PMID- 26659923 OWN - NLM STAT- MEDLINE DCOM- 20160808 LR - 20210202 IS - 1528-0020 (Electronic) IS - 0006-4971 (Print) IS - 0006-4971 (Linking) VI - 127 IP - 8 DP - 2016 Feb 25 TI - Mechanical prophylaxis is a heparin-independent risk for anti-platelet factor 4/heparin antibody formation after orthopedic surgery. PG - 1036-43 LID - 10.1182/blood-2015-06-651620 [doi] AB - Platelet-activating antibodies, which recognize platelet factor 4 (PF4)/heparin complexes, induce spontaneous heparin-induced thrombocytopenia (HIT) syndrome or fondaparinux-associated HIT without exposure to unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH). This condition mostly occurs after major orthopedic surgery, implying that surgery itself could trigger this immune response, although the mechanism is unclear. To investigate how surgery may do so, we performed a multicenter, prospective study of 2069 patients who underwent total knee arthroplasty (TKA) or hip arthroplasty. Approximately half of the patients received postoperative thromboprophylaxis with UFH, LMWH, or fondaparinux. The other half received only mechanical thromboprophylaxis, including dynamic (intermittent plantar or pneumatic compression device), static (graduated compression stockings [GCSs]), or both. We measured anti-PF4/heparin immunoglobulins G, A, and M before and 10 days after surgery using an immunoassay. Multivariate analysis revealed that dynamic mechanical thromboprophylaxis (DMT) was an independent risk factor for seroconversion (odds ratio [OR], 2.01; 95% confidence interval [CI], 1.34-3.02; P = .001), which was confirmed with propensity-score matching (OR, 1.99; 95% CI, 1.17-3.37; P = .018). For TKA, the seroconversion rates in patients treated with DMT but no anticoagulation and in patients treated with UFH or LMWH without DMT were similar, but significantly higher than in patients treated with only GCSs. The proportion of patients with >/=1.4 optical density units appeared to be higher among those treated with any anticoagulant plus DMT than among those not treated with DMT. Our study suggests that DMT increases risk of an anti-PF4/heparin immune response, even without heparin exposure. This trial was registered to www.umin.ac.jp/ctr as #UMIN000001366. CI - (c) 2016 by The American Society of Hematology. FAU - Bito, Seiji AU - Bito S AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; Division of Clinical Epidemiology, NHO Tokyo Medical Center, Tokyo, Japan; FAU - Miyata, Shigeki AU - Miyata S AD - Division of Transfusion Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan; FAU - Migita, Kiyoshi AU - Migita K AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Nakamura, Mashio AU - Nakamura M AD - Department of Cardiology and Nephrology, Mie University Graduate School of Medicine, Mie, Japan; FAU - Shinohara, Kazuhito AU - Shinohara K AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Sato, Tomotaro AU - Sato T AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Tonai, Takeharu AU - Tonai T AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Shimizu, Motoyuki AU - Shimizu M AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Shibata, Yasuhiro AU - Shibata Y AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Kishi, Kazuhiko AU - Kishi K AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Kubota, Chikara AU - Kubota C AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Nakahara, Shinnosuke AU - Nakahara S AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Mori, Toshihito AU - Mori T AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Ikeda, Kazuo AU - Ikeda K AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Ota, Shusuke AU - Ota S AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Minamizaki, Takeshi AU - Minamizaki T AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Yamada, Shigeru AU - Yamada S AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Shiota, Naofumi AU - Shiota N AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; FAU - Kamei, Masataka AU - Kamei M AD - Department of Anesthesiology, National Cerebral and Cardiovascular Center, Osaka, Japan; and. FAU - Motokawa, Satoru AU - Motokawa S AD - Japanese National Hospital Organization (NHO)-Evidence-Based Medicine Study Group for the Clinical Study of Prevention and Actual Situation of Venous Thromboembolism After Total Arthroplasty, Tokyo, Japan; Department of Orthopedic Surgery, NHO Nagasaki Medical Center, Nagasaki, Japan. LA - eng SI - JPRN/UMIN000001366 PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20151209 PL - United States TA - Blood JT - Blood JID - 7603509 RN - 0 (Anticoagulants) RN - 0 (Autoantibodies) RN - 0 (Autoantigens) RN - 0 (Heparin, Low-Molecular-Weight) RN - 0 (Polysaccharides) RN - 37270-94-3 (Platelet Factor 4) RN - 9005-49-6 (Heparin) RN - J177FOW5JL (Fondaparinux) SB - IM CIN - Blood. 2016 Feb 25;127(8):961-2. PMID: 26917737 MH - Aged MH - Anticoagulants/therapeutic use MH - Arthroplasty, Replacement, Hip/*adverse effects MH - Arthroplasty, Replacement, Knee/*adverse effects MH - Autoantibodies/*blood/immunology MH - Autoantigens/immunology MH - Cohort Studies MH - Enzyme-Linked Immunosorbent Assay MH - Female MH - Fondaparinux MH - Heparin/immunology/therapeutic use MH - Heparin, Low-Molecular-Weight/therapeutic use MH - Humans MH - Intermittent Pneumatic Compression Devices MH - Male MH - Middle Aged MH - Platelet Factor 4/immunology MH - Polysaccharides/therapeutic use MH - Stockings, Compression MH - Thromboembolism/*prevention & control PMC - PMC4768427 EDAT- 2015/12/15 06:00 MHDA- 2016/08/09 06:00 PMCR- 2016/02/25 CRDT- 2015/12/15 06:00 PHST- 2015/06/16 00:00 [received] PHST- 2015/12/01 00:00 [accepted] PHST- 2015/12/15 06:00 [entrez] PHST- 2015/12/15 06:00 [pubmed] PHST- 2016/08/09 06:00 [medline] PHST- 2016/02/25 00:00 [pmc-release] AID - S0006-4971(20)30424-9 [pii] AID - 2015/651620 [pii] AID - 10.1182/blood-2015-06-651620 [doi] PST - ppublish SO - Blood. 2016 Feb 25;127(8):1036-43. doi: 10.1182/blood-2015-06-651620. Epub 2015 Dec 9.