• Tuberculosis and Respiratory Diseases
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• 제41권5호
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• pp.537-545
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• 1994

연구배경: 중증 원외폐렴은 1987년 영국흉부학회에서 453명의 원외폐렴환자를 대상으로 전향적조사를 한 이후, 여러 학자들에 의해 조기에 위험군을 찾아내어 치료에 도움을 주려는 노력이 있어 왔다. 외국의 경우 중증 원외폐렴에 관한 많은 보고가 있으나 국내에서는 중증 원외폐렴에 대한 임상양상과 특징이 잘 연구되지 못한 상태이다. 이에 본 관찰에서는 계명대학교 동산병원에 입원하여 중증 원외폐렴으로 중환자실에서 치료중 사망한 환자 10명을 대상으로 임상적 고찰을 하였다. 방법: 1987년 7월 부터 1993년 7월 까지 계명대학교 동산병원에서 면역억제 치료중이거나 폐암으로 인한 이차성 폐렴 그리고 결핵성 폐렴을 제외한 원외폐렴으로 498명이 입원하였다. 중환자실에서 치료를 받은 환자는 77명이었으며 이들중 치료중에 사망한 10예를 대상으로 나이, 성별, 임상소견, 검사실성적, 중환자실 전원이유, 원인균, 항생제치료, 및 입원기간 등을 후향적으로 분석하였다. 결과: 1) 10예중 남자가 7예 여자가 10예로 남자의 발생빈도가 높았고, 연령분포는 20대에서 70대까지의 분포를 보였으나 60대 이상이 7예로 고령에서 가장 많은 분포를 보였으며 평균나이는 56.2세였다. 2) 입원당시 임상양상은 호흡수증가 5예, 저산소혈증 5예, 의식변화 4예, 청색증 4예, 백혈구감소증 4예, 백혈구증가증 4예, 혈청 크레아티닌증가 4예, 저혈압 3예, 저알부민혈증 3예 순으로 관찰되었다. 이학적검사에서 이상소견이 없는 경우가 2예였고 한가지만 이상소견을 가지는 경우가 3예에서 관찰되었다. 검사실성적에서는 모든 환자에서 한가지이상의 이상소견이 관찰되었다. 3) 객담배양 검사에서 E.coli와 Enterobacter species가 각각 한 예씩 검출되었으며, 객담도말검사에서는 그람양성구균만 검출된 경우가 6예, 그람양성구균과 그람음성간균이 함께 검출된 경우가 2예에서 관찰되었다. 4) 중환자실로 전원된 이유로는 저산소혈증 5예, 고탄산혈증 2예, 산혈증 2예, 심장 또는 폐정지 2예, 신부전 2예, 간부전 2예의 순으로 관찰되었다. 5) 사용한 항생제는 aminoglycoside 8예, 1세대 cephalosporin 7예, 3세대 cephalosporin 5예, vancomycin 2예였으며 환자당 평균 2.7종류의 항생제를 사용하였다. 가장 많이 사용한 항생제 조합은 1세대 cephalosporin과 aminoglycoside 였다. 6) 평균 입원일수는 11.2일 이었으며, 7예(70%)에서 5일 이내에 사망하였다. 결론: 대부분의 사망환자는 입원초기에 사망하여 조기 집중치료가 중요할 것으로 생각되며, 고령의 환자는 많은 주의를 요할 것으로 사료된다. 앞으로 조기에 위험군을 확인하기 위한 노력이 필요할 것으로 생각된다.

• Tuberculosis and Respiratory Diseases
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• 제78권3호
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• pp.262-266
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• 2015

Plasmacytomas are extramedullary accumulations of plasma cells originating from soft tissue. Mediastinal plasmacytoma is a rare presentation. A 67-year-old man recovered after antibiotic treatment for community-acquired pneumonia. However, on convalescent chest radiography after 3 months, mass like lesion at the right lower lung field was newly detected. Follow-up chest computed tomography (CT) revealed an increase in the extent of the right posterior mediastinal mass that we had considered to be pneumonic consolidations on previous CT scans. Through percutaneous needle biopsy, we diagnosed IgG kappa type extramedullary plasmacytoma of the posterior mediastinum.

• Tuberculosis and Respiratory Diseases
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• 제84권4호
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• pp.317-325
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• 2021

Background: Hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP) are significant public health issues in the world, but the epidemiological data pertaining to HAP/VAP is limited in Korea. The objective of this study was to investigate the characteristics, management, and clinical outcomes of HAP/VAP in Korea. Methods: This study is a multicenter retrospective cohort study. In total, 206,372 adult patients, who were hospitalized at one of the 13 participating tertiary hospitals in Korea, were screened for eligibility during the six-month study period. Among them, we included patients who were diagnosed with HAP/VAP based on the Infectious Diseases Society of America (IDSA)/American Thoracic Society (ATS) definition for HAP/VAP. Results: Using the IDSA/ATS diagnostic criteria, 526 patients were identified as HAP/VAP patients. Among them, 27.9% were diagnosed at the intensive care unit (ICU). The cohort of patients had a median age of 71.0 (range from 62.0 to 79.0) years. Most of the patients had a high risk of aspiration (63.3%). The pathogen involved was identified in 211 patients (40.1%). Furthermore, multidrug resistant (MDR) pathogens were isolated in 138 patients; the most common MDR pathogen was Acinetobacter baumannii. During hospitalization, 107 patients with HAP (28.2%) had to be admitted to the ICU for additional care. The hospital mortality rate was 28.1% in the cohort of this study. Among the 378 patients who survived, 54.2% were discharged and sent back home, while 45.8% were transferred to other hospitals or facilities. Conclusion: This study found that the prevalence of HAP/VAP in adult hospitalized patients in Korea was 2.54/1,000 patients. In tertiary hospitals in Korea, patients with HAP/VAP were elderly and had a risk of aspiration, so they were often referred to step-down centers.

• Tuberculosis and Respiratory Diseases
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• 제72권2호
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• pp.149-155
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• 2012

Background: This study is to evaluate the effect of systemic corticosteroid on the clinical outcomes and the occurrence of complications in mechanical ventilated patients with severe community-acquired pneumonia (CAP). Methods: We retrospectively assessed the clinical outcomes and complications in patients with severe CAP admitted to ICU between March 1, 2003 and July 28, 2009. Outcomes were measured by hospital mortality after ICU admission, duration of mechanical ventilation (MV), ICU, and hospital stay. Complications such as ventilator associated pneumonia (VAP), catheter related-blood stream infection (CR-BSI), and upper gastrointestinal (UGI) bleeding during ICU stay were assessed. Results: Of the 93 patients, 36 patients received corticosteroids over 7 days while 57 patients did not receive corticosteroids. Age, underlying disease, APACHE II, PSI score, and use of vasopressor were not different between two groups. In-hospital mortality was 30.5% in the steroid group and 36.8% in the non-steroid group (p>0.05). The major complications such as VAP, CR-BSI and UGI bleeding was significantly higher in the steroid group than in the non-steroid group (19.4% vs. 7%, p<0.05). The use of steroids and the duration of ICU stay were significantly associated with the development of major complications during ones ICU stay (p<0.05). Conclusion: Systemic corticosteroid in patients with severe CAP requiring mechanical ventilation may have no beneficial effect on clinical outcomes like duration of ICU stay and in-hospital mortality but may contribute to the development of ICU acquired complications.

• The Korean journal of internal medicine
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• 제39권3호
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• pp.477-487
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• 2024

Background/Aims: Risk factors for progression to critical illness in hospital-acquired coronavirus disease 2019 (COVID-19) remain unknown. Here, we assessed the incidence and risk factors for progression to critical illness and determined their effects on clinical outcomes in patients with hospital-acquired COVID-19. Methods: This retrospective cohort study analyzed patients admitted to the tertiary hospital between January 2020 and June 2022 with confirmed hospital-acquired COVID-19. The primary outcome was the progression to critical illness of hospital-acquired COVID-19. Patients were stratified into high-, intermediate-, or low-risk groups by the number of risk factors for progression to critical illness. Results: In total, 204 patients were included and 37 (18.1%) progressed to critical illness. In the multivariable logistic analysis, patients with preexisting respiratory disease (OR, 3.90; 95% CI, 1.04-15.18), preexisting cardiovascular disease (OR, 3.49; 95% CI, 1.11-11.27), immunocompromised status (OR, 3.18; 95% CI, 1.11-9.16), higher sequential organ failure assessment (SOFA) score (OR, 1.56; 95% CI, 1.28-1.96), and higher clinical frailty scale (OR, 2.49; 95% CI, 1.62-4.13) showed significantly increased risk of progression to critical illness. As the risk of the groups increased, patients were significantly more likely to progress to critical illness and had higher 28-day mortality. Conclusions: Among patients with hospital-acquired COVID-19, preexisting respiratory disease, preexisting cardiovascular disease, immunocompromised status, and higher clinical frailty scale and SOFA scores at baseline were risk factors for progression to critical illness. Patients with these risk factors must be prioritized and appropriately isolated or treated in a timely manner, especially in pandemic settings.

• Clinical and Experimental Pediatrics
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• 제63권12호
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• pp.469-476
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• 2020

The major pathogens that cause atypical pneumonia are Mycoplasma pneumoniae, Chlamydophila pneumoniae, and Legionella pneumophila. Community-acquired pneumonia (CAP) caused by M. pneumoniae or C. pneumoniae is common in children and presents as a relatively mild and self-limiting disease. CAP due to L. pneumophila is very rare in children and progresses rapidly, with fatal outcomes if not treated early. M. pneumoniae, C. pneumoniae, and L. pneumophila have no cell walls; therefore, they do not respond to β-lactam antibiotics. Accordingly, macrolides, tetracyclines, and fluoroquinolones are the treatments of choice for atypical pneumonia. Macrolides are the first-line antibiotics used in children because of their low minimum inhibitory concentrations and high safety. The incidence of pneumonia caused by macrolide-resistant M. pneumoniae that harbors point mutations has been increasing since 2000, particularly in Korea, Japan, and China. The marked increase in macrolide-resistant M. pneumoniae pneumonia (MRMP) is partly attributed to the excessive use of macrolides. MRMP does not always lead to clinical nonresponsiveness to macrolides. Furthermore, severe complicated MRMP responds to corticosteroids without requiring a change in antibiotic. This implies that the hyper-inflammatory status of the host can induce clinically refractory pneumonia regardless of mutation. Empirical macrolide therapy in children with mild to moderate CAP, particularly during periods without M. pneumoniae epidemics, may not provide additional benefits over β-lactam monotherapy and can increase the risk of MRMP.

• 한국임상약학회지
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• 제15권2호
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• pp.75-81
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• 2005

Community acquired pneumonia (CAP) remains a prevalent and potentially life threatening illness. American Thoracic Society and Infectious Disease Society America recommend combination therapies with ${\beta}-lactam$ plus a macrolide or a fluoroquinolone monotherapy for the empirical treatment of CAP. The aim of this study was to compare moxifloxacin monotherapy with cephalosporin plus azithromycin combination therapies. From January 2004 to March 2005, 18 patients in the moxifloxacin group(MG) and 21 patients in the cefuroxime or ceftriaxone plus azithromycin group(CAG) with CAP were retrospectively reviewed with regard to clinical, laboratory and microbiological data. Each patient was stratified into mild (risk class I-II), moderate (risk class III) and severe (risk class VI, V) group according to and PSI (Pneumonia Severity Index) score. Each group was compared for microbiological eradication, clinical assessment, the length of hospital stay. As results, Total 39 patients with CAP were reviewed. The appropriateness of admission was 83.3% in MC vs. 76.2% in CAC. The mean length of the hospital day was for 8.31 days vs. 7.39 days, days switching parenteral to oral antibiotics in 5.19 days vs. 5.28 days, clinical improvement in 2.43 days vs. 2.61 days in MG vs. CAC. Radiological improvement required 3.75 days vs 3.63 days in MG vs. CAG and bacteriological eradication rate at discharge was the same in the both groups. Mortality rate was 11.1% (2 of 18) vs 14.3% (3 of 21) in MG vs. CAG (p=0.77). Drug cost of the mean 5 hospital days requiring parenteral antibiotics was the most inexpensive in moxifloxacin group for the 147,045 won, and ceftriaxone 1g-azithromycin group for the 170,285 won, cefuroxime bid-azithromycin group for the 207,800 won, ceftriaxone 2g-azithromycin group far the 220,570 won, cefuroxime tid-azithromycin group for the 251,700 won. There was no significant statistical difference in clinical, bacterial, radiological cure and hospital days, and switch to oral days. In conclusion, that i.v. moxifloxacin monotherapy was as effective as azithromycin plus cefuroxime or ceftriaxone combination therapies fur the treatment of CAP. In drug cost analysis, moxifloxacin is less expensive than CAG.

• Clinical and Experimental Pediatrics
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• 제61권9호
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• pp.291-300
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• 2018

Purpose: Understanding changes in pathogen and pneumonia prevalence among pediatric pneumonia patients is important for the prevention of infectious diseases. Methods: We retrospectively analyzed data of children younger than 18 years diagnosed with pneumonia at 117 Emergency Departments in Korea between 2007 and 2014. Results: Over the study period, 329,380 pediatric cases of pneumonia were identified. The most frequent age group was 1-3 years old (48.6%) and the next was less than 12 months of age (17.4%). Based on International Classification of Diseases, 10th revision diagnostic codes, confirmed cases of viral pneumonia comprised 8.4% of all cases, pneumonia due to Mycoplasma pneumoniae comprised 3.8% and confirmed cases of bacterial pneumonia 1.3%. The prevalence of confirmed bacterial pneumonia decreased from 3.07% in 2007 and 4.01% in 2008 to 0.65% in 2014. The yearly rate of pneumococcal pneumonia also decreased from 0.47% in 2007 to 0.08% in 2014. A periodic prevalence of M. pneumoniae pneumonia (MP) was identified. Conclusion: The increased number of patients with pneumonia, bacterial pneumonia, pleural effusion, and empyema in 2011 and 2013-2014 resulted from an MP epidemic. We provide evidence that the frequency of confirmed cases of bacterial pneumonia and pneumococcal pneumonia has declined from 2007 to 2014, which can simultaneously reflect the effectiveness of the pneumococcal conjugate vaccine.

• The Korean Journal of Medicine
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• 제99권2호
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• pp.111-115
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• 2024

hMPV는 모든 연령에서 급성 호흡기 질환의 중요한 원인이며 고령, 면역 저하, 특정 동반 질환이 없는 건강한 환자에서도 ARDS를 동반한 중증 폐렴을 유발할 수 있다. 따라서 임상의는 젊고 면역력이 정상인 ARDS 환자에서도 hMPV 감염을 의심할 필요가 있다.

• Tuberculosis and Respiratory Diseases
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• 제54권3호
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• pp.295-303
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• 2003

연구배경 : 국내에서 검출된 폐렴구균의 페니실린 내성률은 약 70%로 알려져 있고, 특히 고도 내성률은 33%로 매우 높은 것으로 알려져 왔다. 내성 균주에 대한 경험적 항생제가 실패할 수 있다는 보고가 있었으나, 내성 여부가 사망률과 무관하다는 반론들도 적지 않았다. 이에 저자들은 폐렴구균에 의한 지역사회획득폐렴에서 페니실린 내성률을 조사하였고, 페니실린에 대한 내성이 치료 실패와 직접적인 연관이 있는지 확인하고자 하였다. 방 법 : 1999년 7월부터 2001년 5월까지 한림대학교 성심병원에 내원한 지역사회 획득 폐렴 환자 중 객담 및 혈액 배양검사를 통해 폐렴구균에 의한 폐렴으로 진단된 42명의 환자를 대상으로 하였다. 배양된 폐렴구균에 대해 E-test를 시행하여 MIC에 따라 감수성, 중등도 내성, 고도 내성으로 분류하여 내성률을 조사하였고, 각 군별로 내성여부에 따른 임상경과를 분석하였다. 결 과 : 폐렴구균에 의한 폐렴으로 진단된 42명의 환자 중 페니실린 감수성 균주($MIC{\leq}0.06{\mu}g/m{\ell}$)는 14예(33.3%), 중등도 내성 균주(MIC $0.1-1{\mu}g/m{\ell}$)는 22예(52.4%), 고도 내성($MIC{\geq}2.0{\mu}g/m{\ell}$) 균주는 6예(14.3%)였다. 경험적 항생제 치료에 대해 감수성 균주에 의한 폐렴 군과 내성 균주에 의한 폐렴 군간에 임상경과는 차이가 없었다. 폐렴구균에 의한 폐렴에서 페니실린에 대한 내성률은 66.7%로 현재까지의 보고와 큰 차이가 없으나 고도내성의 경우 약 33%로 알려진 것에 비해 저자들의 연구에서는 14.3%로 낮게 조사되었다. DRSPTWG의 분류에 따른 내성률은 26.2%에 불과했으며, 고도내성에 해당하는 균주는 없었다. 결 론 : 이와 같은 결과는 폐렴구균에 의한 폐렴의 내성을 정의하는 현재의 기준이 지나치게 낮아 항생제 내성이 높게 나타났기 때문으로 사료되며 기존의 기준에 의한 내성은 경험적 항생제 치료의 예후에 별다른 영향을 주지 못하는 것으로 확인되었다.