Screening and Recall
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Screening and Recall

Policy

Our practice participates in the Manatū Hauora | Ministry of Health's national screening programmes provided by the National Screening Unit:

Pregnancy and newborn screening is usually organised by the mother's lead maternity carer, and/or carried out in hospital, but may be suggested opportunistically if the mother visits the practice before the baby's 6-week check.

In addition to the National Screening Programme, we offer opportunistic screening to help detect diseases early in those who may be at risk, and routine screening for existing conditions.

New clinical staff are trained on the practice's screening and recall processes, including the importance of keeping complete and accurate clinical records, during induction and orientation.

We communicate with patients about screening programmes by text, phone, letter, or another method that best suits the patient.

We aim to reduce inequities and barriers to accessing screening services by regularly reviewing patient data, and offering appropriate screening to all eligible patients.

The nurse manager is responsible for overseeing screening and recalls.

See also Notifying Patients of Results

Enrolling patients onto screening programmes

We identify patients who are eligible for national screening programmes by:

We follow processes appropriate to each screening programme:

We may refer at-risk patients who fall outside of National Screening Programme criteria, for screening. If necessary, we contact patients to obtain their consent to participate in a screening programme.

Information is also available in our waiting room, for patients who wish to self-refer to screening programmes.

Recalling patients

All recalls are managed within Medtech by the nursing team:

Patients who don't respond

If follow up is not carried out by the relevant screening programme, and our attempts to contact a patient have failed, we manage the process accordingly:

Audits

We regularly audit our screening and recall procedures to ensure screening is effective, and to identify inequities and under-screened groups within our patient population. Screening rates by ethnicity are identified, and Māori data is included in our Māori Health Plan.

Clinical governance

Audit outcomes are reviewed by our clinical governance group and may become the subject of a quality improvement (CQI) or equity initiative.

Equity

Some patients opt out of screening, and we understand that for some patients or patient groups, there may be barriers to accessing screening services.

To better enable equitable access to screening, we provide information and support by:

Patients who experience barriers to accessing breast or cervical screening services may be directed to Screening Support Services, to help them find an outreach service, or other alternative provider.

Disruptions

If the practice's screening recall programme is disrupted e.g. during a pandemic, we prioritise patients as follows:

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Topic type Core content
Approved By: Key Contact
Topic ID: 8248

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