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Sickle Cell Disease

Determinants of Blood Pressure in Adults with Sickle Cell Disease

Pre-published Manuscript

This manuscript has been assigned to a volume and issue but has not yet been published. It is either being edited, typeset or is in the proof stage of publication.
In the pre-published stage, this manuscript may contain statements, opinions, and information that have errors in facts, figures, or interpretation. Any final changes in this manuscript will be made at the time of publication and will be reflected in the final electronic version of the issue. The editors and authors and their respective employees are not responsible or liable for the use of any such inaccurate or misleading data, opinion or information contained in the articles in this section.

The Prevalence of Marijuana Smoking in Young Adults with Sickle Cell Disease: A Longitudinal Study

Issue: 
Pages: 
224–7
Synopsis: 
A history of marijuana smoking was common in young adults with sickle cell disease. Usage increased between 2000 and 2004, and was seldom for medicinal purposes.

ABSTRACT

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e-Published: 10 Jun, 2013

Open Splenectomy in Jamaican Children with Sickle Cell Disease

Issue: 
Pages: 
37–41
Synopsis: 
One-hundred and ten splenectomies performed on children with sickle cell disease at the University Hospital of the West Indies are reviewed. There was low morbidity and no mortality. Open splenectomy remains the gold standard for patients with sickle cell disease requiring splenectomy.

ABSTRACT

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e-Published: 06 Jun, 2013

Laparoscopic Cholecystectomy for Chronic Cholecystitis in Jamaican Patients with Sickle Cell Disease: Preliminary Experience

Issue: 
Pages: 
22–4
Synopsis: 
Acute chest syndrome remains a significant problem in patients with sickle cell disease subjected to laparoscopic cholecystectomy.

ABSTRACT

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e-Published: 06 Jun, 2013

Iron Deficiency Anaemia in Jamaican Children, Aged 1–5 Years, with Sickle Cell Disease

Issue: 
Pages: 
292–6
Synopsis: 
Iron deficiency anaemia (IDA) occurs in children with sickle cell disease (SCD) in Jamaica. Further studies are needed to determine whether treatment of IDA in children with SCD reduces morbidity and is associated with clinical benefits such as improvement in neurocognitive function.

ABSTRACT

Objective: The aim of this study was to determine, using a combination of measures, the prevalence of iron deficiency anaemia (IDA) in children under five years-of-age who have sickle cell disease (SCD) and attend the Sickle Cell Clinic (SCU) of the Tropical Medicine Research Institute.

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e-Published: 06 Jun, 2013

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