Literature DB >> 16425722

[Effects of age on causes of hospitalization in children suffering from sickle cell disease].

J R Mabiala-Babela1, S A T Nkanza-Kaluwako, P S Ganga-Zandzou, S Nzingoula, P Senga.   

Abstract

The objective of this work was to assess the frequency the nature of complications and prognosis of the disease in children suffering from sickle cell disease. This retrospective study was conducted from January 2002 to December 2003 among 251 children suffering from sickle cell disease, hospitalized at the Brazzaville Teaching Hospital, Congo. The main hospitalization causes were dominated by the vaso-occlusive crisis (26.7%), anaemic crisis (20.3%) and infections (36.6%). The vaso-occlusive crisis were observed particularly in the 5 year-old children (p < 0.05); the hand-foot syndrome concerned in particular children under 5 years old. Anaemic crisis were found almost exclusively in patients under 5 (p < 0.05). The infections in children under 5 (35.8%) were almost as frequent as in older children (37.4%). Some non infectious complications were only observed in children above 5: cholithiasis, 4 cases; heart failure, 4 cases; hip osteonecrosis, 1 case. Global mortality was 4.8% and higher in children under five (p > 0.05). In addition, the death causes were dominated by anaemic crisis. In conclusion, this study stresses on the need to implement a primary prevention as well as a secondary prevention adapted to age.

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Year:  2005        PMID: 16425722

Source DB:  PubMed          Journal:  Bull Soc Pathol Exot        ISSN: 0037-9085


  6 in total

1.  [Sickle cell disease in stationary phase in 6-59 months children in Lubumbashi: epidemiology and clinical features].

Authors:  Mick Ya Pongombo Shongo; Olivier Mukuku; Toni Kasole Lubala; Augustin Mulangu Mutombo; Gray Wakamb Kanteng; Winnie Sombodi Umumbu; Robert Mbuli Lukamba; Stanislas Okitotsho Wembonyama; Oscar Numbi Luboya
Journal:  Pan Afr Med J       Date:  2014-09-24

2.  [Major sickle cell syndromes and infections associated with this condition in children in Burkina Faso].

Authors:  Sonia Douamba; Kisito Nagalo; Laure Tamini; Ismaël Traoré; Madibèlè Kam; Fla Kouéta; Diarra Yé
Journal:  Pan Afr Med J       Date:  2017-01-04

3.  [Evaluation of hemogram in patients with homozygous sickle cell disease: about 87 cases].

Authors:  Fatima Dahmani; Souad Benkirane; Jaafar Kouzih; Aziz Woumki; Hassan Mamad; Azlarab Masrar
Journal:  Pan Afr Med J       Date:  2016-12-20

4.  [Osteoarticular infections in patients with sickle cell disease in Lubumbashi: epidemiological study focusing on etiology and management].

Authors:  Manix Ilunga Banza; Nathalie Dinganga Kapessa; Augustin Kibonge Mukakala; Christelle Ngoie Ngoie; Yannick Tietie Ben N Dwala; Vincent De Paul Kaoma Cabala; Trésor Kibangula Kasanga; Erick Wakunga Unen
Journal:  Pan Afr Med J       Date:  2021-01-22

5.  Clinical profile of sickle cell disease in children treated at "Cliniques Universitaires de Bukavu" and "Clinique Ami des Enfants", Bukavu, Democratic Republic of the Congo.

Authors:  Viviane Feza Bianga; Mwanza Nangunia; Fernand Manga Oponjo; John Mambo Itongwa; Judicaël Iragi Mushubusha; Moise Mbaluku Colombe; Carmel Mbalo Walemba; Okitosho Wembonyama
Journal:  Pan Afr Med J       Date:  2022-02-03

6.  Sickle-Cell Disease Healthcare Cost in Africa: Experience of the Congo.

Authors:  L O Ngolet; M Moyen Engoba; Innocent Kocko; Alexis Elira Dokekias; Jean-Vivien Mombouli; Georges Marius Moyen
Journal:  Anemia       Date:  2016-02-02
  6 in total

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