Abstract
Background: Sickle cell disease (SCD) patients can receive their ambulatory care from either SCD specialists (caregivers with sickle cell-only clinics) or nonspecialized care centers. Patient satisfaction, an important factor that may influence compliance and outcome, can differ between the two groups because of the perceived quality of care, outcomes or practice style. Methods: We administered a patient satisfaction survey to 308 participants in an SCD prospective cohort study. Of the 308 patients, 133 (43.2%) received the majority of their SCD care at specialized centers, 152 (49.3%) received their care from nonspecialized centers and 26 (7.5) did not provide information. The satisfaction surveys measured general satisfaction (GS), technical quality (TQ), interpersonal manner (IM), communication (CM), financial aspects (FA), time spent with doctor (TA), and accessibility and convenience (AC). Patients reported their levels of satisfaction using a five-point Likert scale. We compared unadjusted group means, as well as means adjusted for potential confounders such as marital status, on patient satisfaction between specialized and nonspecialized centers. Results: SCD patients who received their care from specialized centers had significantly higher mean satisfaction scores, compared to those who received their care from nonspecialized centers: GS 4.00(±0.93) vs. 3.66 (±01.16, p=0.0326), TQ 3.98 (±0.77) vs. 3.65 (±0.91, p=0.0058), AC 3.83 (±0.79) vs.3.51 (±1.02, p=0.0142), FA3.88 (±0.96) vs.3.49 (± 1.25, p=0.0120). There were no statistically significant group differences in IM, TA and CM. Conclusion: SCD patients who received most of their SCD care from specialized centers had somewhat higher satisfaction scores in some areas when compared with patients who received their care from nonspecialized centers.
| Original language | English |
|---|---|
| Pages (from-to) | 886-890 |
| Number of pages | 5 |
| Journal | Journal of the National Medical Association |
| Volume | 99 |
| Issue number | 8 |
| State | Published - Aug 2007 |
Keywords
- Quality of care
- Sickle cell anemia
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