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Coagucheck

Manufactured by Roche
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The CoaguCheck is a compact, portable device designed for monitoring coagulation and prothrombin time (PT) in a healthcare setting. It provides accurate and reliable results to assist healthcare professionals in managing patients' anticoagulation therapy.

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Lab products found in correlation

I stat 1, by Abbott (2 mentions)

4 protocols using coagucheck

1

LVAD Implantation: Standardized Heart Failure Management

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Following LVAD implantation, all patients received a standardized heart failure prevention medical regimen, including neurohormonal antagonists, diuretics, and antiarrhythmic agents, as needed. Antiplatelet therapy with aspirin (100 mg daily) was also implemented on the next day of LVAD implantation and maintained throughout LVAD support unless any bleeding events occurred. Anticoagulation therapy was also immediately implemented after LVAD implantation and maintained throughout LVAD support at the target international normalized ratio of 2.0 to 2.5 for patients with a HeartMateII (Thoratec) or DuraHeart (Terumo Heart) device, and 2.5 to 3.0 for those with a HeartWare (HeartWare), EVAHEART (SunMedical), or Jarvik 2000 (Jarvik Heart) device. In our hospital, patients routinely visit the hospital and check their international normalized ratio every month. If patients have below or above therapeutic ranges, their international normalized ratio is checked every 2 or 3 days with CoaguCheck (Roche) at home until therapeutic the range is stably achieved.
Yoshioka D., Okazaki S., Toda K., Murase S., Saito S., Domae K., Miyagawa S., Yoshikawa Y., Daimon T., Sakaguchi M, & Sawa Y. (2017). Prevalence of Cerebral Microbleeds in Patients With Continuous‐Flow Left Ventricular Assist Devices. Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 6(9), e005955.
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2

Point-of-Care Blood Analysis Protocol

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Testing was performed on fresh whole-blood samples within a biosafety cabinet using point-of-care instruments. Prothrombin time was measured using the Coagucheck (Roche) meter. Electrolyte, acid-base, and hematology parameters were assayed on lithium-heparinized whole blood using the iSTAT-1 (Abbot) with the Chem8+ cartridge.
Winkler E.S., Bailey A.L., Kafai N.M., Nair S., McCune B.T., Yu J., Fox J.M., Chen R.E., Earnest J.T., Keeler S.P., Ritter J.H., Kang L.I., Dort S., Robichaud A., Head R., Holtzman M.J, & Diamond M.S. (2020). SARS-CoV-2 infection of hACE2 transgenic mice causes severe lung inflammation and impaired function. Nature immunology, 21(11), 1327-1335.
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3

Point-of-Care Blood Analysis Protocol

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Testing was performed on fresh whole-blood samples within a biosafety cabinet using point-of-care instruments. Prothrombin time was measured using the Coagucheck (Roche) meter. Electrolyte, acid-base, and hematology parameters were assayed on lithium-heparinized whole blood using the iSTAT-1 (Abbot) with the Chem8+ cartridge.
Winkler E.S., Bailey A.L., Kafai N.M., Nair S., McCune B.T., Yu J., Fox J.M., Chen R.E., Earnest J.T., Keeler S.P., Ritter J.H., Kang L.I., Dort S., Robichaud A., Head R., Holtzman M.J, & Diamond M.S. (2020). SARS-CoV-2 infection of hACE2 transgenic mice causes severe lung inflammation and impaired function. Nature immunology, 21(11), 1327-1335.
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4

Patient INR Self-Testing with Approved Devices

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Patient self-testing of INR with a home monitoring device was performed with Food and Drug Administrationapproved devices: CoaguCheck (Roche, Roche Diagnostics, Mannheim, Germany) and INRatio 2 (Alere Inc., South Waltham, MA).
Schettle S., Schlöglhofer T., Zimpfer D., Schima H., Kaufmann F., Salimbangon A., Wolforth J., Schroeder S., Hards R., Ritchie B., Staley L., Pereira N., Kushwaha S., Maltais S, & Stulak J. (2018). International Analysis of LVAD Point-of-Care Versus Plasma INR: A Multicenter Study. ASAIO journal (American Society for Artificial Internal Organs : 1992), 64(6).
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