Gender | |
male | 39 (55.71) |
female | 31 (44.29) |
Age (years) | 5 (3 months–12 years) |
≤1 | 18 (25.71) |
>1–5 | 21 (30.00) |
>5–12 | 31 (44.29) |
Diagnosis | |
ALL | 23 (32.86) |
AML | 22 (31.43) |
relapsed ALL | 5 (7.14) |
aplastic anaemia | 2 (2.86) |
CGD | 2 (2.86) |
MDS + JMML | 2 (2.86) |
JMML | 2 (2.86) |
CML | 2 (2.86) |
othera | 10 (14.29) |
Bone marrow transplant recipient | |
no | 51 (72.86) |
yes | 19 (27.14) |
Type of bone marrow transplant | |
matched sibling | 4 (21.05) |
unrelated peripheral blood stem cell | 4 (21.05) |
haploidentical | 4 (21.05) |
unrelated cord blood | 3 (15.79) |
matched unrelated donor | 3 (15.79) |
cord blood | 1 (5.26) |
Covariates associated with reduced absorption | |
concurrent PPIb | 14 (20.00) |
concurrent ranitidine | 2 (2.86) |
concurrent metoclopramide | 18 (25.71) |
mucositis | 6 (8.57) |
enteral feeding | 16 (22.86) |
At least one covariate | 38 (54.29) |
Gender | |
male | 39 (55.71) |
female | 31 (44.29) |
Age (years) | 5 (3 months–12 years) |
≤1 | 18 (25.71) |
>1–5 | 21 (30.00) |
>5–12 | 31 (44.29) |
Diagnosis | |
ALL | 23 (32.86) |
AML | 22 (31.43) |
relapsed ALL | 5 (7.14) |
aplastic anaemia | 2 (2.86) |
CGD | 2 (2.86) |
MDS + JMML | 2 (2.86) |
JMML | 2 (2.86) |
CML | 2 (2.86) |
othera | 10 (14.29) |
Bone marrow transplant recipient | |
no | 51 (72.86) |
yes | 19 (27.14) |
Type of bone marrow transplant | |
matched sibling | 4 (21.05) |
unrelated peripheral blood stem cell | 4 (21.05) |
haploidentical | 4 (21.05) |
unrelated cord blood | 3 (15.79) |
matched unrelated donor | 3 (15.79) |
cord blood | 1 (5.26) |
Covariates associated with reduced absorption | |
concurrent PPIb | 14 (20.00) |
concurrent ranitidine | 2 (2.86) |
concurrent metoclopramide | 18 (25.71) |
mucositis | 6 (8.57) |
enteral feeding | 16 (22.86) |
At least one covariate | 38 (54.29) |
Values are n (%) or median (range).
CGD, chronic granulomatous disease; MDS, myelodysplastic syndrome; JMML, juvenile myelomonocytic leukaemia.
Wiskott–Aldrich syndrome, Omenn’s syndrome, anaplastic large cell lymphoma, congenital neutropenia, severe combined immunodeficiency, haemophagocytic lymphohistiocytosis, Hurler’s syndrome, IL-10 receptor-deficient inflammatory bowel disease, Langerhans cell histiocytosis and X-linked adrenoleucodystrophy, each of which were n=1 (1.43%).
Omeprazole or esomeprazole
Gender | |
male | 39 (55.71) |
female | 31 (44.29) |
Age (years) | 5 (3 months–12 years) |
≤1 | 18 (25.71) |
>1–5 | 21 (30.00) |
>5–12 | 31 (44.29) |
Diagnosis | |
ALL | 23 (32.86) |
AML | 22 (31.43) |
relapsed ALL | 5 (7.14) |
aplastic anaemia | 2 (2.86) |
CGD | 2 (2.86) |
MDS + JMML | 2 (2.86) |
JMML | 2 (2.86) |
CML | 2 (2.86) |
othera | 10 (14.29) |
Bone marrow transplant recipient | |
no | 51 (72.86) |
yes | 19 (27.14) |
Type of bone marrow transplant | |
matched sibling | 4 (21.05) |
unrelated peripheral blood stem cell | 4 (21.05) |
haploidentical | 4 (21.05) |
unrelated cord blood | 3 (15.79) |
matched unrelated donor | 3 (15.79) |
cord blood | 1 (5.26) |
Covariates associated with reduced absorption | |
concurrent PPIb | 14 (20.00) |
concurrent ranitidine | 2 (2.86) |
concurrent metoclopramide | 18 (25.71) |
mucositis | 6 (8.57) |
enteral feeding | 16 (22.86) |
At least one covariate | 38 (54.29) |
Gender | |
male | 39 (55.71) |
female | 31 (44.29) |
Age (years) | 5 (3 months–12 years) |
≤1 | 18 (25.71) |
>1–5 | 21 (30.00) |
>5–12 | 31 (44.29) |
Diagnosis | |
ALL | 23 (32.86) |
AML | 22 (31.43) |
relapsed ALL | 5 (7.14) |
aplastic anaemia | 2 (2.86) |
CGD | 2 (2.86) |
MDS + JMML | 2 (2.86) |
JMML | 2 (2.86) |
CML | 2 (2.86) |
othera | 10 (14.29) |
Bone marrow transplant recipient | |
no | 51 (72.86) |
yes | 19 (27.14) |
Type of bone marrow transplant | |
matched sibling | 4 (21.05) |
unrelated peripheral blood stem cell | 4 (21.05) |
haploidentical | 4 (21.05) |
unrelated cord blood | 3 (15.79) |
matched unrelated donor | 3 (15.79) |
cord blood | 1 (5.26) |
Covariates associated with reduced absorption | |
concurrent PPIb | 14 (20.00) |
concurrent ranitidine | 2 (2.86) |
concurrent metoclopramide | 18 (25.71) |
mucositis | 6 (8.57) |
enteral feeding | 16 (22.86) |
At least one covariate | 38 (54.29) |
Values are n (%) or median (range).
CGD, chronic granulomatous disease; MDS, myelodysplastic syndrome; JMML, juvenile myelomonocytic leukaemia.
Wiskott–Aldrich syndrome, Omenn’s syndrome, anaplastic large cell lymphoma, congenital neutropenia, severe combined immunodeficiency, haemophagocytic lymphohistiocytosis, Hurler’s syndrome, IL-10 receptor-deficient inflammatory bowel disease, Langerhans cell histiocytosis and X-linked adrenoleucodystrophy, each of which were n=1 (1.43%).
Omeprazole or esomeprazole
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