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1.
A A Pract ; 17(12): e01717, 2023 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-38088749

RESUMO

A 39-year-old woman with juvenile idiopathic arthritis complicated by nonuremic calciphylaxis presented for pain management of bilateral lower extremity wounds requiring frequent dressing changes. Bilateral single-shot femoral nerve blocks using liposomal bupivacaine and 0.25% bupivacaine were performed. The patient reported decreased pain scores and had reduced opioid use for 72 hours postblock. Repeat, bilateral single-shot femoral nerve blocks with liposomal bupivacaine and 0.25% bupivacaine were performed approximately every 72 hours to maintain adequate analgesia. We conclude that off-label use of liposomal bupivacaine in femoral nerve blocks results in prolonged block duration without adverse effects or tachyphylaxis.


Assuntos
Analgesia , Calciofilaxia , Adulto , Feminino , Humanos , Anestésicos Locais/uso terapêutico , Bupivacaína/uso terapêutico , Calciofilaxia/terapia , Nervo Femoral , Bloqueio Nervoso/métodos , Manejo da Dor/métodos
2.
A A Pract ; 17(4): e01674, 2023 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-37043402

RESUMO

A 36-year-old man with a history of cervical spinal cord stimulator (SCS) lead placement presented with transient right-sided hemiparesis and diplopia that began 2 days after a coughing episode. Imaging revealed lateral and cranial migration of one of the patient's SCS leads. Deactivation of the SCS resulted in rapid improvement of his nonmotor symptoms but did not resolve his motor deficits. The SCS system was surgically explanted, resulting in resolution of the patient's motor symptoms. The unique neurologic symptomatology demonstrated by this patient is a previously undescribed complication of SCS placement and lead migration.


Assuntos
Medula Cervical , Terapia por Estimulação Elétrica , Masculino , Humanos , Adulto , Diplopia/etiologia , Diplopia/terapia , Medula Espinal , Terapia por Estimulação Elétrica/efeitos adversos , Pescoço
4.
Ann Thorac Surg ; 103(4): e323-e325, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28359488

RESUMO

We report a rare case of left atrial paraganglioma with a synchronous carotid body paraganglioma in a 30-year-old man with succinate dehydrogenase B gene mutation. The patient initially presented with a neck mass and palpitations. Laboratory test results showed elevated catecholamine levels. A cardiac paraganglioma was identified by computed tomography, meta-iodobenzylguanidine scintigraphy, and magnetic resonance imaging. Surgical resection of both paragangliomas were performed on two separate occasions. Serum and urine catecholamine levels returned to normal range. On follow-up, there was no recurrence of the cardiac paraganglioma. Radiotherapy was subsequently initiated for recurrence in the carotid body paraganglioma.


Assuntos
Tumor do Corpo Carotídeo/diagnóstico , Tumor do Corpo Carotídeo/terapia , Neoplasias Cardíacas/diagnóstico , Neoplasias Cardíacas/terapia , Adulto , Átrios do Coração , Humanos , Masculino
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