- Coding system
- CTV3 (Read V3)
- Coding system release
- Codelist ID
- Version Tag
- Version ID
Codes indicating a diagnosis of a temporary immunosuppression.
This codelist was derived by the following method:
- Read 2 Codelist provided by LSHTM.
- Codes from Quality Outcome Framework (QOF) were examined and relevant immunosuppression codes extracted
- Codes from SNOMED were taken by searching for relevant immunosuppression terms
These original codes were aimed at creating an "immunosuppression NOS" codelist. The 3 lists were mapped into CTV3 by TPP to create one list. This list was examined by clinicians, and it was determined that it should instead become "temporary immunosuppression", so that it could be applied to only codes that were recorded recently. More details on the process are found in the issue below.
Signed off by
- Liam Smeeth, (April 24, 2020)
- Helen McDonald, (April 23, 2020)
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
|D2015||Pancytopenia - acquired|
|D400.||(Agranulocytosis) or (Kostmann's syndrome) or (neutropenia)|
|D4000||Idiopathic: [agranulocytosis] or [neutropenia]|
|D4002||Drug induced: [agranulocytosis] or [neutropenia]|
|D4003||Radiation: [agranulocytosis] or [neutropenia]|
|D4004||Infection: [agranulocytosis] or [neutropenia]|
|D4008||Acquired: [neutropenia NEC] or [agranulocytosis NEC]|
|D400y||Other specified agranulocytosis|
|X20HQ||Phagocytic cell defect|
|X20HR||Disorder of phagocytic cell number|
|XaXUJ||Immunosuppressant drug therapy|
|XE14D||Neutropenia due to irradiation|
|XE14G||Acquired neutropenia NEC|
|XM0BV||Predominantly B-cell defect|
|XM0BW||Predominantly T-cell defect|
|XM1WJ||Preventing infection of immunocompromised patient|
|XM1WL||Reverse barrier nursing|
|X20HB||Primary immunoglobulin catabolism abnormality|
|X20HD||Familial immunoglobulin hypercatabolism|
|X20HP||Benign combined immunodeficiency|
|BBmC.||[M] T-gamma lymphoproliferative disease|
Codes not in the full codelist are in faint grey.