scholarly journals Response to Letter to the Editor: Impact of Bariatric Surgery on Outcomes of Patients with Sickle Cell Disease: a Nationwide Inpatient Sample Analysis, 2004–2014

2019 ◽  
Vol 29 (8) ◽  
pp. 2624-2624 ◽  
Author(s):  
Thomas R. McCarty ◽  
Prabin Sharma ◽  
Siddhartha Yadav ◽  
Julius N. Ngu ◽  
Basile Njei
2019 ◽  
Vol 29 (6) ◽  
pp. 1789-1796 ◽  
Author(s):  
Prabin Sharma ◽  
Thomas R. McCarty ◽  
Siddhartha Yadav ◽  
Julius N. Ngu ◽  
Basile Njei

Stroke ◽  
2015 ◽  
Vol 46 (suppl_1) ◽  
Author(s):  
Sudharani Busani ◽  
Girish N Nadkarni ◽  
Achint Patel ◽  
Natraj Ammakkanavar ◽  
Hardik kumar shah ◽  
...  

BACKGROUND: The association between Moyamoya disease and sickle cell disease is well recognized in the literature. However, there is limited data on inpatient admission of concurrent sickle cell disease and Moyamoya disease. We sought to determine the trend in incidence of admissions of concurrent Moyamoya and sickle cell disease as well as the most common presentation of these admissions. METHODS: We reviewed the Healthcare Cost and Utilization Project's Nationwide Inpatient Sample (NIS) database from 2000-2011 for concurrent Moyamoya and sickle cell admissions using the ICD 9-CM codes We obtained data on gender, clinical presentation, procedures, co-morbidities and patient outcomes RESULTS: From 2000 to 2011, an estimated patients 756 (weighted (n)=3692) with co-existing Moyamoya disease and sickle cell disease were admitted. The incidence of admission for concurrent disease increased significantly from 0.04/100,000 admissions in 2000 to 0.21/100,000 admissions in 2011(figure 1). This was very significant using the Cochrane Armitage trend test(p<0.001). The most likely reasons for admissions were ischemic stroke(7.2)% followed by hemorrhagic stroke(2.8 and transient ischemic attack(1.2%) (p = 0.0116). The most commonly performed treatment procedures included packed cell transfusion(33.7%) followed by exchange transfusion (8.8%). However there was no significant change in mortality from 2000-2011. CONCLUSION: The number of hospitalizations due to concurrent Moyamoya and sickle cell disease has increased significantly over the last decade and are likely to present with a cerebrovascular accident. Thus, it is important to maintain a high degree of suspicion for Moyamoya disease in sickle cell disease patients presenting with neurological symptoms since this could potentially impact their management.


2020 ◽  
Vol 09 (06) ◽  
pp. 158-164
Author(s):  
Hassan Al-Jafar ◽  
Masouma Al-Ali ◽  
Osama R. Kombar ◽  
Mohammad Alhaifi

PEDIATRICS ◽  
1974 ◽  
Vol 53 (3) ◽  
pp. 447-447
Author(s):  
Thomas R. Walters

This is to express my disappointment in your publication of "Anesthetic Risks in Sickle Cell Trait." Reference words in the abstract such as "sickle cell trait, anesthesia risks, and sudden anesthetic death" expand the implication of the title. There are several criticisms. Case 2 in the Table identifying the five Negro children with sickle cell trait shows hemoglobin electrophoresis results as S-C. Current terminology in sickle cell disease indicates that this patient has a double-heterozygote state, is not a patient with sickle cell trait and, therefore, cannot be included.


1974 ◽  
Vol 133 (4) ◽  
pp. 624-631 ◽  
Author(s):  
T. A. Bensinger

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