Results from transcranial Doppler examination on children and adolescents with sickle cell disease and correlation between the time-averaged maximum mean velocity and hematological characteristics: a cross-sectional analytical study
- PMID: 21755247
- PMCID: PMC10866317
- DOI: 10.1590/s1516-31802011000300003
Results from transcranial Doppler examination on children and adolescents with sickle cell disease and correlation between the time-averaged maximum mean velocity and hematological characteristics: a cross-sectional analytical study
Abstract
Context and objective: Transcranial Doppler (TCD) detects stroke risk among children with sickle cell anemia (SCA). Our aim was to evaluate TCD findings in patients with different sickle cell disease (SCD) genotypes and correlate the time-averaged maximum mean (TAMM) velocity with hematological characteristics.
Design and setting: Cross-sectional analytical study in the Pediatric Hematology sector, Universidade Federal de São Paulo.
Methods: 85 SCD patients of both sexes, aged 2-18 years, were evaluated, divided into: group I (62 patients with SCA/Sß(0) thalassemia); and group II (23 patients with SC hemoglobinopathy/Sß(+) thalassemia). TCD was performed and reviewed by a single investigator using Doppler ultrasonography with a 2 MHz transducer, in accordance with the Stroke Prevention Trial in Sickle Cell Anemia (STOP) protocol. The hematological parameters evaluated were: hematocrit, hemoglobin, reticulocytes, leukocytes, platelets and fetal hemoglobin. Univariate analysis was performed and Pearson's coefficient was calculated for hematological parameters and TAMM velocities (P < 0.05).
Results: TAMM velocities were 137 ± 28 and 103 ± 19 cm/s in groups I and II, respectively, and correlated negatively with hematocrit and hemoglobin in group I. There was one abnormal result (1.6%) and five conditional results (8.1%) in group I. All results were normal in group II. Middle cerebral arteries were the only vessels affected.
Conclusion: There was a low prevalence of abnormal Doppler results in patients with sickle-cell disease. Time-average maximum mean velocity was significantly different between the genotypes and correlated with hematological characteristics.
CONTEXTO E OBJETIVO:: Doppler transcraniano (DTC) detecta risco de acidente vascular cerebral (AVC) em crianças com anemia falciforme (AF). O objetivo foi avaliar os resultados ao DTC nos diferentes genótipos da doença falciforme (DF) e correlacionar a velocidade média-máxima (VMMáx) às características hematológicas.
TIPO DE ESTUDO E LOCAL:: Estudo transversal analítico realizado no setor de Hematopediatria da Universidade Federal de São Paulo.
MÉTODOS:: 85 pacientes com DF, 2-18 anos, ambos os sexos, foram avaliados e divididos em: grupo I (62 com AF ou Sß0 talassemia); e grupo II (23 com hemoglobinopatia SC ou Sß+ talassemia). DTC foi realizado e revisado por um único investigador usando um aparelho de ultrassonografia Doppler com transdutor de 2MHz, conforme critérios do protocolo STOP (Stroke Prevention Trial in Sickle Cell Anemia). As variáveis hematológicas avaliadas foram: hematócrito, hemoglobina, reticulócitos, leucócitos, plaquetas, hemoglobina fetal. Análise univariada e coeficiente de Pearson calculados para parâmetros hematológicos e VMMáx, P < 0,05.
RESULTADOS:: As média das VMMáx foram de 137 ± 28 cm/s e 103 ± 19 cm/s nos grupos I e II, respectivamente. Houve correlação negativa da VMMáx com hematócrito e hemoglobina no grupo I. Houve um (1,6%) resultado anormal e 5 (8,1%) condicionais no grupo I; no grupo II, todos estavam normais. Artérias cerebrais médias foram as únicas acometidas.
CONCLUSÃO:: Houve baixa prevalência de resultados anormais ao DTC em pacientes com DF. A VMMáx foi significativamente diferente entre os genótipos da DF e apresentou correlação com variáveis hematológicas.
Conflict of interest statement
Similar articles
-
Transcranial Doppler in hemoglobin SC disease.Pediatr Blood Cancer. 2017 May;64(5). doi: 10.1002/pbc.26342. Epub 2016 Dec 13. Pediatr Blood Cancer. 2017. PMID: 27957790
-
Transcranial Doppler ultrasonography in children with sickle cell anemia: Clinical and laboratory correlates for elevated blood flow velocities.J Clin Ultrasound. 2014 Feb;42(2):89-95. doi: 10.1002/jcu.22099. Epub 2013 Oct 26. J Clin Ultrasound. 2014. PMID: 24166013 Clinical Trial.
-
Can peak systolic velocities be used for prediction of stroke in sickle cell anemia?Pediatr Radiol. 2005 Jan;35(1):66-72. doi: 10.1007/s00247-004-1282-9. Epub 2004 Oct 23. Pediatr Radiol. 2005. PMID: 15517239 Clinical Trial.
-
How I manage sickle cell patients with high transcranial doppler results.Br J Haematol. 2017 Nov;179(3):377-388. doi: 10.1111/bjh.14850. Epub 2017 Aug 2. Br J Haematol. 2017. PMID: 28771666 Review.
-
Big strokes in small persons.Arch Neurol. 2007 Nov;64(11):1567-74. doi: 10.1001/archneur.64.11.1567. Arch Neurol. 2007. PMID: 17998439 Review.
Cited by
-
Pattern of Cerebral Blood Flow Velocity Using Transcranial Doppler Ultrasonography in Children with Sickle Cell Disorder in Lagos State, Nigeria.Mediterr J Hematol Infect Dis. 2017 Aug 14;9(1):e2017050. doi: 10.4084/MJHID.2017.050. eCollection 2017. Mediterr J Hematol Infect Dis. 2017. PMID: 28894559 Free PMC article.
-
Stroke Avoidance for Children in REpública Dominicana (SACRED): Protocol for a Prospective Study of Stroke Risk and Hydroxyurea Treatment in Sickle Cell Anemia.JMIR Res Protoc. 2017 Jun 2;6(6):e107. doi: 10.2196/resprot.7491. JMIR Res Protoc. 2017. PMID: 28576754 Free PMC article.
-
Transcranial Doppler sonography and the effect of haematopoietic stem cell transplantation in sickle cell disease.Neurol Res Pract. 2022 Apr 4;4(1):12. doi: 10.1186/s42466-022-00175-y. Neurol Res Pract. 2022. PMID: 35369878 Free PMC article.
-
[Transcranial doppler in sickle cell disease (SCD) in Malagasy children].Pan Afr Med J. 2016 Apr 29;23:264. doi: 10.11604/pamj.2016.23.264.7072. eCollection 2016. Pan Afr Med J. 2016. PMID: 27516829 Free PMC article. French.
-
Transcranial doppler as screening method for sickling crises in children with sickle cell anemia: a latin America cohort study.BMC Pediatr. 2022 Jun 27;22(1):368. doi: 10.1186/s12887-022-03429-5. BMC Pediatr. 2022. PMID: 35761209 Free PMC article.
References
-
- Manual de diagnóstico e tratamento de doenças falciformes . Brasília: Anvisa; 2002. Available from: http://www.anvisa.gov.br/divulga/public/sangue/hemoglobinopatia/diagnost.... Accessed in 2011 (Jan 24)
-
- Cançado RD, Jesus JA. A doença falciforme no Brasil (editorial) [Sickle cell disease in Brazil: (editorial)] Rev Bras Hematol Hemoter. 2007;29(3):204–206.
-
- Huttenlocher PR, Moohr JW, Johns L, Brown FD. Cerebral blood flow in sickle cell cerebrovascular disease. Pediatrics. 1984;73(5):615–621. - PubMed
-
- Zago MA, Pinto ACS. Fisiopatologia das doenças falciformes: da mutação genética à insuficiência de múltiplos órgãos [The pathophysiology of sickle cell disease: from the genetic mutation to multiorgan dysfunction] Rev Bras Hematol Hemoter. 2007;29(3):207–214.
-
- Ohene-Frempong K, Weiner SJ, Sleeper LA, et al. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood. 1998;91(1):288–294. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical