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1.
Annals of Laboratory Medicine ; : 235-243, 2016.
Article in English | WPRIM | ID: wpr-56703

ABSTRACT

BACKGROUND: We estimated the prevalence and clinical impact of heterogeneous vancomycin-intermediate Staphylococcus aureus (hVISA). The concordance between macromethod and glycopeptide resistance detection (GRD) E tests was determined. In addition, predictors of clinical outcomes in hospitalized patients with S. aureus bacteremia (SAB) or pneumonia (SAP) were evaluated. METHODS: We obtained 229 consecutive S. aureus isolates from all hospitalized patients at two university hospitals located in Busan and Yangsan, Korea. Standard, macromethod, and GRD E tests were performed. Additionally, we reviewed the medical records of all patients. Among the 229 patients, predictors of clinical outcomes were analyzed for 107 patients with SAB and 39 with SAP. RESULTS: Among the 229 isolates, 34.5% of S. aureus isolates and 50.7% of methicillin-resistant S. aureus isolates exhibited the hVISA phenotype based on the macromethod E test. hVISA was nearly associated with treatment failure in patients with SAB (P=0.054) and was significantly associated with treatment failure in patients with SAP (P=0.014). However, hVISA was not associated with 30-day mortality in patients with SAB or SAP. The concordance between the macromethod and GRD E tests was 84.2%. CONCLUSIONS: hVISA is quite common in the southeastern part of Korea. hVISA is associated with treatment failure in patients with SAP.


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Anti-Bacterial Agents/pharmacology , Bacteremia/drug therapy , Drug Resistance, Bacterial/drug effects , Hospital Mortality , Hospitalization , Methicillin-Resistant Staphylococcus aureus/drug effects , Microbial Sensitivity Tests , Phenotype , Pneumonia/drug therapy , Prevalence , Republic of Korea/epidemiology , Staphylococcus aureus/drug effects , Teicoplanin/pharmacology , Vancomycin/pharmacology
3.
Annals of Laboratory Medicine ; : 380-385, 2014.
Article in English | WPRIM | ID: wpr-216384

ABSTRACT

We performed customer satisfaction surveys for physicians and nurses regarding clinical laboratory services, and for outpatients who used phlebotomy services at a tertiary care unit level to evaluate our clinical laboratory and phlebotomy services. Thus, we wish to share our experiences with the customer satisfaction survey for clinical laboratory and phlebotomy services. Board members of our laboratory designed a study procedure and study population, and developed two types of questionnaire. A satisfaction survey for clinical laboratory services was conducted with 370 physicians and 125 nurses by using an online or paper questionnaire. The satisfaction survey for phlebotomy services was performed with 347 outpatients who received phlebotomy services by using computer-aided interviews. Mean satisfaction scores of physicians and nurses was 58.1, while outpatients' satisfaction score was 70.5. We identified several dissatisfactions with our clinical laboratory and phlebotomy services. First, physicians and nurses were most dissatisfied with the specimen collection and delivery process. Second, physicians and nurses were dissatisfied with phlebotomy services. Third, molecular genetic and cytogenetic tests were found more expensive than other tests. This study is significant in that it describes the first reference survey that offers a survey procedure and questionnaire to assess customer satisfaction with clinical laboratory and phlebotomy services at a tertiary care unit level.


Subject(s)
Humans , Internet , Interviews as Topic , Laboratories , Personal Satisfaction , Phlebotomy , Surveys and Questionnaires , Tertiary Healthcare , User-Computer Interface
4.
Annals of Laboratory Medicine ; : 283-287, 2013.
Article in English | WPRIM | ID: wpr-105284

ABSTRACT

Sphingobacterium spiritivorum has been rarely isolated from clinical specimens of immunocompromised patients, and there have been no case reports of S. spiritivorum infection in Korea to our knowledge. We report a case of S. spiritivorum bacteremia in a 68-yr-old woman, who was diagnosed with acute myeloid leukemia and subsequently received chemotherapy. One day after chemotherapy ended, her body temperature increased to 38.3degrees C. A gram-negative bacillus was isolated in aerobic blood cultures and identified as S. spiritivorum by an automated biochemical system. A 16S rRNA sequencing analysis confirmed that the isolate was S. spiritivorum. The patient received antibiotic therapy for 11 days but died of septic shock. This is the first reported case of human S. spiritivorum infection in Korea. Although human infection is rare, S. spiritivorum can be a fatal opportunistic pathogen in immunocompromised patients.


Subject(s)
Aged , Female , Humans , Anti-Bacterial Agents/therapeutic use , Bacteremia/complications , Bone Marrow Cells/pathology , Fatal Outcome , Immunocompromised Host , Leukemia, Myeloid, Acute/complications , Phylogeny , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Shock, Septic/etiology , Sphingobacterium/classification
5.
Annals of Laboratory Medicine ; : 130-135, 2013.
Article in English | WPRIM | ID: wpr-216010

ABSTRACT

Transformation of MDS into ALL during childhood is extremely rare. We report a rare case of an 8-yr-old girl who presented with refractory cytopenia of childhood (RCC) that transformed into ALL only 3 months after the diagnosis of childhood MDS. Although no cytogenetic abnormalities were observed in conventional karyotype and FISH analysis, we found several deletions on chromosomes 5q, 12q, 13q, and 22q. Partial homozygous deletion of the RB1 gene was observed on microarray analysis, with the bone marrow specimen diagnosed as ALL. This is the first case report of transformation of ALL from childhood MDS in Korea. We also compared the clinical, cytological, and cytogenetic features of 4 previously reported childhood MDS cases that transformed into ALL.


Subject(s)
Child , Female , Humans , Bone Marrow Cells/pathology , Cell Transformation, Neoplastic/genetics , Chromosome Aberrations , Gene Deletion , In Situ Hybridization, Fluorescence , Karyotyping , Myelodysplastic Syndromes/diagnosis , Precursor Cell Lymphoblastic Leukemia-Lymphoma/diagnosis , Retinoblastoma Protein/genetics
6.
Annals of Laboratory Medicine ; : 145-152, 2012.
Article in English | WPRIM | ID: wpr-100684

ABSTRACT

BACKGROUND: Recent studies and case reports have shown that recombinant factor VIIa (rFVIIa) treatment is effective for reversing coagulopathy and reducing blood transfusion requirements in trauma patients with life-threatening hemorrhage. The purpose of this study is to evaluate the effect of rFVIIa treatment on clinical outcomes and cost effectiveness in trauma patients. METHODS: Between January 2007 and December 2010, we reviewed the medical records of patients who were treated with rFVIIa (N=18) or without rFVIIa (N=36) for life-threatening hemorrhage due to multiple traumas at the Emergency Department of Pusan National University Hospital in Busan, Korea. We reviewed patient demographics, baseline characteristics, initial vital signs, laboratory test results, and number of units transfused, and then analyzed clinical outcomes and 24-hr and 30-day mortality rates. Thromboembolic events were monitored in all patients. Transfusion costs and hospital stay costs were also calculated. RESULTS: In the rFVIIa-treated group, laboratory test results and clinical outcomes improved, and the 24-hr mortality rate decreased compared to that in the untreated group; however, 30-day mortality rate did not differ between the groups. Thromboembolic events did not occur in both groups. Transfusion and hospital stay costs in the rFVIIa-treated group were cost effective; however, total treatment costs, including the cost of rFVIIa, were not cost effective. CONCLUSIONS: In our study, rFVIIa treatment was shown to be helpful as a supplementary drug to improve clinical outcomes and reduce the 24-hr mortality rate, transfusion and hospital stay costs, and transfusion requirements in trauma patients with life-threatening hemorrhage.


Subject(s)
Adult , Aged , Aged, 80 and over , Humans , Middle Aged , Factor VIIa/therapeutic use , Hemoglobins/analysis , Hemorrhage/complications , Multiple Trauma/complications , Partial Thromboplastin Time , Platelet Count , Prothrombin Time , Recombinant Proteins/therapeutic use , Retrospective Studies , Treatment Outcome
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