Abstract
Readmission within 30 days of hospital discharge has recently become an important topic of discussion and a measure of quality of care. Factors influencing 30-day readmissions and its impact on patient related outcomes are diverse. Allogeneic hematopoietic cell transplantation (allo-HCT) presents a unique medical setting that may be associated with higher readmission rates. We analyzed factors affecting 30-day readmissions, its impact on patient related outcomes and health care costs in allo-HCT patients.
The study group included 91 consecutive patients with hematological malignancies who underwent related (n=44) or unrelated donor (n=47), peripheral blood allo-HCT after conditioning with fludarabine and busulfan +/- thymoglobulin. Subjects were divided into 2 groups; readmission (R-gp), n=35 if they were readmitted within 30 days of hospital discharge after the index hospitalization for a planned allo-HCT, or to no readmission (NR-gp), n=56. The baseline characteristics did not differ between the 2 groups (Table 1). Overall 38% (n=35) required readmission with a median time to readmission of 14 days (range, 1-29). Causes for readmission included documented infections (n=12), cardio-pulmonary complications (n=10), fever (n=6), gastrointestinal disorders (n=4), and graft-versus-host disease (n=3). Median length of stay was 3 days (range, 1-34). In multivariate analysis only documented infection during the index admission predicted 30-day readmission, OR 5.24; 95% CI 1.42-19.32; p=0.01. Caregiver type (spouse vs. others); and number of caregivers (1 vs. >1) did not influence readmission. With a median follow up of 1 year for surviving patients, the estimated overall survival (OS) was 58% and 67% in the R-gp and NR-gp respectively, OR 1.07, 95% CI 0.55-2.06, p=0.85. The 1-yr non-relapse mortality (NRM) in R-gp and NR-gp was 74% and 84% respectively, OR 1.13, 95% CI 0.42-3.03, p=0.80. The median post-transplant hospital charges (inpatient + outpatient) in the R-gp and NR-gp were 85,115.45 USD (mean 93,925.26, range 32,014.86-242,519.35) and 45,083.09 USD (mean 69,142.6, range 10,714.78-485,456.08), p=0.0002.
In conclusion, except for infections during the index admission, no other baseline demographic, social, disease or treatment related factors influenced 30-day readmissions after allo-HCT. 30-day readmission status did not adversely affect OS or NRM, but it significantly increased the 100-day hospital charges. Acknowledging the limitation of our study included its retrospective nature and small sample size, we conclude that 30-day readmission status does not portend poor post transplant outcomes. However, it is associated with higher health care costs.
Readmission (n=35) | Not Readmitted (n=56) | P-Value | |
Median age (range) | 56 (17-72) | 54 (22-68) | 0.23 |
Male (%) | 21 (60) | 34 (61) | 0.99 |
Malignancy type, n (%) | 0.93 | ||
ALL/AML/MDS | 23 (65.7) | 39 (70) | |
CLL/CML | 2 (5.7) | 3 (5) | |
Hodgkin/NHL/Others | 10 (28.6) | 14 (25) | |
Disease risk, n (%) | 0.18 | ||
Low | 16 (45.7) | 24 (43) | |
Intermediate | 3 (8.6) | 13 (23) | |
High | 16 (45.7) | 19 (34) | |
Disease status, n (%) | 0.49 | ||
Chemosensitive | 23 (66) | 41 (73) | |
Resistant | 12 (34) | 15 (27) | |
Prior number of therapy, median (range) | 2 (1-6) | 2 (0-6) | 0.65 |
Prior radiation therapy, n (%) | 2 (6) | 8 (14) | 0.31 |
Prior autologous transplantation, n (%) | 2 (6) | 6 (11) | 0.71 |
KPS, median (range) | 80 (60-100) | 85 (70-100) | 0.44 |
HCT-CI, median (range) | 2 (0-7) | 1 (0-5) | 0.31 |
Patients receiving ATG, n (%) | 23 (66) | 31 (55) | 0.38 |
Donor type, n (%) | |||
Unrelated | 19 (54) | 28 (50) | 0.83 |
Related | 16 (46) | 28 (50) | |
HLA mismatch, n (%) § | 0.99 | ||
Allele level | 1 (2) | 3 (5) | |
Antigen level | 1 (2) | 1 (2) | |
Infused CD34 cell dose, median (range) ¶ | 6.5 (2.7-12.8) | 6.5 (1.8-15.1) | 0.98 |
Infused CD3 cell dose, median (range) Ŧ | 31.3 (9.6-58.5) | 32.4 (11.5-94.5) | 0.48 |
GVHD prophylaxis, n (%) | 0.83 | ||
MTX + calcineurine inhibitor | 22 (63) | 33 (59) | |
MMF + calcineurine inhibitor | 13 (37) | 23 (41) |
Readmission (n=35) | Not Readmitted (n=56) | P-Value | |
Median age (range) | 56 (17-72) | 54 (22-68) | 0.23 |
Male (%) | 21 (60) | 34 (61) | 0.99 |
Malignancy type, n (%) | 0.93 | ||
ALL/AML/MDS | 23 (65.7) | 39 (70) | |
CLL/CML | 2 (5.7) | 3 (5) | |
Hodgkin/NHL/Others | 10 (28.6) | 14 (25) | |
Disease risk, n (%) | 0.18 | ||
Low | 16 (45.7) | 24 (43) | |
Intermediate | 3 (8.6) | 13 (23) | |
High | 16 (45.7) | 19 (34) | |
Disease status, n (%) | 0.49 | ||
Chemosensitive | 23 (66) | 41 (73) | |
Resistant | 12 (34) | 15 (27) | |
Prior number of therapy, median (range) | 2 (1-6) | 2 (0-6) | 0.65 |
Prior radiation therapy, n (%) | 2 (6) | 8 (14) | 0.31 |
Prior autologous transplantation, n (%) | 2 (6) | 6 (11) | 0.71 |
KPS, median (range) | 80 (60-100) | 85 (70-100) | 0.44 |
HCT-CI, median (range) | 2 (0-7) | 1 (0-5) | 0.31 |
Patients receiving ATG, n (%) | 23 (66) | 31 (55) | 0.38 |
Donor type, n (%) | |||
Unrelated | 19 (54) | 28 (50) | 0.83 |
Related | 16 (46) | 28 (50) | |
HLA mismatch, n (%) § | 0.99 | ||
Allele level | 1 (2) | 3 (5) | |
Antigen level | 1 (2) | 1 (2) | |
Infused CD34 cell dose, median (range) ¶ | 6.5 (2.7-12.8) | 6.5 (1.8-15.1) | 0.98 |
Infused CD3 cell dose, median (range) Ŧ | 31.3 (9.6-58.5) | 32.4 (11.5-94.5) | 0.48 |
GVHD prophylaxis, n (%) | 0.83 | ||
MTX + calcineurine inhibitor | 22 (63) | 33 (59) | |
MMF + calcineurine inhibitor | 13 (37) | 23 (41) |
High resolution HLA typing at the allele level for A, B, C and DRB-1 for all patients.
Cell dose x 106/kg patient body weight
Cell dose x 107/kg patient body weight
No relevant conflicts of interest to declare.
Author notes
Asterisk with author names denotes non-ASH members.
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