TABLE 3.
Type and No. of Additional LT-CCCs | Neuromusculara | Cardiovasculara | Malignancya | |||
---|---|---|---|---|---|---|
Hospital Days | Pb | Hospital Days | Pb | Hospital Days | Pb | |
Median (IQR) hospital days by no. of LT-CCCs | ||||||
1 LT-CCC | 5 (2–15) | <.001 | 6 (2–22) | <.001 | 21 (9–51) | <.001 |
≥2 LT-CCCs | 32 (11–77) | 46 (11–112) | 75 (31–123) | |||
Effect of additional LT-CCCs on hospital days (SE)c,d | ||||||
Hematologic/ Immunologic | +58 (7) | <.001 | +47 (8) | <.001 | +38 (6) | <.001 |
Gastrointestinal | +50 (9) | <.001 | +35 (9) | <.001 | +18 (8) | .02 |
Metabolic | +42 (4) | <.001 | +36 (5) | <.001 | +33 (5) | <.001 |
Renal | +40 (8) | <.001 | +27 (9) | <.01 | +13 (9) | .2 |
Malignancy | +36 (5) | <.001 | +29 (6) | <.001 | NAe | NA |
Respiratory | +32 (6) | <.001 | +22 (7) | <.01 | +3 (9) | .8 |
Cardiovascular | +17 (4) | <.001 | NAe | NA | −9 (6) | .1 |
Congenital/ Genetic | +5 (4) | .2 | −6 (4) | .1 | −22 (7) | <.001 |
Neuromuscular | NAe | NA | −8 (4) | .03 | −29 (5) | <.001 |
NA, not applicable.
Neuromuscular, cardiovascular, and malignancy were selected for presentation because they are the 3 most prevalent conditions among children in the cohort.
P values were obtained from a type III block test on the fixed effect of interest (eg, type of LT-CCC) that was included in generalized linear models; statistical significance is defined as a P value of < .05.
Shown are greater (+) or fewer (−) hospital days with SE experienced in the presence of a specific additional LT-CCC. For example, among children with a neuromuscular LT-CCC, the presence of an additional hematologic/immunologic LT-CCC added 58 (SE 7) hospital days in the last year of life. Hospital days and SE were estimated from generalized linear models.
LT-CCCs are ranked in order from greatest to least added hospital days for children with neuromuscular conditions.
Not applicable, as every child in the cohort of interest has this condition.