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1.
Eur J Pediatr ; 183(7): 2893-2897, 2024 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-38602530

RESUMEN

Patients with immune thrombocytopenia (ITP) usually present with minor mucocutaneous bleeding. Corpus luteum hemorrhage (CLH) is generally asymptomatic but may, rarely, lead to severe intraperitoneal bleeding, mostly in patients with coagulation disorders. CLH causing intraperitoneal bleeding has only been described in few individuals with ITP. The objective of this retrospective observational study was to assess the clinical course and incidence of symptomatic CLH in adolescent females with newly diagnosed or chronic ITP. Additionally, a comprehensive literature review was conducted to scrutinize cases of pediatric female patients with ITP, complicated by CLH. We identified three patients with ITP and hemoperitoneum secondary to CLH. They presented with acute abdominal pain, had severe thrombocytopenia (platelet counts below 20 × 109/L), and required blood transfusions as well as ITP-directed therapy. All the patients were hemodynamically stable and did not require emergency surgical intervention.  Conclusion: CLH could potentially pose a significant complication in the context of adolescent females with ITP, requiring a strong index of suspicion to direct expedient therapy. What is Known: • Immune thrombocytopenia is typically associated with minor bleeding tendency. • Corpus luteum hemorrhage is generally asymptomatic; however, in women with bleeding disorders, it has the potential to result in substantial intra-abdominal bleeding. What is New: • Corpus luteum hemorrhage leading to intra-abdominal bleeding is a potential severe complication of immune thrombocytopenia in adolescent females.


Asunto(s)
Cuerpo Lúteo , Hemorragia , Púrpura Trombocitopénica Idiopática , Adolescente , Femenino , Humanos , Hemoperitoneo/etiología , Hemorragia/etiología , Hemorragia/diagnóstico , Hemorragia/terapia , Enfermedades del Ovario/diagnóstico , Enfermedades del Ovario/etiología , Púrpura Trombocitopénica Idiopática/complicaciones , Púrpura Trombocitopénica Idiopática/terapia , Púrpura Trombocitopénica Idiopática/diagnóstico , Estudios Retrospectivos
2.
Pediatr Rheumatol Online J ; 20(1): 5, 2022 Jan 29.
Artículo en Inglés | MEDLINE | ID: mdl-35093116

RESUMEN

OBJECTIVES: Juvenile idiopathic arthritis (JIA) is the most common childhood rheumatic disease. Intra-articular corticosteroids joint injection (IAJI), with triamcinolone hexacetonide (TH) or triamcinolone acetonide (TA), is an effective additional treatment for oligo and polyarticular JIA. Previous studies have shown the benefits of TH over TA; however, TA is still used in many pediatric rheumatology centers. Our unit has experience with both regimens, and therefore we aimed to compare the efficacy and safety of TA versus TH for JIA patients. METHODS: Chart review of JIA patients who were randomly (based on drug availability) treated with TA or TH IAJI during 2010-2019. Primary outcomes for efficacy were defined as full recovery from arthritis one month after IAJI and a relapse rate of arthritis 3 months after IAJI. Primary outcome for safety was defined as the occurrence of adverse events (AEs) during the follow up period after IAJI. RESULTS: Overall, 292 joints of 102 JIA patients were treated (138 TA/154 TH joints). Complete recovery after one month was documented in 107 (69.6%) of TA treated joints and 96 (69.5%) of TH treated joints (P = 0.232). However, rate of relapse after 3 months was significantly higher for TA treated joints (27 (20.1%) vs. 13 (8.8%), respectively, P < 0.01). No AEs were documented except minor scars at four joint injection sites. CONCLUSION: The recovery from arthritis was similar (~ 70%) with both regimens, however relapse rate was more than double in TA as compared to TH injected joints. These findings are important due to a contemporary shortage of TH in the US market.


Asunto(s)
Artritis Juvenil/tratamiento farmacológico , Inyecciones Intraarticulares , Triamcinolona Acetonida/análogos & derivados , Triamcinolona Acetonida/uso terapéutico , Antiinflamatorios/uso terapéutico , Niño , Preescolar , Femenino , Glucocorticoides/uso terapéutico , Humanos , Lactante , Masculino , Recurrencia
3.
Isr Med Assoc J ; 23(10): 651-656, 2021 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-34672448

RESUMEN

BACKGROUND: Systemic sclerosis (SSc) is a connective tissue disease that may affect the heart and the autonomic nervous system (ANS). There is little knowledge regarding the degree of ANS involvement in SSc patients with unknown cardiac disease. OBJECTIVES: To evaluate cardiac and pupillary autonomic functions in patients before cardiac involvement has emerged. METHODS: The study comprised 19 patients with SSc and 29 healthy controls. Heart rate variability (HRV) analysis for time and frequency domains, as well as deep breathing test and Ewing maneuvers, were performed in all patients. Automated pupillometry for the evaluation of pupillary diameter and pupillary light reflex was completed in 8 SSc patients and 21 controls. RESULTS: Both groups had similar characteristics, except for medications that were more commonly or solely prescribed for SSc patients. Compared with control subjects, the SSc patients had significantly lower HRV parameters of NN50 (15.8 ± 24.4 vs. 33.9 ± 33.1, P = 0.03), pNN50 (4.9 ± 7.4% vs.10.8 ± 10.8%, P = 0.03), and triangular index (11.7 ± 3.4 vs. 15.7 ± 5.8, P = 0.02). Abnormal adaptive responses in heart rate changes were recorded during deep breathing tests and Ewing maneuvers. There was no significant difference in any of the pupillometric indices or other HRV parameters within groups. CONCLUSIONS: SSc patients may manifest cardiac autonomic dysfunction, while their autonomic pupillary function is seemingly spared. The role of certain medications, the significance of differential organ involvement, as well as the prognostic value of our findings should be evaluated in future studies.


Asunto(s)
Enfermedades del Sistema Nervioso Autónomo , Cardiopatías , Frecuencia Cardíaca , Trastornos de la Pupila , Reflejo Pupilar , Esclerodermia Sistémica , Adulto , Enfermedades del Sistema Nervioso Autónomo/diagnóstico , Enfermedades del Sistema Nervioso Autónomo/etiología , Enfermedades del Sistema Nervioso Autónomo/fisiopatología , Estudios de Casos y Controles , Electrocardiografía Ambulatoria/métodos , Femenino , Cardiopatías/diagnóstico , Cardiopatías/etiología , Humanos , Israel/epidemiología , Masculino , Examen Neurológico/métodos , Valor Predictivo de las Pruebas , Pronóstico , Trastornos de la Pupila/diagnóstico , Trastornos de la Pupila/etiología , Esclerodermia Sistémica/complicaciones , Esclerodermia Sistémica/diagnóstico , Esclerodermia Sistémica/fisiopatología
4.
Eur J Rheumatol ; 8(3): 144-149, 2021 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-33372887

RESUMEN

OBJECTIVE: Systemic sclerosis (SSc) is associated with increased cardiac morbidity and mortality. Whether some electrocardiographic markers of arrhythmias predispose to early cardiogenic death in SSc remains controversial. This study evaluated the occurrence of previously reported as well as unstudied markers of repolarization in patients with SSc and assessed their prognostic implications. METHODS: A total of 21 patients with SSc and 31 unaffected controls were included in this prospective study. Electrocardiograms were conducted under strict standards. Repolarization and dispersion parameters and markers of late ventricular potentials were determined using designated computer software. Results of multiple beats were averaged. RESULTS: There were no significant differences between the SSc and control groups in average QT intervals, average corrected QT intervals, average QT interval dispersion (QTd), average QT corrected dispersion (QTcd), and QT dispersion ratio. However, average QT apex dispersion, average JT dispersion, average JT corrected dispersion, and Tpeak-Tend corrected were significantly higher in patients with SSc than in controls. Late ventricular potentials were not found in patients with SSc or in controls. Increased QTd and QTcd were recorded in 1 patient who experienced ventricular arrhythmia before inclusion in the study. None of the remaining patients with SSc or the controls developed arrhythmia during the 9-year follow-up. CONCLUSION: Abnormal repolarization parameters may be observed in patients with SSc. However, their prognostic significance with regard to increased risk for repolarization-associated ventricular arrhythmias and increased cardiac death could not be determined in this study. Our findings endorse additional studies on this matter.

5.
Eur J Rheumatol ; 6(4): 179-183, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31657700

RESUMEN

OBJECTIVE: Systemic sclerosis (SSc) may affect the heart with microvascular dysfunction and lead to an early cardiac death, but the association between certain repolarization indexes and SSc heart disease remains controversial. Our goal was to evaluate a previously unstudied marker of repolarization dynamics, i.e., QT variability, in patients with SSc and to assess its prognostic implications. METHODS: A total of 17 patients with SSc and 21 healthy controls were included into this prospective study. Electrocardiograms were conducted under strict standards. The QT variability index (QTVI), normalized QT variability (QTVN), and power spectral analysis of QT dynamics, considered as markers of ventricular arrhythmias in a number of other disorders, were determined using designated computer software. RESULTS: There was no significant difference in demographic and cardiac important clinical parameters between the groups. Also, the mean QTVI, QTVN, and power spectral analysis parameters were comparable between the patients with SSc and control subjects. At baseline, the QTVI values of 1 patient with SSc, who experienced ventricular arrhythmia prior to inclusion in the study, were considerably higher compared to other patients with SSc. None of the remaining patients with SSc or the control subjects developed arrhythmia during the follow-up of 8 years. CONCLUSION: Higher than normal QTVI may be found in the minority of patients with SSc. The prognostic significance of this finding is unknown, but it may entail an increased risk of ventricular arrhythmias. Therefore, the value of QTVI as a tool for arrhythmia risk stratification in SSc merits further research.

6.
Mycoses ; 61(9): 639-645, 2018 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-29663565

RESUMEN

Invasive fungal infections (IFIs) postliver transplantation are a frequent cause of morbidity and mortality; however, studies reporting on these infections in the paediatric population are scarce. To investigate the incidence and risk factors of IFIs in paediatric liver transplant recipients during the early posttransplantation period (≤3 months). Data were collected for all paediatric liver transplant recipients registered in a national transplantation center from 2004 to 2014. Using a stepwise logistic regression to identify independent risk factors for IFIs, a predictive model was formulated. Ten IFIs were identified in 81 liver transplant recipients (12.3%) all occurring during the first month posttransplantation. Candida species were responsible for nine cases (90%), of which four were non-albicans Candida (44%). Significant risk factors were identified; recipient of multiple blood product transfusions during transplantation, prolonged use of indwelling intravenous catheter, prolonged IV antibiotic treatment, surgical complications, pulse steroid treatment and living donor liver transplantation. The predictive model used two clinical parameters to define high-risk patients: a living donor transplantation and duration of IV antibiotic treatment (area under the ROC curve 0.918). IFIs are a significant complication occurring in the first month posttransplantation. Future studies are required to assess efficacy of targeted antifungal prophylaxis in high risk patients.


Asunto(s)
Infecciones Fúngicas Invasoras/epidemiología , Trasplante de Hígado/efectos adversos , Receptores de Trasplantes , Adolescente , Niño , Preescolar , Femenino , Humanos , Incidencia , Lactante , Masculino , Curva ROC , Factores de Riesgo
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