Literature DB >> 6819042

Causes of death in sickle-cell disease in Jamaica.

A N Thomas, C Pattison, G R Serjeant.   

Abstract

A review of the causes of death in 276 patients with sickle-cell disease showed that although the greatest mortality occurred in the first five years of life, roughly one-quarter were aged over 30. Commonest causes of death in the first ten years included acute splenic sequestration, septicaemia, meningitis, aplastic crises, and gastroenteritis. In older patients cerebrovascular accidents and renal failure became common. The acute chest syndrome affected all age groups about equally but appeared to result predominantly from infection in the young and embolism or thrombosis in the old.

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Year:  1982        PMID: 6819042      PMCID: PMC1499426          DOI: 10.1136/bmj.285.6342.633

Source DB:  PubMed          Journal:  Br Med J (Clin Res Ed)        ISSN: 0267-0623


  5 in total

1.  The pathology of sickle-cell disease in West Africa.

Authors:  G M EDINGTON
Journal:  Trans R Soc Trop Med Hyg       Date:  1955-05       Impact factor: 2.184

2.  Bacterial meningitis and septicemia in sickle cell disease.

Authors:  G D Overturf; D Powars; L J Baraff
Journal:  Am J Dis Child       Date:  1977-07

3.  Acute splenic sequestration crises (ASSC) in young children with sickle cell anemia. Clinical observations in 20 episodes in 14 children.

Authors:  R A Seeler; M Z Shwiaki
Journal:  Clin Pediatr (Phila)       Date:  1972-12       Impact factor: 1.168

4.  Early deaths in Jamaican children with sickle cell disease.

Authors:  D W Rogers; J M Clarke; L Cupidore; A M Ramlal; B R Sparke; G R Serjeant
Journal:  Br Med J       Date:  1978-06-10

5.  Renal function in patients over 40 with homozygous sickle-cell disease.

Authors:  A G Morgan; G R Serjeant
Journal:  Br Med J (Clin Res Ed)       Date:  1981-04-11
  5 in total
  53 in total

1.  Accuracy of the urinary albumin to creatinine ratio as a predictor of albuminuria in adults with sickle cell disease.

Authors:  C S P Lima; P V Bottini; C R Garlipp; A O Santos; F F Costa; S T O Saad
Journal:  J Clin Pathol       Date:  2002-12       Impact factor: 3.411

2.  Complications of sickle cell anaemia in children in Northwestern Tanzania.

Authors:  Hamza Saidi; Luke R Smart; Erasmus Kamugisha; Emmanuela E Ambrose; Deogratias Soka; Robert N Peck; Julie Makani
Journal:  Hematology       Date:  2016-02-17       Impact factor: 2.269

Review 3.  The natural history of sickle cell disease.

Authors:  Graham R Serjeant
Journal:  Cold Spring Harb Perspect Med       Date:  2013-10-01       Impact factor: 6.915

4.  Acute splenic sequestration crisis in a young woman with homozygous sickle cell anaemia.

Authors:  P S Sarma
Journal:  Postgrad Med J       Date:  1989-02       Impact factor: 2.401

5.  Normal haemoglobin electrophoretic pattern in a patient with sickle cell disease and end stage renal failure.

Authors:  J C Marsh; L R Baker; G W Marsh
Journal:  J Clin Pathol       Date:  1988-03       Impact factor: 3.411

6.  Defining Sickle Cell Disease Mortality Using a Population-Based Surveillance System, 2004 through 2008.

Authors:  Susan T Paulukonis; James R Eckman; Angela B Snyder; Ward Hagar; Lisa B Feuchtbaum; Mei Zhou; Althea M Grant; Mary M Hulihan
Journal:  Public Health Rep       Date:  2016 Mar-Apr       Impact factor: 2.792

7.  Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Authors:  A Driss; K O Asare; J M Hibbert; B E Gee; T V Adamkiewicz; J K Stiles
Journal:  Genomics Insights       Date:  2009-07-30

8.  Raised D-dimer levels in acute sickle cell crisis and their correlation with chest X-ray abnormalities.

Authors:  Javeed Dar; Inam Mughal; Hilali Hassan; Taj E Al Mekki; Zivani Chapunduka; Imad S A Hassan
Journal:  Ger Med Sci       Date:  2010-10-08

9.  Clinical presentation of acute chest syndrome in sickle cell disease.

Authors:  C Taylor; F Carter; J Poulose; S Rolle; S Babu; S Crichlow
Journal:  Postgrad Med J       Date:  2004-06       Impact factor: 2.401

10.  Sickle cell disease patients in eastern province of Saudi Arabia suffer less severe acute chest syndrome than patients with African haplotypes.

Authors:  M K Alabdulaali
Journal:  Ann Thorac Med       Date:  2007-10       Impact factor: 2.219

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