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1.
Arch Intern Med ; 160(4): 494-500, 2000 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-10695689

RESUMO

BACKGROUND: There are scant data on the effect of body mass index (BMI) (calculated as weight in kilograms divided by the square of height in meters) on cardiovascular events and death in older patients with hypertension. OBJECTIVE: To determine if low body mass in older patients with hypertension confers an increased risk of death or stroke. PATIENTS: Participants were 3975 men and women (mean age, 71 years) enrolled in 17 US centers in the Systolic Hypertension in the Elderly Program trial, a randomized, double-blind, placebo-controlled clinical trial of lowdose antihypertensive therapy, with follow-up for 5 years. MAIN OUTCOME MEASURES: Five-year adjusted mortality and stroke rates from Cox proportional hazards analyses. RESULTS: There was no statistically significant relation of death or stroke with BMI in the placebo group (P = .47), and there was a U- or J-shaped relation in the treatment group. The J-shaped relation of death with BMI in the treated group (P = .03) showed that the lowest probability of death for men was associated with a BMI of 26.0 and for women with a BMI of 29.6; the curve was quite flat for women across a wide range of BMIs. For stroke, men and women did not differ, and the BMI nadir for both sexes combined was 29, with risk increasing steeply at BMIs below 24. Those in active treatment, however, had lower death and stroke rates compared with those taking placebo. CONCLUSIONS: Among older patients with hypertension, a wide range of BMIs was associated with a similar risk of death and stroke; a low BMI was associated with increased risk. Lean, older patients with hypertension in treatment should be monitored carefully for additional risk factors.


Assuntos
Índice de Massa Corporal , Hipertensão/complicações , Obesidade/complicações , Acidente Vascular Cerebral/mortalidade , Idoso , Idoso de 80 Anos ou mais , Anti-Hipertensivos/uso terapêutico , Método Duplo-Cego , Feminino , Humanos , Hipertensão/tratamento farmacológico , Hipertensão/etiologia , Hipertensão/fisiopatologia , Masculino , Pessoa de Meia-Idade , Modelos de Riscos Proporcionais , Risco , Fatores Sexuais , Acidente Vascular Cerebral/etiologia , Acidente Vascular Cerebral/prevenção & controle , Taxa de Sobrevida , Sístole , Estados Unidos/epidemiologia
2.
Arch Intern Med ; 154(19): 2154-60, 1994 Oct 10.
Artigo em Inglês | MEDLINE | ID: mdl-7944835

RESUMO

BACKGROUND: Little information has been published on the impact of antihypertensive medications on quality of life in older persons. Particular concern has existed that lowering systolic blood pressure in older persons might have adverse consequences on cognition, mood, or leisure activities. METHODS: A multicenter double-blind randomized controlled trial was conducted over an average of 5 years' followup involving 16 academic clinical trial clinics. Participants consisted of 4736 persons (1.06%) selected from 447,921 screenees aged 60 years and older. Systolic blood pressure at baseline ranged from 160 to 219 mm Hg, while diastolic blood pressure was less than 90 mm Hg. Participants were randomized to active antihypertensive drug therapy or matching placebo. Active treatment consisted of 12.5 to 25 mg of chlorthalidone for step 1, while step 2 consisted of 25 to 50 mg of atenolol. If atenolol was contraindicated, 0.05 to 0.10 mg of reserpine could be used for the second-step drug. The impact of drug treatment on measures of cognitive, emotional, and physical function and leisure activities was assessed. RESULTS: Our analyses demonstrate that active treatment of isolated systolic hypertension in the Systolic Hypertension in the Elderly Program cohort had no measured negative effects and, for some measures, a slight positive effect on cognitive, physical, and leisure function. The positive findings in favor of the treatment group were small. There was no effect on measures related to emotional state. Measures of cognitive and emotional function were stable in both groups for the duration of the study. Both treatment groups showed a modest trend toward deterioration of some measures of physical and leisure function over the study period. CONCLUSIONS: The overall study cohort exhibited decline over time in activities of daily living, particularly the more strenuous ones, and some decline in certain leisure activities. However, mood, cognitive function, basic self-care, and moderate leisure activity were remarkably stable for both the active and the placebo groups throughout the entire study. Results of this study support the inference that medical treatment of isolated systolic hypertension does not cause deterioration in measures of cognition, emotional state, physical function, or leisure activities.


Assuntos
Atenolol/efeitos adversos , Clortalidona/efeitos adversos , Transtornos Cognitivos/induzido quimicamente , Transtorno Depressivo/induzido quimicamente , Hipertensão/tratamento farmacológico , Atividades de Lazer , Qualidade de Vida , Reserpina/efeitos adversos , Atividades Cotidianas , Idoso , Idoso de 80 Anos ou mais , Transtornos Cerebrovasculares/epidemiologia , Transtornos Cerebrovasculares/etiologia , Transtornos Cognitivos/epidemiologia , Transtorno Depressivo/epidemiologia , Método Duplo-Cego , Feminino , Seguimentos , Humanos , Hipertensão/complicações , Hipertensão/psicologia , Masculino , Pessoa de Meia-Idade , Autocuidado , Sístole
4.
J Hypertens Suppl ; 2(3): S197-9, 1984 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-6152782

RESUMO

In the 1950s, 223 white patients had varyingly severe hypertension controlled in hospital with ganglioplegic agent and hydralazine. At home, each was instructed to take and record his/her blood pressure (BP) four or five times per day and to bring all BP records to the next treatment visit. Our file of home BP records exactly one year after treatment began was used to divide the patients into: non-compliant; compliant but uncontrolled; controlled. There were 56 non-compliant, 60 compliant but uncontrolled, and 107 controlled patients. Their respective median survival times after beginning therapy were 56.5, 134, and 153 months. Thus, survival was a strong function of compliance and a significant but weaker function of control. The non-compliant quarter of the group survived an average of less than five years, while the controlled half survived an average of more than 12 years.


Assuntos
Hipertensão/mortalidade , Cooperação do Paciente , Determinação da Pressão Arterial , Feminino , Seguimentos , Bloqueadores Ganglionares/uso terapêutico , Humanos , Hidralazina/uso terapêutico , Hipertensão/tratamento farmacológico , Masculino , Pessoa de Meia-Idade , Missouri , Autocuidado , Fatores de Tempo
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