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
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
  • [41] Sleep and fatigue among youth with sickle cell disease: A daily diary study
    Johnston, Julia D.
    Reinman, Laura C.
    Bills, Sarah E.
    Schatz, Jeffrey C.
    JOURNAL OF BEHAVIORAL MEDICINE, 2023, 46 (03) : 440 - 450
  • [42] AAPT Diagnostic Criteria for Chronic Sickle Cell Disease Pain
    Dampier, Carlton
    Palermo, Tonya M.
    Darbari, Deepika S.
    Hassell, Kathryn
    Smith, Wally
    Zempsky, William
    JOURNAL OF PAIN, 2017, 18 (05) : 490 - 498
  • [43] Depression and Anxiety as Moderators of the Pain-Social Functioning Relationship in Youth with Sickle Cell Disease
    Valrie, Cecelia
    Floyd, Alfonso
    Sisler, India
    Redding-Lallinger, Rupa
    Fuh, Beng
    JOURNAL OF PAIN RESEARCH, 2020, 13 : 729 - 736
  • [44] Sleep Moderating the Relationship Between Pain and Health Care Use in Youth With Sickle Cell Disease
    Valrie, Cecelia R.
    Alston, Kristen
    Fuh, Beng
    Redding-Lallinger, Rupa
    Sisler, India
    CLINICAL JOURNAL OF PAIN, 2020, 36 (02) : 117 - 123
  • [45] Prevalence and predictors of chronic pain intensity and disability among adults with sickle cell disease
    Matthie, Nadine
    Jenerette, Coretta
    Gibson, Ashley
    Paul, Sudeshna
    Higgins, Melinda
    Krishnamurti, Lakshmanan
    HEALTH PSYCHOLOGY OPEN, 2020, 7 (01)
  • [46] Optimism predicting daily pain medication use in adolescents with sickle cell disease
    Pence, Laura
    Valrie, Cecelia R.
    Gil, Karen M.
    Redding-Lallinger, Rupa
    Daeschner, Charles
    JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2007, 33 (03) : 302 - 309
  • [47] Criterion and Convergent Validity for 4 Measures of Pain in a Pediatric Sickle Cell Disease Population
    McClellan, Catherine B.
    Schatz, Jeffrey C.
    Mark, Teresa R. M.
    McKelvy, Alvin
    Puffer, Eve
    Roberts, Carla W.
    Sweitzer, Sarah M.
    CLINICAL JOURNAL OF PAIN, 2009, 25 (02) : 146 - 152
  • [48] A Healthcare Improvement Initiative to Increase Multidisciplinary Pain Management Referrals for Youth with Sickle Cell Disease
    Kingsley, Rae Ann
    PAIN MANAGEMENT NURSING, 2020, 21 (05) : 403 - 409
  • [49] Gout and sickle cell disease: not all pain is sickle cell pain
    Gupta, Sarthak
    Yui, Jennifer C.
    Xu, Dihua
    Fitzhugh, Courtney D.
    Clark, Caroline
    Siddiqui, Salahuddin
    Conrey, Anna K.
    Kato, Gregory J.
    Minniti, Caterina P.
    BRITISH JOURNAL OF HAEMATOLOGY, 2015, 171 (05) : 872 - 875
  • [50] A "dyadic dance": pain catastrophizing moderates the daily relationships between parent mood and protective responses and child chronic pain
    Neville, Alexandra
    Griep, Yannick
    Palermo, Tonya M.
    Vervoort, Tine
    Schulte, Fiona
    Yeates, Keith Owen
    Sumpton, Janice E.
    Mychasiuk, Richelle
    Noel, Melanie
    PAIN, 2020, 161 (05) : 1072 - 1082