| Literature DB >> 30405744 |
Seungwon Kwon1, Woo-Sang Jung1, Seungbo Yang1, Chul Jin1, Seung-Yeon Cho1, Seong-Uk Park1, Sang-Kwan Moon1, Jung-Mi Park1, Chang-Nam Ko1, Ki-Ho Cho1, Min-Jeong Park1.
Abstract
Anticoagulant therapy is used to reduce the risk of thromboembolic events in patients with atrial fibrillation. Warfarin has been the traditional anticoagulant but is difficult to use because of its narrow therapeutic window. Recently, newer oral anticoagulants (NOACs) have been developed. However, bleeding continues to be a significant complication. The objective of this study was to assess the safety of acupuncture in patients taking NOACs. The medical records in the Stroke Center at Kyung Hee University Korean Medicine Hospital were retrospectively reviewed to identify patients who had received acupuncture between January 2017 and September 2017. The patients were divided into groups according to whether they were taking an NOAC, an antiplatelet agent, or no anticoagulant therapy. Bleeding-related side effects that occurred immediately after removal of acupuncture needles were recorded. Three hundred and sixteen patients underwent 10,177 acupuncture sessions during the study period. Microbleeding (bleeding that ceased within 30 s) occurred at a rate of 3.9% in the NOAC group, 5.6% in the antiplatelet group, and 5.1% in the control group. There were no between-group differences in the microbleeding rate. No serious adverse events, including major bleeding, were detected. These findings indicate that acupuncture is safe in patients taking NOACs.Entities:
Year: 2018 PMID: 30405744 PMCID: PMC6199863 DOI: 10.1155/2018/8042198
Source DB: PubMed Journal: Evid Based Complement Alternat Med ISSN: 1741-427X Impact factor: 2.629
Checklist for acupuncture-related side effects.
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| The number of microbleeds was checked according to the time of hemostasis 10 s after removal of the acupuncture needle. This procedure was routinely carried out by Korean medicine doctors. Bleeding that stopped within 30 s was defined as “microbleeding.” Multiple bleeding events occurring during one acupuncture session were considered to be one episode of bleeding. |
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| Bleeding that took at least 30 s to stop. |
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| Bruising checked 1–3 h after removing the needles. |
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General patient characteristics.
| Group A (n = 28) | Group B (n = 145) | Group C (n = 143) |
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| Male | 14 (50.0) | 78 (53.8) | 64 (44.8) | 0.308 |
| Female | 14 (50.0) | 67 (46.2) | 79 (55.2) | |
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| 73.14 ± 9.60 | 67.52 ± 11.44 | 62.60 ± 13.42 | <0.001 |
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| Atrial fibrillation | 24 (85.7) | 1 (0.7) | 4 (2.7) | <0.001 |
| Hypertension | 13 (41.9) | 96 (66.2) | 72 (50.3) | 0.005 |
| Diabetes mellitus | 8 (22.2) | 58 (28.2) | 31 (17.8) | 0.048 |
| Hyperlipidemia | 5 (15.2) | 53 (26.8) | 31 (17.8) | 0.071 |
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| Dabigatran | 11 (39.3) | 0 | 0 | |
| Rivaroxaban | 2 (7.1) | 0 | 0 | |
| Apixaban | 15 (53.6) | 0 | 0 | |
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| Aspirin | 1 | 50 (34.5) | 0 | |
| Clopidogrel | 1 | 35 (24.1) | 0 | |
| Triflusal | 0 | 7 (4.8) | 0 | |
| Aspirin + clopidogrel | 0 | 46 (31.7) | 0 | |
| Aspirin + triflusal | 0 | 7 (4.8) | 0 |
The data are shown as the mean ± standard deviation or number (percentage). Group A includes patients taking an NOAC. Group B includes patients taking an antiplatelet agent. Group C includes the controls who were not taking an NOAC or antiplatelet agent. aAnalysis of variance used for age and the chi-squared test for categorical variables.
Side effects of acupuncture in the study groups.
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| (n = 28) | (n = 145) | (n = 143) | ||
| Total number of acupuncture treatments, n | 1076 | 4574 | 4527 | |
| Total number of side effects | 43 (4.0) | 314 (6.9) | 250 (5.5) | <0.001 |
| Microbleeding (10 s ≤ x < 30 s) | 42 (3.9) | 254 (5.6) | 230 (5.1) | 0.084 |
| 10 s ≤ x < 20 s | 42 (3.8) | 217 (4.5) | 203 (4.3) | 0.065 |
| 20 s ≤ x < 30 s | 0 (0.0) | 37 (0.8) | 27 (0.6) | |
| Extensive bleeding | 0 (0.0) | 4 (0.0) | 2 (0.0) | |
| Massive hemorrhage | 0 (0.0) | 0 (0.0) | 0 (0.0) | |
| Bruising | 1 (0.0) | 31 (0.6) | 13 (0.2) | |
| Edema | 0 (0.0) | 22 (0.4) | 4 (0.0) | |
| Faintness or dizziness | 0 (0.0) | 0 (0.0) | 1 (0.0) | |
| Fatigue or exhaustion | 0 (0.0) | 0 (0.0) | 0 (0.0) | |
| Nausea or vomiting | 0 (0.0) | 0 (0.0) | 0 (0.0) | |
| Pneumothorax | 0 (0.0) | 0 (0.0) | 0 (0.0) | |
| Needle fracture | 0 (0.0) | 0 (0.0) | 0 (0.0) | |
| Skin eruption or itching | 0 (0.0) | 0 (0.0) | 0 (0.0) | |
| Pain after needling | 0 (0.0) | 3 (0.0) | 0 (0.0) | |
| Other adverse effects | 0 (0.0) | 0 (0.0) | 0 (0.0) |
The data are shown as the number (percentage). Group A includes patients taking an NOAC. Group B includes patients taking an antiplatelet agent. Group C includes the controls who were not taking an NOAC or antiplatelet agent. aChi-squared test.