Overall mortality · patients with acquired SAA
First‐line allogeneic hematopoietic stem cell transplantation of… showed no clear difference in overall mortality compared with first‐line ciclosporin and/or antithymocyte or antilymphocyte globulin (low certainty).
1 finding from 1 review
Treatment‐related mortality · patients with acquired SAA
1 finding from 1 review
Health‐related quality of life · patients with acquired SAA
1 finding from 1 review
Graft failure · patients with acquired SAA
1 finding from 1 review
No response to IST · patients with acquired SAA
1 finding from 1 review
Graft‐versus‐host disease · patients with acquired SAA
1 finding from 1 review
Secondary clonal disease or malignancies · patients with acquired SAA
First‐line allogeneic hematopoietic stem cell transplantation of… showed no clear difference in secondary clonal disease or malignancies compared with first‐line ciclosporin and/or antithymocyte or antilymphocyte globulin (low certainty).
1 finding from 1 review
Successful stem cell collection · People with haematopoietic stem cell mobilisation for autologous transplantation in malignant lymphoma or multiple myeloma
Plerixafor leads to higher successful stem cell collection compared with placebo (high certainty).
1 finding from 1 review
Adverse events (during stem cell mobilisation and collection) · People with haematopoietic stem cell mobilisation for autologous transplantation in malignant lymphoma or multiple myeloma
Plerixafor showed no clear difference in adverse events (during stem cell mobilisation and collection) compared with placebo (high certainty).
1 finding from 1 review
Intervention not reported
Overall survival (at 36 months) · patients after allogeneic stem cell or bone marrow transplantation
The intervention showed no clear difference in overall survival (at 36 months) (moderate certainty).
1 finding from 1 review
Intervention not reported
Acute GVHD II to IV (90 days) · patients after allogeneic stem cell or bone marrow transplantation
The intervention leads to lower acute GVHD II to IV (90 days) (high certainty).
1 finding from 1 review
Intervention not reported
Overall Chronic GVHD (up to 36 months) · patients after allogeneic stem cell or bone marrow transplantation
The intervention leads to lower overall Chronic GVHD (up to 36 months) (high certainty).
1 finding from 1 review
Intervention not reported
Incidence of relapse (up to 36 months) · patients after allogeneic stem cell or bone marrow transplantation
The intervention showed no clear difference in incidence of relapse (up to 36 months) (moderate certainty).
1 finding from 1 review
Intervention not reported
Non‐relapse mortality (at 36 months) · patients after allogeneic stem cell or bone marrow transplantation
The intervention showed no clear difference in non‐relapse mortality (at 36 months) (moderate certainty).
1 finding from 1 review
Intervention not reported
Graft failure (during study) · patients after allogeneic stem cell or bone marrow transplantation
The intervention showed no clear difference in graft failure (during study) (low certainty).
1 finding from 1 review
Intervention not reported
Adverse Events (during study) · patients after allogeneic stem cell or bone marrow transplantation
1 finding from 1 review
Number of participants with at least 1 bleeding episode · people with haematological disorders undergoing intensive chemotherapy or stem cell transplantation
It is very uncertain whether thrombopoietin mimetics changes number of participants with at least 1 bleeding episode compared with placebo or standard care (very low certainty).
1 finding from 1 review
Intervention not reported
Number of participants with severe or life‐threatening bleeding · people with haematological disorders undergoing intensive chemotherapy or stem cell transplantation
It is very uncertain whether the intervention changes number of participants with severe or life‐threatening bleeding (very low certainty).
1 finding from 1 review
Intervention not reported
Number of days on which bleeding occurred ‐ not reported · people with haematological disorders undergoing intensive chemotherapy or stem cell transplantation
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Time from randomisation to first bleeding episode ‐ not reported · people with haematological disorders undergoing intensive chemotherapy or stem cell transplantation
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found