Deaths in children with sickle cell disease in a pediatrics department in Central Africa

被引:20
|
作者
Koko, J
Dufillot, D
M'Ba-Meyo, J
Gahouma, D
Kani, F
机构
[1] Hop Pediat Owendo, Serv Pediat Gen, Libreville, Gabon
[2] Hop Pediat Owendo, Serv Chirurg Pediat, Libreville, Gabon
[3] Hop Pediat Owendo, Med Biol Lab, Libreville, Gabon
来源
ARCHIVES DE PEDIATRIE | 1998年 / 5卷 / 09期
关键词
anemia; sickle cell; mortality; Gabon; child;
D O I
10.1016/S0929-693X(98)80003-1
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background. - Sickle cell disease is a serious public health problem in Gabon with a relatively high mortality rate. Patients and methods, - Charts of 23 children (nine boys, 14 girls) who died of complications from sickle cell anemia in the department of pediatrics of Owendo Pediatric Hospital (Libreville, Gabon), from January 1, 1990 through December 31, 1992, were analysed retrospectively. Results. - Approximately two-thirds of the children (60.9%) were under 5 years of age. The great majority of patients were from low socio-economic standard families. Of 319 deaths observed during the study period 23 were due to sickle cell disease-associated complications for an overall mortality rare of 7.2% and a related mortality of 3.6%. Commonest causes of deaths were severe anemia (11 cases, ie, 47.8%), which affected predominantly the younger patients between 6 months and 5 years (eight cases), infections (30.4%) and blood transfusion complications (21.7%). Conclusion. - To decrease these mortality rates, appropriate health supervision and well-designed preventive strategies are needed. (C) 1998 Elsevier, Paris.
引用
收藏
页码:965 / 969
页数:5
相关论文
共 50 条
  • [31] Asthma in children with sickle cell disease
    Willen, Shaina M.
    Rodeghier, Mark
    DeBaun, Michael R.
    CURRENT OPINION IN PEDIATRICS, 2019, 31 (03) : 349 - 356
  • [32] Sickle Cell Disease and Plumbism in Children
    Issaivanan, Magimairajan
    Ahmed, Rafat
    Shekher, Monica
    Esernio-Jenssen, Debra
    Manwani, Deepa
    PEDIATRIC BLOOD & CANCER, 2009, 52 (05) : 653 - 656
  • [33] Sickle Cell Disease in the Emergency Department: Complications and Management
    Barriteau, Christina M.
    McNaull, Melissa A.
    CLINICAL PEDIATRIC EMERGENCY MEDICINE, 2018, 19 (02) : 103 - 109
  • [34] Wheezing in children with sickle cell disease
    Glassberg, Jeffrey A.
    Strunk, Robert
    DeBaun, Michael R.
    CURRENT OPINION IN PEDIATRICS, 2014, 26 (01) : 9 - 18
  • [35] Stroke in children with sickle cell disease
    Kirkham F.J.
    deBaun M.R.
    Current Treatment Options in Neurology, 2004, 6 (5) : 357 - 375
  • [36] Malaria continues to select for sickle cell trait in Central Africa
    Elguero, Eric
    Delicat-Loembet, Lucrece M.
    Rougeron, Virginie
    Arnathau, Celine
    Roche, Benjamin
    Becquart, Pierre
    Gonzalez, Jean-Paul
    Nkoghe, Dieudonne
    Sica, Lucas
    Leroy, Eric M.
    Durand, Patrick
    Ayala, Francisco J.
    Ollomo, Benjamin
    Renaud, Francois
    Prugnolle, Franck
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (22) : 7051 - 7054
  • [37] COVID-19 outcomes in sickle cell disease and sickle cell trait
    Christian, Jana
    Lanzkron, Sophie
    Naik, Rakhi P.
    BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2022, 35 (03)
  • [38] The cost of health care for children and adults with sickle cell disease
    Kauf, Teresa L.
    Coates, Thomas D.
    Liu Huazhi
    Mody-Patel, Nikita
    Hartzema, Abraham G.
    AMERICAN JOURNAL OF HEMATOLOGY, 2009, 84 (06) : 323 - 327
  • [39] Central Nervous System Events in Children with Sickle Cell Disease Presenting Acutely with Headache
    Hines, Patrick C.
    McKnight, Therese P.
    Seto, Wendy
    Kwiatkowski, Janet L.
    JOURNAL OF PEDIATRICS, 2011, 159 (03) : 472 - 478
  • [40] Malocclusion and treatment need in children and adolescents with sickle cell disease
    Alves e Luna, Ana Claudia
    Godoy, Fabiana
    de Menezes, Valdenice Aparecida
    ANGLE ORTHODONTIST, 2014, 84 (03) : 467 - 472