Risk factors for high cerebral blood flow velocity and death in Kenyan children with Sickle Cell Anaemia: role of haemoglobin oxygen saturation and febrile illness.

Risk factors for high cerebral blood flow velocity and death in Kenyan children with Sickle Cell Anaemia: role of haemoglobin oxygen saturation and febrile illness.

High cerebral blood flow velocity (CBFv) and low haemoglobin oxygen saturation (SpO(2)) predict neurological complications in sickle cell anaemia (SCA) but any association is unclear. In a cross-sectional study of 105 Kenyan children, mean CBFv was 120 +/- 34.9 cm/s; 3 had conditional CBFv (170-199...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Makani, J, Kirkham, F, Komba, A, Ajala-Agbo, T, Otieno, G, Fegan, G, Williams, T, Marsh, K, Newton, C
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	2009

Παρόμοια τεκμήρια

Cerebral blood flow velocities measured by transcranial Doppler ultrasonography in children with sickle cell disease in Africa.
ανά: Makani, J, κ.ά.
Έκδοση: (2005)

Spectrum of cerebral blood flow velocities measured by transcranial Doppler ultrasonography in children with sickle cell disease in Africa
ανά: Ajala-Agbo, T, κ.ά.
Έκδοση: (2006)

Associations between oxyhaemoglobin desaturation and haematology in African children with sickle cell anaemia
ανά: Ajala-Agbo, T, κ.ά.
Έκδοση: (2006)

Transcranial doppler in sickle cell disease in Africa
ανά: Ajala-Agbo, T, κ.ά.
Έκδοση: (2007)

Nocturnal haemoglobin oxygen saturation variability is associated with vitamin C deficiency in Tanzanian children with sickle cell anaemia
ανά: L'Esperance, V, κ.ά.
Έκδοση: (2010)

Bacteraemia in sickle cell anaemia is associated with low haemoglobin: a report of 890 admissions to a tertiary hospital in Tanzania
ανά: Makani, J, κ.ά.
Έκδοση: (2015)

Nocturnal haemoglobin oxygen desaturation in urban and rural East African paediatric cohorts with and without sickle cell anaemia: a cross-sectional study
ανά: L'Esperance, VS, κ.ά.
Έκδοση: (2015)

An observational study of children with sickle cell disease in Kilifi, Kenya.
ανά: Sadarangani, M, κ.ά.
Έκδοση: (2009)

Bacteraemia in Kenyan children with sickle-cell anaemia: a retrospective cohort and case-control study.
ανά: Williams, T, κ.ά.
Έκδοση: (2009)

Mortality in sickle cell anaemia in Africa: rates and risk factors from a prospective cohort study in Tanzania
ανά: Makani, J, κ.ά.
Έκδοση: (2011)

Malaria as a cause of morbidity and mortality in children with homozygous sickle cell disease on the coast of Kenya
ανά: Komba, A, κ.ά.
Έκδοση: (2009)

Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady-state: a nested case control study of deaths versus survivors.
ανά: Cox, SE, κ.ά.
Έκδοση: (2011)

Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady-state: A nested case control study of deaths versus survivors
ανά: Cox, SE, κ.ά.
Έκδοση: (2011)

Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell Anaemia
ανά: L. Tshilolo, κ.ά.
Έκδοση: (2012-01-01)

FOETAL HAEMOGLOBIN AND DISEASE SEVERITY IN NIGERIAN CHILDREN WITH SICKLE CELL ANAEMIA.
ανά: Oluwagbemiga Adeodu, κ.ά.
Έκδοση: (2017-11-01)

Correlation of the middle cerebral artery blood flow velocity with age and Haemoglobin values of children with Sickle cell anaemia in Uyo
ανά: Ahunanya CN, κ.ά.
Έκδοση: (2024-09-01)

A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia.
ανά: Titilope A Adeyemo, κ.ά.
Έκδοση: (2018-01-01)

Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia.
ανά: Cox, SE, κ.ά.
Έκδοση: (2014)

Relationship of age, anthropometry and haemoglobin concentration with echocardiographic findings in Nigerian children with sickle cell anaemia.
ανά: Animasahun BA, κ.ά.
Έκδοση: (2024-07-01)

Interplay between foetal haemoglobin, micronutrients and oxidative stress biomarkers in sickle cell anaemia children
ανά: Ama Gyasiwaah Owusu-Poku, κ.ά.
Έκδοση: (2022-12-01)

Nutritional status, hospitalization and mortality among patients with sickle cell anaemia in Tanzania
ανά: Cox, SE, κ.ά.
Έκδοση: (2011)

Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study.
ανά: Céline Renoux, κ.ά.
Έκδοση: (2016-01-01)

Sickle cell anaemia in East Africa: Preliminary results from a cohort study.
ανά: Makani, J, κ.ά.
Έκδοση: (2006)

Sickle haemoglobin, haemoglobin C and malaria mortality feedbacks
ανά: Goncalves, B, κ.ά.
Έκδοση: (2016)

Fetal hemoglobin is associated with peripheral oxygen saturation in sickle cell disease in Tanzania.
ανά: Nkya, S, κ.ά.
Έκδοση: (2017)

A Comparison of MRI Quantitative Susceptibility Mapping and TRUST-Based Measures of Brain Venous Oxygen Saturation in Sickle Cell Anaemia
ανά: Russell Murdoch, κ.ά.
Έκδοση: (2022-08-01)

Sickle haemoglobin comes of age
ανά: Graham Serjeant
Έκδοση: (2014-02-01)

Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia
ανά: Sharon E. Cox, κ.ά.
Έκδοση: (2014-01-01)

Perturbations of cerebral hemodynamics in Kenyans with cerebral malaria.
ανά: Newton, C, κ.ά.
Έκδοση: (1996)

Evaluation of the Nitrite Test in Screening for Urinary Tract Infection in Febrile Children with Sickle Cell Anaemia.
ανά: Brown BJ, κ.ά.
Έκδοση: (2024-07-01)

Continuous EEG monitoring in Kenyan children with non-traumatic coma.
ανά: Gwer, S, κ.ά.
Έκδοση: (2012)

Continuous EEG monitoring in Kenyan children with non-traumatic coma
ανά: Gwer, S, κ.ά.
Έκδοση: (2012)

Steady state haemoglobin level increases with the proportion of erythrocyte membrane n-3 fatty acids in sickle cell anaemia
ανά: Okpala, Iheanyi, κ.ά.
Έκδοση: (2004)

Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania
ανά: Siana Nkya, κ.ά.
Έκδοση: (2017-09-01)

An accidental finding of a penile abscess in a febrile sickle cell anaemia child following circumcision
ανά: Aliyu Ibrahim
Έκδοση: (2014-01-01)

Fetal‐haemoglobin enhancing genotype at BCL11A reduces HbA2 levels in patients with sickle cell anaemia
ανά: Titilope A. Adeyemo, κ.ά.
Έκδοση: (2021-08-01)

Nutritional status, hospitalization and mortality among patients with sickle cell anemia in Tanzania.
ανά: Cox, SE, κ.ά.
Έκδοση: (2011)

Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.
ανά: Cox, SE, κ.ά.
Έκδοση: (2014)

Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania
ανά: Cox, SE, κ.ά.
Έκδοση: (2014)

Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania.
ανά: Makani, J, κ.ά.
Έκδοση: (2011)