{"id":3744,"date":"2021-12-14T12:05:07","date_gmt":"2021-12-14T12:05:07","guid":{"rendered":"https:\/\/www.kauveryhospital.com\/ima-newsletters\/?p=3744"},"modified":"2025-04-11T04:07:50","modified_gmt":"2025-04-11T04:07:50","slug":"severe-anaemia-in-a-dialysis-patient","status":"publish","type":"post","link":"https:\/\/www.kauveryhospital.com\/ima-journal\/ima-journal-december-2021\/severe-anaemia-in-a-dialysis-patient\/","title":{"rendered":"Severe Anaemia in a Dialysis Patient"},"content":{"rendered":"<p class=\"caps\">[vc_row][vc_column][vc_column_text]<\/p>\n<p style=\"text-align: justify;\">Mr.S, 54 yrs old gentleman, is on regular dialysis for his chronic renal failure due to Diabetic nephropathy. He was known to have Ischemic heart disease and underwent single vessel angioplasty, few months before. He was on dual anti platelet therapy post angioplasty.<\/p>\n<p style=\"text-align: justify;\">His chronic renal failure was managed by thrice weekly dialysis, dietary support, erythropoietin thrice weekly for his anaemia, calcium supplementation, and sugars were controlled with insulin.<\/p>\n<p style=\"text-align: justify;\">He maintained haemoglobin at 10 grams and there was gradual drop in his haemoglobin. He complained of epigastric pain but there was no hemetemesis or malena.\u00a0 His stool occult blood tested repeatedly was negative and upper and lower GI scopy studies were normal. His serum ferritin was normal, so as Transferrin saturation. His corrected reticulocyte count was &lt; 0.8 % indicating bone marrow dysfunction.<\/p>\n<p style=\"text-align: justify;\">He underwent a bone marrow biopsy and that was consistent with PRCA \u2013 Pure Red Cell Aplasia.<\/p>\n<p style=\"text-align: justify;\"><strong>Management :<\/strong> He underwent screening for Parvovirus ( negative), and his anti EPO antibody (EPO \u2013 Erythropoietin) result was low positive.. He has been initiated on Cyclosporin and steroids and he didn\u2019t need blood transfusion subsequently.<\/p>\n<h2><strong>What is PRCA ?<\/strong><\/h2>\n<p style=\"text-align: justify;\">Pure Red Cell Aplasia is a condition where there is absolute decrease in the production of red cells in the bone marrow. Contrary to Aplastic anemia, here the WBC and the platelet productions are normal. There is marked decrease in reticulocyte numbers, the red cells are normocytic and normochromic and significant reduction or absence of erythroid precursors on bone marrow biopsy.(1)<\/p>\n<h2><strong>PRCA \u2013Etiology<\/strong><\/h2>\n<p style=\"text-align: justify;\">It can be Congenital( Diamond- BlackfanAnemia(2)\u00a0 \u00a0\u2013 associated with physical malformations due to multiple ribosomal gene abnormalities and Pearson syndrome (3)\u2013 a congenital mitochondrial gene defect associated with pancreatic insuffucuency and PRCA )\u00a0OR Acquired.<\/p>\n<p style=\"text-align: justify;\">Acquired PRCA can be primary that is due to antibodies to red cell precursors. Secondary PRCA could be due to auto immune diseases like lupus, haematological malignancies like lymphomas and leukaemia, infections \u2013 classically Parvovirus B 19 (4) , hepatitis B &amp;C, infectious mono nucleosis, variety of drugs, thymomas and sold tumours.<\/p>\n<h2><strong>Clinical manifestations\u00a0 <\/strong><\/h2>\n<p style=\"text-align: justify;\">Are predominantly due to anemia \u2013 easy fatiguability, exertional breathlessness, chest discomfort, palpitations etc. Manifestations could be present related to the underlying secondary causes in secondary PRCA.<\/p>\n<h2><strong>Investigations :<\/strong><\/h2>\n<p style=\"text-align: justify;\">The routine haematological evaluation for anaemia including complete blood count, peripheral smear, reticulocyte count, endoscopy, coomb\u2019s test etc need to be done. The confirmatory incestigation of\u00a0 PRCA is bone marrow study.<\/p>\n<p style=\"text-align: justify;\">This will reveal normal white cell and platelet series but grossly diminished red cell precursors.<\/p>\n<h2><strong><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-3749 size-full\" src=\"https:\/\/www.kauveryhospital.com\/ima-newsletters\/wp-content\/uploads\/2021\/12\/bone-marrow.jpg\" alt=\"\" width=\"638\" height=\"382\" srcset=\"https:\/\/www.kauveryhospital.com\/ima-journal\/wp-content\/uploads\/2021\/12\/bone-marrow.jpg 638w, https:\/\/www.kauveryhospital.com\/ima-journal\/wp-content\/uploads\/2021\/12\/bone-marrow-300x180.jpg 300w\" sizes=\"auto, (max-width: 638px) 100vw, 638px\" \/><\/strong><\/h2>\n<h2><strong>Management of PRCA (Primary)<\/strong><\/h2>\n<p style=\"text-align: justify;\">This involves immuno suppressive medications as it is due to antibody against EPO or erythroid precursors. Among the various drugs tried the best response is obtained with Cyclosporin (5) either alone or in combination with steroids. Other agents tried are Rituximab (6), IVIG, cyclophosphamide.<\/p>\n<p style=\"text-align: justify;\">For refractory disease, plasmapharesis is tried. In patients with chronic kidney disease, renal transplantation is recommended if medical management .<\/p>\n<ol>\n<li>Sawada K, Fujishima N, Hirokawa M.\u00a0Acquired pure red cell aplasia: updated review of treatment.\u00a0<em>Br J Haematol<\/em>. 2008;142(4):505-514<\/li>\n<li>Ruggero D, Shimamura A.\u00a0Marrow failure: a window into ribosome biology.\u00a0<em>Blood<\/em>. 2014;124(18):2784-2792.<\/li>\n<li>Fleming MD.\u00a0The genetics of inherited sideroblasticanemias.\u00a0<em>SeminHematol<\/em>. 2002;39(4):270-281.<\/li>\n<li>Frickhofen N, Chen ZJ, Young NS, Cohen BJ, Heimpel H, Abkowitz JL.\u00a0Parvovirus B19 as a cause of acquired chronic pure red cell aplasia.\u00a0<em>Br J Haematol<\/em>. 1994;87(4):818-824<\/li>\n<li>Means RT, Dessypris EN, Krantz SB.\u00a0Treatment of refractory pure red cell aplasia with cyclosporine A: disappearance of IgG inhibitor associated with clinical response.\u00a0<em>Br J Haematol<\/em>. 1991;78:114-119.<\/li>\n<li>Auner HW, W\u00f6lfler A, Beham-Schmid C, Strunk D, Linkesch W, Sill H.\u00a0Restoration of erythropoiesis by rituximab in an adult patient with primary acquired pure red cell aplasia refractory to conventional treatment.\u00a0<em>Br J Haematol<\/em>. 2002;116(3):727-728.<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<p><strong><img loading=\"lazy\" decoding=\"async\" class=\"size-thumbnail wp-image-1844 alignleft\" src=\"https:\/\/www.kauveryhospital.com\/ima-journal\/wp-content\/uploads\/2021\/03\/Dr-Balasubramaniam-raju-Nephrology2019-03-30-01-34-01pm1-150x150.jpg\" alt=\"Dr. Balasubramaniam Raju\" width=\"150\" height=\"150\" \/>Dr.R.Balasubramaniyam<\/strong><br \/>\nChief Of Nephrology<br \/>\nKauvery Hospital[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column][vc_column_text] Mr.S, 54 yrs old gentleman, is on regular dialysis for his chronic renal failure due to Diabetic nephropathy. He was known to have Ischemic heart disease and underwent single<\/p>\n","protected":false},"author":2,"featured_media":3745,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[36],"tags":[],"class_list":["post-3744","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-ima-journal-december-2021"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Severe Anaemia in a Dialysis Patient<\/title>\n<meta name=\"description\" content=\"Mr.S, 54 yrs old gentleman, is on regular dialysis for his chronic renal failure due to Diabetic nephropathy. 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