QUESTION | NUMBER OF RESPONSES (TOTAL=45) | | | |
|
Number of unique nurse responses (from individual centres) | 45 | UK | 10 | |
USA | 9 | |
Netherlands | 6 | |
Canada | 5 | |
New Zealand | 4 | |
Ireland | 2 | |
Sweden | 2 | |
Australia, Croatia, Denmark, Finland, Germany, Romania, Switzerland | 1 each | |
|
| | | NUMBER OF RESPONSES | % OF RESPONSES |
|
Ever switched clotting factor product? | 45 | Yes | 43 | 95% |
No | 2 | 5% |
|
Reason(s) for switch (more than one answer possible) | 33* | Clinical need | 34 | |
Funder/purchaser changed product | 30 | |
Patient request/preference | 21 | |
|
Was switch protocol-based? | 40* | Yes | 20 | 50% |
No | 20 | 50% |
|
If so, who wrote the protocol? | 24* | Haemophilia team | 15 | 62.5% |
Nurse/nurse specialist | 4 | 16.5% |
Doctors | 5 | 21% |
|
Frequency of blood tests for pharmacokinetics before switch | 26* | Don’t know | 1 | 4% |
No prior testing | 6 | 23% |
Blood testing at least once | 18 | 69% |
Depends on product | 1 | 4% |
|
Frequency of blood tests for pharmacokinetics after switch** | 25* | None | 4 | 16% |
Depends on product | 4 | 16% |
Depends on clinical need | 1 | 4% |
No/inappropriate response | 16 | 64% |
|
Screen for inhibitors before switch? | 43* | Yes | 37 | 86% |
No | 6 | 14% |
|
Was patient association involved? | 43* | Yes | 11 | 26% |
No | 27 | 63% |
Not sure | 5 | 11% |