Intra-aortic balloon pump weaning strategy: rate or volume? Look at the coronary perfusion flow!

Author(s):  
Costanza Natalia Julia Colombo ◽  
Valentino Dammassa ◽  
Francesco Mojoli ◽  
Guido Tavazzi
2004 ◽  
Vol 28 (3) ◽  
pp. 303-309 ◽  
Author(s):  
Toshihide Tsukioka ◽  
Sigeyuki Tomita ◽  
Go Watanabe ◽  
Hirohumi Takemura

Phytomedicine ◽  
2010 ◽  
Vol 17 (13) ◽  
pp. 1006-1015 ◽  
Author(s):  
Xiao Qin Yi ◽  
Ting Li ◽  
Jing Rong Wang ◽  
Vincent Kam Wai Wong ◽  
Pei Luo ◽  
...  

2021 ◽  
pp. 1-11
Author(s):  
Kate O'Donovan

The intra-aortic balloon pump was first introduced for the treatment of cardiogenic shock. It is now the most commonly used form of circulatory support, despite disappointing findings from the intra-aortic balloon pump SHOCK II trial ( Thiele et al, 2012 ). Common placement is via the femoral artery into the aorta, with the tip of the balloon sitting below the left subclavian artery and the distal end above the renal arteries. The balloon is timed to inflate at the beginning of diastole augmenting coronary perfusion and deflate on the R wave just before systole, reducing the afterload. Patients who may be considered for intra-aortic balloon pump insertion are those experiencing ST elevation myocardial infarction or complex ischaemic disease and cardiogenic shock. Despite advances in catheter size and technology, potential complications include bleeding from the insertion site, limb ischaemia and compartment syndrome. Cardiovascular nurses require specialist knowledge and skills concerning balloon console technology, nursing care and potential complications.


Author(s):  
M. Ashraf ◽  
F. Thompson ◽  
S. Miki ◽  
P. Srivastava

Iron is believed to play an important role in the pathogenesis of ischemic injury. However, the sources of intracellular iron in myocytes are not yet defined. In this study we have attempted to localize iron at various cellular sites of the cardiac tissue with the ferrocyanide technique.Rat hearts were excised under ether anesthesia. They were fixed with coronary perfusion with 3% buffered glutaraldehyde made in 0.1 M cacodylate buffer pH 7.3. Sections, 60 μm in thickness, were cut on a vibratome and were incubated in the medium containing 500 mg of potassium ferrocyanide in 49.5 ml H2O and 0.5 ml concentrated HC1 for 30 minutes at room temperature. Following rinses in the buffer, tissues were dehydrated in ethanol and embedded in Spurr medium.The examination of thin sections revealed intense staining or reaction product in peroxisomes (Fig. 1).


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