Transcranial color Doppler in stroke-free adult patients with sickle cell disease

2017 ◽  
Vol 96 (9) ◽  
pp. 1547-1555 ◽  
Author(s):  
G. Graziadei ◽  
F. M. Casoni ◽  
F. Annoni ◽  
I. Cortinovis ◽  
P. Ridolfi ◽  
...  
Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 4085-4085 ◽  
Author(s):  
Giovanna Graziadei ◽  
Francesca Marta Casoni ◽  
Antonella Costa ◽  
Alessia Marcon ◽  
Fabio Triulzi ◽  
...  

Abstract Introduction. Stroke is a severe complication of Sickle Cell Disease (SCD). Ischemic strokes are more frequent among patients younger than 20 years of age, whereas older patients experience hemorrhagic strokes. At present few data are available in adult patients. Aim. To evaluate Magnetic Resonance Imaging/Angiography (MRI/MRA) findings and to correlate with Transcranial Color Doppler Sonography (TCCD) in adult SCD patients. Patients and methods. Fifty-one adult patients with SCD (median age 36.2 years, range 17-69 years; M:F 19:32) were enrolled, including 15 Sickle Cell Anemia (SCA), 24 Sickle Cell Thalassemia (HbS-βThal) and 12 HbS/HbC, all followed in a single tertiary Rare Disease Center in Milan, Italy. The study was approved by Ethic Committee and all subjects gave written informed consent. Clinical history and hematological tests were collected. 3.0 T MRI/MRA was performed to detect cerebral parenchyma lesions and vessels abnormalities. Color and Duplex Doppler Sonography (CDDS) and TransCranial Color Doppler (TCCD) following the STOP protocol but with angle correction were performed by the same physician to evaluate mean Peak Systolic Velocity (PSV) and Pulsatility Index (PI) of the extracranial vessels (ICA and VA) and middle (MCA), anterior (ACA), posterior (PCA) cerebral arteries, carotid siphon (SIPH), vertebral (VA intracranial) and basilar (BAS) arteries. Results. In overall SCD adult patients median Hb levels were 9.9±1.7 g/dL, Hct 28.5±4.5%, HbS% 60±18.5% (range 5.5-90.2%), HbF% 8.5±8.6% (range 0.9-33.8%); 68.6% SCD patients had <4 crises/year, 27.5% >4 crises/year, while 3.9% were completely asymptomatic; 37.3% SCD patients were treated with Hydroxycarbamide (HU); 49% were transfused <4 RBCs Units /year and 19.6% >4 RBCs Units/year, while 31.4% had never been transfused; 21.6% were splenectomized. No patient experienced stroke nor ischemic, neither hemorrhagic, despite history of sickle crises. Out of 51 SCD patients, 51% showed cerebral parenchimal lesions, 33.3% aneurisms of the intracranial vessels, 96.1% vessel tortuosity (25.5% mild and 70.6% severe). In only 2 patients (4%) mild focal stenosis were detected. Comparing the three SCD subgroups, in SCA patients the percentage of cerebral parenchimal lesions (60%), aneurisms (53%) and tortuosity vessels (100%, 13.3% mild and 86.7 severe) were significantly higher than in HbS-βThal and HbS/HbC patients (p<0.01), where cerebral parenchimal lesions were respectively 45.8% and 50%, aneurisms 20.8% and 33.3%, and vessels tortuosity 92.6% (33.3% mild and 58.3% severe) and 100% (25% mild and 75% severe). Considering SCD patients with cerebral parenchimal lesions, MCA TAMM and PSV values were lower (87.30±16.88 cm/sec, p <0.002; 123.32±22.36, p <0.013 respectively) then in SCD group without lesions. SCD patients with aneurism showed lower MCA TAMM and PSV values (87.55±16 cm/sec, p <0.049; 123.02±22.2, p <0.08 respectively) then SCD group without lesions, as well. Same correlations were found in SCA, HbS-βThal and HbS/HbC patients. No statistical differences between PI, Hb, HT and HbS and the overall MRI/MRA abnormalities were found. Considering the other intracranic vessels studied, no correlations were found between TCCD blood flow velocities and MRI/MRA cerebral findings. Conclusions. In the studied group of SCD adult patients MRI/MRA findings are characterized by aneurismal enlargement and tortuosity of cerebral vessels, probably due to age-related brain endothelial damage. MCA TAMM and PSV values were lower in SCD adult patients with cerebral parenchimal lesions and aneurisms, in comparison with ones without, indicating a consequent reduced blood flow velocity. According to our data, we could suggest as potentially pathological cut off MCA TAMM <100 cm/sec and MCA PSV value <125 cm/s, measurement close to the normal, but lower than ones found in SCD adult patients. These threshold intracranial blood flow velocities could be an indication to perform MRI/MRA to evaluate vessel tortuosity and mainly life-threatening aneurysms The correlations observed between TCCD values and MRI/MRA findings require further investigations. Disclosures Cappellini: Novartis, Shire, Cellgene, Sanofi: Advisory board Other.


2019 ◽  
Vol 111 (1) ◽  
pp. 54-61 ◽  
Author(s):  
Monica Ter-Minassian ◽  
Sophie Lanzkron ◽  
Alphonse Derus ◽  
Elizabeth Brown ◽  
Michael A. Horberg

2020 ◽  
Vol 14 (1) ◽  
pp. 263-284
Author(s):  
Aindrea B. Maddray ◽  
Shannon M. Phillips

Background & Purpose: The purpose of this review is to examine instruments that measure providers' perceptions of adult patients with Sickle Cell Disease (SCD), examine instruments that measure adult patients with SCD perceptions of providers' behaviors, and determine optimal instruments to use in evaluating the perceptions of Emergency Department (ED) providers and adult patients with SCD of one another's behaviors after an interaction in the ED. Methods: An integrative review was conducted searching EBSCOhost and PubMed databases using the keywords: measure [OR] measure* [OR] assess* [OR] scale [OR] survey [OR] tool [AND] stigma* [OR] stereotype [OR] prejudice [OR] bias [OR] perception [OR] attitude [OR] discrimination [OR] racism [OR] behavior [AND] interaction [OR] relationship [OR] communication [AND] sickle cell. Initial search located 256 articles, but only 15 articles were included in the final review. Results: Fifteen articles reporting six instruments were reviewed. Four instruments evaluated a provider’s perceptions of patients with SCD behaviors, and two instruments evaluated how patients with SCD perceived provider behaviors. The two patient-focused instruments and three provider-focused instruments were found to be adequately reliable and valid according to the Psychometric Grading Framework (PGF). Conclusions: The findings suggest that the General Perceptions About Sickle Cell Disease Patients Scale would be an optimal instrument to evaluate ED providers' perceptions of adult patients with SCD behaviors. One patient-focused instrument, The Sickle Cell Health-Related Stigma Scale (SCD-HRSS), reported adequate reliability and validity but was not specific to measuring the patient's perceptions of ED providers' behaviors, nor was it administered in the ED environment. The SCD-HRSS Doctors subscale has potential adaptability for use in measuring patients with SCD perceptions of ED provider behaviors in the ED environment.


Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 2106-2106
Author(s):  
Madiha Iqbal ◽  
Tea Reljic ◽  
Ernesto Ayala ◽  
Hemant S. Murthy ◽  
Ambuj Kumar ◽  
...  

Background: Sickle cell disease (SCD) is an inherited hemoglobinopathy which affects over 300,000 children born each year worldwide. In spite of improvement in supportive care in recent years, there is still a lack of effective treatment options. SCD leads to debilitating and cyclic episodes of erythrocyte sickling with progressive organ injury, contributing to lifetime morbidity and shortened life expectancy. Allogeneic HCT (allo-HCT) is a potentially curative therapy for SCD because engraftment is associated with resolution of the clinical phenotype of the disease and abrogation of its complications. Medical literature on allo-HCT for SCD is largely limited to children. Recent studies have evaluated the efficacy of allo-HCT in the adult population. Here, we conduct a systematic review/meta-analysis to assess the totality of evidence pertaining to the efficacy (or lack thereof) of allo-HCT in children and adults. Materials and methods: We performed a comprehensive search of the medical literature using PubMed/Medline, EMBASE and Cochrane library on July 3rd, 2019. We extracted data on clinical outcomes related to benefits (overall [OS] and disease free/event free survival [EFS/DFS]) and harms (non-relapse mortality [NRM] and graft failure [GF]), independently by two authors. Our search strategy identified 1001 references but only 30 studies (n= 1995 patients) were included in this systematic review/meta-analysis. We also performed a sub analysis on clinical outcomes for studies that included only pediatric patients (defined as <18 years) and those in patients ≥18 years of age. Results: Median age for patients enrolled in all the studies was at 10 years. Recurrent veno-occlusive crises represented the most common indication for allo-HCT followed by acute chest syndrome and stroke; nevertheless, most patients had more than one indication. Matched related donors (MRD) were the most common donor source (93%). Bone marrow was the most common source of hematopoietic stem cells (77%). Majority of patients underwent conditioning with myeloablative regimens (77%). Pooled OS rates (n=29 studies, 1681 patients) after allogeneic HCT was 95% (95%CI=93-96%) with low heterogeneity (I2=6.4%) among included studies (Figure 1). Pooled EFS/DFS rates (n=29 studies, 1894 patients) post-allografting was 90% (95%CI=87-93%) with moderate heterogeneity (I2=54%). Pooled NRM rates from 30 studies (1995 patients) was 4% (95%CI=2-6%) with low heterogeneity (I2=29.4%). Pooled GF rates from 28 studies (1851 patients) was 4% (95%CI=2-6%) with moderate heterogeneity (I2=55%). A subset analysis specifically for pediatric patients (n= 11 studies, 1009 patients, median age at 9.7 years) showed a pooled OS rate of 96% (95%CI=94-97%) with low heterogeneity (I2=0%); and for adult patients (n=3 studies, 51 patients, median age at 33.4 years) the pooled OS was 94% (95%CI=80-100%) with moderate heterogeneity (I2=52%). Pooled EFS/DFS for pediatric patients (n= 11 studies, 1009 patients) was at 89 %( 95%CI=84-93%) with moderate heterogeneity (I2=55.1%); and for adult patients (n=2 studies, 30 patients) was at 95% (95%CI=83-100%) with high heterogeneity (I2=96.5%). Pooled NRM from 10 studies with pediatric patients (281 patients) was at 6 % (95%CI=3-10%) with low heterogeneity (I2=0%); and from 3 studies with adult patients (51 patients) was at 1% (95%CI=0-7%) with low heterogeneity (I2=15.1%). Pooled GF from 10 studies with pediatric patients (281 patients) was at 3 % (95%CI=1-7%) with moderate heterogeneity (I2=40%); and from 2 studies with adult patients (30 patients) was at 5% (95%CI=0-17%) with high heterogeneity (I2=95.4%). Conclusions: The results of our systematic review/meta-analysis show excellent OS, EFS/DFS in children and adults undergoing allo-HCT with pooled OS rates exceeding 90%. The main limitation to offering an allo-HCT in SCD remains the availability of a suitable donor as 85% of patients meeting criteria do not have a MRD. We anticipate that with emergence of haploidentical transplantation the number of allo-HCT will increase in the future. GF remains a significant concern in this population and future studies should focus on novel immune suppression strategies to help reduce GF. Disclosures Kharfan-Dabaja: Pharmacyclics: Consultancy; Daiichi Sankyo: Consultancy.


Author(s):  
Susanna A. Curtis ◽  
Balbuena-Merle Raisa ◽  
John D. Roberts ◽  
Jeanne E. Hendrickson ◽  
Joanna Starrels ◽  
...  

2005 ◽  
Vol 19 (12) ◽  
pp. 1668-1669 ◽  
Author(s):  
G. Marakis ◽  
T. E. Pavlidis ◽  
K. Ballas ◽  
S. Rafailidis ◽  
A. Sakantamis

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