Hemochromatosis medical therapy: Difference between revisions

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__NOTOC__
__NOTOC__
{{Hemochromatosis}}
{{Hemochromatosis}}
{{CMG}}; {{AE}}{{SKA}}
{{CMG}} {{shyam}}; {{AE}}{{SKA}}


==Overview==
==Overview==
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'''Following are the recommendations for treating hemochromatosis according to American Association for the Study of Liver Diseases:'''
'''Following are the recommendations for treating hemochromatosis according to American Association for the Study of Liver Diseases:'''


Phlebotomy is recommended option for the patients with iron over load weather they are symptomatic or not.<ref name="pmid2065912">{{cite journal| author=Adams PC, Speechley M, Kertesz AE| title=Long-term survival analysis in hereditary hemochromatosis. | journal=Gastroenterology | year= 1991 | volume= 101 | issue= 2 | pages= 368-72 | pmid=2065912 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2065912  }}</ref><ref name="pmid8613000">{{cite journal| author=Niederau C, Fischer R, Pürschel A, Stremmel W, Häussinger D, Strohmeyer G| title=Long-term survival in patients with hereditary hemochromatosis. | journal=Gastroenterology | year= 1996 | volume= 110 | issue= 4 | pages= 1107-19 | pmid=8613000 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8613000  }}</ref><ref name="pmid16871557">{{cite journal| author=Falize L, Guillygomarc'h A, Perrin M, Lainé F, Guyader D, Brissot P et al.| title=Reversibility of hepatic fibrosis in treated genetic hemochromatosis: a study of 36 cases. | journal=Hepatology | year= 2006 | volume= 44 | issue= 2 | pages= 472-7 | pmid=16871557 | doi=10.1002/hep.21260 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16871557  }}</ref><ref name="pmid8985284">{{cite journal| author=Adams PC, Deugnier Y, Moirand R, Brissot P| title=The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis. | journal=Hepatology | year= 1997 | volume= 25 | issue= 1 | pages= 162-6 | pmid=8985284 | doi=10.1002/hep.510250130 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8985284  }}</ref><ref name="pmid15508107">{{cite journal| author=Kowdley KV| title=Iron, hemochromatosis, and hepatocellular carcinoma. | journal=Gastroenterology | year= 2004 | volume= 127 | issue= 5 Suppl 1 | pages= S79-86 | pmid=15508107 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15508107  }}</ref><ref name="pmid11722996">{{cite journal| author=Brittenham GM, Klein HG, Kushner JP, Ajioka RS| title=Preserving the national blood supply. | journal=Hematology Am Soc Hematol Educ Program | year= 2001 | volume=  | issue=  | pages= 422-32 | pmid=11722996 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11722996  }}</ref><ref name="pmid6940487">{{cite journal| author=Lynch SR, Cook JD| title=Interaction of vitamin C and iron. | journal=Ann N Y Acad Sci | year= 1980 | volume= 355 | issue=  | pages= 32-44 | pmid=6940487 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6940487  }}</ref><ref name="pmid12957298">{{cite journal| author=Bonkovsky HL, Lambrecht RW, Shan Y| title=Iron as a co-morbid factor in nonhemochromatotic liver disease. | journal=Alcohol | year= 2003 | volume= 30 | issue= 2 | pages= 137-44 | pmid=12957298 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12957298  }}</ref><ref name="pmid11910345">{{cite journal| author=Facchini FS, Hua NW, Stoohs RA| title=Effect of iron depletion in carbohydrate-intolerant patients with clinical evidence of nonalcoholic fatty liver disease. | journal=Gastroenterology | year= 2002 | volume= 122 | issue= 4 | pages= 931-9 | pmid=11910345 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11910345  }}</ref><ref name="pmid8047080">{{cite journal| author=Brittenham GM, Griffith PM, Nienhuis AW, McLaren CE, Young NS, Tucker EE et al.| title=Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major. | journal=N Engl J Med | year= 1994 | volume= 331 | issue= 9 | pages= 567-73 | pmid=8047080 | doi=10.1056/NEJM199409013310902 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8047080  }}</ref><ref name="pmid12393526">{{cite journal| author=Brittenham GM, Badman DG, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Workshop| title=Noninvasive measurement of iron: report of an NIDDK workshop. | journal=Blood | year= 2003 | volume= 101 | issue= 1 | pages= 15-9 | pmid=12393526 | doi=10.1182/blood-2002-06-1723 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12393526  }}</ref>
Phlebotomy is recommended option for the patients with iron over load weather they are symptomatic or not.<ref name="pmid2065912">{{cite journal| author=Adams PC, Speechley M, Kertesz AE| title=Long-term survival analysis in hereditary hemochromatosis. | journal=Gastroenterology | year= 1991 | volume= 101 | issue= 2 | pages= 368-72 | pmid=2065912 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2065912  }}</ref><ref name="pmid8613000">{{cite journal| author=Niederau C, Fischer R, Pürschel A, Stremmel W, Häussinger D, Strohmeyer G| title=Long-term survival in patients with hereditary hemochromatosis. | journal=Gastroenterology | year= 1996 | volume= 110 | issue= 4 | pages= 1107-19 | pmid=8613000 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8613000  }}</ref><ref name="pmid16871557">{{cite journal| author=Falize L, Guillygomarc'h A, Perrin M, Lainé F, Guyader D, Brissot P et al.| title=Reversibility of hepatic fibrosis in treated genetic hemochromatosis: a study of 36 cases. | journal=Hepatology | year= 2006 | volume= 44 | issue= 2 | pages= 472-7 | pmid=16871557 | doi=10.1002/hep.21260 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16871557  }}</ref><ref name="pmid8985284">{{cite journal| author=Adams PC, Deugnier Y, Moirand R, Brissot P| title=The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis. | journal=Hepatology | year= 1997 | volume= 25 | issue= 1 | pages= 162-6 | pmid=8985284 | doi=10.1002/hep.510250130 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8985284  }}</ref><ref name="pmid15508107">{{cite journal| author=Kowdley KV| title=Iron, hemochromatosis, and hepatocellular carcinoma. | journal=Gastroenterology | year= 2004 | volume= 127 | issue= 5 Suppl 1 | pages= S79-86 | pmid=15508107 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15508107  }}</ref><ref name="pmid11722996">{{cite journal| author=Brittenham GM, Klein HG, Kushner JP, Ajioka RS| title=Preserving the national blood supply. | journal=Hematology Am Soc Hematol Educ Program | year= 2001 | volume=  | issue=  | pages= 422-32 | pmid=11722996 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11722996  }}</ref><ref name="pmid6940487">{{cite journal| author=Lynch SR, Cook JD| title=Interaction of vitamin C and iron. | journal=Ann N Y Acad Sci | year= 1980 | volume= 355 | issue=  | pages= 32-44 | pmid=6940487 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6940487  }}</ref><ref name="pmid12957298">{{cite journal| author=Bonkovsky HL, Lambrecht RW, Shan Y| title=Iron as a co-morbid factor in nonhemochromatotic liver disease. | journal=Alcohol | year= 2003 | volume= 30 | issue= 2 | pages= 137-44 | pmid=12957298 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12957298  }}</ref><ref name="pmid11910345">{{cite journal| author=Facchini FS, Hua NW, Stoohs RA| title=Effect of iron depletion in carbohydrate-intolerant patients with clinical evidence of nonalcoholic fatty liver disease. | journal=Gastroenterology | year= 2002 | volume= 122 | issue= 4 | pages= 931-9 | pmid=11910345 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11910345  }}</ref><ref name="pmid8047080">{{cite journal| author=Brittenham GM, Griffith PM, Nienhuis AW, McLaren CE, Young NS, Tucker EE et al.| title=Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major. | journal=N Engl J Med | year= 1994 | volume= 331 | issue= 9 | pages= 567-73 | pmid=8047080 | doi=10.1056/NEJM199409013310902 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8047080  }}</ref><ref name="pmid12393526">{{cite journal| author=Brittenham GM, Badman DG, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Workshop| title=Noninvasive measurement of iron: report of an NIDDK workshop. | journal=Blood | year= 2003 | volume= 101 | issue= 1 | pages= 15-9 | pmid=12393526 | doi=10.1182/blood-2002-06-1723 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12393526 }}</ref><ref name="pmid19264677">{{cite journal| author=Hankins JS, McCarville MB, Loeffler RB, Smeltzer MP, Onciu M, Hoffer FA et al.| title=R2* magnetic resonance imaging of the liver in patients with iron overload. | journal=Blood | year= 2009 | volume= 113 | issue= 20 | pages= 4853-5 | pmid=19264677 | doi=10.1182/blood-2008-12-191643 | pmc=2686136 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19264677 }}</ref>


'''1 Starting therapeutic phlebotomy''': Staring blood removal till iron level gets normal.
'''1 Starting therapeutic (induction) phlebotomy''': Staring blood removal till iron level gets normal.
* 1.1 Asymptomatic hemochromatosis:
* 1.1 Asymptomatic hemochromatosis:
* Preferred regime: 1 unit of blood (about 473 mL or 1 pint) is removed per week
* Preferred regime: 1 unit of blood (about 473 mL or 1 pint) is removed per week
Line 27: Line 27:
* 2.3 Check serum ferritin level every 10-12 phlebotomies
* 2.3 Check serum ferritin level every 10-12 phlebotomies
'''3 Dietary restrictions:'''
'''3 Dietary restrictions:'''
* 3.1 Preferred regime: No restrictions.
* 3.1 Preferred regime: No restrictions.  
* 3.2 Alternative regime: avoid iron supplements, avoid vitamin C supplements, avoid alcohol completely
* 3.2 Alternative regime: avoid iron supplements, avoid vitamin C supplements, avoid red meat, avoid alcohol completely
'''4 Non-HEF hemochromaosis:'''
'''4 Non-HEF hemochromaosis:'''
* 4.1 Preferred regime: 1 unit of blood (about 473 mL or 1 pint) is removed per week
* 4.1 Preferred regime: 1 unit of blood (about 473 mL or 1 pint) is removed per week
Line 42: Line 42:
* 5.3.1: Liver biopsy for evaluation not required.
* 5.3.1: Liver biopsy for evaluation not required.
* 5.3.2: Consider follow-up liver biopsy to ascertain adequacy of iron removal.
* 5.3.2: Consider follow-up liver biopsy to ascertain adequacy of iron removal.
====Screening and diagnosis of hemochromatosis.WT, wild type; HII, histologic iron index; CII, chemical iron index; HH, hereditary hemochromatosis<ref name="pmid22675794">{{cite journal| author=Bacon BR| title=Hemochromatosis: discovery of the HFE gene. | journal=Mo Med | year= 2012 | volume= 109 | issue= 2 | pages= 133-6 | pmid=22675794 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22675794  }}</ref><ref name="pmid20492323">{{cite journal| author=Asia-Pacific Working Party on Prevention of Hepatocellular Carcinoma| title=Prevention of hepatocellular carcinoma in the Asia-Pacific region: consensus statements. | journal=J Gastroenterol Hepatol | year= 2010 | volume= 25 | issue= 4 | pages= 657-63 | pmid=20492323 | doi=10.1111/j.1440-1746.2009.06167.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20492323  }}</ref><ref name="pmid25976957">{{cite journal| author=Adams PC| title=Epidemiology and diagnostic testing for hemochromatosis and iron overload. | journal=Int J Lab Hematol | year= 2015 | volume= 37 Suppl 1 | issue=  | pages= 25-30 | pmid=25976957 | doi=10.1111/ijlh.12347 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25976957  }}</ref><ref name="pmid25454304">{{cite journal| author=Salgia RJ, Brown K| title=Diagnosis and management of hereditary hemochromatosis. | journal=Clin Liver Dis | year= 2015 | volume= 19 | issue= 1 | pages= 187-98 | pmid=25454304 | doi=10.1016/j.cld.2014.09.011 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25454304  }}</ref><ref name="pmid23418762">{{cite journal| author=Crownover BK, Covey CJ| title=Hereditary hemochromatosis. | journal=Am Fam Physician | year= 2013 | volume= 87 | issue= 3 | pages= 183-90 | pmid=23418762 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23418762  }}</ref><ref name="pmid25864215">{{cite journal| author=Adams PC, Barton JC, Guo H, Alter D, Speechley M| title=Serum ferritin is a biomarker for liver mortality in the Hemochromatosis and Iron Overload Screening Study. | journal=Ann Hepatol | year= 2015 | volume= 14 | issue= 3 | pages= 348-53 | pmid=25864215 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25864215  }}</ref><ref name="pmid23862168">{{cite journal| author=Adams PC, McLaren CE, Speechley M, McLaren GD, Barton JC, Eckfeldt JH| title=HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L. | journal=Can J Gastroenterol | year= 2013 | volume= 27 | issue= 7 | pages= 390-2 | pmid=23862168 | doi= | pmc=3956024 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23862168  }}</ref><ref name="pmid25314357">{{cite journal| author=Lim A, Speechley M, Adams PC| title=Predicting C282Y homozygote genotype for hemochromatosis using serum ferritin and transferrin saturation values from 44,809 participants of the HEIRS study. | journal=Can J Gastroenterol Hepatol | year= 2014 | volume= 28 | issue= 9 | pages= 502-4 | pmid=25314357 | doi= | pmc=4205907 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25314357  }}</ref>====
{{familytree/start|summary=Algorithm for screening and diagnosis of hemochromatosis.WT, wild type; HII, histologic iron index; CII, chemical iron index; HH, hereditary hemochromatosis.}}
{{familytree| | | | | | | | | | | | |A01| | | | | | | | | |A01=Serum Transferin Saturation<br>TS}}
{{familytree| | | | | | | | | |,|-|-|-|^|-|-|-|.| | | | | | |}}
{{familytree| | | | | | | | | |!| | | | | | | |!| | | | | |}}
{{familytree| | | | | | | | |B01| | | | | |B02| | | | |B01=<50% premenupasal females<br><60% men, postmenupasal women|B02=≥50% premenupasal females<br>≥60% men, postmenupasal women}}
{{familytree| | | | | | | | | |!| | | | | | | |!| | | | |}}
{{familytree| | | | | | | | | |!| | | | | | |Q01| | | | |Q01=1 Repeat Transferin Saturation TS<br>2 Serum Feretin SF}}
{{familytree| | | | | | | | | |!| | |,|-|-|-|-|^|-|-|.| |}}
{{familytree| | | | | | | | |C01| |!| | | | | | | |!| | |C01=Repeat testing every 5 year}}
{{familytree| | | | | | | | |,|-|-|-|'| | | | | | | |!| | |}}
{{familytree| | | | | | | | |!| | | | | | | | | | | |!| |}}
{{familytree| | | | | | | | |D01| | | | | | | | |D02| |D01=TS:<50% premenupasal females<br>TS: <60% men, postmenupasal women<br>SF: 20-250μg/L premenupasal females<br>SF: 10-120μg/L men, postmenupasal women|D02=TS:≥50% premenupasal females<br>TS: ≥60% men, postmenupasal women<br>SF:>200 μg/L premenupasal females<br>SF:>300 μg/L men, postmenupasal women}}
{{familytree| | | | | | | | | |!| | | | | | |,|-|-|-|^|-|-|-|-|.|}}
{{familytree| | | | | | | | |E01| | | | |E02| | | | | | |E03|E01=Repeat TS and SF every 2-3 year|E02=Serum Feretin<1000 μg/L|E03=Serum Feretin>1000 μg/L}}
{{familytree| | | | | | | | | | | | | | | | |!|,|-|-|-|-|-|-|^|-|-|.|}}
{{familytree| | | | | | | | | | | | | | | |F01| | | | | | | | |F02|F01=Geno-typing|F02=Liver biopsy}}
{{familytree| | | | | | | | |,|-|-|v|-|-|-|^|-|-|v|-|-|.| | | | |,|-|^|-|.| |}}
{{familytree| | | | | | | |G01| |G02| | | |G03| |G04| | |G05| |G06|G01=WT/WT genotype|G02=C282Y/WT genotype|G03=C282Y/H63D genotype|G04=C282Y/C282Y genotype|G05=Histological iron index<0.15<br>Chemical iron index<2.0|G06=Histological iron index>0.15<br>Chemical iron index>2.0}}
{{familytree| | | | | | | | |`|-|V|-|'| | | | | |`|-|V|-|'| | | | |!| | |!|}}
{{familytree| | | | | | | | | |H01| | | | | | | |H02| | | | |H03| |H04|H01=Secondray hemochromatosis|H02=Phelebotomy to maintain Serum Feretin|H03=Repeat TS and SF after 2-3 year|H04=Phelebotomy to maintain Serum Feretin}}
{{familytree| | | | | | | | | | |!| | | | | | | | | |!| | |}}
{{familytree| | | | | | | | | |K01| | | | | | | |K02|K01=Screen family with Transferin Saturation & Serum Feretin if atypical HH suspected|K02=Screen family with genotyping}}
{{familytree| | | | | | | | | | | | | | | | | | | | |!| |}}
{{familytree| | | | | | | | | | | | | | | | | | | |J01|J01=Moniter Transferin Saturation & Serum Feretin in subclinical members}}
{{familytree/end}}


==References==
==References==

Latest revision as of 18:33, 1 January 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2]; Associate Editor(s)-in-Chief: Sunny Kumar MD [3]

Overview

The treatment of hemochromatosis depends on levels of iron deposition in body tissues, symptoms and complications due to damaged organs secondary to inflammatory response towards deposition.

Medical Therapy

  • Treatment is initiated when ferritin levels reach 300 micrograms per litre (or 200 in nonpregnant premenopausal women).
  • Treatment of organ damage (heart failure with diuretics and ACE inhibitor therapy).
  • Limiting intake of alcoholic beverages, vitamin C (increases iron absorption in the gut), red meat (high in iron) and potential causes of food poisoning (shellfish, seafood).
  • Increasing intake of substances that inhibit iron absorption, such as high-tannin tea, calcium, and foods containing oxalic and phytic acids (these must be consumed at the same time as the iron-containing foods in order to be effective.

Following are the recommendations for treating hemochromatosis according to American Association for the Study of Liver Diseases:

Phlebotomy is recommended option for the patients with iron over load weather they are symptomatic or not.[1][2][3][4][5][6][7][8][9][10][11][12]

1 Starting therapeutic (induction) phlebotomy: Staring blood removal till iron level gets normal.

  • 1.1 Asymptomatic hemochromatosis:
  • Preferred regime: 1 unit of blood (about 473 mL or 1 pint) is removed per week
  • Alternative regime: 0.5 to 2 units of blood can often be removed from men, whereas it may be possible to remove only 0.5 units of blood from women or frail or elderly patients with other medical problems
  • 1.2 Symptomatic patients with end-organ damage hemochromatosis:
  • 1.3 Preferred regime: 1 unit of blood (about 473 mL or 1 pint) is removed per week
  • 1.4 Stop frequent phlebotomy when serum ferritin reaches 50-100 μg/L

2 Maintenance phlebotomy: When serum ferritin levels in the range of 50 to 100 ng/mL

  • 2.1 Preferred regime: Removing 1 unit of blood (about 473 mL or 1 pint) is removed per 2 months
  • 2.2 Alternative regime: Removing 1 unit of blood (about 473 mL or 1 pint) is removed per 4 months
  • 2.3 Check serum ferritin level every 10-12 phlebotomies

3 Dietary restrictions:

  • 3.1 Preferred regime: No restrictions.
  • 3.2 Alternative regime: avoid iron supplements, avoid vitamin C supplements, avoid red meat, avoid alcohol completely

4 Non-HEF hemochromaosis:

  • 4.1 Preferred regime: 1 unit of blood (about 473 mL or 1 pint) is removed per week
  • 4.2 Alternative regime: In HIC is normal then follow dietary restrictions.

5 Secondary Iron Overload:

  • 5.1 Dyserythropoietic syndromes:
  • 5.1.1 Preferred regimen: Deferoxamine (Desferal) at a dose of 20-40 mg/kg body weight per day
  • 5.1.2 Alternative regime: Deferasirox (Exjade) given orally
  • 5.2 chronic hemolytic anemia:
  • 5.2.1 Preferred regimen: Deferoxamine at a dose of 20-40 mg/kg body weight per day
  • 5.2.2 Alternative regime: Deferasirox given orally
  • 5.3 Liver Biopsy
  • 5.3.1: Liver biopsy for evaluation not required.
  • 5.3.2: Consider follow-up liver biopsy to ascertain adequacy of iron removal.

References

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