1.Delayed Traumatic Subarachnoid Hemorrhage in a Polytraumatized Patient with Disseminated Intravascular Coagulation.
Jiwoong OH ; Wonyeon LEE ; Ji Young JANG ; Pilyoung JUNG ; Sohyun KIM ; Jongyeon KIM ; Jinsu PYEN ; Kum WHANG ; Sungmin CHO
Korean Journal of Critical Care Medicine 2015;30(4):336-342
The precise mechanism involved in DIC and delayed traumatic subarachnoid hemorrhage (DT-SAH) remains unclear in multiple-trauma patients. Hereby, we describe a polytraumatized patient with DIC who died due to DT-SAH. A 75-year-old female patient was admitted to our Emergency Department complaining of abdominal pain and drowsiness after a pedestrian accident. Her initial brain computerized tomography (CT) finding was negative for intracranial injury. However, her abdominal CT scan revealed a collection of retroperitoneal hematomas from internal iliac artery bleeding after a compressive pelvic fracture. This event eventually resulted in shock and DIC. An immediate angiographic embolization of the bleeding artery was performed along with transfusion and anti-thrombin III. Her vital signs were stabilized without neurological change. Fourteen hours after admission, she suddenly became comatose, and her follow-up brain CT scan revealed a dense DT-SAH along the basal cisterns with acute hydrocephalus. This event rapidly prompted brain CT angiography and digital subtraction angiography, which both confirmed the absence of any cerebrovascular abnormality. Despite emergency extraventricular drainage to reverse the hydrocephalus, the patient died three days after the trauma. This paper presents an unusual case of DT-SAH in a polytraumatized patient with DIC.
Abdominal Pain
;
Aged
;
Angiography
;
Angiography, Digital Subtraction
;
Arteries
;
Brain
;
Coma
;
Dacarbazine
;
Disseminated Intravascular Coagulation*
;
Drainage
;
Emergencies
;
Emergency Service, Hospital
;
Female
;
Follow-Up Studies
;
Hematoma
;
Hemorrhage
;
Humans
;
Hydrocephalus
;
Iliac Artery
;
Multiple Trauma
;
Shock
;
Sleep Stages
;
Subarachnoid Hemorrhage, Traumatic*
;
Tomography, X-Ray Computed
;
Vital Signs
2.Delayed Traumatic Subarachnoid Hemorrhage in a Polytraumatized Patient with Disseminated Intravascular Coagulation
Jiwoong OH ; Wonyeon LEE ; Ji Young JANG ; Pilyoung JUNG ; Sohyun KIM ; Jongyeon KIM ; Jinsu PYEN ; Kum WHANG ; Sungmin CHO
The Korean Journal of Critical Care Medicine 2015;30(4):336-342
The precise mechanism involved in DIC and delayed traumatic subarachnoid hemorrhage (DT-SAH) remains unclear in multiple-trauma patients. Hereby, we describe a polytraumatized patient with DIC who died due to DT-SAH. A 75-year-old female patient was admitted to our Emergency Department complaining of abdominal pain and drowsiness after a pedestrian accident. Her initial brain computerized tomography (CT) finding was negative for intracranial injury. However, her abdominal CT scan revealed a collection of retroperitoneal hematomas from internal iliac artery bleeding after a compressive pelvic fracture. This event eventually resulted in shock and DIC. An immediate angiographic embolization of the bleeding artery was performed along with transfusion and anti-thrombin III. Her vital signs were stabilized without neurological change. Fourteen hours after admission, she suddenly became comatose, and her follow-up brain CT scan revealed a dense DT-SAH along the basal cisterns with acute hydrocephalus. This event rapidly prompted brain CT angiography and digital subtraction angiography, which both confirmed the absence of any cerebrovascular abnormality. Despite emergency extraventricular drainage to reverse the hydrocephalus, the patient died three days after the trauma. This paper presents an unusual case of DT-SAH in a polytraumatized patient with DIC.
Abdominal Pain
;
Aged
;
Angiography
;
Angiography, Digital Subtraction
;
Arteries
;
Brain
;
Coma
;
Dacarbazine
;
Disseminated Intravascular Coagulation
;
Drainage
;
Emergencies
;
Emergency Service, Hospital
;
Female
;
Follow-Up Studies
;
Hematoma
;
Hemorrhage
;
Humans
;
Hydrocephalus
;
Iliac Artery
;
Multiple Trauma
;
Shock
;
Sleep Stages
;
Subarachnoid Hemorrhage, Traumatic
;
Tomography, X-Ray Computed
;
Vital Signs
3.Tetrahydrobiopterin Inhibits PDGF-stimulated Migration and Proliferation in Rat Aortic Smooth Muscle Cells via the Nitric Oxide Synthase-independent Pathway.
Xiaowen JIANG ; Bokyung KIM ; Haiyue LIN ; Chang Kwon LEE ; Junghwan KIM ; Hyun KANG ; Pilyoung LEE ; Seung Hyo JUNG ; Hwan Myung LEE ; Kyung Jong WON
The Korean Journal of Physiology and Pharmacology 2010;14(3):177-183
Tetrahydrobiopterin (BH4), an essential cofactor for nitric oxide synthase (NOS) activity, is known to play important roles in modulating both NO and superoxide production during vascular diseases such as atherosclerosis. However, the role of BH4 in functions of vascular smooth muscle cells is not fully known. In this study, we tested the effects of BH4 and dihydrobiopterin (BH2), a BH4 precursor, on migration and proliferation in response to platelet-derived growth factor-BB (PDGF-BB) in rat aortic smooth muscle cells (RASMCs). Cell migration and proliferation were measured using a Boyden chamber and a 5-bromo-2'-deoxyuridine incorporation assay, respectively, and these results were confirmed with an ex vivo aortic sprout assay. Cell viability was examined by 2,3-bis [2-methoxy-4-nitro-5-sulfophenyl]-2H-tetrazolium-5-carboxanilide assays. BH4 and BH2 decreased PDGF-BB-induced cell migration and proliferation in a dose-dependent manner. The inhibition of cell migration and proliferation by BH4 and BH2 was not affected by pretreatment with N G-nitro-L-arginine methyl ester, a NOS inhibitor. Moreover, the sprout outgrowth formation of aortic rings induced by PDGF-BB was inhibited by BH4 and BH2. Cell viability was not inhibited by BH4 and BH2 treatment. The present results suggest that BH4 and BH2 may inhibit PDGF-stimulated RASMC migration and proliferation via the NOS-independent pathway. Therefore, BH4 and its derivative could be useful for the development of a candidate molecule with an NO-independent anti-atherosclerotic function.
Animals
;
Atherosclerosis
;
Biopterin
;
Bromodeoxyuridine
;
Cell Movement
;
Cell Survival
;
Muscle, Smooth
;
Muscle, Smooth, Vascular
;
Myocytes, Smooth Muscle
;
Nitric Oxide
;
Nitric Oxide Synthase
;
Proto-Oncogene Proteins c-sis
;
Rats
;
Superoxides
;
Vascular Diseases