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The patient is 26-year-old man with severe nephrotic syndrome &#40;NS&#41; due to FSGS&#44; a cellular variant&#44; diagnosed 10 months earlier&#46; The patient received treatment with steroids&#44; cyclophosphamide&#44; cyclosporine and mycophenolate&#44; with no response&#44; maintaining a proteinuria of 15&#8211;33<span class="elsevierStyleHsp" style=""></span>g&#47;day&#46; He was admitted the Hospital on 3 occasions for extreme generalised oedema&#44; with ascites&#44; effusion in the testicular region&#44; no pleural effusion&#44; and during the last admission the patient required ultrafiltration for oedema and oligoanuria&#44; with no response to an intravenous albumin infusion&#46; Four months later&#44; he was re-admitted due to a new episode of extreme generalised oedema&#44; with Cr 2&#46;3<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; proteinuria 49&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;day&#44; serum albumin 1&#46;6<span class="elsevierStyleHsp" style=""></span>g&#47;dl and total protein 3&#46;7<span class="elsevierStyleHsp" style=""></span>g&#47;dl&#46; Plasmapheresis was performed through a right femoral transient venous catheter&#44; performing 3 sessions&#44; extracting 3300<span class="elsevierStyleHsp" style=""></span>ml of plasma and infusing 1800<span class="elsevierStyleHsp" style=""></span>ml of 5&#37; albumin and 1500<span class="elsevierStyleHsp" style=""></span>ml of fresh frozen plasma &#40;FFP&#41; every other day&#46; Anticoagulation was performed with 3500<span class="elsevierStyleHsp" style=""></span>IU of subcutaneous bemiparin every 24<span class="elsevierStyleHsp" style=""></span>h&#46; The patient maintained diuresis and had no episodes of hypotension&#46; On the third day&#44; the patient noticed pain in the left thigh&#44; together with an increase in its volume of the extremity&#59; the Doppler ultrasound showed bilateral iliofemoral venous thrombosis&#46; The coagulation study showed D-dimer 14&#44;895<span class="elsevierStyleHsp" style=""></span>ng&#47;ml&#44; fibrinogen 8&#46;9<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; prothrombin activity at 77&#37;&#44; antithrombin III at 49&#37; and platelets 534&#44;000&#47;mm<span class="elsevierStyleSup">3</span>&#46; Proteinuria rose to 71&#46;3<span class="elsevierStyleHsp" style=""></span>g&#47;day during admission&#44; and serum albumin initially rose to 2&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;dl and then decreased rapidly and remained at 1&#8211;1&#46;3<span class="elsevierStyleHsp" style=""></span>g&#47;dl&#46; Antithrombin III &#40;1000<span class="elsevierStyleHsp" style=""></span>IU&#47;day&#41; was administered for 10 days&#44; achieving serum antithrombin III levels around 70&#37; by discharge&#46; The venous catheter was removed after the third round of plasmapheresis&#59; the patient was anticoagulated with 7500<span class="elsevierStyleHsp" style=""></span>IU of subcutaneous bemiparin&#47;day and discharged on acenocoumarol&#46; Creatinine stayed at 1&#46;6<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#46; Nine months later&#44; the Doppler ultrasound was repeated&#44; showing the complete permeability of the iliac and femoral axis&#46; Plasmapheresis did not affect the subsequent changes in proteinuria&#46; Rituximab and tacrolimus were subsequently administered&#44; but&#44; 13 months later&#44; the patient entered the haemodialysis programme due to severe kidney failure &#40;Cr 12&#46;2<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#41;&#44; with no changes in proteinuria &#40;25<span class="elsevierStyleHsp" style=""></span>g&#47;day&#41;&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">It has been postulated that the most important predictive factor for the development of thrombosis in NS is a degree of proteinuria<a class="elsevierStyleCrossRefs" href="#bib0080"><span class="elsevierStyleSup">6&#44;7</span></a> at which hepatic synthesis can no longer compensate&#59; this entails an imbalance between coagulation-regulating proteins and fibrinolysis&#46;<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">8&#44;9</span></a> Plasmapheresis would theoretically allow restautration of the balance this imbalance&#44; in addition to removing the postulated permeabilising agent that mediates the podocyte lesion in FSGS&#46; The curious nature of our case lies in the fact that the thrombosis coincided with the performance of plasmapheresis&#44; an observation that we have not found described in the literature&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Several factors may have facilitated the thrombosis&#46; Ultrafiltration can cause haemoconcentration&#44; which may have raised levels of procoagulant factors&#59; this could have promoted the thrombosis by a similar mechanism as in children following dehydration&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a> Replacement of FFP with plasmapheresis provides all the coagulation factors&#44; as well as antithrombotic factors &#40;antithrombin III&#44; proteins C and S&#41;&#44; while with 5&#37; albumin we could increase serum albumin levels slightly&#44; and so the thrombotic risk should be reduced&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> However&#44; we observed that the antithrombin III levels during thrombosis were low&#59; it is therefore possible that plasma infusion in cases of severe NS does not completely restore the coagulation&#47;fibrinolysis imbalance&#46; There is nothing in the literature describing how coagulation factors change after plasma replacement&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Our case provides several interesting and practical reflections&#46; First&#44; should specific preventive anticoagulation be used when plasmapheresis is to be performed in a case of nephrotic syndrome&#63; The dose of LMWH may need to be higher than that normally used if there is no nephrotic syndrome&#44; given the low levels of antithrombin III&#44; coupled with elevated procoagulant factors&#44; plus the loss of LMWH via the kidneys compared with heparin sodium&#46; Antithrombin III levels should be monitored before starting plasmapheresis and after each session&#44; since it may not normalise&#44; despite plasma infusion&#44; as happened in our case&#46; We do not know whether a LMWH with a higher molecular weight or with a longer half-life would be more effective or suitable for preventing venous thrombosis in cases with severe NS&#46;</p></span>"
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Letter to the Editor
Development of deep vein thrombosis during treatment with plasmapheresis
Desarrollo de trombosis coincidiendo con la realización de plasmaféresis
Maria Teresa Jaldo Rodríguez, Francisco J. Borrego Utiel
Corresponding author
fborregou@senefro.org

Corresponding author.
, Josefa Borrego Hinojosa, Maria Pilar Pérez del Barrio
Servicio de Nefrología, Complejo Hospitalario de Jaén, Jaén, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">In primary focal segmental glomerulosclerosis &#40;FSGS&#41; the response to drug treatment is 30&#8211;70&#37;&#44; depending on factors such as histological type&#44; degree of proteinuria&#44; presence of kidney failure or degree of resistance to steroid treatment&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;2</span></a> Plasmapheresis is used as rescue therapy when there is no response to drugs&#44; results are variable and there are&#44; frequent relapses&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4</span></a> Plasmapheresis&#44; accompanied by immunoadsorption in post-transplant relapse of FSGS&#44; achieves good results with minimal complications&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Here we report a case of venous thrombosis that occurred while performing plasmapheresis on a patient with FSGS&#46; The patient is 26-year-old man with severe nephrotic syndrome &#40;NS&#41; due to FSGS&#44; a cellular variant&#44; diagnosed 10 months earlier&#46; The patient received treatment with steroids&#44; cyclophosphamide&#44; cyclosporine and mycophenolate&#44; with no response&#44; maintaining a proteinuria of 15&#8211;33<span class="elsevierStyleHsp" style=""></span>g&#47;day&#46; He was admitted the Hospital on 3 occasions for extreme generalised oedema&#44; with ascites&#44; effusion in the testicular region&#44; no pleural effusion&#44; and during the last admission the patient required ultrafiltration for oedema and oligoanuria&#44; with no response to an intravenous albumin infusion&#46; Four months later&#44; he was re-admitted due to a new episode of extreme generalised oedema&#44; with Cr 2&#46;3<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; proteinuria 49&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;day&#44; serum albumin 1&#46;6<span class="elsevierStyleHsp" style=""></span>g&#47;dl and total protein 3&#46;7<span class="elsevierStyleHsp" style=""></span>g&#47;dl&#46; Plasmapheresis was performed through a right femoral transient venous catheter&#44; performing 3 sessions&#44; extracting 3300<span class="elsevierStyleHsp" style=""></span>ml of plasma and infusing 1800<span class="elsevierStyleHsp" style=""></span>ml of 5&#37; albumin and 1500<span class="elsevierStyleHsp" style=""></span>ml of fresh frozen plasma &#40;FFP&#41; every other day&#46; Anticoagulation was performed with 3500<span class="elsevierStyleHsp" style=""></span>IU of subcutaneous bemiparin every 24<span class="elsevierStyleHsp" style=""></span>h&#46; The patient maintained diuresis and had no episodes of hypotension&#46; On the third day&#44; the patient noticed pain in the left thigh&#44; together with an increase in its volume of the extremity&#59; the Doppler ultrasound showed bilateral iliofemoral venous thrombosis&#46; The coagulation study showed D-dimer 14&#44;895<span class="elsevierStyleHsp" style=""></span>ng&#47;ml&#44; fibrinogen 8&#46;9<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; prothrombin activity at 77&#37;&#44; antithrombin III at 49&#37; and platelets 534&#44;000&#47;mm<span class="elsevierStyleSup">3</span>&#46; Proteinuria rose to 71&#46;3<span class="elsevierStyleHsp" style=""></span>g&#47;day during admission&#44; and serum albumin initially rose to 2&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;dl and then decreased rapidly and remained at 1&#8211;1&#46;3<span class="elsevierStyleHsp" style=""></span>g&#47;dl&#46; Antithrombin III &#40;1000<span class="elsevierStyleHsp" style=""></span>IU&#47;day&#41; was administered for 10 days&#44; achieving serum antithrombin III levels around 70&#37; by discharge&#46; The venous catheter was removed after the third round of plasmapheresis&#59; the patient was anticoagulated with 7500<span class="elsevierStyleHsp" style=""></span>IU of subcutaneous bemiparin&#47;day and discharged on acenocoumarol&#46; Creatinine stayed at 1&#46;6<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#46; Nine months later&#44; the Doppler ultrasound was repeated&#44; showing the complete permeability of the iliac and femoral axis&#46; Plasmapheresis did not affect the subsequent changes in proteinuria&#46; Rituximab and tacrolimus were subsequently administered&#44; but&#44; 13 months later&#44; the patient entered the haemodialysis programme due to severe kidney failure &#40;Cr 12&#46;2<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#41;&#44; with no changes in proteinuria &#40;25<span class="elsevierStyleHsp" style=""></span>g&#47;day&#41;&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">It has been postulated that the most important predictive factor for the development of thrombosis in NS is a degree of proteinuria<a class="elsevierStyleCrossRefs" href="#bib0080"><span class="elsevierStyleSup">6&#44;7</span></a> at which hepatic synthesis can no longer compensate&#59; this entails an imbalance between coagulation-regulating proteins and fibrinolysis&#46;<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">8&#44;9</span></a> Plasmapheresis would theoretically allow restautration of the balance this imbalance&#44; in addition to removing the postulated permeabilising agent that mediates the podocyte lesion in FSGS&#46; The curious nature of our case lies in the fact that the thrombosis coincided with the performance of plasmapheresis&#44; an observation that we have not found described in the literature&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Several factors may have facilitated the thrombosis&#46; Ultrafiltration can cause haemoconcentration&#44; which may have raised levels of procoagulant factors&#59; this could have promoted the thrombosis by a similar mechanism as in children following dehydration&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a> Replacement of FFP with plasmapheresis provides all the coagulation factors&#44; as well as antithrombotic factors &#40;antithrombin III&#44; proteins C and S&#41;&#44; while with 5&#37; albumin we could increase serum albumin levels slightly&#44; and so the thrombotic risk should be reduced&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> However&#44; we observed that the antithrombin III levels during thrombosis were low&#59; it is therefore possible that plasma infusion in cases of severe NS does not completely restore the coagulation&#47;fibrinolysis imbalance&#46; There is nothing in the literature describing how coagulation factors change after plasma replacement&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Our case provides several interesting and practical reflections&#46; First&#44; should specific preventive anticoagulation be used when plasmapheresis is to be performed in a case of nephrotic syndrome&#63; The dose of LMWH may need to be higher than that normally used if there is no nephrotic syndrome&#44; given the low levels of antithrombin III&#44; coupled with elevated procoagulant factors&#44; plus the loss of LMWH via the kidneys compared with heparin sodium&#46; Antithrombin III levels should be monitored before starting plasmapheresis and after each session&#44; since it may not normalise&#44; despite plasma infusion&#44; as happened in our case&#46; We do not know whether a LMWH with a higher molecular weight or with a longer half-life would be more effective or suitable for preventing venous thrombosis in cases with severe NS&#46;</p></span>"
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ISSN: 20132514
Original language: English
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