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1.
Blood Coagul Fibrinolysis ; 35(1): 23-26, 2024 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-37994629

RESUMEN

Interpretation of coagulation mixing studies is complicated by interference arising from direct oral anticoagulants (DOACs), which are increasingly prescribed. In this retrospective study, we reviewed 1035 consecutive coagulation mixing studies performed from 2017 to 2021. Three hundred and ninety-nine cases with normal prothrombin time (PT) and activated partial thromboplastin time (aPTT) were excluded. aPTT mixing studies were performed at time 0 and after 60 min of incubation. We confirmed the presence of interfering factors with additional laboratory testing, medication records, and medical history. Mixing corrected most prolonged PT samples (93%), but 32 cases showed incomplete correction. Of these 32 cases, 18 were confounded by DOAC use, and 3 by factor V (FV) inhibitor. We observed an unusual pattern of prolongation of aPTT after incubation, which was previously considered a characteristic of specific factor inhibitors, most commonly FVIII inhibitor. However, we found that lupus anticoagulant (28%) and DOAC (25%) contributed to this pattern similarly as specific factor inhibitors (28%). Coagulation laboratories should be aware of interference arising from DOACs and other factors in PT/aPTT mixing studies, especially in some unusual correction patterns.


Asunto(s)
Anticoagulantes , Coagulación Sanguínea , Humanos , Anticoagulantes/farmacología , Anticoagulantes/uso terapéutico , Pruebas de Coagulación Sanguínea/métodos , Tiempo de Tromboplastina Parcial , Tiempo de Protrombina , Estudios Retrospectivos
2.
Science ; 377(6601): 109-115, 2022 07.
Artículo en Inglés | MEDLINE | ID: mdl-35771907

RESUMEN

Implantable devices capable of targeted and reversible blocking of peripheral nerve activity may provide alternatives to opioids for treating pain. Local cooling represents an attractive means for on-demand elimination of pain signals, but traditional technologies are limited by rigid, bulky form factors; imprecise cooling; and requirements for extraction surgeries. Here, we introduce soft, bioresorbable, microfluidic devices that enable delivery of focused, minimally invasive cooling power at arbitrary depths in living tissues with real-time temperature feedback control. Construction with water-soluble, biocompatible materials leads to dissolution and bioresorption as a mechanism to eliminate unnecessary device load and risk to the patient without additional surgeries. Multiweek in vivo trials demonstrate the ability to rapidly and precisely cool peripheral nerves to provide local, on-demand analgesia in rat models for neuropathic pain.


Asunto(s)
Implantes Absorbibles , Bloqueo Nervioso , Neuralgia , Manejo del Dolor , Nervios Periféricos , Animales , Materiales Biocompatibles , Bloqueo Nervioso/instrumentación , Neuralgia/terapia , Manejo del Dolor/instrumentación , Nervios Periféricos/fisiopatología , Ratas
3.
Lab Med ; 51(3): 310-314, 2020 May 06.
Artículo en Inglés | MEDLINE | ID: mdl-31665395

RESUMEN

A 70-year-old female with a history of hypertension and left A2 segment aneurysm was scheduled for pipeline embolization device (PED) placement. Preinterventional antiplatelet prophylaxis included aspirin and ticagrelor. Unexpectedly, after 13 days of treatment, VerifyNow showed a P2Y12 reaction unit (PRU) value of 216, approximately >5 times the mean PRU of other patients on aspirin and ticagrelor. We confirmed platelet reactivity and ticagrelor resistance with light transmission aggregometry. Antiplatelet therapy was switched to prasugrel, and aspirin was continued. Eight days later, the P2Y12 reaction value (PRU) was 164. PED was placed without complications. Unlike clopidogrel, ticagrelor is a direct P2Y12 inhibitor that does not require metabolism to an active metabolite. Ticagrelor resistance is very rarely reported. To the best of our knowledge, there has been no case of ticagrelor resistance reported in the context of pre-PED placement prophylaxis.


Asunto(s)
Plaquetas/fisiología , Embolización Terapéutica , Pruebas de Función Plaquetaria/métodos , Clorhidrato de Prasugrel/uso terapéutico , Ticagrelor/uso terapéutico , Anciano , Equipos y Suministros , Femenino , Humanos , Agregación Plaquetaria , Ejercicio Preoperatorio , Estudios Prospectivos , Receptores Purinérgicos P2Y12/metabolismo , Resultado del Tratamiento
4.
Pathol Int ; 68(2): 123-127, 2018 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-29222812

RESUMEN

We report a colonic adenocarcinoma associated with diffuse submucosal deposition of a peculiar spheroid-type amyloid identified in the colon, terminal ileum, and appendix. A 65-year-old woman with past medical histories of hypertension, and chronic obstructive pulmonary disease, presented to the emergency room with cramping abdominal pain and nausea. A computed tomography (CT) scan of abdomen showed right colonic volvulus. Emergency right hemicolectomy was performed. The specimen showed colonic adenocarcinoma with focal submucosal invasion (pT1) arising from a villotubular adenoma. A diffuse submucosal spheroid-type amyloid deposition (resembling corpora amylacea-like structures with Liesegang ring formation) was identified in the colon, ileum, and appendix. Electron microscopy examination of this unusual spheroidal-type material further confirmed the presence of amyloid fibrils. Analysis by liquid chromatography-mass spectrometry detected AL (lambda) type amyloidosis in this specimen. Tests for monoclonal gammopathy were not performed because patient consent was not obtained. In tissue section evaluation, however, no plasma cell neoplasm was identified. Cases with isolated AL amyloid deposition in the gastrointestinal tract have been reported rarely, and there is no case report of colonic adenocarcinoma associated with primary amyloid deposition in the English literature.


Asunto(s)
Adenocarcinoma/patología , Amiloidosis/patología , Colon/patología , Neoplasias del Colon/patología , Adenocarcinoma/diagnóstico , Adenoma/complicaciones , Adenoma/patología , Anciano , Amiloide/metabolismo , Femenino , Humanos
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