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1.
Am J Emerg Med ; 35(6): 819-822, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28148468

ABSTRACT

BACKGROUND: Abdominal pain is common in children, but expeditious diagnosis of life- or organ-threatening diseases can be challenging. An evidence-based definition of tachycardia in children was established recently, but its diagnostic utility has not yet been studied. OBJECTIVE: To test the hypothesis that abdominal pain with tachycardia may pose a higher likelihood of life- or organ-threatening diseases in children. METHODS: A nested case-control study was conducted in a pediatric emergency department in 2013. Tachycardia was defined as a resting heart rate of more than 3 standard deviations above the average for that age. Life- or organ-threatening diseases were defined as "disorders that might result in permanent morbidity or mortality without appropriate intervention." A triage team recorded vital signs before emergency physicians attended patients. Patients with tachycardia (cases) and without tachycardia (controls) were systematically matched for age, sex, and month of visit. The groups were compared for the presence of life- or organ-threatening diseases. RESULTS: There were 1683 visits for abdominal pain, 1512 of which had vital signs measured at rest. Eighty-three patients experienced tachycardia, while 1429 did not. Fifty-eight cases and 58 controls were matched. Life- or organ-threatening diseases were more common in the case group (19%) than the control group (5%, p=0.043). The relative risk of tachycardia to the presence of the diseases was 3.7 (95% confidence interval 1.2-12.0). CONCLUSION: Tachycardia significantly increased the likelihood of life- or organ-threatening diseases. Tachycardia in children with abdominal pain should alert emergency physicians to the possibility of serious illness.


Subject(s)
Abdominal Pain/diagnosis , Tachycardia/epidemiology , Triage , Adolescent , Case-Control Studies , Child , Child, Preschool , Emergency Service, Hospital , Female , Hospitals, Pediatric , Humans , Japan , Male , Tachycardia/diagnosis , Vital Signs
2.
Clin Rheumatol ; 35(11): 2749-2756, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27596741

ABSTRACT

At the national level, IgA vasculitis-related hospitalizations among children in the USA are scarce. Furthermore, nationwide epidemiology and hospital course of children with IgA vasculitis have not been fully described in the USA, and disparities by race/ethnicity remain unknown. Hospital discharge records of patients aged 19 years or younger were obtained from the 2003, 2006, 2009, and 2012 Kids' Inpatient Database, and they were weighted to estimate the annual hospitalization rates with respect to age, gender, and race/ethnicity in the USA. Annual hospitalization rates were calculated using weighted case estimates and US census data. Negative binomial regression was used to ascertain the factors associated with length of hospital stay. Total annual hospitalization rates showed a significant decreasing trend, ranging from 2.45 per 100,000 children in 2003 to 1.89 per 100,000 children in 2012 (p < 0.001). The peak ages of the hospitalized children with IgA vasculitis were 2 and 7 years, and male-to-female ratios were 1.38-1.44. Factors associated with length of hospital stay were patients' ages (10-14 and 15-19 years), race/ethnicity (Hispanic, Asian, and Pacific Islander), comorbid electrolyte abnormality, GI hemorrhage, intussusception, renal symptoms, and GI symptoms. The annual hospitalization rates for IgA vasculitis are declining in the USA across multiple age groups. GI and renal manifestations are associated with increased length of hospital stay.


Subject(s)
Hospitalization/statistics & numerical data , Immunoglobulin A , Vasculitis/epidemiology , Adolescent , Child , Child, Preschool , Female , Humans , Incidence , Infant , Length of Stay , Male , United States/epidemiology , Vasculitis/therapy , Young Adult
3.
J Allergy Clin Immunol Pract ; 4(6): 1227-1231, 2016.
Article in English | MEDLINE | ID: mdl-27372599

ABSTRACT

BACKGROUND: Obesity and asthma are common health problems in the United States. OBJECTIVE: The objective of this study was to evaluate the clinical and economic burdens of obesity on hospitalized children with acute asthma exacerbation in 2012. METHODS: Hospital discharge records of patients aged 2 to 18 years with a diagnosis of asthma were obtained from the 2012 Kids' Inpatient Database, wherein the data were compiled by the Agency for Healthcare Research and Quality. The discharge records were weighted to estimate the number of hospitalizations because of asthma exacerbations in the United States. To classify whether the patient was obese or not, we used the International Classification of Diseases, Ninth Revision, Clinical Modification code 278.0x. We compared the odds of using noninvasive or invasive mechanical ventilation, mean total charges for inpatient service, and length of hospital stay between obese and nonobese patients. RESULTS: A total of 74,338 patient discharges were extracted. Of these, 3,494 discharges were excluded because of chronic medical conditions. Using discharge weight variables, we estimated a total of 100,157 hospitalizations with asthma exacerbations among children aged between 2 and 18 years in 2012. Obesity was significantly associated with higher odds of using mechanical ventilation (odds ratio 1.59, 95% CI 1.28-1.99), higher mean total hospital charges (adjusted difference: $1588, 95% CI $802-$2529), and longer mean length of hospital stay (0.24 days, 95% CI 0.17-0.32 days) compared with nonobesity. CONCLUSIONS: These findings suggest that obesity is a significant risk factor of severe asthma exacerbation that requires mechanical ventilation, and obesity is an economically complicating factor.


Subject(s)
Asthma/epidemiology , Obesity/epidemiology , Adolescent , Asthma/economics , Child , Child, Preschool , Female , Hospital Costs , Humans , Length of Stay , Male , Obesity/economics , Odds Ratio , Respiration, Artificial/statistics & numerical data , Retrospective Studies , Risk Factors , United States/epidemiology
4.
J Child Neurol ; 31(10): 1257-64, 2016 09.
Article in English | MEDLINE | ID: mdl-27280723

ABSTRACT

Pediatric convulsive status epilepticus with fever is common in the emergency setting but leads to severe neurological sequelae in some patients. To explore the epidemiology of convulsive status epilepticus with fever, a retrospective cohort covering all convulsive status epilepticus cases with fever seen in the emergency department of a tertiary care children's hospital were consecutively collected. Of the 381 consecutive cases gathered, 81.6% were due to prolonged febrile seizure, 6.6% to encephalopathy/encephalitis, 0.8% to meningitis, and 7.6% to epilepsy. In addition, seizures were significantly longer in encephalopathy/encephalitis cases than in prolonged febrile seizure cases (log rank test, P < .001). These results provide for the first time the pretest probability of final diagnoses in children with convulsive status epilepticus with fever in the emergency setting, and will help optimize the management of pediatric patients presenting to the emergency department with convulsive status epilepticus with fever.


Subject(s)
Emergency Service, Hospital , Fever/complications , Fever/epidemiology , Status Epilepticus/complications , Status Epilepticus/epidemiology , Child, Preschool , Cross-Sectional Studies , Diagnosis, Differential , Emergency Service, Hospital/statistics & numerical data , Female , Fever/diagnosis , Fever/therapy , Humans , Infant , Kaplan-Meier Estimate , Male , Meningitis/complications , Meningitis/diagnosis , Meningitis/epidemiology , Meningitis/therapy , Retrospective Studies , Seizures, Febrile/complications , Seizures, Febrile/diagnosis , Seizures, Febrile/epidemiology , Seizures, Febrile/therapy , Status Epilepticus/diagnosis , Status Epilepticus/therapy
5.
Emerg Med J ; 33(8): 533-7, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27044947

ABSTRACT

OBJECTIVE: Assessment of abnormal vital signs in triage is a challenge in the paediatric emergency department (PED), since vital signs may reflect anxiety, fever or pain rather than the clinical deterioration of the child. We aimed to evaluate the efficacy of subjective 'down-triage' (change of the initially determined acuity levels) of Japanese Triage and Acuity Scale (JTAS). METHODS: This is a retrospective cohort study of patients in PED up to 15 years of age at a tertiary paediatric medical centre in Japan during a 1-year period. At the end of every JTAS triage process, PED nurses were allowed to 'down-triage' acuity levels of well-appearing patients with abnormal HR or RR, which were presumably attributable to fever, crying or being upset. We compared predictive performance of the triage system before and after 'down-triage' using admission rate as the primary outcome. RESULTS: Among 37 961 PED visits during the study period, we analysed 37 219 records. A total of 17 089 patients (45.9%) were 'down-triaged' after their initial triage allocation upon arrival. Admission rates after 'down-triage' (83%, 33%, 7%, 1% and 3% for levels 1-5, respectively), compared with those of unmodified initial level (16%, 11%, 6%, 2% and 6% for levels 1-5, respectively), had a better apparent relevance with the anticipated admission rates of Canadian Triage and Acuity Scale. CONCLUSIONS: Modification of JTAS through 'down-triage' by experienced staff improves prediction of disposition in a PED. Further research is needed to determine an objective protocol for 'down-triage' to ensure safe practice in a PED.


Subject(s)
Emergency Service, Hospital/organization & administration , Triage/methods , Vital Signs , Adolescent , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Japan , Male , Retrospective Studies
6.
Pediatr Int ; 58(5): 382-385, 2016 May.
Article in English | MEDLINE | ID: mdl-27005513

ABSTRACT

Cases of infection with hypervirulent Klebsiella pneumoniae are gradually increasing in number, and cause life-threatening community-acquired infection even in immunocompetent patients. A 14-year-old boy developed septic hip arthritis due to hypervirulent K. pneumoniae (sequence type 23, serotype K1, magA positive). The patient initially seemed to have been successfully treated with antibiotics and surgical intervention, but septic arthritis developed into osteomyelitis of the femoral head and myositis, which required long-term antibiotic therapy and additional surgical intervention. This is the first pediatric case of hypervirulent K. pneumoniae septic hip arthritis. Treatment plans should mainly consist of antibiotic therapy and surgical intervention. Clinicians, even pediatricians, in developed countries should be aware of the increasing incidence of hypervirulent Klebsiella pneumoniae infection.

8.
Pediatr Int ; 57(4): 783-5, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26177232

ABSTRACT

Staphylococcus lugdunensis is a known pathogen of infective endocarditis, but not of urinary tract infection. We report a previously healthy neonate without congenital anomalies of the kidney and urinary tract who developed urinary tract infection due to Staphylococcus lugdunensis, illustrating that Staphylococcus lugdunensis can cause urinary tract infection even in those with no urinary tract complications.


Subject(s)
Staphylococcal Infections/microbiology , Staphylococcus lugdunensis/isolation & purification , Urinary Tract Infections/microbiology , Anti-Bacterial Agents/therapeutic use , Female , Humans , Infant, Newborn , Staphylococcal Infections/diagnosis , Staphylococcal Infections/drug therapy , Urinary Tract Infections/diagnosis , Urinary Tract Infections/drug therapy
9.
Pediatr Int ; 57(2): e56-8, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25712264

ABSTRACT

We herein describe the case of a 27-day-old male infant who was brought to the emergency room for intermittent crying, and swelling of the left scrotum. Based on the clinical findings, necrotizing fasciitis was suspected, and surgical intervention was successfully completed within a few hours of admission. Streptococcus agalactiae type Ia was cultured from the drained abscess, and was considered the causative pathogen. To our knowledge, this is the first report of neonatal necrotizing fasciitis caused by S. agalactiae. Prompt diagnosis and immediate surgical debridement are crucial in the initial management of this disease.


Subject(s)
Fasciitis, Necrotizing/microbiology , Genital Diseases, Male/microbiology , Scrotum/microbiology , Streptococcal Infections/microbiology , Streptococcus agalactiae/isolation & purification , Anti-Bacterial Agents/therapeutic use , Cefmetazole/therapeutic use , Fasciitis, Necrotizing/diagnosis , Fasciitis, Necrotizing/surgery , Genital Diseases, Male/diagnosis , Genital Diseases, Male/surgery , Humans , Infant, Newborn , Male , Scrotum/pathology , Streptococcal Infections/drug therapy
10.
Pediatr Neurol ; 51(6): 837-9, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25301225

ABSTRACT

BACKGROUND: Type 2 Gaucher disease is the most severe neuronopathic form of Gaucher disease and is characterized by severe neurodegeneration with brainstem involvement and organ failure. Prediction or diagnosis of type 2 Gaucher disease before the development of neurological complications is difficult. PATIENT: A 5-month-old female infant presented with deafness without other neurological abnormalities. Auditory brainstem response analysis revealed the absence of later wave components. Two months later, muscular rigidity became evident, followed by the development of opisthotonus and strabismus. Rapid progression of splenomegaly led to the diagnosis of type 2 Gaucher disease. CONCLUSIONS: Abnormal auditory brainstem response findings may already exist before the development of severe brainstem abnormalities such as muscular rigidity and opisthotonus in type 2 Gaucher disease. When patients present with deafness and absent later wave components on auditory brainstem response, type 2 Gaucher disease should be included in the differential diagnosis even in the absence of other neurological abnormalities.


Subject(s)
Evoked Potentials, Auditory, Brain Stem/physiology , Gaucher Disease/physiopathology , Deafness/etiology , Deafness/physiopathology , Female , Gaucher Disease/complications , Gaucher Disease/diagnosis , Humans , Infant , Splenomegaly/etiology , Splenomegaly/pathology
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