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2.
J Toxicol Clin Toxicol ; 22(2): 177-85, 1984.
Article in English | MEDLINE | ID: mdl-6502789

ABSTRACT

Forty-five cases of ciguatera poisoning in Puerto Rico (P.R.) are described. These cases represent all those reported to the P.R. Poison Control Center in 1982. Most of the cases were reported in the spring and summer months. The most common fish ingested was the grouper. The clinical presentation of acute and long term symptoms was similar to that reported in other geographical areas, except the incidence of paresthesias. Paresthesias were reported in 11% of the patients reported to the poison center. A companion telephone survey indicated that persons in P.R. that do not eat fish do so because of fear of ingesting the toxin. Our findings indicate an overall familial contact with the ciguatera toxin in Puerto Rico at 7%. This study is the first to document that ciguatera is a common poisoning reported to the Poison Control Center in Puerto Rico. Our findings also support other authors contentions of geographical variations in clinical symptomatology.


Subject(s)
Ciguatera Poisoning , Gastroenteritis/chemically induced , Marine Toxins/poisoning , Adolescent , Adult , Animals , Attitude to Health , Child , Epidemiologic Methods , Feeding Behavior , Female , Fishes, Poisonous , Gastroenteritis/epidemiology , Gastroenteritis/physiopathology , Humans , Male , Middle Aged , Poison Control Centers , Puerto Rico , Seasons
3.
Bol. Asoc. Méd. P. R ; Bol. Asoc. Méd. P. R;76(4): 151-6, 1984.
Article in English | LILACS | ID: lil-20972
10.
s.l; s.n; 1980. 4 p.
Non-conventional in English | Sec. Est. Saúde SP, HANSEN, Hanseníase Leprosy, SESSP-ILSLACERVO, Sec. Est. Saúde SP | ID: biblio-1240699

ABSTRACT

Before 1950 no reliable or safe therapy existed for systemic and invasive mycoses, and only traditional and empirical topical preparations were available for dermatomycoses. Two distinct eras of rapid progress in antifungal therapy followed: first, in the 1950's came the introduction of the polyenes, nystatin and pimaricin for cutaneous, vaginal and intestinal candidiasis, and amphotericin B for the treatment of severe systemic mycoses. The second phase saw the successful introduction and clinical use of 5-fluorocytosine and several imidazole derivatives some twenty years later, at a time when the vast increase in iatrogenic systemic mycoses caused by opportunistic fungi had created an urgent and pressing need for new agents in addition to those still effective.


Subject(s)
Humans , Amphotericin B/therapeutic use , Antifungal Agents/therapeutic use , Blastomycosis/drug therapy , Candidiasis/drug therapy , Flucytosine/therapeutic use , Imidazoles/therapeutic use , Mycoses/drug therapy , Natamycin/therapeutic use , Nystatin/therapeutic use , Polyenes/therapeutic use
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