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Table 4 Future directions for the MyChristie-MyHealth project

From: Patient and clinician-reported experiences of using electronic patient reported outcome measures (ePROMs) as part of routine cancer care

Area

Key learning points

Future directions

Action plan

Patient experience

Regular collection of ePROMs as part of routine cancer care is acceptable and feasible

Gain experience data from non-completers

Repeat experience study evaluating non-completers

 

ePROMs make patients feel more involved in their care

Ongoing feedback from patients to develop service

ePROMs patient coordinator as point of contact in clinic

Clinician experience

ePROMs support communication and patient engagement

Further clinician experience data needed

Clinician experience review (aim 100% feedback)

 

Integration into the electronic patient record (EPR) is essential

Explore reasons for non-engagement with ePROMs

 

Developing MyChristie-MyHealth service to improve patient centered care

ePROMs help patients feel more involved in their care and consultations more patient focused

Roll out of ePROMS into all disease groups and clinics

 
 

Increased need of virtual follow-up during/since the COVID pandemic

Use of ePROMs for adaptive/virtual follow-up

 
  

Develop ‘ad-hoc’ ePROMs service with real-time clinical review

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