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...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Makani, J, Kirkham, F, Komba, A, Ajala-Agbo, T, Otieno, G, Fegan, G, Williams, T, Marsh, K, Newton, C
التنسيق:	Journal article
اللغة:	English
منشور في:	2009

مواد مشابهة

Cerebral blood flow velocities measured by transcranial Doppler ultrasonography in children with sickle cell disease in Africa.
حسب: Makani, J, وآخرون
منشور في: (2005)

Spectrum of cerebral blood flow velocities measured by transcranial Doppler ultrasonography in children with sickle cell disease in Africa
حسب: Ajala-Agbo, T, وآخرون
منشور في: (2006)

Associations between oxyhaemoglobin desaturation and haematology in African children with sickle cell anaemia
حسب: Ajala-Agbo, T, وآخرون
منشور في: (2006)

Transcranial doppler in sickle cell disease in Africa
حسب: Ajala-Agbo, T, وآخرون
منشور في: (2007)

Nocturnal haemoglobin oxygen saturation variability is associated with vitamin C deficiency in Tanzanian children with sickle cell anaemia
حسب: L'Esperance, V, وآخرون
منشور في: (2010)

Bacteraemia in sickle cell anaemia is associated with low haemoglobin: a report of 890 admissions to a tertiary hospital in Tanzania
حسب: Makani, J, وآخرون
منشور في: (2015)

Nocturnal haemoglobin oxygen desaturation in urban and rural East African paediatric cohorts with and without sickle cell anaemia: a cross-sectional study
حسب: L'Esperance, VS, وآخرون
منشور في: (2015)

An observational study of children with sickle cell disease in Kilifi, Kenya.
حسب: Sadarangani, M, وآخرون
منشور في: (2009)

Bacteraemia in Kenyan children with sickle-cell anaemia: a retrospective cohort and case-control study.
حسب: Williams, T, وآخرون
منشور في: (2009)

Mortality in sickle cell anaemia in Africa: rates and risk factors from a prospective cohort study in Tanzania
حسب: Makani, J, وآخرون
منشور في: (2011)

Malaria as a cause of morbidity and mortality in children with homozygous sickle cell disease on the coast of Kenya
حسب: Komba, A, وآخرون
منشور في: (2009)

Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady-state: a nested case control study of deaths versus survivors.
حسب: Cox, SE, وآخرون
منشور في: (2011)

Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady-state: A nested case control study of deaths versus survivors
حسب: Cox, SE, وآخرون
منشور في: (2011)

Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell Anaemia
حسب: L. Tshilolo, وآخرون
منشور في: (2012-01-01)

FOETAL HAEMOGLOBIN AND DISEASE SEVERITY IN NIGERIAN CHILDREN WITH SICKLE CELL ANAEMIA.
حسب: Oluwagbemiga Adeodu, وآخرون
منشور في: (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
حسب: Ahunanya CN, وآخرون
منشور في: (2024-09-01)

A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia.
حسب: Titilope A Adeyemo, وآخرون
منشور في: (2018-01-01)

Relationship of age, anthropometry and haemoglobin concentration with echocardiographic findings in Nigerian children with sickle cell anaemia.
حسب: Animasahun BA, وآخرون
منشور في: (2024-07-01)

Interplay between foetal haemoglobin, micronutrients and oxidative stress biomarkers in sickle cell anaemia children
حسب: Ama Gyasiwaah Owusu-Poku, وآخرون
منشور في: (2022-12-01)

Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia.
حسب: Cox, SE, وآخرون
منشور في: (2014)

Nutritional status, hospitalization and mortality among patients with sickle cell anaemia in Tanzania
حسب: Cox, SE, وآخرون
منشور في: (2011)

Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study.
حسب: Céline Renoux, وآخرون
منشور في: (2016-01-01)

Sickle cell anaemia in East Africa: Preliminary results from a cohort study.
حسب: Makani, J, وآخرون
منشور في: (2006)

Sickle haemoglobin, haemoglobin C and malaria mortality feedbacks
حسب: Goncalves, B, وآخرون
منشور في: (2016)

Fetal hemoglobin is associated with peripheral oxygen saturation in sickle cell disease in Tanzania.
حسب: Nkya, S, وآخرون
منشور في: (2017)

A Comparison of MRI Quantitative Susceptibility Mapping and TRUST-Based Measures of Brain Venous Oxygen Saturation in Sickle Cell Anaemia
حسب: Russell Murdoch, وآخرون
منشور في: (2022-08-01)

Sickle haemoglobin comes of age
حسب: Graham Serjeant
منشور في: (2014-02-01)

Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia
حسب: Sharon E. Cox, وآخرون
منشور في: (2014-01-01)

Perturbations of cerebral hemodynamics in Kenyans with cerebral malaria.
حسب: Newton, C, وآخرون
منشور في: (1996)

Evaluation of the Nitrite Test in Screening for Urinary Tract Infection in Febrile Children with Sickle Cell Anaemia.
حسب: Brown BJ, وآخرون
منشور في: (2024-07-01)

Steady state haemoglobin level increases with the proportion of erythrocyte membrane n-3 fatty acids in sickle cell anaemia
حسب: Okpala, Iheanyi, وآخرون
منشور في: (2004)

Continuous EEG monitoring in Kenyan children with non-traumatic coma.
حسب: Gwer, S, وآخرون
منشور في: (2012)

Continuous EEG monitoring in Kenyan children with non-traumatic coma
حسب: Gwer, S, وآخرون
منشور في: (2012)

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

Fetal‐haemoglobin enhancing genotype at BCL11A reduces HbA2 levels in patients with sickle cell anaemia
حسب: Titilope A. Adeyemo, وآخرون
منشور في: (2021-08-01)

Nutritional status, hospitalization and mortality among patients with sickle cell anemia in Tanzania.
حسب: Cox, SE, وآخرون
منشور في: (2011)

Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.
حسب: Cox, SE, وآخرون
منشور في: (2014)

Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania
حسب: Cox, SE, وآخرون
منشور في: (2014)

Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania.
حسب: Makani, J, وآخرون
منشور في: (2011)

Malaria protection due to sickle haemoglobin depends on parasite genotype
حسب: Band, G, وآخرون
منشور في: (2021)