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. 2019 Nov 12;8(22):e012655. doi: 10.1161/JAHA.119.012655

Table 1.

Baseline Patient Demographics, Clinical Characteristics, and Clinical Histories of the CKD and HF Cohorts Stratified by the RAASi Dose Achieved During the Majority of Patients’ Follow‐Up Period

Variable CKD Cohort HF Cohort
RAASi Dose Achieved During the Majority (≥75%) of Follow‐Up RAASi Dose Achieved During the Majority (≥75%) of Follow‐Up
Non‐RAASi (n=71 008) <50% of ESC‐Recommended Dose (n=27 935)a ≥50% of ESC‐Recommended Dose (n=26 596)a P Value (ANOVA/χ2) Non‐RAASi (n=6063) <50% of ESC‐Recommended Dose (n=4568)a ≥50% of ESC‐Recommended Dose (n=2758)a P Value (ANOVA/χ2)
Baselineb patient demographics and clinical characteristics
Age, y, mean (SD) 71.77 (14.20) 74.84 (10.79) 71.43 (10.36) <0.01c 74.97 (15.83) 75.5 (12.48) 68.93 (12.74) <0.01c
Female 46 320 (65.22) 16 492 (59.04) 14 776 (55.56) <0.01c 3007 (49.59) 2015 (44.11) 906 (32.85) <0.01c
Current smoker 10 599 (14.92) 3681 (13.18) 3705 (13.93) <0.01c 702 (11.58) 807 (17.67) 582 (21.10) <0.01c
BMI, kg/m2, mean (SD) 27.02 (5.59) 28.28 (5.69) 29.80 (5.88) <0.01c 26.49 (6.90) 27.49 (6.42) 29.73 (6.66) <0.01c
SBP, mm Hg, mean (SD) 134.33 (18.36) 138.58 (19.92) 143.45 (19.90) <0.01c 128.17 (20.75) 125.91 (20.70) 132.98 (21.92) <0.01c
eGFR, mL/min/1.73 m2, mean (SD) 51.43 (8.47) 51.23 (10.45) 51.98 (8.65) <0.01c 63.38 (19.52) 64.7 (17.74) 67.75 (15.40) <0.01c
Serum potassium, mEq/L, mean (SD) 4.44 (0.53) 4.49 (0.52) 4.49 (0.51) <0.01c 4.28 (0.60) 4.42 (0.55) 4.42 (0.51) <0.01c
Serum phosphorus, mEq/L, mean (SD) 1.14 (1.00) 1.15 (1.59) 1.11 (0.20) 0.18 1.17 (0.26) 1.16 (0.23) 1.15 (0.21) 0.46
Clinical history within 5 y before initial CKD/HF diagnosis
Diabetes mellitus 5234 (7.37) 4410 (15.79) 5843 (21.97) <0.01c 715 (11.79) 637 (13.94) 524 (19.00) <0.01c
MI 872 (1.23) 1467 (5.25) 1090 (4.10) <0.01c 234 (3.86) 532 (11.65) 388 (14.07) <0.01c
PVD 1059 (1.49) 749 (2.68) 771 (2.90) <0.01c 121 (2.00) 159 (3.48) 83 (3.01) <0.01c
Stroke 3835 (5.40) 1817 (6.50) 1426 (5.36) <0.01c 352 (5.80) 329 (7.20) 135 (4.89) 0.01c
Arrhythmia 4315 (6.08) 2663 (9.53) 2020 (7.60) <0.01c 830 (13.69) 1144 (25.04) 651 (23.60) <0.01c
CPD 6199 (8.73) 2818 (10.09) 2526 (9.50) <0.01c 562 (9.27) 721 (15.78) 398 (14.43) <0.01c
Metastatic tumor 1640 (2.31) 599 (2.14) 508 (1.91) <0.01c 89 (1.47) 93 (2.04) 50 (1.81) 0.08
Rheumatic disease 2307 (3.25) 942 (3.37) 732 (2.75) <0.01c 126 (2.08) 135 (2.96) 68 (2.47) 0.02c
Peptic ulcer 568 (0.80) 239 (0.86) 211 (0.79) 0.64 55 (0.91) 54 (1.18) 23 (0.83) 0.24
Cancer 7074 (9.96) 2513 (9.00) 2068 (7.78) <0.01c 516 (8.51) 527 (11.54) 220 (7.98) <0.01c
Baselineb medication usage
β‐Blockers 11 332 (15.96) 8737 (31.28) 8864 (33.33) <0.01c 999 (16.47) 2636 (57.71) 1877 (68.06) <0.01c
Statins 19 163 (26.98) 15 562 (55.71) 15 734 (59.16) <0.01c 1040 (17.15) 2354 (51.53) 1731 (62.76) <0.01c
Bronchodilators 7329 (10.32) 3377 (12.09) 2608 (9.81) <0.01c 727 (11.99) 960 (21.02) 474 (17.19) <0.01c
Diuretics 16 736 (23.57) 12 911 (46.22) 13 998 (52.63) <0.01c 2001 (33.00) 3691 (80.80) 2117 (76.76) <0.01c
NSAIDs 9589 (13.50) 2441 (8.74) 2535 (9.53) <0.01c 283 (4.67) 217 (4.75) 131 (4.75) 0.97
Calcium channel blockers 11 778 (16.58) 7775 (27.83) 10 547 (39.66) <0.01c 627 (10.34) 522 (11.43) 589 (21.36) <0.01c
OADs 2869 (4.04) 3226 (11.55) 4186 (15.74) <0.01c 226 (3.73) 450 (9.85) 392 (14.21) <0.01c
Insulin 765 (1.08) 795 (2.85) 1088 (4.09) <0.01c 61 (1.01) 109 (2.39) 93 (3.37) <0.01c

Data are shown as n (%) except as noted. ANOVA and χ2 test were used to evaluate differences between HbA1c groups for continuous and categorical variables, respectively. BMI indicates body mass index; CKD, chronic kidney disease; CPD, cardiopulmonary disease; eGFR, estimated glomerular filtration rate; ESC, European Society of Cardiology; HF, heart failure; MI, myocardial infarction; OADs, oral antidiabetics; PVD, peripheral vascular disease; RAASi, renin–angiotensin–aldosterone system inhibitors; SBP, systolic blood pressure.

a

The numbers of patients at <50% and ≥50% of the recommended dose do not add up to the total cohort size because patients who spent most of their time on 0% dose and those who do not have a clear majority of time spent at a given dose level are not shown in the table but are included in the total cohort.

b

Baseline for RAASi patients is time of each patient's first RAASi prescription after their CKD or HF event and for non‐RAASi patients is time of first CKD or HF event.

c

P<0.05.