Daily changes in pain, mood and physical function in youth hospitalized for sickle cell disease pain

被引:26
|
作者
Zempsky, William T. [1 ,2 ]
Palermo, Tonya M. [3 ]
Corsi, John M. [1 ]
Lewandowski, Amy S. [3 ]
Zhou, Chuan [3 ]
Casella, James F. [4 ]
机构
[1] Connecticut Childrens Med Ctr, Hartford, CT 06106 USA
[2] Univ Connecticut, Sch Med, Farmington, CT USA
[3] Univ Washington, Sch Med, Seattle, WA USA
[4] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
来源
PAIN RESEARCH & MANAGEMENT | 2013年 / 18卷 / 01期
关键词
Adolescents; Functional assessment; Pain assessment; Physical functioning; Sickle cell disease; Vaso-occlusive episode; ACTIVITY LIMITATIONS INTERVIEW; CHILDREN; VALIDATION; ADOLESCENTS; IMPAIRMENT; DISABILITY; QUALITY; SCALE;
D O I
10.1155/2013/487060
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Youth with sickle cell disease (SCD) are commonly hospitalized for treatment of painful vaso-occlusive episodes (VOE). However, limited data are available concerning the course of hospitalization for these children and adolescents and, in particular, whether daily changes occur in pain, emotional status and physical function. OBJECTIVES: To characterize changes in daily pain intensity, physical function and mood over the course of hospitalization, and to determine whether specific clinical characteristics were associated with these changes. METHODS: Daily ratings of pain (0 to 10 numerical rating scale) and mood (Positive and Negative Affect Scale for Children) were completed by 25 youth (11 to 20 years of age) with SCD over a total of 152 days (mean [+/- SD] = 6.7 +/- 5.6 days) of hospitalization. Trained raters determined each youth's daily physical function. RESULTS: Linear mixed modelling was used to examine changes in pain, mood and physical function during hospital stay. The rate of change over the course of hospitalization was significant for reductions in pain intensity (P<0.001) and improvements in physical (motor) function (P=0.001). Positive affect over time was significantly associated with subjects' physical function scores (B 0.24 [95% CI 0.12 to 0.35]) but not with their pain scores. In contrast, negative affect was positively associated with pain and inversely associated with physical function scores (B 1.58 [95% CI 0.23 to 2.93]). CONCLUSIONS: The results of the present study demonstrated that children made daily improvements in physical function and pain over hospitalization for VOE. Mood was related to changes in pain and physical recovery. Assessment of physical function and mood during hospitalization may help guide strategies to better understand the pain experience in youth with SCD hospitalized with VOE.
引用
收藏
页码:33 / 38
页数:6
相关论文
共 50 条
  • [1] Pain, mood, and functional status in youth with sickle cell disease hospitalized for pain
    Zempsky, W.
    O'Hara, E.
    Santanelli, J.
    Palermo, T.
    JOURNAL OF PAIN, 2013, 14 (04): : S2 - S2
  • [2] Physical Activity and Pain in Youth With Sickle Cell Disease
    Karlson, Cynthia W.
    Delozier, Alexandria M.
    Seals, Samantha R.
    Britt, Anna B.
    Stone, Amanda L.
    Reneker, Jennifer C.
    Jackson, Erin A.
    McNaull, Melissa M.
    Credeur, Daniel P.
    Welsch, Michael A.
    FAMILY & COMMUNITY HEALTH, 2020, 43 (01) : 1 - 9
  • [3] NOVEL APPROACH TO DESCRIBING PAIN IMPACT ON FUNCTION OF SICKLE CELL YOUTH HOSPITALIZED FOR VASOOCCLUSIVE PAIN
    Santanelli, James P.
    Zempsky, William T.
    Casella, James
    New, Tamara
    Smith-Whitley, Kim
    O'Hara, Emily A.
    AMERICAN JOURNAL OF HEMATOLOGY, 2013, 88 (12) : E38 - E38
  • [4] Widespread Pain Among Youth With Sickle Cell Disease Hospitalized With Vasoocclusive Pain: A Different Clinical Phenotype?
    Zempsky, William T.
    Wakefield, Emily O.
    Santanelli, James P.
    New, Tamara
    Smith-Whitley, Kimberly
    Casella, James F.
    Palermo, Tonya M.
    CLINICAL JOURNAL OF PAIN, 2017, 33 (04): : 335 - 339
  • [5] Is pain body surface area a valid method to assess pain in hospitalized youth with sickle cell disease?
    Santanelli, I.
    Zempsky, W.
    O'Hara, E.
    New, T.
    Smith-Whitley, K.
    Casella, J.
    JOURNAL OF PAIN, 2014, 15 (04): : S2 - S2
  • [6] Pain and stress in sickle cell disease: An analysis of daily pain records
    Porter, LS
    Gil, KM
    Sedway, JA
    Ready, J
    Workman, E
    Thompson, RJ
    INTERNATIONAL JOURNAL OF BEHAVIORAL MEDICINE, 1998, 5 (03) : 185 - 203
  • [7] Pain and stress in sickle cell disease: An analysis of daily pain records
    Laura S. Porter
    Karen M. Gil
    Jan A. Sedway
    Jawana Ready
    Elizabeth Workman
    Robert J. Thompson
    International Journal of Behavioral Medicine, 1998, 5 : 185 - 203
  • [8] Daily assessment of pain in adults with sickle cell disease
    Smith, Wally R.
    Penberthy, Lynne T.
    Bovbjerg, Viktor E.
    McClish, Donna K.
    Roberts, John D.
    Dahman, Bassarn
    Aisiku, Imoigele P.
    Levenson, James L.
    Roseff, Susan D.
    ANNALS OF INTERNAL MEDICINE, 2008, 148 (02) : 94 - 101
  • [9] Pain in children and adolescents with sickle cell disease: An analysis of daily pain diaries
    Gil, KM
    Porter, L
    Ready, J
    Workman, E
    Sedway, J
    Anthony, KK
    CHILDRENS HEALTH CARE, 2000, 29 (04) : 225 - 241
  • [10] Daily Pain, Physical Activity, and Home Fluid Intake in Pediatric Sickle Cell Disease
    Karlson, CynthiaW.
    Baker, Anna M.
    Bromberg, Maggie H.
    Elkin, Thomas David
    Majumdar, Suvankar
    Palermo, Tonya M.
    JOURNAL OF PEDIATRIC PSYCHOLOGY, 2017, 42 (03) : 335 - 344