Skip to main content

Table 7 Identified pains and (desired) gains for ‘what to do with outcomes’

From: The needs of key-stakeholders for evaluating client’s experienced quality of home care: a qualitative approach

Category

Pains

Gains

What to do with outcomes

▪ Little is done with outcomes, not transparent (I,F,P)

▪ No concrete points-of-improvement are being formed (I,F,P)

▪ Difficult jargon used in discussing outcomes of measurement (I)

▪ Outcomes do not reflect content evaluation (I)

▪ Outcomes only discussed by district nurse with direct caregiver (F)

▪ Unrealistic expectations of outcomes (F)

▪ Unrelated outcomes to nursing or personal care services (F)

▪ Only extreme outcomes are communicated in teams (P)

▪ Provide client insight into evaluation with both verbal and written outcomes (I)

▪ Discover specific points-of-attention for client (I)

▪ Discuss outcomes of evaluation with district nurses (F)

▪ Evaluation not aimed to solve all care difficulties, but rather to discuss them (F)

Desired gains

Help stimulate caregiver to reflect on care provision (F,P)

Discuss outcome evaluation in team and decide what to feedback to client (I,P)

Share outcomes in team to define point-of-actions together (F, P)

Help caregiver to check for unrecognized assumptions or biases in care process (F)

Give daily update on positive and negative experiences in team (F)

Access client file and outcomes remotely (F)

Create client awareness for organizational restrictions on care services (F)

Share outcomes evaluation in organization in multiple formats (e.g. figures and practical solutions) (P)

  1. Mentioned by C Clients, I Informal caregivers, F formal caregivers, P managers/policy officers