Eylem Seç
Assessment of Patient-reported Health-related Quality of Life among Hospitalized Adults with Sickle Cell Disease
Başlık:
Assessment of Patient-reported Health-related Quality of Life among Hospitalized Adults with Sickle Cell Disease
Yazar:
Esham, Kimberly S., author.
ISBN:
9780438031258
Yazar Ek Girişi:
Fiziksel Tanımlama:
1 electronic resource (72 pages)
Genel Not:
Source: Masters Abstracts International, Volume: 57-06M(E).
Advisors: Susan K. Parsons Committee members: Farzad Noubary; Angie M. Rodday.
Özet:
Sickle cell disease (SCD) is an inherited condition characterized by painful vaso-occlusive (VOC) episodes that lead to poor health-related quality of life and premature mortality. Currently, pain assessment is performed by the Numeric Rating Scale (NRS), with which patients rate the intensity of pain from 0 (no pain) to 10 (worst imaginable pain). Newer patient-reported outcomes (PROs) measures that assess the multidimensional impact of pain among adults with SCD have been preliminarily validated in ambulatory populations. This study described the VOC experience among hospitalized adults with VOC, using two PRO tools, the Patient-Reported Outcomes Measurement Information system (PROMIS) Global Health and the Adult Sickle Cell Quality of Life Measurement System (ASCQ-Me).
Adults with SCD hospitalized with VOC at two academic centers in New England from April 2016-October 2017 were eligible. Participants completed PROMIS Global Health and ASCQ-Me assessments at admission and seven days after hospital discharge. We calculated means and standard deviations for the NRS and PRO scores. We described feasibility in terms of proportion of assessment ascertainment. Healthcare utilization outcomes included hospital length of stay (LOS) and 30-day readmission rates. Using multivariable linear regression, we used sociodemographic, clinical characteristics, and the novel PRO scores to predict hospital LOS.
Forty-two of 44 eligible patients (95.5%) consented and completed all admission assessments. The mean age was 30.2 years, 60% were women, 76% were black, non-Hispanic, and 64% had hemoglobin SS. Twenty-seven participants (64%) completed all assessments seven days after discharge. Seven (47%) of the missing assessments were due to hospital readmission within one week. Sixty percent of patients had four or more VOCs in the last 12 months. These participants were more likely to be younger, of non-Hispanic race, have hemoglobin SS, be prescribed hydroxyurea, and on disability. They tended to have higher pain intensity and lower ASCQ-Me scores.
All mean ASCQ-Me and PROMIS Global scores were below population norms, with the exception of Sleep Impact. There was statistically significant improvement in mean NRS (p<0.01) and PROMIS Physical Health (p<0.05) at seven days following discharge. The overall 30-day readmission rate was 40.5% and mean LOS 8.5 days. The clinical prediction model demonstrated that 29% of the variability in LOS was accounted for by the relationship of Hb SS genotype, presence of dependent children at home, and PROMIS Global Physical Health score.
Administering PROs among adults with SCD hospitalized for VOC is feasible and informative. Participants reported recurrent, prolonged and severe VOCs. PROMIS and ASCQ-Me scores indicated substantial suffering as compared to the general U.S. and outpatient SCD populations. The striking 30-day readmission rate (40.5%) highlights that hospitalized adults with SCD are a particularly vulnerable population.
Notlar:
School code: 0845
Mevcut:*
Yer Numarası | Demirbaş Numarası | Shelf Location | Lokasyon / Statüsü / İade Tarihi |
---|---|---|---|
XX(689379.1) | 689379-1001 | Proquest E-Tez Koleksiyonu | Arıyor... |
On Order
Liste seç
Bunu varsayılan liste yap.
Öğeler başarıyla eklendi
Öğeler eklenirken hata oldu. Lütfen tekrar deneyiniz.
:
Select An Item
Data usage warning: You will receive one text message for each title you selected.
Standard text messaging rates apply.