Real-world effectiveness of remote monitoring of the international normalized ratio in patients undergoing heart valve replacement using the CoaguChek® INRange system with a remote data transmission module
- Authors: Provatorov S.I.1, Osokina A.K.1, Shchinova A.M.1, Barabanova T.I.2, Shestova I.I.2, Mel'nikova E.N.2
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Affiliations:
- Chazov National Medical Research Center of Cardiology
- Tula Regional Clinical Cardiological Dispensary
- Issue: Vol 26, No 12 (2024): Коморбидность в клинике внутренних болезней
- Pages: 851-857
- Section: Articles
- URL: https://bakhtiniada.ru/2075-1753/article/view/289173
- DOI: https://doi.org/10.26442/20751753.2024.12.203065
- ID: 289173
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Abstract
Background. Systems for self-determination of international normalized ratio (INR) may increase adherence to regular monitoring of hemostasis parameters in patients taking vitamin K antagonists. However, evidence of the effectiveness of self-determination of INR in real-world clinical practice in Russia is limited.
Aim. To compare the effectiveness of remote monitoring of INR using the CoaguChek® INRange coagulometer in patients who have undergone mechanical heart valve implantation with traditional INR control by measuring it in the outpatient department laboratory.
Materials and methods. A prospective study enrolled 101 patients receiving warfarin after a mitral or aortic mechanical heart valve prosthesis implantation. In Group 1 (n=51), conventional laboratory INR control was used; in Group 2 (n=50), patients monitored INR by themselves using a CoaguChek® INRange coagulometer. The follow-up duration was 1 year.
Results. Patients in Groups 1 and 2 did not differ in INR: 2.62 [2.45; 2.85] vs 2.6 [2.5; 2.8], respectively (data are presented as the median [1st to 3rd quartile]), and the time of INR in the therapeutic range: 66.7% [50; 78.6] vs 67.7% [53.2; 80.6]. The intervals between INR determinations in Group 1 were significantly longer: 30.5 [29.5; 31] days vs 20 [13; 25] days.
Conclusion. The CoaguChek® INRange system enables remote patient monitoring during continuous warfarin therapy and achievement of the target INR with a time in the therapeutic range comparable to that for patients with INR measurements in outpatient laboratories.
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##article.viewOnOriginalSite##About the authors
Sergei I. Provatorov
Chazov National Medical Research Center of Cardiology
Email: osk@rambler.ru
ORCID iD: 0000-0002-7936-3634
D. Sci. (Med.)
Russian Federation, MoscowAnna K. Osokina
Chazov National Medical Research Center of Cardiology
Author for correspondence.
Email: osk@rambler.ru
ORCID iD: 0000-0001-8127-4609
Cand. Sci. (Med.)
Russian Federation, MoscowAleksandra M. Shchinova
Chazov National Medical Research Center of Cardiology
Email: osk@rambler.ru
ORCID iD: 0000-0002-3631-5026
Cand. Sci. (Med.)
Russian Federation, MoscowTatiana I. Barabanova
Tula Regional Clinical Cardiological Dispensary
Email: osk@rambler.ru
ORCID iD: 0009-0000-8565-9952
cardiologist
Russian Federation, TulaIrina I. Shestova
Tula Regional Clinical Cardiological Dispensary
Email: osk@rambler.ru
ORCID iD: 0000-0002-2341-8181
cardiologist
Russian Federation, TulaElena N. Mel'nikova
Tula Regional Clinical Cardiological Dispensary
Email: osk@rambler.ru
ORCID iD: 0009-0007-5296-5946
Deputy Chief doctor
Russian Federation, TulaReferences
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