2.Clinical manifestations of pneumonia according to the causative organism in patients in the intensive care unit.
Jung Kyu LEE ; Jinwoo LEE ; Young Sik PARK ; Chang Hoon LEE ; Jae Joon YIM ; Chul Gyu YOO ; Young Whan KIM ; Sung Koo HAN ; Sang Min LEE
The Korean Journal of Internal Medicine 2015;30(6):829-836
BACKGROUND/AIMS: Whether the causative organism influences the clinical course of pneumonia in the intensive care unit (ICU) is controversial. We assessed the clinical manifestations and prognosis of pneumonia according to the causative pathogens in patients in a medical ICU. METHODS: A retrospective observational study was performed in a medical ICU. Among 242 patients who were admitted to the ICU, 103 who were treated for pneumonia were analyzed. RESULTS: The causative pathogen was identified in 50 patients (49.0%); 22 patients (21.6%) had multidrug-resistant (MDR) pathogens. The distribution of causative micro-organisms was Staphylococcus aureus (20%), Pseudomonas species (16%), Klebsiella pneumoniae (14%), and Acinetobacter baumannii (12%). No significant difference in ICU mortality rate, duration of ICU stay, duration of mechanical ventilation, or frequencies of re-intubation and tracheostomy were detected based on the identification of any pathogen. In sub-analyses according to the pneumonia classification, the number of pathogens identified did not differ between pneumonia types, and a higher incidence of identified MDR pathogens was detected in the hospital-acquired pneumonia group than in the community-acquired or healthcare- acquired pneumonia groups. However, the clinical outcomes of pneumonia according to identification status and type of pathogen did not differ significantly between the groups. CONCLUSIONS: Neither the causative micro-organism nor the existence of MDR pathogens in critically ill patients with pneumonia was associated with the clinical outcome of pneumonia, including ICU mortality. This result was consistent regardless of the pneumonia classification.
Acinetobacter Infections/diagnosis/*microbiology/mortality/therapy
;
Aged
;
Anti-Bacterial Agents/therapeutic use
;
Critical Illness
;
Drug Resistance, Multiple, Bacterial
;
Female
;
Hospital Mortality
;
Humans
;
Intensive Care Units
;
Klebsiella Infections/diagnosis/*microbiology/mortality/therapy
;
Length of Stay
;
Male
;
Middle Aged
;
Pneumonia, Bacterial/diagnosis/*microbiology/mortality/therapy
;
Proportional Hazards Models
;
Pseudomonas Infections/diagnosis/*microbiology/mortality/therapy
;
Respiration, Artificial
;
Retrospective Studies
;
Risk Factors
;
Staphylococcal Infections/diagnosis/*microbiology/mortality/therapy
;
Time Factors
;
Tracheostomy
;
Treatment Outcome
3.Controlling infection and spread of carbapenems-resistant Klebsiella pneumoniae among burn patients.
Chinese Journal of Burns 2015;31(1):5-8
The emergence and spread of carbapenems-resistant Klebsiella pneumoniae (CRKP) in burn ward is an important threat to burn management. CRKP isolates are resistant to almost all available antibiotics and are susceptible only to polymyxins and tigecycline. The mechanism of the drug resistance of CRKP is associated with the plasmid-encoded carbapenemase Klebsiella pneumoniae carbapenemase (KPC), a carbapenem-hydrolyzing β-lactamase. Antibiotics which can currently be used to treat CRKP infection include polymyxins, tigecycline, and some aminoglycosides. The efficacy of using antibiotics in combination is better than that of single-agent therapy for the treatment of CRKP infection in bloodstream. In order to control CRKP infection in burn patients, strategies for preventing CRKP dissemination in burn ward are strongly advocated.
Anti-Bacterial Agents
;
therapeutic use
;
Bacterial Proteins
;
Burns
;
drug therapy
;
Carbapenems
;
pharmacology
;
Drug Resistance, Bacterial
;
Humans
;
Klebsiella Infections
;
drug therapy
;
microbiology
;
prevention & control
;
Klebsiella pneumoniae
;
drug effects
;
Microbial Sensitivity Tests
;
Minocycline
;
analogs & derivatives
;
therapeutic use
;
beta-Lactam Resistance
;
beta-Lactamases
4.Causative Pathogens of Febrile Neutropaenia in Children Treated for Acute Lymphoblastic Leukaemia.
Joyce Cm LAM ; Jie Yang CHAI ; Yi Ling WONG ; Natalie Wh TAN ; Christina Tt HA ; Mei Yoke CHAN ; Ah Moy TAN
Annals of the Academy of Medicine, Singapore 2015;44(11):530-534
INTRODUCTIONTreatment of acute lymphoblastic leukaemia (ALL) using intensive chemotherapy has resulted in high cure rates but also substantial morbidity. Infective complications represent a significant proportion of treatment-related toxicity. The objective of this study was to describe the microbiological aetiology and clinical outcome of episodes of chemotherapy-induced febrile neutropaenia in a cohort of children treated for ALL at our institution.
MATERIALS AND METHODSPatients with ALL were treated with either the HKSGALL93 or the Malaysia-Singapore (Ma-Spore) 2003 chemotherapy protocols. The records of 197 patients who completed the intensive phase of treatment, defined as the period of treatment from induction, central nervous system (CNS)-directed therapy to reinduction from June 2000 to January 2010 were retrospectively reviewed.
RESULTSThere were a total of 587 episodes of febrile neutropaenia in 197 patients, translating to an overall rate of 2.98 episodes per patient. A causative pathogen was isolated in 22.7% of episodes. An equal proportion of Gram-positive bacteria (36.4%) and Gram-negative bacteria (36.4%) were most frequently isolated followed by viral pathogens (17.4%), fungal pathogens (8.4%) and other bacteria (1.2%). Fungal organisms accounted for a higher proportion of clinically severe episodes of febrile neutropaenia requiring admission to the high-dependency or intensive care unit (23.1%). The overall mortality rate from all episodes was 1.5%.
CONCLUSIONFebrile neutropaenia continues to be of concern in ALL patients undergoing intensive chemotherapy. The majority of episodes will not have an identifiable causative organism. Gram-positive bacteria and Gram-negative bacteria were the most common causative pathogens identified. With appropriate antimicrobial therapy and supportive management, the overall risk of mortality from febrile neutropaenia is extremely low.
Candidiasis ; epidemiology ; Chemotherapy-Induced Febrile Neutropenia ; epidemiology ; microbiology ; Child ; Cohort Studies ; Escherichia coli Infections ; epidemiology ; Gram-Negative Bacterial Infections ; epidemiology ; Gram-Positive Bacterial Infections ; epidemiology ; Humans ; Influenza, Human ; epidemiology ; Klebsiella Infections ; epidemiology ; Mycoses ; epidemiology ; Precursor Cell Lymphoblastic Leukemia-Lymphoma ; drug therapy ; Pseudomonas Infections ; epidemiology ; Retrospective Studies ; Singapore ; epidemiology ; Staphylococcal Infections ; epidemiology ; Virus Diseases ; epidemiology
5.Native valve endocarditis due to extended spectrum beta-lactamase producing Klebsiella pneumoniae.
Hyun Ae JUNG ; Young Eun HA ; Damin KIM ; Jihyun PARK ; Cheol In KANG ; Doo Ryeon CHUNG ; Seung Woo PARK ; Ki Ik SUNG ; Jae Hoon SONG ; Kyong Ran PECK
The Korean Journal of Internal Medicine 2014;29(3):398-401
No abstract available.
Aged
;
Anti-Bacterial Agents/therapeutic use
;
Aortic Valve/*microbiology/surgery/ultrasonography
;
Cross Infection/diagnosis/*microbiology/therapy
;
Diffusion Magnetic Resonance Imaging
;
Endocarditis, Bacterial/diagnosis/*microbiology/therapy
;
Heart Valve Prosthesis Implantation
;
Humans
;
Klebsiella Infections/diagnosis/*microbiology/therapy
;
Klebsiella pneumoniae/drug effects/*enzymology/pathogenicity
;
Male
;
Microbial Sensitivity Tests
;
Predictive Value of Tests
;
Sepsis/diagnosis/*microbiology/therapy
;
Treatment Outcome
;
beta-Lactamases/*metabolism
6.Pathologic bacterial distribution and antibiotic resistance in induced sputum of infants aged from 1 to 3 months with lower respiratory tract infection.
Man-Feng ZUO ; He-Lin LIU ; Mu-Liang ZHU ; Qiong-Zhang SHU ; Ling JIANG
Chinese Journal of Contemporary Pediatrics 2014;16(12):1226-1230
OBJECTIVETo investigate the pathologic bacterial distribution and their antibiotic resistance in infants aged from 1 to 3 months with lower respiratory tract infection, so as to provide instructions for clinical application of antibiotics.
METHODSInduced sputum was extracted from 622 cases of hospitalized infants aged from 1 to 3 months with lower respiratory tract infection between January 2013 and December 2013, and microbial sensitivity test was performed with agar diffusion sensitivity test.
RESULTSA total of 379 (60.9%) strains of bacteria were isolated from induced sputum in the 622 infants. The Gram-negative strains were detected in 325 strains (85.8%), and the Gram-positive strains were found in 50 strains (13.2%) in the 379 strains. The others were Fungal strains (4 strains, 1.1%). The Gram-negative bacteria included Escherichia coli (31.1%) and Klebsiella pneumoniae (18.2%), with extended-spectrum β-lactamases (ESBLs) production of 48.3% and 52.2% respectively. The average rate of antibiotic resistance for ESBLs-producing bacteria was 53%. ESBLs-producing bacteria were highly resistant (100%) to ampicillin and cefotaxime, but sensitive to carbapenems. Staphylococcus aureus (10.0%) was the dominant bacteria in Gram-positive bacteria. A lower proportion of methicillin-resistant Staphylococcus aureus (1.8%) was observed, however the resistance rate of methicillin-resistant Staphylococcus aureus to β-lactam antibiotics were 100%.
CONCLUSIONSEscherichia coli and Klebsiella pneumoniae are the main pathogenic bacteria causing lower respiratory tract infection in infants aged from 1 to 3 months. ESBLs-producing bacteria accounted for over 48%, and the antibiotic resistance rate were more than 53% in these infants. These results provide a basis for the first empirical clinical use of antimicrobial in infants with lower respiratory tract infection.
Drug Resistance, Bacterial ; Escherichia coli ; isolation & purification ; Female ; Humans ; Infant ; Klebsiella pneumoniae ; isolation & purification ; Male ; Respiratory Tract Infections ; drug therapy ; microbiology ; Sputum ; microbiology
7.Bloodstream infection with carbapenem-resistant Klebsiella pneumoniae and multidrug-resistant Acinetobacter baumannii: a case report.
Hong-min ZHANG ; Da-Wei LIU ; Xiao-ting WANG ; Yun LONG ; Huan CHEN
Chinese Medical Sciences Journal 2014;29(1):51-54
IN the presence of septic shock, every hour in delaying the administration of effective antibiotics is associated with a measurable increase in mortality. This is especially true for neutropenic patients with septic shock.1 As there is a higher incidence of involving multi-drug resistant pathogens for neutropenic patients, the decision on antibiotics regime remains a challenge for physicians.2 Immunosuppression and previous antibacterial use are factors that promote the spread of multi-drug resistant pathogens, and the possibility of co-existing multi-drug resistant pathogens should be suspected when treating patients with these risk factors who developed refractory shock. Here we present a case with neutropenic fever and refractory shock whose blood culture yielded multi-drug resistant Acinetobacter baumannii and carbapenem- resistant Klebsiella pneumoniae.
Acinetobacter Infections
;
blood
;
drug therapy
;
microbiology
;
Acinetobacter baumannii
;
drug effects
;
isolation & purification
;
Adult
;
Bacteremia
;
blood
;
drug therapy
;
microbiology
;
Carbapenems
;
administration & dosage
;
pharmacology
;
therapeutic use
;
Drug Resistance, Multiple, Bacterial
;
Fatal Outcome
;
Humans
;
Klebsiella Infections
;
blood
;
drug therapy
;
microbiology
;
Klebsiella pneumoniae
;
drug effects
;
isolation & purification
;
Male
;
Shock, Septic
;
blood
;
drug therapy
;
microbiology
8.The First Case of Septicemia Caused by Imipenem-Susceptible, Meropenem-Resistant Klebsiella pneumoniae.
Shizuo KAYAMA ; Norifumi SHIGEMOTO ; Ryuichi KUWAHARA ; Takashi ISHINO ; Kentaro IMON ; Makoto ONODERA ; Michiya YOKOZAKI ; Hiroki OHGE ; Motoyuki SUGAI
Annals of Laboratory Medicine 2013;33(5):383-385
No abstract available.
Aged
;
Drug Resistance, Bacterial
;
Humans
;
Imipenem/pharmacology/therapeutic use
;
Klebsiella Infections/diagnosis/drug therapy/*microbiology
;
Klebsiella pneumoniae/drug effects/isolation & purification/*physiology
;
Male
;
Microbial Sensitivity Tests
;
Phenotype
;
Sepsis/diagnosis/drug therapy/*microbiology
;
Thienamycins/pharmacology/therapeutic use
9.A case of necrotizing pancreatitis subsequent to transcatheter arterial chemoembolization in a patient with hepatocellular carcinoma.
Song I BAE ; Jong Eun YEON ; Jong Mee LEE ; Ji Hoon KIM ; Hyun Jung LEE ; Sun Jae LEE ; Sang Jun SUH ; Eileen L YOON ; Hae Rim KIM ; Kwan Soo BYUN ; Tae Seok SEO
Clinical and Molecular Hepatology 2012;18(3):321-325
Necrotizing pancreatitis is one of the rare complications of transcatheter arterial chemoembolization (TACE). Necrotizing pancreatitis after TACE may result from the development of ischemia caused by regurgitation of embolic materials into the vessels supplying the pancreas. We report a case of post-TACE necrotizing pancreatitis with abscess formation in a patient with hepatocellular carcinoma. The patient had suffered hepatic artery injury due to repetitive TACE; during his 25th TACE procedure he had submitted to selective catheterization of the feeding vessel from the dorsal pancreatic artery with a cytotoxic agent and Gelfoam particles. The patient complained of abdominal pain after the TACE procedure, and a CT scan led to a diagnosis of necrotizing pancreatitis with abscess formation. The pancreatic abscess progressed despite general management of the pancreatitis, including antibiotics. Percutaneous catheter drainage was performed, and the symptoms of the patient improved.
Abscess/microbiology
;
Aged
;
Anti-Bacterial Agents/therapeutic use
;
Carcinoma, Hepatocellular/*complications/*therapy
;
Chemoembolization, Therapeutic/*adverse effects
;
Cholangiopancreatography, Endoscopic Retrograde
;
Citrobacter freundii/isolation & purification
;
Drainage
;
Drug Resistance, Multiple, Bacterial
;
Enterobacteriaceae Infections/drug therapy
;
Hepatitis B/complications
;
Humans
;
Klebsiella/isolation & purification
;
Klebsiella Infections/drug therapy
;
Liver Cirrhosis/etiology
;
Liver Neoplasms/*complications/*therapy
;
Male
;
Necrosis/*diagnosis/etiology
;
Pancreatitis/*diagnosis/etiology
;
Tomography, X-Ray Computed
10.Splenic Abscess: A Single Institution Study and Review of the Literature.
Won Suk LEE ; Sang Tae CHOI ; Keon Kuk KIM
Yonsei Medical Journal 2011;52(2):288-292
PURPOSE: The aim of this study was to review our experience with splenic abscesses, with respect to the relevant aspects of splenic abscesses and treatment outcomes. MATERIALS AND METHODS: We reviewed the cases of 18 patients who had splenic abscesses and who were treated at our hospital from November 1993 to December 2008. RESULTS: The most common symptom at presentation was abdominal pain in 12 patients (66.7%). The median duration from symptom onset until establishment of a diagnosis was 22 days. Streptococcus viridians was the most common pathogen (27.8%), follow by Klebsiella pneumoniae (22.2%). The mortality rate during the inpatient period and the previous 90 days was 16.6%. Three of four patients with Klebsiella pneumoniae showed a single abscess pocket. Four patients (22.2%) underwent percutaneous drainage, eight (44.5%) recieved antibiotic treatment only and six (33.3%) underwent splenectomy. CONCLUSION: There is no gold standard for treating splenic abscesses. Treatment should be customized for each patient.
Abscess/diagnosis/drug therapy/microbiology/surgery/*therapy
;
Adult
;
Aged
;
Anti-Bacterial Agents/therapeutic use
;
Drainage
;
Female
;
Humans
;
Klebsiella Infections/diagnosis/drug therapy/microbiology/surgery
;
Klebsiella pneumoniae
;
Male
;
Middle Aged
;
Splenectomy
;
Splenic Diseases/diagnosis/drug therapy/*microbiology/surgery
;
Streptococcal Infections/diagnosis/drug therapy/microbiology/surgery
;
Treatment Outcome
;
Viridans Streptococci
;
Young Adult

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