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4.
Harefuah ; 140(6): 471-2, 567, 2001 Jun.
Article in Hebrew | MEDLINE | ID: mdl-11420842

ABSTRACT

We report a case of a 22 year old man with a history of bronchial asthma, suffering from diarrhea, eosinophilic ascites and prominent blood and bone marrow eosinophilia. The patient responded to corticosteroid treatment. Later, hydroxyurea was added to this treatment because of recurrence of eosinophilia, ascites and hepatosplenomegaly. Eosinophilic ascites is rarely the outstanding symptom of the hypereosinophilic syndrome. Following the exclusion of other reasons for eosinophilia, concomitant unexplained hepatosplenomegaly suggested the diagnosis of a hyperereosinophilic syndrome.


Subject(s)
Ascitic Fluid/etiology , Eosinophilia/etiology , Hypereosinophilic Syndrome/diagnosis , Hypereosinophilic Syndrome/drug therapy , Adult , Asthma/complications , Asthma/physiopathology , Diagnosis, Differential , Humans , Hydroxyurea/therapeutic use , Male
6.
Harefuah ; 136(11): 857-9, 915, 1999 Jun 01.
Article in Hebrew | MEDLINE | ID: mdl-10955129

ABSTRACT

Paroxysmal atrial fibrillation (AF), a frequent cause of repeated hospitalization, is effectively treated with propafenone. The time to conversion to sinus rhythm is a consideration when managing AF in the emergency room. We investigated the conversion rates of paroxysmal AF by 3 different oral propafenone (P) regimens, in terms of time to conversion. 188 patients with onset of AF within 48 hours were treated with propafenone (P): 48 received 600 mg as a first oral dose followed after 8 hrs by 150 mg (Group A); 82 received 300 mg as a first dose, followed by the same dose 3 and again 8 hrs later (B); 58 received 150 mg every 3 hrs, up to a total dose of 600 mg (C). P was stopped when sinus rhythm was achieved. Rates of conversion to sinus rhythm after 3 hrs in the 3 groups were: 46%, 41% and 26% respectively; after 8 hrs: 77%, 78% and 70%; and after 12 hrs: 81%, 84% and 76%. Treatment was discontinued in 8. There was excessive QRS widening (> 25% of the basal value) in 1 in group A, 1 in group B and 2 in group C; wide-QRS tachycardia occurred in 4 in group B. In Group A there was a higher rate of early successful conversion, with a lower incidence of side-effects than with the other regimens.


Subject(s)
Anti-Arrhythmia Agents/therapeutic use , Atrial Fibrillation/drug therapy , Propafenone/therapeutic use , Administration, Oral , Anti-Arrhythmia Agents/administration & dosage , Atrial Fibrillation/physiopathology , Emergency Medical Services , Female , Humans , Male , Middle Aged , Propafenone/administration & dosage , Time Factors
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