1.Reconstruction for the complication of old elbow injuries.
Moon Sang CHUNG ; Goo Hyun BAEK ; Kook Hyeung CHO
The Journal of the Korean Orthopaedic Association 1993;28(5):1628-1647
No abstract available.
Elbow*
2.Significance of preoperative biliary drainage in pancreaticoduodenal resection.
Sang Soo JIN ; Suck Ju CHO ; Hyun Jong KIM ; Young Kook CHO
Journal of the Korean Surgical Society 1991;40(1):37-43
No abstract available.
Drainage*
3.The Effect of Intratracheal Pulmonary Ventilation on the Decrease of Dead Space in Rabbits with Acute Respiratory Failure.
Korean Journal of Anesthesiology 1999;36(4):723-728
BACKGROUND: A technique that improves the efficiency of alveolar ventilation should decrease the pressure required and reduce the potential for lung injury during mechanical ventilation. High PaCO2 can be permitted to lower airway pressures as in permissive hypercapnia (PH). Intratracheal pulmonary ventilation (ITPV) was developed to allow a decrease in physiological dead space during mechanical ventilation. We compared the effect of hybrid ventilation (HV) as a modification of ITPV with PH on the decrease of tidal volume and airway pressures in rabbits with acute respiratory failure. METHODS: Tracheostomy was performed in 7 rabbits ventilated under volume-controlled mode in the supine position. Arterial blood gas analysis, airway pressures, and dead space ventilation were measured at respiratory rate of 20/min as control values. Oleic acid (OA) of 0.06 ml/kg was injected to induce acute respiratory failure. Tidal volume (VT) was elevated to maintain PaCO2 in the normal range. The same parameters were measured as OA values. Then VT was reduced to the control level to allow PH. HV was initiated by inserting a reverse thrust catheter (RTC) into the endotracheal tube. HV consists of a pressure-controlled mode of mechanical ventilation and ITPV while flushing fresh gas continuously via the RTC. Respiratory parameters were compared under control, OA, PH and HV conditions. RESULTS: Oleic acid injection decreased PaO2 from 401+/-35 mmHg to 129+/-39 mmHg, increased VT from 42+/-5 ml to 52+/-10 ml, and increased VD/VT ratio from 0.65+/-0.07 to 0.71+/-0.07. During PH, the increase in PaCO2 was accompanied by the increase in VD/VT ratio from 0.71+/-0.07 to 0.79+/-0.03 and by the decrease of peak inspiratory pressure (PIP) from 19.4+/-4.0 cmH2O to 16.8+/-3.1 cmH2O. PaCO2 was lowered from 50+/-5 mmHg in PH to 39+/-5 mmHg in HV with a lower VT. VD/VT ratio in HV was as low as that in control. CONCLUSION: HV is an effective and easy-to-use ventilatory modality to reduce PaCO2 and airway pressures by the reduction in VD/VT ratio in acute respiratory failure model.
Blood Gas Analysis
;
Catheters
;
Flushing
;
Hydrogen-Ion Concentration
;
Hypercapnia
;
Lung Injury
;
Oleic Acid
;
Pulmonary Ventilation*
;
Rabbits*
;
Reference Values
;
Respiration, Artificial
;
Respiratory Insufficiency*
;
Respiratory Rate
;
Supine Position
;
Tidal Volume
;
Tracheostomy
;
Ventilation
4.A Case of Encephalopathy Presented with Motor Aphasia and Quadriplegia Following Intrathecal Methotrexate .
Seon Woo LEE ; Eun Hye PARK ; Hyun Sang CHO ; Jae Kook CHA ; Hae Ran LEE
Journal of the Korean Pediatric Society 2001;44(9):1066-1069
Intrathecal administration of methotrexate(IT-MTX) has constituted the standard approach to prophylaxis and treatment of central nevous system(CNS) leukemia. We experienced a quadriplegia and motor aphasia in a 14-year-old boy following repeated IT-MTX for the prophylaxis of meningeal leukemia. He was diagnosed as ALL without CNS involvement and treated by CCG- 1882 protocol. IT-MTX was administered for CNS prophylaxis. The patient began complaining of urinary incontinence, motor aphasia and weakness in his right leg from 12 days after the 5th dose of the IT-MTX therapy. Even though the IT-MTX was discontinued, loss of muscle power progressed upward resulting in quadriplegia. The patient showed slow and partial recovery on right extremities over 3 months. We report this case with brief review of literature.
Adolescent
;
Aphasia, Broca*
;
Extremities
;
Humans
;
Leg
;
Leukemia
;
Male
;
Methotrexate*
;
Quadriplegia*
;
Urinary Incontinence
5.The Morphometric Study of the Pons and Cerebellum in Korean using MRI.
Hyun Sook KIM ; In Hyuk CHUNG ; Dong lk KIM ; Young Kook CHO ; Mi Jin YUN
Journal of the Korean Radiological Society 1995;33(5):687-692
PURPOSE: To evaluate the size of normal pons and cerebellum in vivo and the change in size according to age, and to compare those with measurement of the diseased pons and cerebellum. MATERIALS AND METHODS: 121 normal adults(M:F=54:67), 5 patients with OPCD and 19 patients with WallerJan degeneration were studied. The normal group was divided into 5 subgroups according to the age (ranged from 20 to 72 years). 1.5T GE Signa MR unit was used. On axial plane, the AP(A) and transverse(B) diameters of the pons, the size of the middle cerebellar peduncle(C), and transverse diameter of the posterior fossa(D) and the cerebellum(E) were measured. On midsagittal plane, the longitudinal(F) and AP(G) diameters of the basis pontis were measured. The ratios of E/D and F/G were calculated. The student t test was used for statistical analysis. RESULTS: C, E and F/G were 15.5mm+/-1.3, 99.8mm+/-4.3 and 1.63+/-.10, respectively. F/G, H/I, and H/J were larger in male(p<.01). All data of the pons showed no statistically significant differences among age groups. E of the seventh decades was shorter than that of the third decades(p<.05). C(12.7 mm+/-1.4) in OPCD and F/G(1. 81+/-.10) in Wallerian degeneration(p<.01) showed the most significant differences when they were compared to the normal. CONCLUSION: Although the cerebellum decreased in size with age, the pons maintained its size up to eighth' decades. The measurement of middle cerebellar peduncle on axial plane (C) and the ratio of basis pontis on midsagittal plane (F/G) were important in the evaluation of OPCD and WallerJan degeneration, respectively.
Cerebellum*
;
Humans
;
Magnetic Resonance Imaging*
;
Pons*
6.Analysis of routine test results for the diagnosis of paraxysmal nocturnal hemoglobinuria.
Sun Hee KIM ; Sung Sup PARK ; Chong Hyun YOON ; Han Ik CHO ; Byoung Kook KIM
Korean Journal of Clinical Pathology 1993;13(2):225-231
No abstract available.
Diagnosis*
;
Hemoglobinuria*
7.CT and MR findings of primitive neuroectodermal tumor.
Shin Ho KOOK ; In One KIM ; Kee Hyun CHANG ; Moon Hee HAN ; Byung Kyu CHO
Journal of the Korean Radiological Society 1991;27(4):503-508
No abstract available.
Neuroectodermal Tumors, Primitive*
8.A comparison of urologic complications between extravesical and modified politano ureteroneocystostomy in living donor renal transplantation.
Tae Kook KIM ; Won Hyun CHO ; Chul Hee PARK ; Soo Hyung LEE ; Sung Bae PARK ; Hyun Chul KIM
The Journal of the Korean Society for Transplantation 1993;7(1):179-185
No abstract available.
Humans
;
Kidney Transplantation*
;
Living Donors*
9.Analysis of Multiorgan Failure in Brain-Dead Patients.
Hyun Sung CHO ; Chung Su KIM ; Yang Ja KANG ; Kook Hyun LEE
Korean Journal of Anesthesiology 1997;32(5):787-792
BACKGROUND: Brain death is irreversible coma due to injury of brain hemisphere and brain stem regardless of any treatment. In brain-dead patients, diabetes insipidus, hypothermia, acute respiratory failure, and multiorgan failure occur due to brain stem compression injury. The primary goal of organ donor management is maintenance of optimal physiologic environment for organs prior to donation. This study is performed for suggesting the guideline of the prediction and management of multiorgan failure in the brain-dead patient. METHODS: We analyzed 16 brain-dead patients waiting for organ donation in the intensive care unit. The causes of brain death among the donors consisted of closed head injury in 8 patients, subarachnoid hemorrhage in 4, drowning in 1, aplastic anemia in 1, asthmatic attack in 1 and falling-down injury in 1. PaO2/FIO2 (arterial oxygen tension/fractional inspired O2 concentration) was analyzed to demonstrate the progress of respiratory failure. Body temperature, vital signs, urine output, serum osmolarity, urine osmolarity, serum K+, serum Na+, AST(aspartate aminotransferase), ALT(alanine aminotransferase), total bilirubin, BUN(blood urea nitrogen) and creatinine were also analyzed in all patients. RESULTS: Diabetes insipidus were found in 15 patients, hypothermia in 8, renal dysfunction in 2, hepatic dysfunction in 0, and acute respiratory failure in 2 at the time of arrival to intensive care unit. Diabetes insipidus was found in 16patients, hypothermia in 0, renal dysfunction in 0, hepatic dysfunction in 0, and acute respiratory failure in 9 at 16 hours after arrival to intensive care unit. CONCLUSIONS: We concluded that hepatic and renal functions were well preserved for long time after brain death and brain-dead patients rapidly progressed to acute respiratory failure. It can be suggested that organ procurement should be performed as soon as possible after brain death was confirmed for successeful organ transplantation.
Anemia, Aplastic
;
Bilirubin
;
Body Temperature
;
Brain
;
Brain Death
;
Brain Stem
;
Creatinine
;
Diabetes Insipidus
;
Drowning
;
Head Injuries, Closed
;
Humans
;
Hypothermia
;
Intensive Care Units
;
Lung
;
Multiple Organ Failure
;
Organ Transplantation
;
Osmolar Concentration
;
Oxygen
;
Respiratory Insufficiency
;
Subarachnoid Hemorrhage
;
Tissue and Organ Procurement
;
Tissue Donors
;
Transplants
;
Urea
;
Vital Signs
10.Protective Action of Purinergic and Cholinergic Agonists on the Ischemic Myocardium in the Rat.
Jae Ha KIM ; Sang Duck PARK ; Jeong Min JU ; Hyun KOOK ; Jeong Gwan CHO ; Ok Kyu PARK
Korean Circulation Journal 1998;28(7):1141-1153
BACKGROUND: Purinergic and cholinergic agonists elicit negative-inotropic and chronotropic effects, anticip-ating their protective action from the damage of overloaded myocardium. However, the actions of the agents during the ischemic insults are not yet clearly informed. The aim of this study was to investigate the role of the purinergic and cholinergic agonists on the simulated ischemic myocardium of the rat atrial fiber preparations. METHOD: Various action potential parameters (maximum diastolic potential MDP;action potential amplitude APA;velocity of phase 0 depolarization dV/dtmax;action potential duration APD90) were measured and compared in electrically paced, normal (NPSS) and modified physiological salt solution (MPSS) superfused rat atrial fibers in vitro, using conventional 3M-KCl microelectrode technique. Ischemia-simulated modified physiologic solutions were prepared by changing the solution's composition. RESULTS: Hypoxic-and/or hyperkalemic-MPSS decreased all the action potential (AP) variables. However, no significant changes of the AP variables were developed by the acidic-or glucose-free MPSS. Adenosine (Ado) and cyclopentyladenosine (CPA) only decreased the APD90 in a dose-dependent manner. Acetylcholine (Ach) and carbachol (Cch) hyperpolarized the MDP, increased the dV/dtmax with certain doses, and decreased the APD90 dose-depen-dently. The potency for APD90-decrease was greater in order, CPA>Cch>Ach>Ado. Ado and CPA did not affect the hypoxic, hypokalemic MPSS-induced dV/dtmax-decrease. On the other hand, Ach and Cch sig-nificantly inhibited the dV/dtmax-decrease by the hypoxic hypokalemic-MPSS. Ado, CPA, Ach and Cch sig-nificantly augmented the hypoxic, hypokalemic MPSS-induced APD90-decrease. The inhibition by the Ach and Cch on the MPSS-induced dV/dtmax-decrease was not affected by DPCPX, but atropine significantly attenuated the inhibition by the cholinergic agonists. DPCPX inhibited the augmentation by the Ado and CPA on the MPSS induced APD90-decrease, and atropine inhibited the effect of the cholinergic agonists. CONCLUSION: Both purinergic and cholinergic agonists not only shorten the AP duration by themselves but also enhance the AP-shortening effect elicited by the ischemia, and therefore, it is inferred that both agonists prevent further tissue damage from the ischemic insults.
Acetylcholine
;
Action Potentials
;
Adenosine
;
Animals
;
Atropine
;
Carbachol
;
Cholinergic Agonists*
;
Hand
;
Ischemia
;
Microelectrodes
;
Myocardium*
;
Rats*