Table 1 Characteristics of studies in the chronic heart failure population
StudyPopulationP‡Patient characteristicsNo of patients (no of events)Mean (SD) follow-up (years)Mean (SD) SBP(mm Hg)NYHA classMean (SD) EFMean ageMale(%)Aetiology (%)β‡A‡C‡D‡Hazard ratio for death
Lee 20065DIG database; RCTNoPatients with stable HF and normal sinus rhythm5747 (2066)3.2Not recordedII (64%) III (36%)28 (9)6377Ischaemic (72) Hypertensive (8) Valvular (2) Idiopathic (19) Alcoholic (3)U95U810.89 (0.86 to 0.91) per 10 mm Hg increase
Davos 200312589 Consecutive patients presenting to HF clinicYesDiagnosis of HF on clinical and echo/RV diagnosis589 (208)4.4 (2.1)122.9 (34.8)I (101) II (230) III(152) IV(42)30.9 (0.73)6588Not recorded748.516.284.60.99 (0.98 to 0.99) per 1 mm Hg increase
Robbins 199913Consecutive patients with HF referred for metabolic stress testingYesPatients 18–70 with chronic HF under evaluation for heart transplantation. Exclusion criteria—β blocker or IV ionotropes470 (71)1.5111 (18)Not recorded20 (27)527147 CAD086U791.4 (1.06 to 1.85) per 18 mm Hg decrease
Huynh 200614RCTYesPatients >70 years old. recently discharged with HF with ⩾1 risk factors for early hospital readmission282 (269)14158 (52)2.4 (1.0)42.5 (19.1)7936Ischaemic (56)116441841.0 (0.99 to 1.0) per 1 mm Hg increase
Koike 200015Consecutive patients with cardiac disease referred for CPXYesConsecutive patients with known cardiac disease. Exclusion criteria—UA, MI within 1 month, documented lung or cerebrovascular disease249 (29)9.1 (1.7)140 (24)I (46) II (45) III (9)Not recorded5660IHD (34) Valvular (24) Hypertensive (23) Other (19)UUUU1.01 (0.99 to 1.023) per 1 mm Hg decrease
Rickli 200316Consecutive patients referred to HF clinicYesHF with LVEF <40 and able to perform a CPX test202 (44)2.4 (1.7)103 (17)I (7) II (101) III (90) IV (4)28 (7)5286CAD (53) DCM (34) Valvular (2) Hypertension (2) Other or combined (9)4599†U900.8 (0.65 to 0.98) per 10 mm Hg increase
Cicoira 200117Consecutive patients referred to heart failure clinicYesAge >70 with a history of dyspnoea and symptomatic exercise tolerance. Optimised medical regimen188 (61)1.5 (0.6)133 (22)Mean 2.3 (0.8)38 (17) (n = 105)7771Ischaemic (66) IDCM (14) Valvular (7) Restrictive (5) HCM (2)1585U720.98 (0.96 to 0.99) per 1 mm Hg increase
Terrovitis 200618RCTYesNYHA class II–IV, LVEF ⩽35% on radionuclide ventriculography160 (55)2114 (18)I (6) III (45) III (42) IV (7)20 (9)560.85Ischaemic (46) Non-ischaemic (54)28UU910.98 (0.96 to 0.99) per 1 mm Hg increase
Pousset 200019RCTYesClinically stable CHF, LVEF <45% with at least 1 month on constant treatment. Exclusions—MI in past 3 months117 (14)0.64 (0.38)123 (23)I (7) II (62) III (25) IV (6)28 (10)5579IDCM (64) CAD (28) Anthracycline induced (3) Hypertension (3) Valvular (3)1791U820.35 (0.18 to 0.69) per 23 mm Hg increase
Walsh 199720Patients enrolled in clinical trials of heart failure drugsYesSymptomatic HF for at least 2 months with cardiomegaly on CXR. LVEF <35 or an increase in LVEDV >5.5 and fractional shortening <30%84 (43)1.9120* (94–180)II (56) III (44)Not recorded64*88CAD (65) Non-ischaemic cardiomyopathy (35)U23U1000.97 (0.96 to 0.98) per 1 mm Hg increase
  • *Median (range); †99% were receiving ACE inhibitors or angiotensin receptor blockers; ‡A, ACEi; β, β blockers; C, CCB; D, diuretics; P, prospective.

  • ACEi, angiotensin converting enzyme inhibitors; CAD, coronary artery disease; CPX, cardiopulmonary exercise test; CCB, calcium channel blockers; CHF, chronic heart failure; DCM, dilated cardiomyopathy; EF, ejection fraction; HCM, hypertrophic cardiomyopathy; HF, heart failure; IDCM, ischaemic dilated cardiomyopathy; IHD, ischaemic heart disease; IV, intravenous; LVEDV, left ventricular end-diastolic volume; LVEF, left ventricular ejection fraction; MI, myocardial infarction; NYHA, New York Heart Association; RCT, randomised control trial; RV, radionucleotide ventriculography; SBP, systolic blood pressure; U, unknown value (data not recorded in original study); UA, unstable angina.