CLINICAL AND ECHOCARDIOGRAPHIC DISEASE IN PATIENTS STARTING END-STAGE RENAL-DISEASE THERAPY

被引:1076
|
作者
FOLEY, RN
PARFREY, PS
HARNETT, JD
KENT, GM
MARTIN, CJ
MURRAY, DC
BARRE, PE
机构
[1] MEM UNIV NEWFOUNDLAND,HLTH SCI CTR,DIV NEPHROL,ST JOHNS,NF A1B 3V6,CANADA
[2] SALVAT ARMY GRACE GEN HOSP,DIV NEPHROL,ST JOHNS,NF,CANADA
[3] MCGILL UNIV,ROYAL VICTORIA HOSP,DIV NEPHROL,MONTREAL,PQ H3A 1A1,CANADA
关键词
D O I
10.1038/ki.1995.22
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
End-stage renal disease (ESRD) patients have a high cardiovascular mortality rate. Precise estimates of the prevalence, risk factors and prognosis of different manifestations of cardiac disease are unavailable. In this study a prospective cohort of 433 ESRD patients was followed from the start of ESRD therapy for a mean of 41 months. Baseline clinical assessment and echocardiography were performed on all patients. The major outcome measure was death while on dialysis therapy. Clinical manifestations of cardiovascular disease were highly prevalent at the start of ESRD therapy: 14% had coronary artery disease, 19% angina pectoris, 31% cardiac failure, 7% dysrhythmia and 8% peripheral vascular disease. On echocardiography 15% had systolic dysfunction, 32% left ventricular dilatation and 74% left ventricular hypertrophy. The overall median survival time was 50 months. Age, diabetes mellitus, cardiac failure, peripheral vascular disease and systolic dysfunction independently predicted death in all time frames. Coronary artery disease was associated with a worse prognosis in patients with cardiac failure at baseline. High left ventricular cavity volume and mass index were independently associated with death after two years. The independent associations of the different echocardiographic abnormalities were: systolic dysfunction-older age and coronary artery disease; left ventricular dilatation-male gender, anemia, hypocalcemia and hyperphosphatemia; left ventricular hypertrophy-older age, female gender, wide arterial pulse pressure, low blood urea and hypoalbuminemia. We conclude that clinical and echocardiographic cardiovascular disease are already present in a very high proportion of patients starting ESRD therapy and are independent mortality factors.
引用
收藏
页码:186 / 192
页数:7
相关论文
共 50 条
  • [31] TREATMENT OF END-STAGE RENAL-DISEASE
    VELEZ, R
    CHARLTON, J
    HELLER, R
    NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (06): : 356 - 357
  • [32] END-STAGE RENAL-DISEASE DIALYSIS
    KEMPH, JP
    PSYCHIATRIC CLINICS OF NORTH AMERICA, 1982, 5 (02) : 407 - 417
  • [33] HISPANICS WITH END-STAGE RENAL-DISEASE
    RADECKI, SE
    NISSENSON, AR
    ANNALS OF INTERNAL MEDICINE, 1994, 121 (09) : 723 - 724
  • [34] MALIGNANCY IN END-STAGE RENAL-DISEASE
    SLIFKIN, RF
    GOLDBERG, J
    NEFF, MS
    BAEZ, A
    MATTOO, N
    GUPTA, S
    TRANSACTIONS AMERICAN SOCIETY FOR ARTIFICIAL INTERNAL ORGANS, 1977, 23 : 34 - 40
  • [35] PHARMACODYNAMICS OF ZIDOVUDINE IN PATIENTS WITH END-STAGE RENAL-DISEASE
    PAOLI, I
    DAVE, M
    COHEN, BD
    NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (12): : 839 - 840
  • [36] CARDIAC OPERATIONS IN PATIENTS WITH END-STAGE RENAL-DISEASE
    KAUL, TK
    FIELDS, BL
    REDDY, MA
    KAHN, DR
    ANNALS OF THORACIC SURGERY, 1994, 57 (03): : 691 - 696
  • [37] NITRENDIPINE IN PATIENTS WITH END-STAGE RENAL-DISEASE AND HYPERTENSION
    BAMBAUER, R
    JUTZLER, GA
    WEBER, U
    WALTER, R
    KELLER, HE
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1988, 12 : S133 - S135
  • [38] EXERCISE TOLERANCE OF END-STAGE RENAL-DISEASE PATIENTS
    SAGIV, M
    RUDOY, J
    ROTSTEIN, A
    FISHER, N
    BENARI, J
    NEPHRON, 1991, 57 (04): : 424 - 427
  • [39] SILICONE SENSITIZATION IN PATIENTS WITH END-STAGE RENAL-DISEASE
    ACCHIARDO, SR
    SMALLEY, DL
    SHAKLIN, DR
    BURK, L
    SMITH, SJ
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1994, 5 (03): : 430 - 430
  • [40] BIOAVAILABILITY OF LABETALOL IN PATIENTS WITH END-STAGE RENAL-DISEASE
    LUKE, DR
    AWNI, WM
    HALSTENSON, CE
    OPSAHL, JA
    MATZKE, GR
    THERAPEUTIC DRUG MONITORING, 1992, 14 (03) : 203 - 208