De l’intérêt de la corticothérapie nasale dans la rhinite allergique de l’enfant

Glucocorticosteroids are the most powerful anti-inflammatory medications available and, since the 70s, their local application has become an essential element in the treatment of allergic rhinitis. Thanks to an increased efficacy, a lower biodistribution and a better tolerability, the modern molecules are not only more and more proposed as first choice in adults, but they also find their place in the treatment of allergic children. However, following different reports, some caution must be taken in daily practice. Finally, guidelines for the treatment of allergic rhinitis have been recently published in order to standardize the management of allergic rhinitis and to specify the place of each therapeutic option.     

L’hypo-albuminémie contribue-t-elle à l’aggravation de l’insuffisance cardiaque ?

BackgroundHypoalbuminemia has now emerged as a powerful prognosticator in heart failure regardless of age, clinical presentation, left ventricular ejection fraction and usual prognostic markers. Growing evidence is that this prognostic value persists after adjusting for causative factors for hypoalbuminemia such as malnutrition, inflammation and liver dysfunction.ObjectiveTo address the prognostic relevance of hypoalbuminemia in frail elderly patients with well-characterized cardiogenic pulmonary edema at high risk for adverse outcome, beyond causative factors for low serum albumin levels. Serum albumin was measured after clinical stabilization to avoid hypervolemia.ResultsIn all, 67 patients with a mean age of 86 years were included. Hospital mortality was 30%. Patients who died and who survived were similar in age, ejection fraction, BNP concentration, serum creatinine, serum hemoglobin, total bilirubin and prealbumin. Patients who died had lower serum albumin levels (P < 0.001), higher blood urea nitrogen (P = 0.03) and higher C-reactive protein (P = 0.02). In multivariate analysis, serum albumin was the sole independent predictor of hospital death (P < 0.01), after adjusting for malnutrition (prealbumin P = ns), inflammation (C-reactive protein P = ns) and liver dysfunction (total bilirubin P = ns).ConclusionSerum albumin is a powerful prognosticator in frail elderly patients with acute cardiogenic pulmonary edema even after adjusting for main causative factors. These results suggest that hypoalbuminemia may contribute to the worsening of heart failure given the physiological properties of serum albumin that includes antioxidant activity and plasma colloid osmotic pressure action. Further studies are critically needed to address the relevance of prevention and correction of hypoalbuminemia in heart failure.     

Maladie de Gaucher de type 1 simulant une thrombopénie immunologique : intérêt de l’hyperferritinémie et de l’hypergammaglobulinémie dans le bilan d’une thrombopénie isolée

IntroductionGaucher disease type 1 is a rare genetic disease. It can cause thrombocytopenia. Current guidelines do not support bone marrow examination in front of isolated thrombocytopenia if no evidence suggests malignant hemopathy. This strategy aiming at sparing unnecessary investigations makes such rare diseases more difficult to diagnose.Case reportA 31-year-old woman was diagnosed with immune thrombocytopenia according to current guidelines. She presented later with mild splenomegaly. Bone marrow aspirate smears showed Gaucher cells. Gaucher disease was then confirmed. Looking backward, initial biological clues (hyperferritinemia, hypergammaglobulinemia) should have enabled to consider the diagnosis.ConclusionGaucher disease type 1 can be responsible for apparently isolated thrombocytopenia. The disease must be looked for if the thrombocytopenia is associated with unexplained hypergammaglobulinemia or hyperferritinemia. Diagnosing immune thrombocytopenia without bone marrow sample requires to systematically pay attention to any clinical or biological abnormality, not to ignore rare differential diagnoses.     

Les tests cutanés dans l’exploration de l’allergie à la pénicilline

Allergy to penicillin is reported to occur in up to 8% of the patients who receive this class of drugs. 80 to 85% of the patients with a positive clinical history to penicillin will nevertheless tolerate penicillin with no adverse effect. Of the remaining 15 to 20%, only a few will develop a severe adverse reaction, and these patients can be identified by skin tests with derivatives of penicillin used at optimal concentrations according to a protocol that is effective and safe. Skin tests to penicillin are positive in 25% of patients with a history of an immediate reaction to penicillin; they are more frequently positive in those who have had a severe reaction. In addition to being able to identify patients who are at risk for a severe reaction when they take penicillin, skin tests can also provide immunological evidence of the origin of delayed clinical reactions such as maculopapular rashes. Such rashes, a frequent and benign manifestation of penicillin allergy, are usually caused by the widely used aminopenicillins. Intradermal skin tests (IDR) and late phase (patch) tests can demonstrate allergy to betalactamines in 5 to 45% of patients with negative skin tests to major and minor determinants of penicillin. When skin tests are positive, provocation tests are not recommended. On the other hand, when the skin tests are negative, an oral provocation test should be done, but such tests can result in an immediate clinical reaction, which may be severe in 3 to 10% of cases.     

Diagnostic et prise en charge de l’anémie hémolytique auto-immune à l’exclusion des formes secondaires à une cause néoplasique. Adéquation de la prise en charge au PNDS octobre 2009

Objectives

Describe the management of Acquired Immune Haemolytic Anaemia (AIHA) and correlate with the current guidelines published in 2009. The secondary objective was to calculate the positive predictive value of the Direct Antiglobulin Test (DAT) for the diagnosis of AIHA.

Dépistage opportuniste de l’anévrysme de l’aorte abdominale lors de l’échocardiographie chez le patient coronarien : utile ou futile ?

Abdominal aortic aneurysm is a chronic degenerative disease that is usually silent until rupture occurs and this complication is still associated in contemporary era with a high rate of mortality. Screening programmes for abdominal aortic aneurysm have been shown to be effective in reducing global mortality in the screened population but these programmes are poorly implemented in the Western countries. As coronary artery disease and abdominal aorta aneurysmal disease share many risk factors, the cardiologist is centrally positioned in the screening strategy, not only to identify patients with higher risk of developing abdominal aortic aneurysm, but also to perform an opportunistic screening during echocardiography. This paper summarises evidence about the feasibility, indications, modalities, benefits and risks related to the opportunistic screening for abdominal aortic aneurysm during echocardiography with a particular emphasis on the population of patients with coronary artery disease.