Table 1.
Four follow-up options for HEU children explored in surveys of parents/carers and health-care professionals.
Option | Description |
---|---|
Clinic contact | Annual follow-up visit at pediatric clinic with data (no names) sent to the NSHPC. Parents/carers would need to inform the clinic of contact detail changes |
Telephone contact | Pediatric clinic staff would call parent/carer annually to collect brief information about the child’s general health. Responses entered on a form and sent to NSHPC (no names). Parents/carers would need to inform the clinic of contact detail changes |
Postal contact | NSHPC would be provided with contact details of parent/carer by the clinic when the child was discharged from routine care. A short form on the child’s health would be sent to parent/carer annually for completion and return to NSHPC (no reference to HIV anywhere on the form or correspondence). Parents/carers would need to inform the NSHPC of contact detail changes |
No direct contact | NSHPC uses child’s NHS number to link to routinely available health information. No further contact with clinic or NSHPC needed after child is discharged |