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2010 review - Patient-Reported Outcomes Measurement - University ...

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Responsiveness of the DASI was illustrated in the study by King (2000), with significant<br />

improvement in functional status for both genders. Significant score changes were reported<br />

for the CABG group in a study comparing outcomes among three groups of patients with<br />

advanced CAD (Kandzari et al., 2001; MOSS study). Significant improvement in DASI<br />

scores post-revascularisation was reported for the Canadian (but not the US) group in the<br />

GUSTO-IIb QoL substudy (Kaul et al., 2004). The DASI also demonstrated responsiveness<br />

in the survival study by Koch et al. (2007); however, distribution of scores was skewed, with<br />

a clustering of scores at the higher end of the range, suggesting the measure lacks precision<br />

for patients with better functional capacity.<br />

Interpretability of the DASI was supported in the 1997 study by Hlatky and colleagues where<br />

a small change in score (2.7 units) was found to be clinically meaningful.<br />

Ease of application, or feasibility, of the DASI is noted (Nelson et al., 1991).<br />

d. Heart Surgery Symptom Inventory, HSSI (LaPier & Jung, 2002)<br />

The HSSI was developed to provide a measure of functional status and QoL for patients in<br />

the subacute stage of recovery from CABG (from two to six months post-surgery). It covers a<br />

broader range of symptoms than most cardiac-specific measures, which focus principally on<br />

angina and dyspnoea. In its current form it is not appropriate for pre-operative assessments<br />

owing to the large number of surgery-specific items (LaPier & Jung, 2002). The developers<br />

suggest it could be readily adapted for use in the immediate post-operative period (up to two<br />

months) and/or during long-term recovery, i.e. beyond six months (LaPier & Jung, 2002);<br />

however, it has not yet been evaluated for this purpose (LaPier, 2006; LaPier & Wilson,<br />

2006).<br />

Three studies (the most recent being from 2007) and a <strong>review</strong> article were identified which<br />

evaluated the HSSI in US patients having undergone CABG.<br />

Content was derived from previously published qualitative studies, clinicians, and patients<br />

recovering from CABG; a preliminary list of items was revised and added to by a panel of<br />

specialist physical therapists (LaPier & Jung, 2002). The final version of the instrument<br />

comprises 76 items in five symptom categories - namely, cardiac; general (includes sleep,<br />

fatigue, sexual functioning, cognitive functioning); trunk (includes incision/drain site pain,<br />

wound healing); lower extremity (for those receiving grafts harvested from the saphenous<br />

vein); upper extremity (for recipients of radial artery grafts). Respondents are asked to assess<br />

symptoms over the previous week, selecting from five Likert-type response options. Domain<br />

scores are summed to produce a total, with lower scores indicating greater severity of<br />

symptoms.<br />

Internal consistency was supported by significant correlations between domain and total<br />

scores, and most inter-domain scores, in a study with a small sample of patients who had<br />

undergone CABG six months previously (LaPier, 2006). However, individual item-domain<br />

and item-total correlations ranged 0.01-0.85, with several values falling well below the norm<br />

of 0.20 (LaPier, 2006). Test-retest reliability was supported by significant correlations<br />

between HSSI scores on two administrations; however, these were conducted on the same<br />

day, and results could therefore be subject to recall bias (LaPier, 2006).<br />

26

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