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1.
Cancer ; 116(17): 4197-205, 2010 Sep 01.
Article in English | MEDLINE | ID: mdl-20533566

ABSTRACT

BACKGROUND: The use of central venous catheters (CVCs) has greatly improved the quality of care in children with cancer, yet these catheters may cause serious infectious and thrombotic complications. The aim of this prospective registry study was to assess the host and CVC-related risk factors for CVC-created thrombotic complications. METHODS: Patients undergoing CVC insertion for chemotherapy were followed prospectively for CVC complications. At the time of enrollment, demographic, clinical, and CVC-related data, and family history of thrombosis were collected. Survival and Cox regression analyses were performed. RESULTS: A total of 423 CVCs were inserted into 262 patients for a total of 76,540 catheter days. The incidence of CVC-related deep-vein thrombosis (DVT) was 0.13 per 1000 catheter-days (95% confidence interval [CI], 0.06-0.24). Insertion of peripherally inserted central catheters (PICCs) and insertion in an angiography suite significantly increased the risk of symptomatic CVC-related DVT. The incidence of CVC occlusion was 1.35 per 1000 catheter-days (95% CI, 1.1-1.63). Positive family history of thrombosis significantly increased the risk of CVC occlusion (hazard ratio [HR], 2.16; 95% CI, 1.2-3.8). The CVC-related risk factors were insertion of Hickman catheters, insertion in angiography suite, and proximal-tip location. Patients developing at least 1 episode of both CVC occlusion and infection had an increased risk for developing symptomatic CVC-related DVT (HR, 4.15; 95% CI, 1.2-14.4). CONCLUSIONS: Both patient-related and CVC-related factors are associated with higher risk of symptomatic thrombotic complications. These risk factors could be used in the clinical setting and in developing future studies for CVC thromboprophylaxis.


Subject(s)
Antineoplastic Agents/administration & dosage , Catheterization, Central Venous/adverse effects , Neoplasms/complications , Thrombosis/epidemiology , Adolescent , Catheterization, Central Venous/instrumentation , Child , Child, Preschool , Humans , Infant , Neoplasms/drug therapy , Risk Factors , Thrombosis/etiology
2.
Eur J Clin Microbiol Infect Dis ; 25(4): 247-53, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16511679

ABSTRACT

Exserohilum is a dematiaceous fungus that may cause a spectrum of diseases in humans, including skin and corneal infection, invasive disease, and allergic fungal sinusitis. The aim of this work is to describe two new cases of Exserohilum infection and to review the literature. The review yielded 33 cases of Exserohilum infection, of which 23 were reported since 1993. Most occurred in regions with hot climates, such as India, Israel, and the southern USA. Impaired immunity was present in the majority of patients with invasive and skin infections, whereas local trauma and atopy were the predisposing factors in those with corneal infections and allergic fungal sinusitis, respectively. Surgical debridement was the principal mode of therapy for allergic fungal sinusitis. Amphotericin B was the initial single antifungal agent used in all cases of invasive disease; the response rate was low but improved with the addition of triazole agents. Outcome appeared to be better than for other mold infections and depended mainly on the underlying diseases.


Subject(s)
Ascomycota/pathogenicity , Mycoses/diagnosis , Mycoses/microbiology , Adolescent , Adult , Amphotericin B/therapeutic use , Antifungal Agents/therapeutic use , Ascomycota/cytology , Ascomycota/isolation & purification , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Mycoses/epidemiology , Mycoses/therapy , Nasal Mucosa/microbiology , Nasal Mucosa/pathology , Treatment Outcome
3.
Rheumatology (Oxford) ; 40(5): 585-7, 2001 May.
Article in English | MEDLINE | ID: mdl-11371671

ABSTRACT

Lupus anticoagulants are closely related to systemic lupus erythemathosus (SLE) and to thrombotic events. We describe a 12 year-old girl with a bilateral intramuscular haemorrhage of the gastrocnemius muscles as her main initial presentation of juvenile SLE. Laboratory work-up revealed lupus anticoagulant-hypoprothrombinaemia syndrome (LAHS) with very low levels of factor II due to autoantibodies. She showed a good initial clinical and laboratory response to prednisone therapy, however steroid dependency developed. To the best of our knowledge, this is the first case reported of juvenile SLE presenting with LAHS.


Subject(s)
Hemorrhage/etiology , Lupus Coagulation Inhibitor/analysis , Lupus Erythematosus, Systemic/complications , Lupus Erythematosus, Systemic/diagnosis , Muscle, Skeletal/pathology , Antiphospholipid Syndrome/diagnosis , Child , Diagnosis, Differential , Female , Humans , Lupus Erythematosus, Systemic/drug therapy , Magnetic Resonance Imaging , Prednisone/therapeutic use , Syndrome
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