Table 1.

Patient characteristics; N=70

Gender
 male39 (55.71)
 female31 (44.29)
Age (years)5 (3 months–12 years)
 ≤118 (25.71)
 >1–521 (30.00)
 >5–1231 (44.29)
Diagnosis
 ALL23 (32.86)
 AML22 (31.43)
 relapsed ALL5 (7.14)
 aplastic anaemia2 (2.86)
 CGD2 (2.86)
 MDS + JMML2 (2.86)
 JMML2 (2.86)
 CML2 (2.86)
 othera10 (14.29)
Bone marrow transplant recipient
 no51 (72.86)
 yes19 (27.14)
Type of bone marrow transplant
 matched sibling4 (21.05)
 unrelated peripheral blood stem cell4 (21.05)
 haploidentical4 (21.05)
 unrelated cord blood3 (15.79)
 matched unrelated donor3 (15.79)
 cord blood1 (5.26)
Covariates associated with reduced absorption
 concurrent PPIb14 (20.00)
 concurrent ranitidine2 (2.86)
 concurrent metoclopramide18 (25.71)
 mucositis6 (8.57)
 enteral feeding16 (22.86)
At least one covariate38 (54.29)
Gender
 male39 (55.71)
 female31 (44.29)
Age (years)5 (3 months–12 years)
 ≤118 (25.71)
 >1–521 (30.00)
 >5–1231 (44.29)
Diagnosis
 ALL23 (32.86)
 AML22 (31.43)
 relapsed ALL5 (7.14)
 aplastic anaemia2 (2.86)
 CGD2 (2.86)
 MDS + JMML2 (2.86)
 JMML2 (2.86)
 CML2 (2.86)
 othera10 (14.29)
Bone marrow transplant recipient
 no51 (72.86)
 yes19 (27.14)
Type of bone marrow transplant
 matched sibling4 (21.05)
 unrelated peripheral blood stem cell4 (21.05)
 haploidentical4 (21.05)
 unrelated cord blood3 (15.79)
 matched unrelated donor3 (15.79)
 cord blood1 (5.26)
Covariates associated with reduced absorption
 concurrent PPIb14 (20.00)
 concurrent ranitidine2 (2.86)
 concurrent metoclopramide18 (25.71)
 mucositis6 (8.57)
 enteral feeding16 (22.86)
At least one covariate38 (54.29)

Values are n (%) or median (range).

CGD, chronic granulomatous disease; MDS, myelodysplastic syndrome; JMML, juvenile myelomonocytic leukaemia.

a

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%).

b

Omeprazole or esomeprazole

Table 1.

Patient characteristics; N=70

Gender
 male39 (55.71)
 female31 (44.29)
Age (years)5 (3 months–12 years)
 ≤118 (25.71)
 >1–521 (30.00)
 >5–1231 (44.29)
Diagnosis
 ALL23 (32.86)
 AML22 (31.43)
 relapsed ALL5 (7.14)
 aplastic anaemia2 (2.86)
 CGD2 (2.86)
 MDS + JMML2 (2.86)
 JMML2 (2.86)
 CML2 (2.86)
 othera10 (14.29)
Bone marrow transplant recipient
 no51 (72.86)
 yes19 (27.14)
Type of bone marrow transplant
 matched sibling4 (21.05)
 unrelated peripheral blood stem cell4 (21.05)
 haploidentical4 (21.05)
 unrelated cord blood3 (15.79)
 matched unrelated donor3 (15.79)
 cord blood1 (5.26)
Covariates associated with reduced absorption
 concurrent PPIb14 (20.00)
 concurrent ranitidine2 (2.86)
 concurrent metoclopramide18 (25.71)
 mucositis6 (8.57)
 enteral feeding16 (22.86)
At least one covariate38 (54.29)
Gender
 male39 (55.71)
 female31 (44.29)
Age (years)5 (3 months–12 years)
 ≤118 (25.71)
 >1–521 (30.00)
 >5–1231 (44.29)
Diagnosis
 ALL23 (32.86)
 AML22 (31.43)
 relapsed ALL5 (7.14)
 aplastic anaemia2 (2.86)
 CGD2 (2.86)
 MDS + JMML2 (2.86)
 JMML2 (2.86)
 CML2 (2.86)
 othera10 (14.29)
Bone marrow transplant recipient
 no51 (72.86)
 yes19 (27.14)
Type of bone marrow transplant
 matched sibling4 (21.05)
 unrelated peripheral blood stem cell4 (21.05)
 haploidentical4 (21.05)
 unrelated cord blood3 (15.79)
 matched unrelated donor3 (15.79)
 cord blood1 (5.26)
Covariates associated with reduced absorption
 concurrent PPIb14 (20.00)
 concurrent ranitidine2 (2.86)
 concurrent metoclopramide18 (25.71)
 mucositis6 (8.57)
 enteral feeding16 (22.86)
At least one covariate38 (54.29)

Values are n (%) or median (range).

CGD, chronic granulomatous disease; MDS, myelodysplastic syndrome; JMML, juvenile myelomonocytic leukaemia.

a

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%).

b

Omeprazole or esomeprazole

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