Caring for Simon: A Case Study in Care for an Infant with Trisomy 18

被引:0
|
作者
Crosier, Sheryl [1 ]
Bruns, Deborah A. [1 ]
Crosier, Sheryl [1 ]
机构
[1] So Illinois Univ, Carbondale, IL 62901 USA
来源
JOGNN-JOURNAL OF OBSTETRIC GYNECOLOGIC AND NEONATAL NURSING | 2012年 / 41卷
关键词
trisomy; 18; NICU care team; cardiac anomalies; decision making; collaboration;
D O I
10.1111/j.1552-6909.2012.01363_31.x
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
[No abstract available]
引用
收藏
页码:S181 / S181
页数:1
相关论文
共 50 条
  • [31] Survival, Medical Care and Quality of Life in Children with Trisomy 13 and 18
    Kusztrich, A.
    Hueseman, D.
    Garten, L.
    Neitzel, H.
    Buehrer, C.
    KLINISCHE PADIATRIE, 2016, 228 (05): : 240 - 244
  • [32] Congenital Anomalies Associated with Trisomy 18 or Trisomy 13: A Registry-Based Study in 16 European Countries, 2000-2011
    Springett, Anna
    Wellesley, Diana
    Greenlees, Ruth
    Loane, Maria
    Addor, Marie-Claude
    Arriola, Larraitz
    Bergman, Jorieke
    Cavero-Carbonell, Clara
    Csaky-Szunyogh, Melinda
    Draper, Elizabeth S.
    Garne, Ester
    Gatt, Miriam
    Haeusler, Martin
    Khoshnood, Babak
    Klungsoyr, Kari
    Lynch, Catherine
    Dias, Carlos Matias
    McDonnell, Robert
    Nelen, Vera
    O'Mahony, Mary
    Pierini, Anna
    Queisser-Luft, Annette
    Rankin, Judith
    Rissmann, Anke
    Rounding, Catherine
    Stoianova, Sylvia
    Tuckerz, David
    Zymak-Zakutnia, Natalya
    Morris, Joan K.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (12) : 3062 - 3069
  • [33] Constellation of congenital abnormalities in an infant: A new syndrome or tissue-specific mosaicism for trisomy 18?
    Shashi, V
    Golden, WL
    vonKapHerr, C
    Wilson, WG
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1996, 62 (01): : 38 - 41
  • [34] Caffeine for the Treatment of Central Apnea in Trisomy 18: A Case Study in the Novel Use of Methylxanthines in Palliative Transport
    Ariagno, Sydney
    Thorvilson, Megan
    Andersen, Lezlie
    Collura, Christopher
    JOURNAL OF PALLIATIVE MEDICINE, 2022, 25 (05) : 840 - 843
  • [35] An infant with trisomy 9 and partial trisomy 12 derived from maternal balanced translocation: A case report and literature review
    Ming, Shengjin
    Zhou, Zhumei
    Huang, Yao
    Huang, Ying
    Zhong, Jinping
    Li, Yingli
    JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2024, 52 (11)
  • [36] Hepatoblastoma associated with trisomy 18 syndrome: A case report and a review of the literature
    Maruyama, K
    Ikeda, H
    Koizumi, T
    PEDIATRICS INTERNATIONAL, 2001, 43 (03) : 302 - 305
  • [37] TRISOMY 18 PRESENTING WITH MEGACYSTIS AND INCREASED NUCHAL TRANSLUCENCY: A CASE REPORT
    Sakin, Onder
    Kars, Blent
    Demir, Cenk
    Turhan, Omer Talip
    Vatansever, Dogan
    JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, 2015, 78 (04): : 137 - 139
  • [38] The health-care experiences of families given the prenatal diagnosis of trisomy 18
    Walker, L. V.
    Miller, V. J.
    Dalton, V. K.
    JOURNAL OF PERINATOLOGY, 2008, 28 (01) : 12 - 19
  • [39] Teaching motor responses to a child with trisomy 18: A preliminary study
    Kusano, Maria Elisa
    Schmidt, Andreia
    BEHAVIORAL INTERVENTIONS, 2022, 37 (03) : 791 - 804
  • [40] Survival of children with trisomy 13 and trisomy 18: A multi-state population-based study
    Meyer, Robert E.
    Liu, Gang
    Gilboa, Suzanne M.
    Ethen, Mary K.
    Aylsworth, Arthur S.
    Powell, Cynthia M.
    Flood, Timothy J.
    Mai, Cara T.
    Wang, Ying
    Canfield, Mark A.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (04) : 825 - 837