A Case of an Increase in Prothrombin Time-International Normalized Ratio by Interaction Between Warfarin and Baloxavir Marboxil in a Patient on Implantable Ventricular Assist Device.


Journal

Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques
ISSN: 1482-1826
Titre abrégé: J Pharm Pharm Sci
Pays: Switzerland
ID NLM: 9807281

Informations de publication

Date de publication:
2021
Historique:
entrez: 18 1 2021
pubmed: 19 1 2021
medline: 27 10 2021
Statut: ppublish

Résumé

Baloxavir marboxil (BM) is a novel drug with a cap-dependent endonuclease inhibitory action for influenza A or B; it is highly safe and requires just a single oral dose. Patients with severe heart failure use implantable ventricular assist device (iVAD) until transplantation, but they have an increased risk of thrombosis development. Their warfarin is administered based on point-of-care testing (POCT) with a strict control of prothrombin time-international normalized ratio (PT-INR). Here, we report a case of a patient with iVAD whose PT-INR was significantly increased from the target range after BM administration. The patient was a 45-year-old man and transplanted with iVAD; warfarin treatment was started when his PT-INR target range was 3.0-3.5. At home, he frequently self-measured PT-INR by POCT and precisely controlled the warfarin dose. He had a fever, was diagnosed with influenza A and was administered BM 40 mg. Thereafter, his PT-INR continued to increase, reaching 4.8 on day 12 of BM administration, exceeding his target range; warfarin was skipped for 1 day. In this case, based on the history of BM administration and clinical course, the increase in PT-INR could be due to BM. Considering the interaction between warfarin and BM, we suspected a possibility of competition for protein-binding sites. Increased PT-INR in the patient was detected early by POCT and thus severe bleeding was avoided. Strict monitoring of PT-INR when using BM in patients taking warfarin is of clinical importance.

Sections du résumé

BACKGROUND
Baloxavir marboxil (BM) is a novel drug with a cap-dependent endonuclease inhibitory action for influenza A or B; it is highly safe and requires just a single oral dose. Patients with severe heart failure use implantable ventricular assist device (iVAD) until transplantation, but they have an increased risk of thrombosis development. Their warfarin is administered based on point-of-care testing (POCT) with a strict control of prothrombin time-international normalized ratio (PT-INR).
CASE REPORT
Here, we report a case of a patient with iVAD whose PT-INR was significantly increased from the target range after BM administration. The patient was a 45-year-old man and transplanted with iVAD; warfarin treatment was started when his PT-INR target range was 3.0-3.5. At home, he frequently self-measured PT-INR by POCT and precisely controlled the warfarin dose. He had a fever, was diagnosed with influenza A and was administered BM 40 mg. Thereafter, his PT-INR continued to increase, reaching 4.8 on day 12 of BM administration, exceeding his target range; warfarin was skipped for 1 day. In this case, based on the history of BM administration and clinical course, the increase in PT-INR could be due to BM. Considering the interaction between warfarin and BM, we suspected a possibility of competition for protein-binding sites. Increased PT-INR in the patient was detected early by POCT and thus severe bleeding was avoided.
CONCLUSION
Strict monitoring of PT-INR when using BM in patients taking warfarin is of clinical importance.

Identifiants

pubmed: 33460556
doi: 10.18433/jpps31375
doi:

Substances chimiques

Anticoagulants 0
Dibenzothiepins 0
Morpholines 0
Pyridones 0
Triazines 0
baloxavir 4G86Y4JT3F
Warfarin 5Q7ZVV76EI

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

37-40

Auteurs

Keiko Kurosawa (K)

Department of Pharmaceutical Sciences, Tohoku University Hospital, Sendai, Miyagi Japan.

Shinya Takasaki (S)

Department of Pharmaceutical Sciences, Tohoku University Hospital, Sendai, Miyagi Japan.

Hisaki Suzuki (H)

Department of Pharmaceutical Sciences, Tohoku University Hospital, Sendai, Miyagi Japan.

Yuji Sato (Y)

Department of Pharmaceutical Sciences, Tohoku University Hospital, Sendai, Miyagi Japan.

Masatoshi Akiyama (M)

Department of Cardiovascular Surgery, Tohoku University Hospital, Sendai, Miyagi Japan.

Miki Akiba (M)

Organ Transplantation Center, Tohoku University Hospital, Sendai, Miyagi Japan.

Yoshikatsu Saiki (Y)

Department of Cardiovascular Surgery, Tohoku University Hospital, Sendai, Miyagi Japan.

Nariyasu Mano (N)

Department of Pharmaceutical Sciences, Tohoku University Hospital, Sendai, Miyagi Japan.

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