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Transcranial Doppler examination in patients with sickle cell anemia

Yıl 2025, Cilt: 50 Sayı: 3, 761 - 769
https://doi.org/10.17826/cumj.1671978

Öz

Purpose: This study aimed to evaluate cerebral blood flow velocities using transcranial Doppler in children with sickle cell anemia, compared to healthy controls, in order to assess stroke risk among sickle cell patients.
Materials and Methods: A total of 80 children participated in this prospective study, which included 40 children with sickle cell anemia (16 girls, 24 boys) and a control group of 40 healthy children (22 girls, 18 boys). The age range of participants was from 3 to 20 years. Cerebral blood flow measurements were performed using a transcranial Doppler (TCD) ultrasonography through the transtemporal and occipital acoustic windows. Time-averaged maximum mean velocity (TAMMV), Resistive Index (RI) and Pulsation Index (PI) of the Middle Cerebral Artery (MCA), Anterior Cerebral Artery (ACA), Posterior Cerebral Artery (PCA), vertebral arteries and basilar artery were recorded.
Results: Children with sickle cell anemia demonstrated significantly elevated cerebral blood flow velocities in both the carotid and vertebrobasilar systems when compared to the control group. In the patient group, the mean±SD TAMMV values were 107.7±23.1 cm/s in the right MCA and 113.3±28.2 cm/s in the left MCA, whereas in the control group, these values were 77.9±16.4 cm/s and 78.1±14.8 cm/s, respectively. In three patients (7.5%) with sickle cell anemia, MCA TAMMV exceeded 170 cm/s. A negative correlation was observed between age and cerebral blood flow velocities. Additionally, RI and PI values for all examined vessels were significantly higher in the patient group compared to controls.
Conclusion: Transcranial Doppler ultrasonography is a valuable, non-invasive modality for assessing stroke risk in children with sickle cell anemia. Routine screening using TCD may facilitate timely preventive interventions.

Etik Beyan

This prospective study was approved by the Ethics Committee of Çukurova University Faculty of Medicine (Approval date/number:2011/07).

Kaynakça

  • Söylemez-Gökyer D, Kayaaltı Z. Türkiye’de orak hücreli anemi dağılımı, patofizyolojisi ve demir toksisitesi. Marmara Pharmaceutical Journal. 2016;20:92-9.
  • Karacaoğlu P, Boğa C. Orak hücre hastalığı epidemiyolojik özellikler ve mortalite çalışmaları. Turkiye Klinikleri Hematology-Special Topics. 2019;12:1-5.
  • Arcasoy A. Canatan D. Dünyada ve Türkiye’de Talasemi ve Hemoglobinopatiler. Antalya, Ulusal Hemoglobinopati Konseyi-Sağlık Bakanlığı, 2003.
  • Yüregir G, Donma O, Dikmen N, Isbir T, Cinar M. Population studies of hemoglobin S and other variants in Cukurova, the southern part of Turkey. Nihon Ketsueki Gakkai zasshi. 1987;50:757-65.
  • Kılınç Y, Akmanlar N, Kümi M, Köker I. The incidences of hemoglobinopathies and thalassemias in cord blood of newborns from Çukurova province. Med Bull İstanbul Medical Faculty. 1992;25:9-14.
  • Kaviany S, Barnawi Z, LaBelle J. Curative therapies for sickle cell disease. Pediat Ann. 2024;53:e56-e61.
  • Bender MA, Carlberg K. Sickle Cell Disease. In: GeneReviews®. University of Washington, Seattle, Seattle (WA), 1993.
  • Ohene-Frempong K, Weiner SJ, Sleeper LA, Miller ST, Embury S, Moohr JW et al. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood. 1998;91:288-94.
  • Serjeant GR. The natural history of sickle cell disease. Cold Spring Harb Perspect Med. 2013;3:a011783.
  • Adams RJ. Toward a stroke-free childhood in sickle cell disease: the 2013 Sherman Lecture. Stroke. 2013;44:2930-34.
  • DeBaun MR, Armstrong FD, McKinstry RC, Ware RE, Vichinsky E, Kirkham FJ. Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia. Blood. 2012;119:4587-96.
  • Aaslid R, Markwalder T-M, Nornes H. Noninvasive transcranial doppler ultrasound recording of flow velocity in basal cerebral arteries. J neurosurgery. 1982;57:769-74.
  • Adams RJ, Aaslid R, El Gammal T, Nichols FT, McKie V. Detection of cerebral vasculopathy in sickle cell disease using transcranial doppler ultrasonography and magnetic resonance imaging. Case report. Stroke. 1988;19:518-20.
  • Rasulo FA, Bertuetti R, Robba C, Lusenti F, Cantoni A, Bernini M et al. The accuracy of transcranial Doppler in excluding intracranial hypertension following acute brain injury: a multicenter prospective pilot study. Crit Care. 2017;21:1-8.
  • Diringer MN, Bleck TP, Claude Hemphill J, Menon D, Shutter L, Vespa P et al. Critical care management of patients following aneurysmal subarachnoid hemorrhage: recommendations from the neurocritical care society’s multidisciplinary consensus conference. Neurocrit Care. 2011;15:211-40.
  • Deana C, Biasucci DG, Aspide R, Brasil S, Vergano M, Leonardis F et al. Transcranial doppler and color‐coded doppler use for brain death determination in adult patients: a pictorial essay. J Ultrasound Med. 2024;43:979-92.
  • Adams RJ, Brambilla DJ, Granger S, Gallagher D, Vichinsky E, Abboud MR et al. Stroke and conversion to high risk in children screened with transcranial doppler ultrasound during the stop study. Blood. 2004;103:3689-94.
  • Seibert J, Glasier CM, Kirby RS, Allison JW, James CA, Becton DL et al. Transcranial Doppler, MRA, and MRI as a screening examination for cerebrovascular disease in patients with sickle cell anemia: an 8-year study. Pediatr Radiol. 1998;28:138-42.
  • Society SC. Standards for the clinical care of adults with sickle cell disease in the UK. Sickle Cell Society. 2018.
  • Adams R, McKie VC, Carl E, Nichols FT, Perry R, Brock K et al. Long‐term stroke risk in children with sickle cell disease screened with transcranial doppler. Ann Neurol. 1997;42:699-704.
  • Adams RJ, McKie VC, Hsu L, Files B, Vichinsky E, Pegelow C et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography. N Engl J Med. 1998;339:5-11.
  • Nichols FT, Jones AM, Adams RJ. Stroke prevention in sickle cell disease (stop) study guidelines for transcranial Doppler testing. J Neuroimaging. 2001;11:354-62.
  • Wang WC. Sickle cell anemia and other sickling syndromes. In: Greer JP, Foerster J, Rodgers GM, Paraskevas F, Glader B, Ar- ber DA, Means RT (eds). Wintrobe’s Clinical Hematology. Philadelphia: Lippincot Williams and Wilkins, 2009: 1038-82.
  • Connes P, Verlhac S, Bernaudin F. Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia. Br J Haematol. 2013;161:484-98.
  • Sabarense AP, Silva CM, Muniz MBdSR, Viana MB. Follow-up of children with sickle cell anemia screened with transcranial doppler and enrolled in a primary prevention program of ischemic stroke. Hematol Transfus Cell Ther. 2022;44:478-84.
  • Adams R, McKie V, Nichols F, Carl E, Zhang D-L, McKie K et al. The use of transcranial ultrasonography to predict stroke in sickle cell disease. N Engl J Med. 1992;326:605-10.
  • Asbeutah AM, Zahra AM, Al‐Abboh H, AlMajran AA, Adekile A. Repeat transcranial doppler ultrasound imaging in kuwaiti children with sickle cell disease after a 10‐year interval: A prospective, cohort study. Health Sci Rep. 2023;6:e1159.
  • Asbeutah AM, Asbeutah SA, Zahra A, AlMajran AA, Adekile A. Longitudinal assessment of transcranial doppler imaging in children with sickle cell disease without neurological symptoms. BMC pediatrics. 2024;24:684.
  • Silva GS, Vicari P, Figueiredo MS, Carrete H, Idagawa MH, Massaro AR. Brain magnetic resonance imaging abnormalities in adult patients with sickle cell disease: correlation with transcranial Doppler findings. Stroke. 2009;40:2408-12.
  • Idro R, Boehme A, Kawooya M, Munube D, Bangirana P, Opoka R et al. Brain magnetic resonance imaging and angiography findings in ugandan children with sickle cell anemia; a cross sectional study. J Stroke and Cerebrovasc Dis. 2022;31:106343.
  • De Ligt LA, Fijnvandraat K, Biemond BJ, Heijboer H. Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: A retrospective analysis. Haematologica. 2024;109:3009-12.

Orak hücre anemili çocuklarda transkraniyal Doppler incelemesi

Yıl 2025, Cilt: 50 Sayı: 3, 761 - 769
https://doi.org/10.17826/cumj.1671978

Öz

Amaç: Bu çalışmanın amacı, orak hücre anemili çocuklarla sağlıklı çocuklar arasında transkraniyal Doppler ultrasonografi ile beyin kan akım hızlarını karşılaştırarak, orak hücre anemili bireylerde inme geçirme riskini değerlendirmektir.
Gereç ve Yöntem: Prospektif olarak tasarlanan bu çalışmaya, 40 orak hücre anemili çocuk (16 kız, 24 erkek) ve 40 sağlıklı çocuk (22 kız, 18 erkek) olmak üzere toplam 80 çocuk dahil edilmiştir. Katılımcıların yaşları 3 ile 20 arasında değişmektedir. Beyin kan akımı ölçümleri, transtemporal ve oksipital pencerelerden transkraniyal Doppler cihazı kullanılarak gerçekleştirilmiştir. Orta Serebral Arter (OSA), Anterior Serebral Arter (ASA), Posterior Serebral Arter (PSA), vertebral arterler ve baziler arterin zaman ortalamalı maksimum ortalama hızı (TAMMV), Rezistif İndeks (RI) ve Pulsatilite İndeksi (PI) değerleri kaydedilmiştir.
Bulgular: Orak hücre anemili çocuklarda, kontrol grubuna kıyasla hem karotis sisteminde hem de vertebrobaziler sistemde beyin kan akım hızlarının anlamlı derecede arttığı saptanmıştır. Hasta grubunda sağ OSA TAMMV ortalaması ± SS 107,7 ± 23,1 cm/s, sol OSA TAMMV 113,3 ± 28,2 cm/s olarak ölçülmüştür. Kontrol grubunda ise bu değerler sırasıyla 77,9 ± 16,4 cm/s ve 78,1 ± 14,8 cm/s bulunmuştur. Orak hücre anemili üç çocukta (%7,5), OSA kan akım hızı 170 cm/s’nin üzerinde bulunmuştur. Serebral arterlerin ortalama kan akım hızları ile yaş arasında negatif korelasyon tespit edilmiştir. Ayrıca, hasta grubunda tüm damarlar için RI ve PI değerleri kontrol grubuna göre anlamlı derecede yüksek bulunmuştur.
Sonuç: Transkraniyal Doppler ultrasonografi, orak hücre anemili çoçuklarda inme riskinin değerlendirilmesinde değerli ve invaziv olmayan bir yöntemdir. Transkraniyal Doppler kullanılarak yapılan rutin taramalar, zamanında koruyucu müdahalelerin uygulanmasını kolaylaştırabilir.

Etik Beyan

Bu prospektif çalışma Çukurova Üniversitesi Tıp Fakültesi Etik Kurulu tarafından onaylanmıştır (Onay tarihi/sayısı: 2011/07).

Kaynakça

  • Söylemez-Gökyer D, Kayaaltı Z. Türkiye’de orak hücreli anemi dağılımı, patofizyolojisi ve demir toksisitesi. Marmara Pharmaceutical Journal. 2016;20:92-9.
  • Karacaoğlu P, Boğa C. Orak hücre hastalığı epidemiyolojik özellikler ve mortalite çalışmaları. Turkiye Klinikleri Hematology-Special Topics. 2019;12:1-5.
  • Arcasoy A. Canatan D. Dünyada ve Türkiye’de Talasemi ve Hemoglobinopatiler. Antalya, Ulusal Hemoglobinopati Konseyi-Sağlık Bakanlığı, 2003.
  • Yüregir G, Donma O, Dikmen N, Isbir T, Cinar M. Population studies of hemoglobin S and other variants in Cukurova, the southern part of Turkey. Nihon Ketsueki Gakkai zasshi. 1987;50:757-65.
  • Kılınç Y, Akmanlar N, Kümi M, Köker I. The incidences of hemoglobinopathies and thalassemias in cord blood of newborns from Çukurova province. Med Bull İstanbul Medical Faculty. 1992;25:9-14.
  • Kaviany S, Barnawi Z, LaBelle J. Curative therapies for sickle cell disease. Pediat Ann. 2024;53:e56-e61.
  • Bender MA, Carlberg K. Sickle Cell Disease. In: GeneReviews®. University of Washington, Seattle, Seattle (WA), 1993.
  • Ohene-Frempong K, Weiner SJ, Sleeper LA, Miller ST, Embury S, Moohr JW et al. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood. 1998;91:288-94.
  • Serjeant GR. The natural history of sickle cell disease. Cold Spring Harb Perspect Med. 2013;3:a011783.
  • Adams RJ. Toward a stroke-free childhood in sickle cell disease: the 2013 Sherman Lecture. Stroke. 2013;44:2930-34.
  • DeBaun MR, Armstrong FD, McKinstry RC, Ware RE, Vichinsky E, Kirkham FJ. Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia. Blood. 2012;119:4587-96.
  • Aaslid R, Markwalder T-M, Nornes H. Noninvasive transcranial doppler ultrasound recording of flow velocity in basal cerebral arteries. J neurosurgery. 1982;57:769-74.
  • Adams RJ, Aaslid R, El Gammal T, Nichols FT, McKie V. Detection of cerebral vasculopathy in sickle cell disease using transcranial doppler ultrasonography and magnetic resonance imaging. Case report. Stroke. 1988;19:518-20.
  • Rasulo FA, Bertuetti R, Robba C, Lusenti F, Cantoni A, Bernini M et al. The accuracy of transcranial Doppler in excluding intracranial hypertension following acute brain injury: a multicenter prospective pilot study. Crit Care. 2017;21:1-8.
  • Diringer MN, Bleck TP, Claude Hemphill J, Menon D, Shutter L, Vespa P et al. Critical care management of patients following aneurysmal subarachnoid hemorrhage: recommendations from the neurocritical care society’s multidisciplinary consensus conference. Neurocrit Care. 2011;15:211-40.
  • Deana C, Biasucci DG, Aspide R, Brasil S, Vergano M, Leonardis F et al. Transcranial doppler and color‐coded doppler use for brain death determination in adult patients: a pictorial essay. J Ultrasound Med. 2024;43:979-92.
  • Adams RJ, Brambilla DJ, Granger S, Gallagher D, Vichinsky E, Abboud MR et al. Stroke and conversion to high risk in children screened with transcranial doppler ultrasound during the stop study. Blood. 2004;103:3689-94.
  • Seibert J, Glasier CM, Kirby RS, Allison JW, James CA, Becton DL et al. Transcranial Doppler, MRA, and MRI as a screening examination for cerebrovascular disease in patients with sickle cell anemia: an 8-year study. Pediatr Radiol. 1998;28:138-42.
  • Society SC. Standards for the clinical care of adults with sickle cell disease in the UK. Sickle Cell Society. 2018.
  • Adams R, McKie VC, Carl E, Nichols FT, Perry R, Brock K et al. Long‐term stroke risk in children with sickle cell disease screened with transcranial doppler. Ann Neurol. 1997;42:699-704.
  • Adams RJ, McKie VC, Hsu L, Files B, Vichinsky E, Pegelow C et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography. N Engl J Med. 1998;339:5-11.
  • Nichols FT, Jones AM, Adams RJ. Stroke prevention in sickle cell disease (stop) study guidelines for transcranial Doppler testing. J Neuroimaging. 2001;11:354-62.
  • Wang WC. Sickle cell anemia and other sickling syndromes. In: Greer JP, Foerster J, Rodgers GM, Paraskevas F, Glader B, Ar- ber DA, Means RT (eds). Wintrobe’s Clinical Hematology. Philadelphia: Lippincot Williams and Wilkins, 2009: 1038-82.
  • Connes P, Verlhac S, Bernaudin F. Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia. Br J Haematol. 2013;161:484-98.
  • Sabarense AP, Silva CM, Muniz MBdSR, Viana MB. Follow-up of children with sickle cell anemia screened with transcranial doppler and enrolled in a primary prevention program of ischemic stroke. Hematol Transfus Cell Ther. 2022;44:478-84.
  • Adams R, McKie V, Nichols F, Carl E, Zhang D-L, McKie K et al. The use of transcranial ultrasonography to predict stroke in sickle cell disease. N Engl J Med. 1992;326:605-10.
  • Asbeutah AM, Zahra AM, Al‐Abboh H, AlMajran AA, Adekile A. Repeat transcranial doppler ultrasound imaging in kuwaiti children with sickle cell disease after a 10‐year interval: A prospective, cohort study. Health Sci Rep. 2023;6:e1159.
  • Asbeutah AM, Asbeutah SA, Zahra A, AlMajran AA, Adekile A. Longitudinal assessment of transcranial doppler imaging in children with sickle cell disease without neurological symptoms. BMC pediatrics. 2024;24:684.
  • Silva GS, Vicari P, Figueiredo MS, Carrete H, Idagawa MH, Massaro AR. Brain magnetic resonance imaging abnormalities in adult patients with sickle cell disease: correlation with transcranial Doppler findings. Stroke. 2009;40:2408-12.
  • Idro R, Boehme A, Kawooya M, Munube D, Bangirana P, Opoka R et al. Brain magnetic resonance imaging and angiography findings in ugandan children with sickle cell anemia; a cross sectional study. J Stroke and Cerebrovasc Dis. 2022;31:106343.
  • De Ligt LA, Fijnvandraat K, Biemond BJ, Heijboer H. Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: A retrospective analysis. Haematologica. 2024;109:3009-12.
Toplam 31 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Çocuk Hematolojisi ve Onkolojisi, Radyoloji ve Organ Görüntüleme
Bölüm Araştırma
Yazarlar

Seda Nida Karaküçük 0000-0002-3789-6571

Süreyya Soyupak 0000-0001-8680-4752

Hatice İlgen Şaşmaz 0000-0001-9361-9838

Gülşah Seydaoğlu 0000-0002-0899-894X

Yayımlanma Tarihi 25 Eylül 2025
Gönderilme Tarihi 9 Nisan 2025
Kabul Tarihi 30 Ağustos 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 50 Sayı: 3

Kaynak Göster

MLA Karaküçük, Seda Nida vd. “Transcranial Doppler examination in patients with sickle cell anemia”. Cukurova Medical Journal, c. 50, sy. 3, ss. 761-9, doi:10.17826/cumj.1671978.