The donor effect of sickle cell trait on host NO bioavailability following red blood cell transfusion

Nitric Oxide ◽  
2014 ◽  
Vol 42 ◽  
pp. 136-137
Author(s):  
David Osei-Hwedieh ◽  
Tamir Kanias ◽  
Janet Lee ◽  
Mark Gladwin
Author(s):  
Shilpa Jain ◽  
Mark T. Gladwin

Sickle cell disease crises are precipitated by an acute occlusion of microvessels, which can lead to end organ ischaemia reperfusion injury and acute haemolysis. Acute fat emboli syndrome, acute lung injury (the acute chest syndrome), acute pulmonary hypertension, and cor pulmonale, haemorrhagic and occlusive stroke, and systemic infection represent the most common life-threatening complications observed in current ICU practice. General principles of management in all patients admitted to the critical care unit are hydration, antibiotics, pain control, and maintenance of oxygenation and ventilation. Red blood cell transfusion therapy is the treatment of choice for most complications of sickle cell disease requiring intensive care management. Transfusion of sickle negative, leukoreduced red blood cells, phenotypically matched for Rhesus and Kell antigens is the minimum standard of care in sickle cell disease patients as they have a high incidence of red blood cell alloimmunization.


2005 ◽  
Vol 55 (6) ◽  
pp. 385-387 ◽  
Author(s):  
Philippe Connes ◽  
Fagnété Sara ◽  
Marie-Dominique Hardy-Dessources ◽  
Maryse Etienne-Julan ◽  
Olivier Hue

Author(s):  
Nazanin Heidari ◽  
Foad Halvaji ◽  
Parisa Rezaei Mofrad ◽  
Mohammad Ali Jalali Far ◽  
Mohammad Taha Jalali ◽  
...  

1990 ◽  
Vol 5 (3) ◽  
pp. 215-222 ◽  
Author(s):  
James A. Mercy ◽  
Clark W. Heath ◽  
Mark L. Rosenberg

A review of police records for the nine-year period from 1974 to 1982 identified 20 men who died following restraint by an upper-body control hold while in the custody of a large, urban police department. Using evidence from autopsy findings and police reports of events immediately preceding death, we concluded that control-hold use was associated with death in 19 of the 20 cases. This investigation points to three factors potentially associated with control hold-related death that deserve further investigation: Phencyclidine (PCP) use, sickle cell trait, and stress-related arrhythmias in the heart. PCP was detected in blood or other tissues from 6 of 17 decedents tested. Intravascular red blood cell sickling was found at autopsy in 4 of 14 black decedents (29%). Four decedents had some indication of cardiovascular abnormalities.


2010 ◽  
Vol 299 (3) ◽  
pp. H908-H914 ◽  
Author(s):  
Julien Tripette ◽  
Gylna Loko ◽  
Abdoulaye Samb ◽  
Bertin Doubi Gogh ◽  
Estelle Sewade ◽  
...  

This study compared the hemorheological responses of a group of sickle cell trait (SCT) carriers with those of a control (Cont) group in response to 40 min of submaximal exercise (exercise intensity, 55% aerobic peak power) performed in two conditions: one with water offered ad libitum, i.e., the hydration (Hyd) condition, and one without water, i.e., the dehydration (Dehyd) condition. Blood and plasma viscosities, as well as red blood cell rigidity, were determined at rest, at the end of exercise, and at 2 h recovery with a cone plate viscometer at high shear rate and 37°C. The SCT and Cont groups lost 1 ± 0.7 and 1.6 ± 0.6 kg of body weight, respectively, in the Dehyd condition, indicating a significant effect of water deprivation compared with the Hyd condition, in which body weight remained unchanged. Plasma viscosity increased with exercise and returned to baseline during recovery independently of the group and condition. As previously demonstrated, resting blood viscosity was greater in the SCT carriers than in the Cont group. Blood viscosity increased by the end of exercise and returned to baseline at 2 h recovery in the Cont group in both conditions. The blood viscosity of SCT carriers did not change in response to exercise in the Dehyd condition and remained elevated at 2 h recovery. This extended hyperviscosity, in association with other biological changes induced by exercise, could be considered as a risk factor for exercise-related events in SCT carriers, similar to vasoocclusive crises, notably during the recovery. In contrast, the Hyd condition normalized the hyperviscosity and red blood cell rigidity of the SCT carriers, with blood viscosity values reaching the same lower values as those found in the Cont group during the recovery. Adequate hydration of SCT carriers should be strongly promoted to reduce the clinical risk associated with potential hyperviscosity complications.


2018 ◽  
Vol 38 (3) ◽  
pp. 200-202
Author(s):  
Prateek Kumar Panda

Vaso-occlusive crises in sickle cell disease commonly involve bone marrow of the long bones and vertebrae. Involvement of bones with less marrow space, including the bones of the orbit, is reported rarely in the literature. The present case is a six year old boy, a known case of sickle cell disease, who presented with acute onset right upper and lower eyelid swelling, restriction of extraocular movement and pain. USG orbit showed a retro-orbital haemorrhage compressing on the orbit, probably due to orbital bone infarction. The child was managed successfully with red blood cell transfusion and intravenous antibiotics, without steroids and surgical intervention. This report highlights the importance of maintaining a high index of suspicion in patients with known sickle cell disease presenting with pain, orbital swelling and restriction of ocular movement. Timely red blood cell transfusion only may be sufficient for uneventful recovery, without steroids or surgical intervention. Expedient diagnosis of orbital compression syndrome in children with sickle cell disease is crucial because this is a potentially sight-threatening entity. 


2020 ◽  
Vol 24 (3) ◽  
pp. 107-111
Author(s):  
Ricci Jo Ackley ◽  
A. Hallie Lee-Stroka ◽  
Barbara J. Bryant ◽  
David F. Stroncek ◽  
Karen M. Byrne

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