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. 2020 Nov 14;159(4):1630–1641. doi: 10.1016/j.chest.2020.10.075

Table 3.

Percentage and Adjusted ORs Predicting the Odds of Potential Poor-Quality Metrics by Facility Typea

Variable Community Cancer Program (n = 10,597) Comprehensive Community Cancer Program (n = 71,271) Integrated Network Program (n = 15,849) Academic Cancer Program (n = 37,047) NCI Program (n = 18,139)
Postoperative mortality
 30 d 3.6 2.7 2.3 2.2 1.4
 OR (95% CI) 2.36 (2.00-2.78) 1.78 (1.55-2.03) 1.46 (1.23-1.72) 1.61 (1.40-1.87) 1
 60 d 5.2 4.0 3.4 3.2 2.0
 OR (95% CI) 2.35 (2.05-2.69) 1.76 (1.57-1.97) 1.47 (1.28-1.69) 1.60 (1.42-1.80) 1
 90 d 6.3 4.9 4.1 4.0 2.6
 OR (95% CI) 2.24 (1.98-2.53) 1.70 (1.54-1.88) 1.39 (1.23-1.57) 1.54 (1.38-1.71) 1
 120 d 7.2 5.8 4.9 4.6 3.0
 OR (95% CI) 2.18 (1.95-2.45) 1.71 (1.56-1.88) 1.41 (1.26-1.58) 1.53 (1.38-1.69) 1
Positive margin 6.12 5.15 4.72 4.44 3.57
 OR (95% CI) 1.65 (1.48-1.85) 1.41 (1.29-1.54) 1.26 (1.13-1.41) 1.23 (1.12-1.35) 1
Wedge resection 14.00 12.13 10.87 13.19 12.53
 OR (95% CI) 1.19 (1.10-1.27) 1.01 (0.96-1.06) 0.93 (0.87-0.99) 1.07 (1.01-1.13) 1
pNX rate 7.29 5.18 3.65 4.45 2.67
 OR (95% CI) 2.96 (2.63-3.33) 2.10 (1.90-2.32) 1.53 (1.35-1.74) 1.69 (1.52-1.87) 1
< 10 lymph nodes resectedb 73.26 67.56 61.29 59.62 47.68
 OR (95% CI) 2.97 (2.80-3.15) 2.28 (2.19-2.36) 1.67 (1.59-1.75) 1.60 (1.53-1.66) 1
Non-evidence-based use of adjuvant radiation therapyc 4.45 2.91 2.65 2.58 1.77
 OR (95% CI) 2.49 (2.13-2.92) 1.70 (1.49-1.93) 1.49 (1.27-1.75) 1.42 (1.24-1.63) 1
Non-evidence-based use of adjuvant chemotherapyd 9.80 8.33 8.21 7.64 6.99
 OR (95% CI) 1.44 (1.30-1.61) 1.30 (1.20-1.41) 1.22 (1.10-1.34) 1.08 (0.99-1.18) 1

Data are presented as percentage unless otherwise indicated. NCI = National Cancer Institute. P < .0001 for all comparisons.

a

Adjusted for age at diagnosis, race or ethnicity, sex, year of diagnosis, insurance, geographic region of the facility, comorbidity score, and clinical stage.

b

Among patients with pathologic stage I-II, including patients with 0 lymph nodes, excluding patients with unknown number of nodes.

c

Defined as use in patients with pathologic N0 and N1 and negative resection margins.

d

Defined as use in patients with pathologic stage I with tumor size ≤ 4 cm and negative resection margins.