Rietzsch, H.* ; Panzner, I.* ; Selisko, T.* ; Julius, U.* ; Jabs, N.* ; Reimann, M.* ; Bonifacio, E.* ; Bornhäuser, M.* ; Bornstein, S.R.*
    
 
    
        
Heparin-induced Extracorporal LDL precipitation (H.E.L.P) in diabetic foot syndrome - preventive and regenerative potential?
    
    
        
    
    
        
        Horm. Metab. Res. 40, 487-490 (2008)
    
    
		
		
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			Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
		
     
    
		
		
			
				Peripheral arterial disease is more aggressive in concomitant diabetes posing an increased risk for critical limb ischemia and subsequent limb loss. The majority of therapies available are not effective to prevent amputation in patients with severe disease. The current observational study reports the effect of the heparin-induced extracorporal LDL-precipitation (H.E.L.P.) as a novel therapeutic approach in patients with severe diabetic foot syndrome. Seventeen diabetic patients with septic foot lesions recruited from the diabetic outpatient clinic underwent H.E.L.P. apheresis regularly until fibrinogen levels were stabilized at 3 g/l or infection was controllable as evidenced by alleviation of necrosis. Patients were subsequently followed up for 2 to 73 months. Fibrinogen levels were reduced by 68% after H.E.L.P. treatment. No severe complications were noted. Necrosis could be confined in sixteen patients. Minor amputations were indicated in twelve patients. Three patients underwent major amputations of the lower limb and two patients received surgical reconstruction. In conclusion, H.E.L.P. apheresis may offer an alternative therapeutic option to diabetic patients with critically ischemic feet and appears to have a beneficial major/minor amputation ratio.
			
			
				
			
		 
		
			
				
					
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        Artikel: Journalartikel
    
 
    
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        Wissenschaftlicher Artikel
    
 
    
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        englisch
    
 
    
        Veröffentlichungsjahr
        2008
    
 
    
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        0018-5043
    
 
    
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        1439-4286
    
 
    
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	    Band: 40,  
	    Heft: 7,  
	    Seiten: 487-490 
	    Artikelnummer: ,  
	    Supplement: ,  
	
    
 
  
        
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        Peer reviewed
    
 
    
        Institut(e)
        Institute of Pancreatic Islet Research (IPI)
    
 
    
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        Erfassungsdatum
        2008-12-31