total (n = 117) | Offline group (n = 60) | Online group (n = 57) | P | OR (95% CI) |
|---|---|---|---|---|---|
| TTR, mean ± SD (%) | 49.4 ± 27.2 | 39.6 ± 23.1 | 61.0 ± 26.5 | < 0.01 | 0.980 (0.965, 0.994) |
| Minor bleeding events, n (%) | 20 (17.1) | 17 (28.3) | 3 (5.3) | < 0.01 | 7.116 (1.666, 17.391) |
| Major bleeding events, n (%) | 1 (0.8) | 1 (1.7) | 0 (0) | > 0.99 | 0.983 (0.951, 1.016) |
| Thromboembolic events, n (%) | 2 (1.7) | 1 (1.7) | 1 (1.8) | > 0.99 | 0.949 (0.058, 15.543) |
| Warfarin-related emergency department visits, n (%) | 18 (15.4) | 14 (23.3) | 1 (1.8) | 0.02 | 17.043 (2.159, 134.514) |
| Warfarin-related hospital admissions, n (%) | 2 (1.7) | 1 (1.7) | 1 (1.8) | > 0.99 | 0.949 (0.058, 15.543) |
OR odds ratio, CI confidence interval, SD standard deviation
Fig. 2Composition of clinical events
The distribution of INR values
| Outcomes | Total (n = 582) | Offline group (n = 359) | Online group (n = 223) | P |
|---|---|---|---|---|
| Extreme subtherapeutic, n (%) | 149 (25.6) | 99 (27.5) | 50 (22.4) | 0.17 |
| Subtherapeutic, n (%) | 39 (8.4) | 36 (10.2) | 13 (5.8) | 0.08 |
| Therapeutic, n (%) | 264 (45.4) | 144 (40.1) | 120 (53.8) | < 0.01 |
| Supratherapeutic, n (%) | 120 (20.6) | 80 (22.2) | 40 (17.9) | 0.21 |
| Extreme supratherapeutic, n (%) | 0 (0.0) | 0 (0.0) | 0 (0.0) | > 0.99 |
INR international normalized ratio