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. 2016 Aug 16;21(1):208–214. doi: 10.1007/s10995-016-2110-1

Table 1.

Transplant indication prevalence (N = 94,539 respondent families)

Indicationa Families reporting transplant indication (%)b Families reporting transplant indication (not in child donor) (%)b
Non-Hodgkin’s lymphoma 323 (0.34) 314 (0.33)
Hodgkin’s lymphoma 290 (0.31) 287 (0.30)
Acute lymphoblastic leukemia 328 (0.35) 263 (0.28)
Sarcoma 144 (0.15) 125 (0.13)
Acute myelogenous leukemia 113 (0.12) 106 (0.11)
Sickle cell disease 121 (0.13) 105 (0.11)
Beta thalassemia major 97 (0.10) 90 (0.10)
Chronic lymphocytic leukemia 88 (0.09) 85 (0.09)
Chronic myelogenous leukemia 82 (0.09) 82 (0.09)
Neuroblastoma 90 (0.10) 61 (0.06)
Multiple myeloma 60 (0.06) 58 (0.06)
Severe aplastic anemia 49 (0.05) 45 (0.05)
Myelodysplastic syndrome 20 (0.02) 19 (0.02)
Diamond–Blackfan anemia 10 (0.01) 9 (0.01)
Fanconi anemia 8 (0.01) 6 (0.01)
Hurler syndrome 0 (0.00) 0 (0.00)
Families reporting at least 1 transplant indication 1823 (1.93) 1655 (1.75)
Unique families reporting at least 1 transplant indication 1757 (1.86)c 1546 (1.64)c

aFamilies may report more than one indication. Ordered by percent of families reporting indication (not in child donor)

bAdjusted using inverse probability weighting based on respondent age, age of child, and number of cord blood units

cPercent represents total unique families reporting at least one transplant indication divided by the total families responding. This total is lower than the sum of all specific transplant indications reported because families with more than 1 transplant indication were only counted once here