Evaluation of the Psychological Problems in Children with Sickle Cell Anemia and Their Families

被引:22
|
作者
Unal, Selma [1 ]
Toros, Fevziye [2 ]
Kutuk, Meryem Ozlem [2 ]
Uyaniker, Mevhibe Gulen [1 ]
机构
[1] Mersin Univ, Fac Med, Sect Pediat Hematol, Dept Pediat, TR-33079 Mersin, Turkey
[2] Mersin Univ, Fac Med, Dept Child Psychiat, TR-33079 Mersin, Turkey
关键词
anxiety; depression; family; psychological problems; sickle cell anemia; DISEASE; ADOLESCENTS; INVENTORY; PAIN; PERFORMANCE; ANXIETY;
D O I
10.3109/08880018.2010.540735
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sickle cell anemia (SCA) is a chronic disease and it would be expected that the children with SCA are at high risk of developing psychosocial problems. In this study the authors intended to evaluate both the psychiatric problems among SCA patients and their families and put forward the relation between the clinical findings and psychiatric problems. Forty children were included in the study. The patients were classified according to their histories of painful crises in the past 1 year. The children who have had a history of painful crisis 1-4, 5-10, and over 10 times were classified as group 1, group 2, and group 3, respectively. The depression levels of the children in group 3 were higher than group 1 (P = .018). The state of the anxiety level of the children and Beck Anxiety Inventory of the mothers were higher in group 3 than in group 1 (P = .004). In addition, anxiety levels of the mothers who had children with social limitations and painful episodes were higher than the anxiety levels of the mothers who had children without social limitations and painful episodes (P = .006 and P = .004, respectively). We found a relationship between the anxiety and depression levels in children and the anxiety, depression, and marital adjustment levels in mothers. In conclusion, the frequency of psychological disorders appears to increase in patients with SCA, as with many chronic diseases. Especially, the patients who had higher frequencies of painful crises and their mothers had increased depression and state anxiety levels. Thus, the patients with SCA and their families should be evaluated regularly in terms of psychological disorders.
引用
收藏
页码:321 / 328
页数:8
相关论文
共 50 条
  • [41] Cerebral vasculopathy in children with sickle cell anemia
    Fasano, Ross M.
    Meier, Emily R.
    Hulbert, Monica L.
    BLOOD CELLS MOLECULES AND DISEASES, 2015, 54 (01) : 17 - 25
  • [42] Microangiopathic glomerulopathy in children with sickle cell anemia
    Vogler, C
    Wood, E
    Lane, P
    Ellis, E
    Cole, B
    Thorpe, C
    PEDIATRIC PATHOLOGY & LABORATORY MEDICINE, 1996, 16 (02): : 275 - 284
  • [43] Airway Hyperresponsiveness in Children With Sickle Cell Anemia
    Field, Joshua J.
    Stocks, Janet
    Kirkham, Fenella J.
    Rosen, Carol L.
    Dietzen, Dennis J.
    Semon, Trisha
    Kirkby, Jane
    Bates, Pamela
    Seicean, Sinziana
    DeBaun, Michael R.
    Redline, Susan
    Strunk, Robert C.
    CHEST, 2011, 139 (03) : 563 - 568
  • [44] Pubertal patterns in children with sickle cell anemia: A case-control study in Cameroon
    Betoko, Ritha Mbono
    Sap, Suzanne
    Alima, Anastasie Yanda
    Chelo, David
    Nengom, Jocelyn Tony
    Simon, Dominique
    Chevenne, Didier
    Ndombo, Paul Koki
    ARCHIVES DE PEDIATRIE, 2023, 30 (07): : 466 - 470
  • [45] Cardiac abnormalities in children with sickle cell anemia
    Batra, AS
    Acherman, RJ
    Wong, WY
    Wood, JC
    Chan, LS
    Ramicone, E
    Ebrahimi, M
    Wong, PC
    AMERICAN JOURNAL OF HEMATOLOGY, 2002, 70 (04) : 306 - 312
  • [46] Evaluation of Hearing and Balance Functions of Patients with Sickle Cell Anemia
    Sarac, Elif Tugba
    Boke, Bilgehan
    Okuyucu, Semsettin
    AUDIOLOGY AND NEURO-OTOLOGY, 2018, 23 (02) : 122 - 125
  • [47] Advanced clinical parameters: A complementary hydroxyurea adherence evaluation in sickle cell anemia treatment
    Moreira, Isabela Delfino
    Machado Lessa, Carem Luana
    Goncalves Rocha, Gueverson Leonardo
    Schmitz, Laura Dewes
    Jahnke, Viviane Schmitt
    Fogliatto, Laura Maria
    Werlang, Maria Cristina
    Rotta, Liane Nanci
    EUROPEAN JOURNAL OF HAEMATOLOGY, 2022, 109 (06) : 736 - 748
  • [48] Epidemiology of sickle cell nephropathy in sickle cell anemia children, Saudi Arabia
    AlAmeer, Mahdi R.
    Alsarhan, Batool K.
    Alsarhan, Leen K.
    Albeshi, Saeed M.
    Alhenaki, Ghazlan A.
    Alqhtani, Muhanned M.
    Alasmari, Hind R.
    Alabdali, Areej H.
    Alsaleh, Taghreed A.
    Alyami, Nouf M.
    Almansour, Arwa M.
    Ahnqaadi, Amna K.
    Alhazmi, Alaa A.
    MEDICAL SCIENCE, 2021, 25 (112) : 1486 - 1493
  • [49] Orofacial manifestations in patients with sickle cell anemia
    Costa Mendes, Patricia Helena
    Fonseca, Naiara Goncalves
    Barbosa Martelli, Daniela Reis
    Ferreti Bonan, Paulo Rogerio
    Yamamoto de Almeida, Lana Kei
    de Melo, Luciana Antunes
    Martelli Junior, Hercilio
    QUINTESSENCE INTERNATIONAL, 2011, 42 (08): : 701 - 709
  • [50] Characterization of a cohort of Angolan children with sickle cell anemia treated with hydroxyurea
    Santos, Brigida
    Ginete, Catarina
    Goncalves, Elisangela
    Delgadinho, Mariana
    Miranda, Armandina
    Faustino, Paula
    Arez, Ana Paula
    Brito, Miguel
    BLOOD CELLS MOLECULES AND DISEASES, 2024, 105