Preemptive warfarin dose reduction after initiation of sulfamethoxazole-trimethoprim or metronidazole

被引:9
|
作者
Powers, Anna [1 ]
Loesch, Erin B. [1 ]
Weiland, Anthony [1 ]
Fioravanti, Nicole [2 ]
Lucius, David [1 ]
机构
[1] Dayton Vet Affairs Med Ctr, 4100 West 3rd St 119, Dayton, OH 45428 USA
[2] Cincinnati Vet Affairs Med Ctr, Cincinnati, OH USA
关键词
Anticoagulation; Drug-interaction; INR control; Metronidazole; Sulfamethoxazole-trimethoprim; Warfarin; NONVALVULAR ATRIAL-FIBRILLATION; OLDER-ADULTS; ANTICOAGULATION; PRESCRIPTION; VETERANS; THERAPY; EVENTS; RANGE;
D O I
10.1007/s11239-017-1497-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To evaluate the utility of a preemptive warfarin dose reduction at the time of initiation of either sulfamethoxazole-trimethoprim or metronidazole, a retrospective chart review of patients who received an outpatient prescription for warfarin and either sulfamethoxazole-trimethoprim and/or metronidazole from July 1, 2011 to July 1, 2015 was conducted. Clinical outcomes compared Veterans who had a warfarin dose reduction and those who did not within 120 h (5 days) of antibiotic initiation. The primary outcome compared the pre-and post-antibiotic International Normalized Ratio (INR) of patients in the intervention group (warfarin dose reduction) with those in the control group (no intervention). Secondary outcomes assessed incidence of thromboembolic and major bleeding events within 30 days of antibiotic completion. Fifty patients were assessed. Forty-nine patients had at least one follow-up appointment; 126 follow-up visits were evaluated. There was a statistically significant difference for the change in therapeutic INR at the first follow-up appointment (p = 0.029) for those patients in the control group. On average, the patients in the intervention group required fewer follow-up visits (p = 0.019). There were no statistically significant differences for the overall rate of therapeutic INR values between groups, as well as no instances of a thromboembolic or major bleeding events during the follow-up period. Clinically significant differences were observed for patients who received a preemptive warfarin dose reduction upon initiation of sulfamethoxazole-trimethoprim or metronidazole. Patients in the intervention group required fewer follow-up appointments and were more likely maintain a therapeutic INR within the 30 days following the antibiotic course. Results of this study will be presented the at Pharmacy and Therapeutics committee in an effort to seek approval for policy development to initiate a local preemptive warfarin dose adjustment as a standard of practice.
引用
收藏
页码:88 / 93
页数:6
相关论文
共 46 条
  • [21] Safety and efficacy of prophylaxis for Pneumocystis jirovecii pneumonia involving trimethoprim-sulfamethoxazole dose reduction in kidney transplantation
    G. V. Ramesh Prasad
    Jill Beckley
    Mohit Mathur
    Madhushankar Gunasekaran
    Michelle M. Nash
    Lindita Rapi
    Michael Huang
    Jeffrey S. Zaltzman
    BMC Infectious Diseases, 19
  • [22] Propylene Glycol Toxicity Resulting In Severe Lactic Acidosis After Standard Dose Trimethoprim/sulfamethoxazole Infusion
    Bulathsinghala, M.
    Keefer, K.
    Van de Louw, A.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 193
  • [23] Low-dose trimethoprim–sulfamethoxazole for Pneumocystis jiroveci pneumonia prophylaxis after allogeneic hematopoietic SCT
    T Muto
    M Takeuchi
    T Kawaguchi
    S Tanaka
    S Tsukamoto
    S Sakai
    Y Takeda
    D Abe
    C Ohwada
    E Sakaida
    N Shimizu
    K Yokote
    T Iseki
    C Nakaseko
    Bone Marrow Transplantation, 2011, 46 : 1573 - 1575
  • [24] Safety and efficacy of prophylaxis for Pneumocystis jirovecii pneumonia involving trimethoprim-sulfamethoxazole dose reduction in kidney transplantation
    Prasad, G. V. Ramesh
    Beckley, Jill
    Mathur, Mohit
    Gunasekaran, Madhushankar
    Nash, Michelle M.
    Rapi, Lindita
    Huang, Michael
    Zaltzman, Jeffrey S.
    BMC INFECTIOUS DISEASES, 2019, 19 (1)
  • [25] MINI-DOSE TRIMETHOPRIM WITH SULFAMETHOXAZOLE PREVENTS PNEUMOCYSTIS AND TOXOPLASMOSIS INFECTIONS AFTER HEART-TRANSPLANTATION
    KEOGH, A
    MACDONALD, P
    RICHENS, D
    HARVISON, A
    SPRATT, P
    TRANSPLANTATION PROCEEDINGS, 1992, 24 (05) : 2263 - 2263
  • [26] Trimethoprim-sulphamethoxazole and metronidazole as prophylaxis in colorectal surgery:: A study of bioavailability after an oral single dose
    Raab, Y
    Rasmussen, I
    Odenholt, I
    Påhlman, L
    EUROPEAN JOURNAL OF SURGERY, 2001, 167 (01) : 46 - 49
  • [27] Prediction of the warfarin maintenance dose after completion of the 10 mg initiation nomogram
    le Gal, G.
    Carrier, M.
    Tierney, S.
    Majeed, H.
    Rodger, M.
    Wells, P. S.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2009, 7 : 269 - 269
  • [28] Low-dose trimethoprim-sulfamethoxazole for Pneumocystis jiroveci pneumonia prophylaxis after allogeneic hematopoietic SCT
    Muto, T.
    Takeuchi, M.
    Kawaguchi, T.
    Tanaka, S.
    Tsukamoto, S.
    Sakai, S.
    Takeda, Y.
    Abe, D.
    Ohwada, C.
    Sakaida, E.
    Shimizu, N.
    Yokote, K.
    Iseki, T.
    Nakaseko, C.
    BONE MARROW TRANSPLANTATION, 2011, 46 (12) : 1573 - 1575
  • [29] Pharmacokinetics of sulfamethoxazole and trimethoprim in Pacific white shrimp, Litopenaeus vannamei, after oral administration of single-dose and multiple-dose
    Ma, Rongrong
    Wang, Yuan
    Zou, Xiong
    Hu, Kun
    Sun, Beibei
    Fang, Wenhong
    Fu, Guihong
    Yang, Xianle
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2017, 52 : 90 - 98
  • [30] DOSE DEPENDENT HYPONATREMIA ASSOCIATED WITH HIGH-DOSE TRIMETHOPRIM-SULFAMETHOXAZOLE FOR TREATMENT OF DISSEMINATED NOCARDIA INFECTION AFTER KIDNEY TRANSPLANTATION
    Kovvuru, Karthik
    Rivera, Franco H. Cabeza
    Cheungpasitporn, Wisit
    AMERICAN JOURNAL OF KIDNEY DISEASES, 2018, 71 (04) : 559 - 559