1.A Case of Rhabdomyolysis Associated with Phenytoin Loading.
Kyoungsub KIM ; Sun Ah CHOI ; Gyu Sik KIM ; Jeong Hee CHO ; Jun Hong LEE
Journal of the Korean Neurological Association 2006;24(6):630-632
No abstract available.
Phenytoin*
;
Rhabdomyolysis*
2.A Case of Rhabdomyolysis Associated with Phenytoin Loading.
Kyoungsub KIM ; Sun Ah CHOI ; Gyu Sik KIM ; Jeong Hee CHO ; Jun Hong LEE
Journal of the Korean Neurological Association 2006;24(6):630-632
No abstract available.
Phenytoin*
;
Rhabdomyolysis*
3.A Case of Phenytoin Induced Toxic Epidermal Necrolysis.
Hae Joung JOUNG ; Wea Kyoun SHIN ; Mee Kyung NAMKUNG ; Jae Seung YANG ; Jong Soo KIM ; Dong Sik BANG
Journal of the Korean Pediatric Society 1990;33(9):1306-1311
No abstract available.
Phenytoin*
;
Stevens-Johnson Syndrome*
4.The Clinical Study on the Predictability of Time from Toxic Level to Therapeutic Concentration on Phenytoin Toxicity.
Hyeon Mi PARK ; Young Ju LEE ; Hee Tae KIM ; Seung Hyun KIM ; Ju Han KIM ; Myung Ho KIM ; Tae Soon MOON ; Dong Jin SHIN ; In Jin JANG ; Sang Gu SHIN
Journal of the Korean Neurological Association 1996;14(2):440-447
It is important to predict time to reach therapeutic concentration in phenytoin toxicity. In tradition, frequent drug monitoring is inevitable until the therapeutic serum level is reached. A method of estimating Vmax and Vd of phenytoin with application to estimating time to reach therapeutic concentration of phenytoin is described. We evaluated the usefulness of that method in twelve patients with phenytoin toxicity whose initial levels ranging from 27.7 to 74.0 ug/ml. We compaired the observed time defined as the time of returning from the initial toxic level to the optimum therapeutic level by serial measurement of serum concentration with the calculated time by using the modified Michaelis-Menten equation (Km x In (C1/C2) +Cl-C2=Vmax/vd x T). We determined individual patient's Vmax (maximal metabolic rate of concentration), Vd(volume of distribution of concentration), and Km(constants of Michaelis-Menten equation) for phenytoin, using data obtained from two consecutive serum concentration and known value of Km in Korean. And then, we calculated the decline time of phenytoin. The calculated decline time did not differ significantly from observed decline time (P=0.830). It is possible to predict the time to the therapeutic range and to reduce the unnecessarily frequent drug monitoring.
Drug Monitoring
;
Humans
;
Phenytoin*
5.Steroid Therapy in Phenytoin Hypersensitivity Syndrome Patient.
Young Ok KIM ; Jung Pil SUH ; Eun Il KIM ; Seok Goo CHO ; Chang Don LEE ; Jong Yuk YI ; Do Sung YOO ; Dal Soo KIM
Journal of Korean Neurosurgical Society 2000;29(12):1673-1676
No abstract available.
Humans
;
Hypersensitivity*
;
Phenytoin*
6.Primarily results of quantification of serum phenytoin in patients with epilepsy
Journal of Practical Medicine 2002;435(11):38-40
This study was carried out on 36 blood samples of epileptic patients, between the ages of 6 and 15, in Army Hospital 103 during 9/2000 - 6/2001, who used a monotherapy - phenytoin. The results of quantitative analysis of serum concentration of drug in the treatment range, under the treatment range and above the treatment range among patients with disease free was 72.41%, 13.78% and 13.8%. 80% of patients used phenytorin at dose of 5-8mg/kg/day had a serum concentration in the treatment range. The dose of phenytoin can be increased increasingly in cases without responding to the treatment while the drug concentration closely reached the treatment range until the defects found.
Serum
;
Phenytoin
;
Epilepsy
7.The Effect of Diphenylhydantoin on the Action of Ouabain.
Korean Circulation Journal 1971;1(2):23-26
The effect of diphenylhydantoin on LD 50 of ouabain was investigated in frogs, using "one hour frog method". LD50 of ouabain in control group was 1.90 microg/10g. A dose of 100 microg/10g diphenylhydantion did not affect the systemic manifestations of the frogs, but increase the LD50 of ouabain to 2.60 microg/10g. The difference of LD50 of ouabain and potency ratio between control group and diphenylhydantoin-treated group was statistically significant.
Lethal Dose 50
;
Ouabain*
;
Phenytoin*
8.Phenytoin-Dexamethasone Interaction.
Kwang Seob PARK ; Hyuck PARK ; Jong Jin LEE ; Cahrles D SANDS ; Dong Youl RHEE
Journal of Korean Neurosurgical Society 1987;16(2):447-452
A possible drug interaction between phenytoin and dexamethasone was evaluated by comparing serum phenytoin concentrations in 34 patients receiving both drugs with those if a control group 19 patients receiving phenytoin only. Serum phenytoin concentrations obtained 24 hours after a loading dose of 15mg per kilogram body weight administrated intravenously were examined. The serum concentrations of phenytoin were checked by homogenous enzyme immunoassay(EMIT) method. The total amounts of dexamethasone administered during the 24 hours period ranged from 10 to 40mg. The average serum phenytoin concentration was 12.08+/-2.78 microgram/ml in patients receiving both drugs, as compared to 8.58+/-2.72 microgram/ml in patients receiving phenytoin only(p<0.005). Our results suggest that serum phenytoin concentrations in patients receiving both drugs were higher than in patients receiving phenytoin only.
Body Weight
;
Dexamethasone
;
Drug Interactions
;
Humans
;
Phenytoin
9.Focal Seizures as a First Manifestation of Nonketotic Hyperglycemia.
Journal of the Korean Neurological Association 1991;9(4):477-480
I report two elderly females who developed repetitive focal seizures as their first manifestations of nonketotic hyperglycemia In the second patient, the seizures were constantly induced by active or passive movements of the involved arm. With a control of the hyperglycemia, the seizures stopped in both cases. Contrary to previous reports, the focal seizures of the second case seemed to respond to parenteral administration of phenytoin.
Aged
;
Arm
;
Female
;
Humans
;
Hyperglycemia*
;
Phenytoin
;
Seizures*
10.A Case of Purple Glove Syndrome.
Lina LEE ; Oh Young KWON ; Kyoung Soo LEE ; Hee Young KANG ; Ki Jong PARK ; Nack Cheon CHOI ; Byeong Hoon LIM
Journal of the Korean Neurological Association 2002;20(5):548-550
Purple glove syndrome is a complication of the intravenous infusion of phenytoin. It is characterized by progressive distal edema, discoloration and pain. The mechanism of purple glove syndrome is poorly understood, but the chemical properties of intravenous phenytoin and the extravasation of that are possible causes. We present a woman with purple glove syndrome, whose symptoms were subsided gradually with conservative management.
Edema
;
Female
;
Humans
;
Infusions, Intravenous
;
Phenytoin