1.New therapeutic techniques and strategies in pulmonary rehabilitation.
Yonsei Medical Journal 1993;34(3):201-211
Patients with chronic obstructive pulmonary disease (COPD) or those with paralytic restrictive pulmonary syndromes caused by progressive neuromuscular disease, kyphoscoliosis or traumatic quadriplegia may require frequent hospitalization because of respiratory impairment and have increased morbidity and mortality. Pulmonary rehabilitation has been shown to decrease the frequency of hospitalization, ameliorate symptoms, increase exercise tolerance, and in one study, prolong life for individuals with COPD. It is now recognized that principles of pulmonary rehabilitation can also be used to avoid hospitalization, intubation, tracheostomy and bronchoscopy while enhancing quality of life, decreasing cost, and greatly prolonging life for individuals with paralytic restrictive syndromes and global alveolar hypoventilation as well.
Female
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Human
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Lung Diseases/*rehabilitation
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Lung Diseases, Obstructive/rehabilitation
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Male
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Neuromuscular Diseases/complications
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Respiration, Artificial
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Respiratory Insufficiency/etiology/rehabilitation
2.Evaluation of Two Lateral-Flow Chromatographic Membrane Immunoassays for Rapid Detection of Influenza Virus in Limited Respiratory Specimens.
Le Thi Quynh MAI ; Pham Thi HIEN ; Nguyen Le Khanh HANG ; J S OH ; G W HA ; J A KWON ; C K LEE ; K N LEE
Journal of Laboratory Medicine and Quality Assurance 2005;27(2):243-249
BACKGROUND: The diagnosis of influenza based on clinical grounds alone may be inaccurate, because the presenting symptoms of influenza are similar to those caused by other infectious agents. We evaluate two influenza rapid tests, SD BIOLINE Influenza Ag (Standard Diagnostic inc., Yongin, Korea) and QuickVueTM Influenza Test (Quidel corporation, San Diego, USA) with influenza virus culture and RT-PCR. METHODS: The two commercially available rapid test kits, SD BIOLINE Influenza Ag and QuickVueTM Influenza Test, for influenza virus detection were evaluated with 189 respiratory specimens collected during Dec. 2004 to Nov. 2005 in Vietnam and compared with viral culture and RT-PCR. RESULTS: Overall, the SD BIOLINE Influenza Ag and QuickVueTM Influenza Test showed high sensitivities (88.4% and 82.6%, respectively) and high specificities (99.0% and 99.0%, respectively), high positive predictive value (PPV) (98.7% and 98.6%, respectively) and high negative predictive value (NPV) (91.1% and 87.2%, respectively). CONCLUSION: Both SD BIOLINE Influenza Ag and QuickVueTM Influenza Test were easy to perform and showed high sensitivity and can be used as an additional tool for rapid diagnosis of influenza virus.
Diagnosis
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Gyeonggi-do
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Immunoassay*
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Influenza, Human*
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Membranes*
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Orthomyxoviridae*
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Sensitivity and Specificity
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Vietnam
3.The Benefits of Combination Therapy with Esomeprazole and Rebamipide in Symptom Improvement in Reflux Esophagitis: An International Multicenter Study.
Su Jin HONG ; Soo Heon PARK ; Jeong Seop MOON ; Woon Geon SHIN ; Jae Gyu KIM ; Yong Chan LEE ; Dong Ho LEE ; Jae Young JANG ; Jae J KIM ; Hang Lak LEE ; Sang Woo LEE ; Young HWANGBO ; Jianming XU ; Bangmao WANG ; Zhanxiong XUE ; Fei LIU ; Yaozong YUAN ; Somchai LEELAKUSOLVONG ; Frederick DY
Gut and Liver 2016;10(6):910-916
BACKGROUND/AIMS: To investigate the effects of esomeprazole and rebamipide combination therapy on symptomatic improvement in patients with reflux esophagitis. METHODS: A total of 501 patients with reflux esophagitis were randomized into one of the following two treatment regimens: 40 mg esomeprazole plus 300 mg rebamipide daily (combination therapy group) or 40 mg esomeprazole daily (monotherapy group). We used a symptom questionnaire that evaluated heartburn, acid regurgitation, and four upper gastrointestinal symptoms. The primary efficacy end point was the mean decrease in the total symptom score. RESULTS: The mean decreases in the total symptom score at 4 weeks were estimated to be −18.1±13.8 in the combination therapy group and −15.1±11.9 in the monotherapy group (p=0.011). Changes in reflux symptoms from baseline after 4 weeks of treatment were −8.4±6.6 in the combination therapy group and −6.8±5.9 in the monotherapy group (p=0.009). CONCLUSIONS: Over a 4-week treatment course, esomeprazole and rebamipide combination therapy was more effective in decreasing the symptoms of reflux esophagitis than esomeprazole monotherapy.
Esomeprazole*
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Esophagitis, Peptic*
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Heartburn
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Humans
4.The Benefits of Combination Therapy with Esomeprazole and Rebamipide in Symptom Improvement in Reflux Esophagitis: An International Multicenter Study.
Su Jin HONG ; Soo Heon PARK ; Jeong Seop MOON ; Woon Geon SHIN ; Jae Gyu KIM ; Yong Chan LEE ; Dong Ho LEE ; Jae Young JANG ; Jae J KIM ; Hang Lak LEE ; Sang Woo LEE ; Young HWANGBO ; Jianming XU ; Bangmao WANG ; Zhanxiong XUE ; Fei LIU ; Yaozong YUAN ; Somchai LEELAKUSOLVONG ; Frederick DY
Gut and Liver 2016;10(6):910-916
BACKGROUND/AIMS: To investigate the effects of esomeprazole and rebamipide combination therapy on symptomatic improvement in patients with reflux esophagitis. METHODS: A total of 501 patients with reflux esophagitis were randomized into one of the following two treatment regimens: 40 mg esomeprazole plus 300 mg rebamipide daily (combination therapy group) or 40 mg esomeprazole daily (monotherapy group). We used a symptom questionnaire that evaluated heartburn, acid regurgitation, and four upper gastrointestinal symptoms. The primary efficacy end point was the mean decrease in the total symptom score. RESULTS: The mean decreases in the total symptom score at 4 weeks were estimated to be −18.1±13.8 in the combination therapy group and −15.1±11.9 in the monotherapy group (p=0.011). Changes in reflux symptoms from baseline after 4 weeks of treatment were −8.4±6.6 in the combination therapy group and −6.8±5.9 in the monotherapy group (p=0.009). CONCLUSIONS: Over a 4-week treatment course, esomeprazole and rebamipide combination therapy was more effective in decreasing the symptoms of reflux esophagitis than esomeprazole monotherapy.
Esomeprazole*
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Esophagitis, Peptic*
;
Heartburn
;
Humans
5.The Impact of Cigarette Smoking on the Frequency of and Qualitative Differences in KRAS Mutations in Korean Patients with Lung Adenocarcinoma.
Hye Ryun KIM ; Jung Ryun AHN ; Jin Gu LEE ; Doo Hee BANG ; Sang Jun HA ; Yun Kyoung HONG ; Sun Mi KIM ; Ki Chang NAM ; Sun Young RHA ; Ross A SOO ; Gregory J RIELY ; Joo Hang KIM ; Byoung Chul CHO
Yonsei Medical Journal 2013;54(4):865-874
PURPOSE: This study was designed to determine the relationship of cigarette smoking to the frequency and qualitative differences among KRAS mutations in lung adenocarcinomas from Korean patients. MATERIALS AND METHODS: Detailed smoking histories were obtained from 200 consecutively enrolled patients with lung adenocarcinoma according to a standard protocol. EGFR (exons 18 to 21) and KRAS (codons 12/13) mutations were determined via direct-sequencing. RESULTS: The incidence of KRAS mutations was 8% (16 of 200) in patients with lung adenocarcinoma. KRAS mutations were found in 5.8% (7 of 120) of tumors from never-smokers, 15% (6 of 40) from former-smokers, and 7.5% (3 of 40) from current-smokers. The frequency of KRAS mutations did not differ significantly according to smoking history (p=0.435). Never-smokers were significantly more likely than former or current smokers to have a transition mutation (G-->A or C-->T) rather than a transversion mutation (G-->T or G-->C) that is known to be smoking-related (p=0.011). In a Cox regression model, the adjusted hazard ratios for the risk of progression with epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) were 0.24 (95% CI, 0.14-0.42; p<0.001) for the EGFR mutation and 1.27 (95% CI, 0.58-2.79; p=0.537) for the KRAS mutation. CONCLUSION: Cigarette smoking did not influence the frequency of KRAS mutations in lung adenocarcinomas in Korean patients, but influenced qualitative differences in the KRAS mutations.
Adenocarcinoma/drug therapy/etiology/*genetics/pathology
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Adult
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Aged
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Aged, 80 and over
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Asian Continental Ancestry Group/genetics
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Female
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Humans
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Incidence
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Lung Neoplasms/drug therapy/etiology/*genetics/pathology
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Male
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Middle Aged
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*Mutation
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Mutation Rate
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Proportional Hazards Models
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Proto-Oncogene Proteins/*genetics
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Receptor, Epidermal Growth Factor/antagonists & inhibitors/genetics
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Smoking/adverse effects/*genetics
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Treatment Outcome
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ras Proteins/*genetics
6.Incidental Statin Use and the Risk of Stroke or Transient Ischemic Attack after Radiotherapy for Head and Neck Cancer
Daniel ADDISON ; Patrick R LAWLER ; Hamed EMAMI ; Sumbal A JANJUA ; Pedro V STAZIAKI ; Travis R HALLETT ; Orla HENNESSY ; Hang LEE ; Bálint SZILVESZTER ; Michael LU ; Negar MOUSAVI ; Matthew G NAYOR ; Francesca N DELLING ; Javier M ROMERO ; Lori J WIRTH ; Annie W CHAN ; Udo HOFFMANN ; Tomas G NEILAN
Journal of Stroke 2018;20(1):71-79
BACKGROUND AND PURPOSE: Interventions to reduce the risk for cerebrovascular events (CVE; stroke and transient ischemic attack [TIA]) after radiotherapy (RT) for head and neck cancer (HNCA) are needed. Among broad populations, statins reduce CVEs; however, whether statins reduce CVEs after RT for HNCA is unclear. Therefore, we aimed to test whether incidental statin use at the time of RT is associated with a lower rate of CVEs after RT for HNCA. METHODS: From an institutional database we identified all consecutive subjects treated with neck RT from 2002 to 2012 for HNCA. Data collection and event adjudication was performed by blinded teams. The primary outcome was a composite of ischemic stroke and TIA. The secondary outcome was ischemic stroke. The association between statin use and events was determined using Cox proportional hazard models after adjustment for traditional and RT-specific risk factors. RESULTS: The final cohort consisted of 1,011 patients (59±13 years, 30% female, 44% hypertension) with 288 (28%) on statins. Over a median follow-up of 3.4 years (interquartile range, 0.1 to 14) there were 102 CVEs (89 ischemic strokes and 13 TIAs) with 17 in statin users versus 85 in nonstatins users. In a multivariable model containing known predictors of CVE, statins were associated with a reduction in the combination of stroke and TIA (hazard ratio [HR], 0.4; 95% confidence interval [CI], 0.2 to 0.8; P=0.01) and ischemic stroke alone (HR, 0.4; 95% CI, 0.2 to 0.8; P=0.01). CONCLUSIONS: Incidental statin use at the time of RT for HNCA is associated with a lower risk of stroke or TIA.
Cohort Studies
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Data Collection
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Female
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Follow-Up Studies
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Head and Neck Neoplasms
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Head
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Humans
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Hydroxymethylglutaryl-CoA Reductase Inhibitors
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Ischemic Attack, Transient
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Neck
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Proportional Hazards Models
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Radiotherapy
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Risk Factors
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Stroke