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1.
Allergy Asthma Proc ; 36(5): 407-11, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26314823

RESUMO

Hematopoietic stem cell transplantation (HSCT) outcomes in X-linked severe combined immune deficiency are most effective when performed with patients <3 months of age and without coexisting morbidity, and with donor cells from a matched sibling. Even under such favorable circumstances, outcomes can be suboptimal, and full cellular engraftment may not be complete, which results in poor B or natural killer cell function. Protein losing enteropathies can accompany persistent immune deficiency disorders with resultant low serum globulins (immunoglobulin A [IgA], IgG, IgM) and lymphopenia. Patients with immune disorders acquire infections that can be predicted by their immune dysfunction. Fungal infections are typically noted in neutropenic (congenital or acquired) and T-cell deficient individuals. Coexisting fungal infections are rare, even in hosts who are immunocompromised, and they require careful evaluation. Antifungal treatment may result in drug-drug interactions with significant complications.


Assuntos
Bronquiectasia/diagnóstico , Budesonida/uso terapêutico , Síndrome de Cushing/diagnóstico , Combinação Fluticasona-Salmeterol/uso terapêutico , Transplante de Células-Tronco Hematopoéticas , Histoplasma/imunologia , Histoplasmose/diagnóstico , Itraconazol/uso terapêutico , Enteropatias Perdedoras de Proteínas/diagnóstico , Imunodeficiência Combinada Severa/diagnóstico , Adolescente , Bronquiectasia/etiologia , Bronquiectasia/terapia , Budesonida/efeitos adversos , Criança , Quimerismo/induzido quimicamente , Síndrome de Cushing/imunologia , Interações Medicamentosas , Combinação Fluticasona-Salmeterol/efeitos adversos , Transplante de Células-Tronco Hematopoéticas/efeitos adversos , Histoplasma/efeitos dos fármacos , Histoplasmose/etiologia , Histoplasmose/terapia , Humanos , Doença Iatrogênica , Terapia de Imunossupressão , Recém-Nascido , Itraconazol/efeitos adversos , Masculino , Linhagem , Enteropatias Perdedoras de Proteínas/etiologia , Enteropatias Perdedoras de Proteínas/terapia , Imunodeficiência Combinada Severa/complicações , Imunodeficiência Combinada Severa/terapia , Aumento de Peso/imunologia
2.
Pediatr Cardiol ; 33(5): 739-43, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22349671

RESUMO

Cardiac involvement, such as pericarditis, myocarditis, and endocarditis, is seen in juvenile idiopathic arthritis. Although there have been some reports about right-ventricular systolic and diastolic functions of adults with rheumatoid arthritis and left-ventricular systolic and diastolic functions of children with JIA, there have been no studies about RV functions of children with JIA. The aim of this study was to determine RV functions in children with JIA. We performed conventional echocardiography and tissue Doppler imaging measurements of the right ventricle of patients with JIA. All patients were in sinus rhythm at the time of examination without overt LV heart failure and with normal LV ejection fraction. Fifty-five children with the diagnosis of JIA and 33 healthy control subjects were included in the study. Peak systolic, early, and late diastolic tricuspid annular velocities were significantly decreased in JIA patients compared with healthy controls (p < 0.05). Isovolumic accelaration (IVA), as a measure of myocardial acceleration during isovolumic contraction of the right ventricle, was also significantly lower in JIA patients than in healthy controls (p < 0.05). RV systolic and diastolic functions, in addition to the previously shown LV functions, are affected in JIA patients. IVA decreases in JIA patients and may be used as an alternative, noninvasive parameter for the assessment of RV systolic function in children with JIA.


Assuntos
Artrite Juvenil/fisiopatologia , Disfunção Ventricular Direita/diagnóstico por imagem , Disfunção Ventricular Direita/fisiopatologia , Estudos de Casos e Controles , Distribuição de Qui-Quadrado , Criança , Ecocardiografia Doppler , Feminino , Humanos , Masculino
3.
J Allergy Clin Immunol Pract ; 9(10): 3679-3685.e1, 2021 10.
Artigo em Inglês | MEDLINE | ID: mdl-34102347

RESUMO

BACKGROUND: Inner-city children are disproportionately affected by asthma and sleep-disordered breathing (SDB). However, little is known about the association of SDB symptoms with asthma morbidity in this vulnerable population. OBJECTIVE: Assess the relationship between snoring frequency and asthma morbidity. METHODS: This study was part of the School Inner-City Asthma Study, a longitudinal prospective cohort study of children with persistent asthma who attended schools in the Northeast United States from 2008 to 2013. Participants had baseline assessments of asthma symptoms, snoring, and allergy status. Caregivers completed quarterly surveys for 12 months on symptoms of asthma, snoring, and health care outcomes. Snoring frequency (non-, rare-, sometimes-, habitual-snoring) and its relationship with asthma symptoms and asthma morbidity were assessed by mixed-effects models. RESULTS: There were 1186 observations from 339 subjects. Mean age was 7.9 years; roughly half were male, and most were of minority race. Half were overweight or obese, and 65.5% had atopy. At initial snoring assessment, 24.8% reported habitual snoring, but report of snoring frequency varied over the study period. Multivariate analyses revealed increased odds of maximum asthma symptom days for habitual snoring compared with nonsnoring (1.58; 95% CI, 1.19-2.10; P < .002) and all other snoring categories. Habitual snoring was associated with greater odds of health care utilization (incidence rate ratio, 1.72; 95% CI, 1.10-2.69; P = .02) and worse asthma control (odds ratio, 1.49; 95% CI, 1.05-2.11; P = .03) compared with nonsnoring. CONCLUSIONS: Snoring is common among inner-city school-age children with asthma, and habitual snoring is associated with increased asthma symptom burden and health care utilization.


Assuntos
Asma , Ronco , Asma/epidemiologia , Criança , Estudos Transversais , Humanos , Masculino , Morbidade , Prevalência , Estudos Prospectivos , Instituições Acadêmicas , Ronco/epidemiologia , Inquéritos e Questionários
4.
Pediatr Int ; 52(5): 749-53, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20487369

RESUMO

BACKGROUND: We aimed to evaluate the cause, clinical profile, and short-term outcome of status epilepticus cases that were admitted to our pediatric emergency unit between 1 January and 31 December 2008. METHODS: We studied the clinical features of 59 seizures that occurred in 56 patients aged between 3 months and 15 years with the diagnosis of status epilepticus. We observed the clinical course and outcome of 53 cases for 6 to 18 months. The correlation between the cause of the seizure and the patient's age at the time of status epilepticus was evaluated as well as the correlation between the risk of seizure recurrence and family history of seizure, the neurological status of the patient prior to seizure and the presence of epilepsy. RESULTS: The most common cause of status epilepticus is febrile illness in children younger than 2 years and idiopathic/cryptogenic and remote symptomatic causes in children older than 2 years. The rate of recurrence of seizure was significantly higher in cases with existing neurological abnormalities, prior epilepsy and seizures with remote symptomatic causes. The most common triggering factors of status epilepticus development in cases with epilepsy were noncompliance for anti-epileptic drugs and infectious fever. CONCLUSIONS: In our study, the risk factors for seizure recurrence were the presence of prior epilepsy, existence of neurological abnormalities and remote symptomatic causes. We argue that improving the compliance of patients and their families to take medicine appropriately and training them in how to cope with febrile illnesses may decrease the recurrence of seizures.


Assuntos
Estado Epiléptico/diagnóstico , Estado Epiléptico/epidemiologia , Adolescente , Distribuição por Idade , Anticonvulsivantes/uso terapêutico , Criança , Pré-Escolar , Estudos de Coortes , Intervalos de Confiança , Serviço Hospitalar de Emergência , Feminino , Seguimentos , Humanos , Lactente , Masculino , Recidiva , Medição de Risco , Índice de Gravidade de Doença , Distribuição por Sexo , Estado Epiléptico/tratamento farmacológico , Resultado do Tratamento , Turquia
5.
North Clin Istanb ; 7(1): 67-70, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32232207

RESUMO

Kawasaki disease is the second most common cause of childhood vasculitis. Cutaneous manifestation, which is the diagnostic criteria of Kawasaki disease, may show atypical course and causes conflict in diagnosis for physicians. A 14-month-old girl treated with intravenous immunoglobulin after diagnosed with KD. Target lesions and a vesicular rash developed on the whole body during the course of the disease. Methylprednisolone was added to the treatment. All atypical skin lesions and disease findings were improved using IVIG and subsequent methylprednisolone therapy. Cutaneous signs of KD may show atypical course. Thus, it may lead to confusion in diagnosis with Stevens-Johnson syndrome.

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