1.Clinical Study on the Effect of Carteolol in Patients with Cardiac Neurosis.
Jong Hoa BAE ; Young Moo RO ; Wee Hyun PARK
Korean Circulation Journal 1987;17(1):169-173
Fiftyeight patients with cardiac neurosis were studied to evaluate the effects of Carteolol 10mg/day. Systolic blood pressure was declined to 122.7+/-17.2mmHg from 137.1+/-23.2mmHg, diastolic blood pressure was declined to 79.6+/-11.1mmHg from 88.2+/-17.5mmHg. Pulse rate was decreased from 83.0+/-10.2 to 73.9+/-6.8per minute. The most frequent subjective symptom was palpitation (74.1%) and effectiveness of therapy for subjective symptom was 91.4%, for usefulness was 93.1%. There was no significant serious side reaction observed. We concluded that Carteolol therapy for the patients with cardiac neurosis could be useful and safe with a small dosage.
Blood Pressure
;
Carteolol*
;
Heart Rate
;
Humans
;
Neurocirculatory Asthenia*
4.Cutaneous asthenia (Ehlers-Danlos syndrome) in a Korean short-haired cat.
Sang Hyuk SEO ; Miru CHOI ; Changbaig HYUN
Korean Journal of Veterinary Research 2016;56(1):53-55
A 1-year-old Korean domestic short-haired cat presented with skin hyperextensibility and a severely macerated wound on the skin of the dorsal part of the neck. Diagnostic studies including histopathology and skin extensibility index revealed congenital cutaneous asthenia (Ehlers-Danlos syndrome). In this cat, the skin wounds and defects were successfully managed with standard wound management and cosmetic surgery. Although skin hyperextensibility is persistent, the cat has lived well without other complications to date. To the best of our knowledge, this is the first report of cutaneous asthenia in a cat in Korea.
Animals
;
Asthenia*
;
Cats*
;
Ehlers-Danlos Syndrome
;
Joint Instability
;
Korea
;
Neck
;
Skin
;
Surgery, Plastic
;
Wounds and Injuries
5.Surgical Treatment of Thymoma.
Chi Uk HONG ; Joo Cheol PARK ; Myung Chun KIM ; Kyu Seok CHO ; Seh Young YOO
The Korean Journal of Thoracic and Cardiovascular Surgery 1997;30(1):61-66
Between January 1986 and December 1995, 24 patients were treated surgically for thymoma. There were 17 males and 7 females, and their ages ranged from 23 to 69 years old and mean age was 49 years. Thymomas were associated with fourteen my asthenia gravis, and classified histologically as lymphocytic in 12 patients, mixed in 8, epithelial in 4, and classified clinically as stage I in 11, stage II in 4, stage III in 8 and stage VI in 1 patient. Eleven patients with non-invasive thymoma had received surgical resection, and 10 out of 13 patients with invasive thymoma were able to undergo complete resection. A partial resection or tissue biopsy followed by radiation or chemotherapy was done with the remaining three patients. Three died, four had improvement of symptom, two had relapse and fifteen had no symptom during follow up ranged from 25 days to 60 months. In fourteen cases of thymoma with myasthenia gravis, one died due to myasthenic crisis, two showed symptom aggravation, six had less medical treatment and five patients had medical treatment as same as dosage received preoperatively.
Aged
;
Asthenia
;
Biopsy
;
Drug Therapy
;
Female
;
Follow-Up Studies
;
Humans
;
Male
;
Myasthenia Gravis
;
Recurrence
;
Thymoma*
6.Hypotensive Efficacy and Safety of Ramipril on the Patients with Essential Hypertension.
Won Sang YOO ; Sung Woon KWON ; Chang Young LIM ; Sang Hyun PARK ; Suck Koo CHOI ; Dong Chul LEE
Korean Circulation Journal 1991;21(4):774-780
Thirty three patients with mild to moderate essential hypertension were administered ramipril, a new ACe inhibitor, 2.5-5mg once daily for 6 weeks to evaluate the hypotensive efficacy and safety. The results were as follows : 1) The patients consisted of 18 males, 15 females, aged 54 on average and classified as mild in 19 and moderate in 14 patients. 2) At the end of 6 weeks trial, blood pressure dropped 13/6mmHg on average, rewarding 70% effectiveness and normalized below 150/90mmHg in 39%. 3) The most frequent side reaction was dry cough in 5 patients(15%) followed by asthenia, GI trouble, dizziness, edema, eye injection and one case of GPT elevation which normalized after completion of trial. 4) The rating of safety of safety was 79% and of overall usefulness was 73%. In conclusion, ramipril 5mg once daily regimen is well tolerated and effective in the treatment of mild to moderated essential hypertension.
Asthenia
;
Blood Pressure
;
Cough
;
Dizziness
;
Edema
;
Female
;
Humans
;
Hypertension*
;
Male
;
Ramipril*
;
Reward
7.Effect of terazosin on blood pressure and serum lipids in nild to moderate hypertension.
Jong Pil KIM ; In Koo KANG ; Seung Cheol SHIM ; Ock Chan LEE ; Kyung Soo KIM ; Jeong Hyun KIM ; Heon Kil IM ; Bang Hun LEE ; Chung Kyun LEE
Korean Circulation Journal 1993;23(3):454-460
BACKGROUND: We evaluated the antihypertensive effect, safety and effect on serum lipids of terazosin, second generation alpha1-blocker. METHODS: Terazosin 1-4mg was adminstered once daily in 20 patients for 12 weeks with dose titration every 2 weeks. RESULTS: 1) The systolic and diastolic blood pressure were decreased from 170.0+/-13.0/104.0+/-6.0mmHg to 144.0+/-13.3/88.0+/-5.6mmHg(p<0.01), but the heart rate and body weight were independant of terazosin administration. 2) Total cholesterol was decreased significantly from 209.9+/-33.5mg/dL to 194.6+/-30.1mg/dL after 12 weeks treatment(p<0.05), triglyceride was decreased significantly from 185.4+/-37.0mg/dL to 168.9+/-35.0mg/dL(p<0.05). and LDL-cholesterol was decreased significantly from 134.5+/-31.9mg/dL to 122.7+/-29.9mg/dL(p<0.05), but HDL-cholesterol was increased significantly from 37.8+/-5.6mg/dL to 40.6+/-5.5mg/dL(p<0.05). 3) The adverse effects of terazosin were dizziness in 2, headache in 2, asthenia in 1, peripheral edema in 1 and skin rash in 1 patient, but were not troublesome enough to stop medication. CONCLUSIONS: Terazosin 1-4mg once daily regimen was effective and safe as an antihypertensive agent, and moreover terazosin has favorable effects on serum lipids.
Asthenia
;
Blood Pressure*
;
Body Weight
;
Cholesterol
;
Dizziness
;
Edema
;
Exanthema
;
Headache
;
Heart Rate
;
Humans
;
Hypertension*
;
Triglycerides
8.Effect of Dose Escalation with Single Opioid, Fentanyl Matrix in Patients Not Controlling Cancer Pain: A Multicenter, Prospective, Observational Study in Korea.
Sung Ae KOH ; Kyung Hee LEE ; Mi Jung KIM ; Kyu Taek LEE ; Seung Woo PARK ; Seung Hyun NAM ; Hun Mo RYOO
Cancer Research and Treatment 2013;45(4):263-269
PURPOSE: End-of-dose failure (EOD) is a clinically common observation and many cancer patients increase the frequency of opioid administration. Fentanyl matrix use is known to be effective in patients with chronic cancer pain. To measure the effectiveness of increase in a single dose of fentanyl matrix in patients whose pain was not controlled sufficiently, we perform this study. MATERIALS AND METHODS: A multi-center, open-label, prospective, observational study was conducted in 30 hospitals in Korea, between August and December 2008. RESULTS: A total of 452 patients were enrolled; 404 patients completed the study. The mean pain intensity decreased from 5.27 at the first visit to 3.37 at the end of the trial. There was a significant difference in pain intensity (p < 0.001) between the first and last visits. The percentage of pain intensity difference was 30.1%. The prevalence of EOD at the first visit was 73% from the 452 enrolled patients. After the use of fentanyl patch, EOD decreased from 73% to 56%. Pain intensity of patients experiencing EOD was 5.64 at the baseline compared to 4.27 in patients without EOD. On final visit, pain intensity in patients with and without EOD was 4.02 and 2.54, respectively. The observed adverse events were mainly nausea, asthenia, constipation and diarrhea. CONCLUSION: This study demonstrated that increasing dose of fentanyl patch decreased pain intensity and decreased the rate of patients experiencing EOD. Thus, fentanyl patch may be an effective modality in cancer patients whose pain was previously not controlled sufficiently; the side effects were as could be expected with an opioid.
Asthenia
;
Constipation
;
Diarrhea
;
Fentanyl*
;
Humans
;
Korea*
;
Nausea
;
Observational Study*
;
Prevalence
;
Prospective Studies*
9.A Phase II Study of Weekly Paclitaxel Plus Gemcitabine as a Second-Line Therapy in Patients with Metastatic or Recurrent Small Cell Lung Cancer.
Tak YUN ; Heung Tae KIM ; Ji Youn HAN ; Sung Jin YOON ; Hyae Young KIM ; Byung Ho NAM ; Jin Soo LEE
Cancer Research and Treatment 2016;48(2):465-472
PURPOSE: Paclitaxel (P) and gemcitabine (G) are clinically synergistic in small cell lung cancer (SCLC). We evaluated the efficacy of PG as a salvage treatment for SCLC patients whose disease progressed after a platinum-containing regimen. MATERIALS AND METHODS: Eligibility included histologically confirmed SCLC, one dimensionally measurable disease, Eastern Cooperative Oncology Group performance status 0-2, and progressive disease after platinum-based chemotherapy. Treatment consisted of P (80 mg/m2) and G (1,000 mg/m2) on days 1 and 8 of each cycle of 21 days until disease progression. RESULTS: Thirty-three patients seen between December 2005 and February 2009 were selected into this study. Thirty patients (91%) had received irinotecan-platinum, and three had received etoposide-platinum. Sixteen patients (49%) had a treatment-free interval of less than 3 months. The overall response rate was 30.3% (29.4% in sensitive relapse and 31.3% in refractory relapse). The median time to progression was 12.0 weeks and median overall survival (OS) 31.0 weeks, with a 1-year OS rate of 30.3%. Toxicities were moderate and manageable with 18.2% grade (G) 4 neutropenia, 24.2% G3 thrombocytopenia, 6.1% G3 sensory neuropathy, and 3% G3 asthenia. One patient developed febrile neutropenia. CONCLUSION: Second-line paclitaxel and gemcitabine were well-tolerated and moderately active in SCLC patients previously treated with platinum-based chemotherapy.
Asthenia
;
Disease Progression
;
Drug Therapy
;
Febrile Neutropenia
;
Humans
;
Neutropenia
;
Paclitaxel*
;
Recurrence
;
Small Cell Lung Carcinoma*
;
Thrombocytopenia
10.Treatment of Cardiac Neurosis with Propranolol (Inderal(R)).
Hee Sung SONG ; Shin Kwon PARK ; Jin Young RO ; Soon Kyu SUH
Korean Circulation Journal 1972;2(2):57-64
Thirty-seven cases of cardiac neurosis were treated with propranolol (Inderal(R)) and following results were obtained. 1) Symptoms, such as palpitation, dyspnea, chest tightness and chest pain were disappeared or improved in all cases. 2) Heart rate reduced significantly after treatment from 99.8 per minutes to 74.8 per minutes. 3) Systolic blood pressure reduced significantly after treatment from 147.6 mmHg to 131.4 mmHg. but diastolic blood pressure were not reduced significantly. These results indicated that propranolol is recommendable medicine for improving cardiac symptoms and tachycardia in cardiac neurosis.
Blood Pressure
;
Chest Pain
;
Dyspnea
;
Heart Rate
;
Neurocirculatory Asthenia*
;
Propranolol*
;
Tachycardia
;
Thorax