Table 2.
Cox regression and Fine-Gray competing risk regression analysis of non-neoplastic and neoplastic mortality risk over 22 years of follow-up after ACS with the interaction for risks between the six geographic areas (n = 541).
| Variable | Unadjusted | Fully adjusted* | ||||
|---|---|---|---|---|---|---|
| HR (95% CI) | Z | p | HR (95% CI) | Z | p | |
| Cox regression | ||||||
| Non-neoplastic mortality (n = 321) | ||||||
| urban-rural areas | 0.8 (0.7–1.0) | -1.8 | 0.08 | 0.9 (0.7–1.1) | -1.2 | 0.24 |
| southern-northern provinces | 1.1 (1.0–1.3) | 1.6 | 0.10 | 1.0 (0.8–1.1) | -0.4 | 0.71 |
| Interaction (urban/rural areas and south to north provinces) | 1.0 (0.7–1.2) | -0.3 | 0.74 | 1.1 (0.9–1.4) | 0.8 | 0.41 |
| Neoplastic mortality (n = 99) | ||||||
| urban-rural areas | 1.1 (0.7–1.7) | 0.5 | 0.59 | 1.3 (0.8–1.9) | 1.1 | 0.27 |
| southern-northern provinces | 1.1 (0.9–1.4) | 1.1 | 0.29 | 1.0 (0.8–1.3) | 0.3 | 0.74 |
| Interaction (urban/rural areas and south to north provinces) | 1.9 (1.1–3.0) | 2.4 | 0.01 | 2.1 (1.3–3.4) | 2.9 | 0.003 |
| Fine-Gray competing risk regression analysis | ||||||
| SHR (95% CI) | Z | p | SHR (95% CI) | Z | p | |
| Non-neoplastic mortality (n = 321) | ||||||
| urban-rural areas | 0.8 (0.7–1.0) | -1.8 | 0.07 | 0.8 (0.7–1.1) | -1.4 | 0.17 |
| southern-northern provinces | 1.1 (1.0–1.2) | 1.2 | 0.25 | 1.0 (0.8–1.1) | -0.2 | 0.82 |
| Interaction (urban/rural areas and south to north provinces) | 0.9 (0.7–1.1) | -0.9 | 0.38 | 0.9 (0.7–1.2) | -0.5 | 0.60 |
| Neoplastic mortality (n = 99) | ||||||
| urban-rural areas | 1.2 (0.8–1.8) | 0.9 | 0.32 | 1.3 (0.8–1.9) | 1.2 | 0.25 |
| southern-northern provinces | 1.1 (0.8–1.3) | 0.5 | 0.60 | 1.1 (0.9–1.4) | 0.8 | 0.45 |
| Interaction (urban/rural areas and south to north provinces) | 1.8 (1.1–3.0) | 2.4 | 0.01 | 1.9 (1.1–3.0) | 2.6 | 0.01 |
CI, confidence interval; HR, hazard ratio; SHR, sub-hazard ratio.
P-values were calculated for log-transformed data. *Adjusted for age, sex, smoking, education level, alcohol consumption, baseline serum cholesterol, presence of heart failure at admission, and anti-platelet and beta-blockers time-intensity treatment per cent during follow-up.