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1.
Int J Infect Dis ; 125: 97-102, 2022 Dec.
Article in English | MEDLINE | ID: mdl-36180033

ABSTRACT

OBJECTIVES: The incidence of infections caused by extended-spectrum beta-lactamase (ESBL)-producing bacteria has increased. This study aimed to clarify the risk factors and treatment strategies for febrile urinary tract infection (fUTI) caused by ESBL-producing bacteria in Japanese children. METHODS: A retrospective observational study was conducted in 21 hospitals among children aged <16 years diagnosed with an fUTI between 2008 and 2017. Clinical data of children with fUTI caused by ESBL-producing and non-ESBL-producing bacteria were compared. RESULTS: Of the 2049 cases of fUTI, 147 (7.2%) were caused by ESBL-producing bacteria. Children in the ESBL group were more likely to have a history of recent antibiotic use or prophylactic antibiotic use, and experience recurrent UTIs (P <0.001) compared with those in the non-ESBL group. Of the 124 cases of fUTI due to ESBL-producing bacteria that were reviewed, 20 and 100 had concordant and discordant antibiotic use, respectively, and four had unknown antibiotic susceptibility. The median time from the start of treatment to fever resolution was 24 hours and did not differ significantly by therapy group (P = 0.39). CONCLUSION: ESBL-producing bacteria should be considered in children with recurrent UTIs and recent antibiotic use. Most children with fUTI experience clinical improvement regardless of the choice of antibiotic.


Subject(s)
Urinary Tract Infections , beta-Lactamases , Child , Humans , Japan/epidemiology , Urinary Tract Infections/drug therapy , Urinary Tract Infections/epidemiology , Urinary Tract Infections/microbiology , Enterobacteriaceae , Retrospective Studies , Anti-Bacterial Agents/therapeutic use , Risk Factors
2.
Int J Infect Dis ; 104: 97-101, 2021 Mar.
Article in English | MEDLINE | ID: mdl-33383218

ABSTRACT

BACKGROUND: Febrile urinary tract infection (fUTI) is the most common serious bacterial infection in children. Despite this, there have been no studies examining the clinical features of pediatric fUTI in Japan. The purpose of this study was to describe the clinical characteristics of fUTI in Japanese children. METHODS: A multicenter, retrospective, observational study was conducted at 21 hospitals in Japan. Children under the age of 15 years who were diagnosed with fUTI between 2008 and 2017 were included. The diagnostic criteria were a temperature over 38 °C and the presence of a single bacterial pathogen in urine culture. Patient characteristics were obtained from medical records. RESULTS: In total, 2,049 children were included in the study. The median age was 5 months, and 59.3% were male. It was found that 87.0% of the males and 53.2% of the females were under 1 year of age. The main causative pathogens identified were Escherichia coli and Enterococcus spp., accounting for 76.6% and 9.8% of infections, respectively. CONCLUSIONS: There was a male predominance of fUTI in Japanese children, particularly in infants. Enterococcus spp. were the second most frequent causative pathogen; therefore, Gram staining of urine samples is strongly recommended before initiating antibiotic therapy.


Subject(s)
Bacteriuria/diagnosis , Adolescent , Bacteria/isolation & purification , Child , Child, Preschool , Female , Fever , Humans , Infant , Japan , Male , Retrospective Studies
3.
Hum Pathol ; 41(9): 1276-85, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20708459

ABSTRACT

The nephritis-associated plasmin receptor is a recently identified nephritogenic antigen associated with acute poststreptococcal glomerulonephritis and proposed to play a pathogenic role, but its precise glomerular localization in acute poststreptococcal glomerulonephritis has not been elucidated. We therefore analyzed renal biopsy sections from 10 acute poststreptococcal glomerulonephritis patients by using immunofluorescence staining with anti-nephritis-associated plasmin receptor antibody and various markers of glomerular components. Nephritis-associated plasmin receptor was detected in the glomeruli of all patients, and double staining for nephritis-associated plasmin receptor and collagen IV showed nephritis-associated plasmin receptor to be predominantly on the inner side of the glomerular tufts. Nephritis-associated plasmin receptor-positive areas within glomerular tufts were further characterized with markers for neutrophils, mesangial cells, endothelial cells, and macrophages. In 6 of the patients, nephritis-associated plasmin receptor staining was seen mainly in neutrophils and to a lesser degree in mesangial and endothelial cells. In the other 4 patients, nephritis-associated plasmin receptor staining was seen mainly in mesangial cells and to a lesser degree in neutrophils and endothelial cells. In all patients, macrophages showed little staining. Elevated plasmin activity in glomerular neutrophils was identified by combining in situ zymography staining for plasmin activity and immunofluorescence staining for neutrophils. The glomerular localizations of nephritis-associated plasmin receptor and another nephritogenic antigen, streptococcal pyrogenic exotoxin B, were compared by double immunofluorescence staining and found to be similar. These findings indicate the nephritogenic potential of nephritis-associated plasmin receptor and offer valuable information with respect to the pathogenic mechanism of acute poststreptococcal glomerulonephritis.


Subject(s)
Antigens, Bacterial/metabolism , Glomerulonephritis/metabolism , Kidney Glomerulus/pathology , Receptors, Cell Surface/metabolism , Streptococcal Infections/metabolism , Acute Disease , Adolescent , Adult , Bacterial Proteins/metabolism , Biomarkers/metabolism , Child , Exotoxins/metabolism , Female , Glomerular Mesangium/metabolism , Glomerular Mesangium/pathology , Glomerulonephritis/microbiology , Humans , Kidney Glomerulus/metabolism , Male , Microscopy, Fluorescence , Middle Aged , Neutrophils/metabolism , Neutrophils/pathology , Young Adult
4.
Nephrol Dial Transplant ; 23(7): 2254-9, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18223261

ABSTRACT

BACKGROUND: A pathogenic role of intraglomerular plasmin bound to nephritogenic antigen (nephritis-associated plasmin receptor, NAPlr) and resistant to physiologic inhibitors such as alpha(2)-antiplasmin (alpha(2)-AP) has recently been proposed in acute poststreptococcal glomerulonephritis (APSGN). To confirm this concept, we analysed the urinary profile of plasmin cascade in APSGN patients. METHODS: Urine samples from 10 patients with APSGN, 12 patients with IgA nephropathy (IgAN), 10 patients with streptococcal infection without nephritis (SI) and 10 healthy control subjects were analysed. The alpha(2)-AP-resistant plasmin activity was assessed by a chromogenic assay after alpha(2)-AP was added to each urine sample. Urinary plasminogen activator (PA) and plasmin were further analysed by polyacrylamide gel zymography. Urinary NAPlr was assessed by western blot analysis in selected samples. RESULTS: Urinary alpha(2)-AP-resistant plasmin activity corrected for creatinine concentration (units/g x creatinine) was significantly higher in patients with APSGN (2.99 +/- 0.63) than in patients with IgAN (1.02 +/- 0.20, P < 0.01), SI (0.79 +/- 0.17, P < 0.01), or in healthy control subjects (0.73 +/- 0.18, P < 0.01). This tendency was confirmed by casein gel zymography. However urinary PA activity assessed by plasminogen-casein gel zymography did not differ between groups. NAPlr was detected in the urine of APSGN patients. CONCLUSIONS: We found elevated urinary plasmin activity resistant to alpha(2)-AP, which may be due to urinary excretion of NAPlr in patients with APSGN. This result supports the pathogenic role of the NAPlr-plasmin complex in the development of APSGN. Furthermore, alpha(2)-AP-resistant urinary plasmin activity may be useful as a diagnostic marker for APSGN.


Subject(s)
Fibrinolysin/drug effects , Fibrinolysin/urine , Glomerulonephritis/microbiology , Glomerulonephritis/urine , Streptococcal Infections/complications , Streptococcal Infections/urine , alpha-2-Antiplasmin/pharmacology , Acute Disease , Adolescent , Adult , Biomarkers/urine , Case-Control Studies , Child , Child, Preschool , Creatinine/urine , Glomerulonephritis/diagnosis , Glomerulonephritis, IGA/urine , Humans , Middle Aged , Receptors, Peptide/metabolism , Streptococcal Infections/diagnosis
6.
J Am Soc Nephrol ; 15(7): 1785-93, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15213266

ABSTRACT

The role of nephritis-associated antigen as a virulence factor for acute poststreptococcal glomerulonephritis (APSGN) remains to be fully clarified. Nephritis-associated plasmin receptor (NAPlr) was previously isolated from group A streptococcus (GAS) and shown to bind plasmin(ogen). The nucleotide sequence of the naplr gene from GAS isolates obtained from patients with APSGN was determined. The sequence of the putative open reading frame (1011 bp) showed 99.8% identity among isolated strains. Homology screen revealed an exact match with streptococcal glyceraldehyde-3-phosphate dehydrogenase (GAPDH). NAPlr exhibited GAPDH activity in zymography, and it activated the complement pathway in vitro. In APSGN kidney biopsy specimens, NAPlr was observed mainly in the early stage of the disease (1 to 14 d after onset) but was not colocalized with either C3 or IgG as assessed by double immunofluorescence staining. Sera of patients with APSGN, patients with GAS infection without renal involvement, nonrenal pediatric patients, and healthy adults as controls were assayed for anti-NAPlr antibody titers. Anti-NAPlr antibodies were present most frequently in APSGN sera, and antibody titers were also significantly higher than in patients with GAS infection alone or in other control patients. Moreover, antibody titers remained elevated during the entire 10-yr follow-up period.


Subject(s)
Glomerulonephritis/etiology , Glomerulonephritis/immunology , Nephritis/pathology , Receptors, Peptide/biosynthesis , Streptococcal Infections/immunology , Adolescent , Adult , Age Factors , Aged , Amino Acid Sequence , Base Sequence , Biopsy , Child , Child, Preschool , Complement Activation , Complement C3/metabolism , Dose-Response Relationship, Drug , Female , Follow-Up Studies , Humans , Immunoglobulin G/chemistry , Kidney/metabolism , Kidney/pathology , Male , Microscopy, Fluorescence , Middle Aged , Molecular Sequence Data , Open Reading Frames , Sequence Analysis, DNA , Time Factors
7.
Pediatr Infect Dis J ; 23(12): 1175-6, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15626965

ABSTRACT

A healthy 7-year-old girl developed emotional incontinence and amnesia associated with mumps encephalitis. Her neurologic findings markedly improved after treatment of daily injection of thyrotropin-releasing hormone tartrate without any adverse effects. Although magnetic resonance imaging revealed no abnormal findings, the findings of Tc-hexamethylpropyleneamine oxime single photon emission computed tomography demonstrated abnormality of left temporooccipital area thought to be responsible for her symptoms.


Subject(s)
Affective Symptoms/drug therapy , Amnesia/drug therapy , Encephalitis, Viral/complications , Mumps/complications , Thyrotropin-Releasing Hormone/therapeutic use , Child , Female , Humans , Magnetic Resonance Imaging , Technetium Tc 99m Exametazime , Tomography, Emission-Computed, Single-Photon
9.
Brain Dev ; 24(2): 98-101, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11891101

ABSTRACT

We herein report a 4-year-old boy with Miller Fisher syndrome (MFS) who presented with transient coma in addition to the typical triad of internal and external ophthalmoplegia, cerebellar ataxia and areflexia after an influenza type B infection. The electroencephalogram findings revealed intermittently generalized slow wave bursts. The cerebrospinal fluid revealed high protein and a lack of any cellular response. The serum anti-GQ1b IgG antibody was elevated in the acute phase and disappeared in the convalescent phase. The transient coma with the triad of MFS in this patient indicated an extended brainstem lesion including a reticular formation, which is also the responsible lesion of Bickerstaff brainstem encephalitis (BBE), but the magnetic resonance imaging repeatedly showed no abnormal finding. Our patient suggested the involvement of central nervous system in addition to the peripheral nerve injury in MFS. He also suggested that MFS and BBE may belong to the same group of disorders as syndrome of ophthalmoplegia, ataxia and areflexia (SOAA).


Subject(s)
Brain Stem , Coma/etiology , Encephalitis/etiology , Miller Fisher Syndrome/complications , Brain Stem/pathology , Brain Stem/physiopathology , Child, Preschool , Coma/pathology , Coma/physiopathology , Electroencephalography , Encephalitis/pathology , Encephalitis/physiopathology , Humans , Magnetic Resonance Imaging , Male , Miller Fisher Syndrome/pathology , Miller Fisher Syndrome/physiopathology
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