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1.
J Infect Chemother ; 19(1): 20-3, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22740189

RESUMO

Malaria is one of the most common and serious infectious diseases in the tropics and subtropics. For high-risk travelers to endemic regions, malaria chemoprophylaxis is recommended. Internationally, atovaquone-proguanil (A/P), mefloquine (MEF), or doxycycline (DOX) are the prescribed malaria chemoprophylactic drugs. However, A/P and DOX are not approved in Japan. Therefore, the data on A/P for malaria chemoprophylaxis in Japanese travelers are not clear. We analyzed questionnaire survey data obtained in Hibiya Clinic to assess the safety and tolerability of A/P and compare them with those of MEF for non-immune Japanese travelers. A/P was given to 278 travelers and MEF to 38 travelers. The mean duration of each prophylaxis is for 20.0 ± 9.6 and 59.0 ± 15.9 days, respectively. Nine travelers discontinued prophylaxis: 5 in the A/P prescribed group (A/P group) and 4 in the MEF prescribed group (MEF group), and the rate of discontinuation was significantly less in the A/P group. The frequency of adverse events was significantly less in the A/P group than in the MEF group [52 cases (18.8 %) vs. 14 cases (36.8 %), respectively]. In particular, the frequency of psychoneurotic adverse events was significantly less in the A/P group. These results suggest that A/P is better tolerated and has fewer adverse events than MEF in non-immune Japanese travelers.


Assuntos
Antimaláricos/uso terapêutico , Atovaquona/uso terapêutico , Malária/prevenção & controle , Mefloquina/uso terapêutico , Proguanil/uso terapêutico , Viagem , Adolescente , Adulto , Idoso , Antimaláricos/efeitos adversos , Atovaquona/efeitos adversos , Quimioprevenção , Criança , Combinação de Medicamentos , Feminino , Humanos , Japão , Masculino , Mefloquina/efeitos adversos , Pessoa de Meia-Idade , Proguanil/efeitos adversos , Inquéritos e Questionários , Adulto Jovem
2.
Clin Exp Hypertens ; 35(8): 582-8, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23496265

RESUMO

BACKGROUND: This 12-month study compared the effects of a combination of losartan 50 mg and hydrochlorothiazide 12.5 mg with a maximum dose of losartan (100 mg) in hypertensive patients with diabetes. METHODS: This was a multicenter randomized open-label study. RESULTS: A similar reduction in systolic/diastolic blood pressure from baseline to month 3 was observed in both groups. There was also a similar decrease in UACR in both groups. A significant decrease in uric acid was observed in the maximum-dose group only. eGFR decreased in the combination group after 1 year. CONCLUSIONS: The combination of losartan and a diuretic may be a useful option in such hypertensive patients with diabetes, provided that metabolic parameters are closely monitored. In patients with hyperuricemia and impaired renal function, a maximum dose of losartan may be more beneficial.


Assuntos
Anti-Hipertensivos/uso terapêutico , Diabetes Mellitus Tipo 2/complicações , Hidroclorotiazida/uso terapêutico , Hipertensão/tratamento farmacológico , Losartan/uso terapêutico , Idoso , Albuminúria/complicações , Relação Dose-Resposta a Droga , Quimioterapia Combinada , Feminino , Humanos , Hipertensão/complicações , Hiperuricemia/complicações , Masculino , Pessoa de Meia-Idade , Insuficiência Renal Crônica/complicações , Resultado do Tratamento , Ácido Úrico/sangue
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