scholarly journals The role of Platelet Rich Plasma and other orthobiologics in bone healing and fracture management: A systematic review

Author(s):  
M.S. Jamal ◽  
E.T. Hurley ◽  
H. Asad ◽  
A. Asad ◽  
T. Taneja
Injury ◽  
2008 ◽  
Vol 39 ◽  
pp. S45-S57 ◽  
Author(s):  
N.C. Keramaris ◽  
G.M. Calori ◽  
V.S. Nikolaou ◽  
E.H. Schemitsch ◽  
P.V. Giannoudis

2019 ◽  
Vol 35 (3) ◽  
pp. 961-976.e3 ◽  
Author(s):  
Michael P. Fice ◽  
J. Chance Miller ◽  
Robert Christian ◽  
Charles P. Hannon ◽  
Niall Smyth ◽  
...  

Injury ◽  
2009 ◽  
Vol 40 (2) ◽  
pp. 158-162 ◽  
Author(s):  
X.L. Griffin ◽  
C.M. Smith ◽  
M.L. Costa

BMC Medicine ◽  
2016 ◽  
Vol 14 (1) ◽  
Author(s):  
Ippokratis Pountos ◽  
Michalis Panteli ◽  
Anastasios Lampropoulos ◽  
Elena Jones ◽  
Giorgio Maria Calori ◽  
...  

1980 ◽  
Vol 44 (01) ◽  
pp. 006-008 ◽  
Author(s):  
D Bergqvist ◽  
K-E Arfors

SummaryIn a model using an isolated rabbit mesenteric preparation microvessels were transected and the time until haemostatic plugs formed was registered. Perfusion of platelet rich plasma gave no haemostasis whereas whole blood did. Addition of chlorpromazine or adenosine to the whole blood significantly prolonged the time for haemostasis, and addition of ADP to the platelet rich plasma significantly shortened it. It is concluded that red cells are necessary for a normal haemostasis in this model, probably by a combination of a haemodynamic and ADP releasing effect.The fundamental role of platelets in haemostatic plug formation is unquestionable but there are still problems concerning the stimulus for this process to start. Three platelet aggregating substances have been discussed – thrombin, adenosine diphosphate (ADP) and collagen. Evidence speaking in favour of thrombin is, however, very minimal, and the discussion has to be focused on collagen and ADP. In an in vitro system using polyethylene tubings we have shown that "haemostasis" can be obtained without the presence of collagen but against these results can be argued that it is only another in vitro test for platelet aggregation (1).To be able to induce haemostasis in this model, however, the presence of red blood cells is necessary. To further study this problem we have developed a model where haemostatic plug formation can be studied in the isolated rabbit mesentery and we have briefly reported on this (2).Thus, it is possible to perfuse the vessels with whole blood as well as with platelet rich plasma (PRP) and different pharmacological agents of importance.


1981 ◽  
Vol 46 (02) ◽  
pp. 538-542 ◽  
Author(s):  
R Pilo ◽  
D Aharony ◽  
A Raz

SummaryThe role of arachidonic acid oxygenated products in human platelet aggregation induced by the ionophore A23187 was investigated. The ionophore produced an increased release of both saturated and unsaturated fatty acids and a concomitant increased formation of TxA2 and other arachidonate products. TxA2 (and possibly other cyclo oxygenase products) appears to have a significant role in ionophore-induced aggregation only when low concentrations (<1 μM) of the ionophore are employed.Testosterone added to rat or human platelet-rich plasma (PRP) was shown previously to potentiate platelet aggregation induced by ADP, adrenaline, collagen and arachidonic acid (1, 2). We show that testosterone also potentiates ionophore induced aggregation in washed platelets and in PRP. This potentiation was dose and time dependent and resulted from increased lipolysis and concomitant generation of TxA2 and other prostaglandin products. The testosterone potentiating effect was abolished by preincubation of the platelets with indomethacin.


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