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== Overview ==
== Overview ==
Secondary Prevention strategies for Gout include dietary and life style modifications. Dietary and life style modifications are indicated for preventing gout flares. Consuming less  purine rich food, fructose rich foods, cherries, vitamin C, increasing low fat dairy product consumption, avoiding red meat go in favour of reducing acute gout flares. Decreasing alcohol consumption, smoking cessation, weight loss, controlling underlying chronic conditions like [[Diabetes mellitus]], [[Hypertension]] favour decrease in gout flares.


== Secondary Prevention ==
== Secondary prevention ==
===Medications===
 
* [[Allopurinol]] and [[azathioprine]] (Imuran) used together present a risk of a potentially fatal [[drug interaction]], a severe risk of allopurinol use which is of importance to transplant patients being treated with azathioprine for [[immunosuppression]].[http://www.medsafe.govt.nz/Profs/PUarticles/azathioprine.htm]
 
* [[Febuxostat]] ((2-[3-cyano-4-isobutoxyphenyl]-4-methylthiazole-5-carboxylic acid) - a non-purine inhibitor of xanthine oxidase seems to be an alternative that is superior to allopurinol; it is currently in [[Clinical trials#Phase III| Phase III trials]].<ref>{{cite journal | author = Becker M, Schumacher H, Wortmann R, MacDonald P, Eustace D, Palo W, Streit J, Joseph-Ridge N | title = Febuxostat compared with allopurinol in patients with hyperuricemia and gout | journal = N Engl J Med | volume = 353 | issue = 23 | pages = 2450&ndash;61 | year = 2005 | id = PMID 16339094}}</ref>
 
* [[Probenecid]], a uricosuric drug that promotes the excretion of uric acid in urine, is also commonly prescribed - often in conjunction with [[colchicine]]. The drug [[fenofibrate]] (which is used in treating [[hyperlipidemia]]) also exerts a beneficial uricosuric effect.<ref>{{cite journal | author = Bardin T | title = Fenofibrate and losartan | journal = Ann Rheum Dis | volume = 62 | issue = 6 | pages = 497&ndash;8 | year = 2003 | id = PMID 12759281 | url=http://ard.bmjjournals.com/cgi/content/full/62/6/497}}</ref>
 
* As arterial hypertension quite often coexists with gout, treating it with [[losartan]], an [[angiotensin II receptor antagonist]], might have an additional beneficial effect on uric acid plasma levels. This way losartan can offset the negative side-effect of [[thiazide]]s (a group of [[diuretic]]s used for [[arterial hypertension|high blood pressure]]) on uric acid metabolism in patients with gout.
 
* It is suspected that in many cases gout may be secondary to untreated [[sleep apnea]], when oxygen-starved cells break down and release purines as a by-product. Treatment for apnea can be effective in lessening incidence of acute gout attacks.<ref>{{cite journal | author = Abrams B | title = Gout is an indicator of sleep apnea | journal = Sleep | volume = 28 | issue = 2 | pages = 275 | year = 2005 | id = PMID 16171252}}</ref>
 
* A study in 2004 suggests that animal flesh sources of purine, such as beef and seafood, greatly increase the risk of developing gout. However, high-purine vegetable sources did not. Dairy products such as milk and cheese significantly reduced the chances of gout. The study followed over 40000 men over a period of 12 years, in which 1300 cases of gout were reported.<ref name="Choi et al 2004">{{cite journal | author = Choi H, Atkinson K, Karlson E, Willett W, Curhan G | title = Purine-rich foods, dairy and protein intake, and the risk of gout in men | journal = N Engl J Med | volume = 350 | issue = 11 | pages = 1093&ndash;103 | year = 2004 | id = PMID 15014182 | url=http://www.nutritionaustralia.org/News_in_Nutrition/Journal_Articles/purine%20rich%20foods.pdf | format=PDF}}</ref>
 
* PEG-uricase, a polyethylene glycol ("PEG") conjugate of recombinant porcine uricase (urate oxidase), which breaks down the uric acid deposits is being studied in [[clinical trial#Phase III|Phase III clinical trials]] for the treatment of severe, treatment-refractory gout in the United States in 2006.[http://www.savientpharma.com/pipeline/puricase.asp Pipeline]
 
*[[Sodium bicarbonate]] (baking soda) is an old remedy,<ref>The British Pharmaceutical Codex.  Published by direction of the Council of the Pharmaceutical Society of Great Britain, 1911. [http://www.henriettesherbal.com/eclectic/bpc1911/sodium.html Sodium]</ref> thought to work by raising blood pH (lowering blood acidity).  However, the added sodium may be inappropriate for some people.
 
*Research from the University of British Columbia suggests long-term coffee consumption is associated with a lower risk of gout.<ref>{{cite journal | author = Hyon K. Choi, Walter Willett, Gary Curhan | title =
Coffee consumption and risk of incident gout in men: A prospective study | journal = Arthritis & Rheumatism | volume = 56 | issue = 6 | pages = 2049&ndash;2055 | year = 2007 | id = PMID 17530645}}</ref> <ref>{{cite journal | author = Choi HK, Curhan G. | title =
Coffee, tea, and caffeine consumption and serum uric acid level: The third national health and nutrition examination survey | journal = Arthritis & Rheumatism | volume = 57 | issue = 5 | pages = 816&ndash;821 | year = 2007 | id = PMID 17530681 }}</ref>


===Diet===
Clinical practice guidelines are available:
* American College of Physicians (ACP)<ref name="pmid27802508">{{cite journal| author=Qaseem A, Harris RP, Forciea MA, Clinical Guidelines Committee of the American College of Physicians. Denberg TD, Barry MJ | display-authors=etal| title=Management of Acute and Recurrent Gout: A Clinical Practice Guideline From the American College of Physicians. | journal=Ann Intern Med | year= 2017 | volume= 166 | issue= 1 | pages= 58-68 | pmid=27802508 | doi=10.7326/M16-0570 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27802508  }}  [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=&cmd=prlinks&id=28241287 Review in: Ann Intern Med. 2017 Feb 21;166(4):JC14] </ref>


''See Saag and Choi, 2006, an open-access review article, for detailed references and further information.''<ref>{{cite journal |author=Saag KG, Choi H |title=Epidemiology, risk factors, and lifestyle modifications for gout |journal=Arthritis Res. Ther. |volume=8 Suppl 1 |issue= |pages=S2 |year=2006 |pmid=16820041 |doi=10.1186/ar1907 |url=http://arthritis-research.com/content/8/S1/S2 }}</ref>
* American College of Rheumatology (ACR). https://www.rheumatology.org/Practice-Quality/Clinical-Support/Clinical-Practice-Guidelines/Gout


The serum level of uric acid is the primary risk factor for gout. The serum level is the result of both intake (diet) and output (excretion).
=== Life style modifications[edit | edit source] ===


====Reduce intake of purines====
* weight reduction reduces serum uric acid levels.
* Limiting alcohol intake and abstinence from alcohol in acute flares.
* All general lifestyle changes( like smoking cessation, increased physical activity, limiting telivision watching, eating healthy, etc.) that play role in control of chronic diseases are found to be more beneficial in gout
* Prevention and optimal management of chronic diseases and metabolic syndromes, cardiovascular events


The solubility threshold for uric acid is approximately 6.7 mg/dl;  above this threshold crystals may form.  Healthy subjects in the Normative Aging Study who had serum levels of uric acid over 9.0 mg/dl suffered a 22% incidence of gout over six years, compared to less than one percent for those with 7.0-8.9 mg/dl. The average uric acid level in men is 5.0 mg/dl, and substitution of a purine-free formula diet reduces this to 3.0 mg/dl. A purine-restricted diet lowers the level nearly as much (1-2 mg/dl).
===== Dietary changes[edit | edit source] =====


A diet low in purines reduces the serum level of uric acid. Notable sources of dietary purines include:
* Decreased levels of meat and sea food consumption and increased intake of low fat or non fat containing dairy products decreases gout attacks, where as foods rich in purine should be limited to moderate amounts.
*beer (high in [[guanosine]]
* Increased dietary consumption of cherries decreases gout attacks.
* Limiting high [[Fructose]] corn syrup intake reduces attacks of gout.


'''Protein''' is a crude proxy for purines;  a more precise proxy is '''muscle'''.  Apart from the notable dietary purines above, the main source of dietary purines is [[DNA]] and [[RNA]], via their bases [[adenine]] and [[guanine]].  All sources of dietary protein supply some purines, but some sources provide far more purines than others.  Meat (particularly dark meat) and seafood are high in purine because [[muscle]] cells are packed with [[mitochondrion|mitochondria]], which have their own DNA and RNA.  In a large prospective study, high consumption of meat and seafood were found associated with an elevated risk of gout onset (41% and 50%, respectively).  High consumption of dairy products, high in protein but very low in DNA and RNA, was associated with a 44% ''decrease'' in the incidence of gout.  Consumption of the more purine-rich vegetables or a high protein diet per se had no significant correlation.
=== Urate-lowering protocols ===
A nurse-driven protocol led to 95% of patients ( versus 30% in usual care) having a target serum uric acid level <360 μmol/L (6 mg/dL) within one year<ref name="pmid30343856">{{cite journal| author=Doherty M, Jenkins W, Richardson H, Sarmanova A, Abhishek A, Ashton D | display-authors=etal| title=Efficacy and cost-effectiveness of nurse-led care involving education and engagement of patients and a treat-to-target urate-lowering strategy versus usual care for gout: a randomised controlled trial. | journal=Lancet | year= 2018 | volume= 392 | issue= 10156 | pages= 1403-1412 | pmid=30343856 | doi=10.1016/S0140-6736(18)32158-5 | pmc=6196879 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30343856 }} </ref>. The protocol was:
* Allopurinol: "started at 100 mg once per day and titrated upwards in 100 mg increments every 3–4 weeks according to serum urate concentrations, to a maximum of 900 mg once per day"
* Flare prophylaxis: colchicine prophylaxis was optional
* Results: more flares in the first year in the treatment group; less flares in treatment group during the second year


Consumption of '''beer''' is associated with a 49% increase in relative risk per daily 12-oz serving.  By contrast, consumption of spirits was associated with only a 15% increase in relative risk, and no association at all was found with consumption of wine.
A pharmacist-driven protocol led to 35% of patients ( versus 13% in usual care) having a target serum uric acid level <360 μmol/L (6 mg/dL) within 30 weeks<ref name="pmid27352414">{{cite journal| author=Goldfien R, Pressman A, Jacobson A, Ng M, Avins A| title=A Pharmacist-Staffed, Virtual Gout Management Clinic for Achieving Target Serum Uric Acid Levels: A Randomized Clinical Trial. | journal=Perm J | year= 2016 | volume= 20 | issue= 3 | pages= 15-234 | pmid=27352414 | doi=10.7812/TPP/15-234 | pmc=4991910 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27352414 }} </ref>. The protocol was:
* Allopurinol: "100 mg/day (if the estimated glomerular filtration rate was less than 30 mL/min, the starting dose was 50 mg/day), unless there was a known allergy or other contraindication to allopurinol. After any change in ULT, subjects were instructed to return for laboratory assessment (sUA, alanine aminotransferase, complete blood cell count, and estimated glomerular filtration rate) in 2 weeks to 3 weeks, and report any adverse drug reactions or gout flares. Dose titration was in increments of 100 mg/day. The titration process was continued in an iterative fashion until a target sUA level was achieved and maintained"
* After each dose change: "sUA, alanine aminotransferase, complete blood cell count, and estimated glomerular filtration rate"


Some '''medical drugs''' are purine-based.  Notable among these are the purine-analog [[antimetabolite]] drugs, sometimes used as [[chemotherapy]] agents.
* Flare prophylaxis: "in most cases consisted of daily oral colchicine or any nonsteroidal anti-inflammatory drug"


====Increase output of uric acid====


Ingestion of 500 mg of [[Vitamin C]] per day has been shown to bring about a 0.5 mg/dl decrease in serum uric acid through increased excretion. Some Gout sufferers have recently found that taking up to 1,000 mg of Vitamin C, combined with a small dosage (approx. 10-15 mg./day) of [[Lithium]] have had very beneficial effects on their uric acid levels.
A target serum uric acid level of ''''<0.20 mmoles/liter (3.3 mg/dl)'''' for erosive gout achieved no clear benefit:<ref name="pmid34927391">{{cite journal| author=Dalbeth N, Doyle AJ, Billington K, Gamble GD, Tan P, Latto K | display-authors=etal| title=Intensive Serum Urate Lowering With Oral Urate-Lowering Therapy for Erosive Gout: A Randomized Double-Blind Controlled Trial. | journal=Arthritis Rheumatol | year= 2022 | volume= 74 | issue= 6 | pages= 1059-1069 | pmid=34927391 | doi=10.1002/art.42055 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=34927391  }} </ref>
 
* Allopurinol: "in those in whom allopurinol was well tolerated, the allopurinol dose was increased every month by 50–100 mg daily (increment dependent on the eGFR), to a maximum dose of 900 mg daily"
Vitamin C, taken in high doses, can help decrease blood uric acid levels, but should not be taken without a doctor's supervision. Note that there is a small subset of people with gout who will actually get worse with high levels of vitamin C. Also, a single high dose can free up too much uric acid and cause kidney stones. (University of Maryland Medical Center for Integrative Medicine).
* Flare prophylaxis: "antiinflammatory prophylaxis against gout flares using colchicine (0.5 mg once daily) or naproxen (250 mg twice daily) was used for those who had experienced gout flares in the preceding 3 months"
 
====Other approaches====
 
Additional dietary recommendations can be made which reduce gout indirectly, by reducing gout risk factors such as [[obesity]], [[hypertension]], [[cardiovascular disease]], [[diabetes]], and [[metabolic syndrome]].
 
'''The following suggestions do not meet with universal approval among medical practitioners.'''
 
Low [[purine]] diet:
* To lower uric acid:
** cherries were reported to reduce uric acid in a small study.<ref>{{cite journal |author=Jacob RA, Spinozzi GM, Simon VA, ''et al'' |title=Consumption of cherries lowers plasma urate in healthy women |journal=J. Nutr. |volume=133 |issue=6 |pages=1826-9 |year=2003 |pmid=12771324 |doi=}}</ref><ref>{{cite journal |author=BLAU LW |title=Cherry diet control for gout and arthritis |journal=Tex. Rep. Biol. Med. |volume=8 |issue=3 |pages=309-11 |year=1950 |pmid=14776685 |doi=}}</ref>
** [[celery]] extracts (celery or celery seed either in capsule form or as a tea) is believed by many to reduce uric acid levels (although these are also [[diuretic]]s). Celery extracts have been reported to act synergistically with anti-inflammatory drugs.<ref>{{cite journal |author=Whitehouse MW, Butters DE |title=Combination anti-inflammatory therapy: synergism in rats of NSAIDs/corticosteroids with some herbal/animal products |journal=Inflammopharmacology |volume=11 |issue=4 |pages=453-64 |year=2003 |pmid=15035799 |doi=10.1163/156856003322699636}}</ref>
** Cheese has been recommended as a low-purine food,<ref>{{cite journal |author=Harris MD, Siegel LB, Alloway JA |title=Gout and hyperuricemia |journal=American family physician |volume=59 |issue=4 |pages=925-34 |year=1999 |pmid=10068714 |doi= |url=http://newcms.aafp.org/afp/990215ap/925.html}}</ref> and dairy products have been found to reduce the risk of gout.
*Food to avoid:
**foods high in [[purine]]s
*** limit food high in protein such as meat, fish, poultry, or [[tofu]] to 8 ounces (226 grams) a day. Avoid entirely during a flare up. Tofu has been proposed as a safe source of protein for gout patients due to its small and transient effect on plasma urate levels.<ref>{{cite journal |author=Yamakita J, Yamamoto T, Moriwaki Y, Takahashi S, Tsutsumi Z, Higashino K |title=Effect of Tofu (bean curd) ingestion and on uric acid metabolism in healthy and gouty subjects |journal=Adv. Exp. Med. Biol. |volume=431 |issue= |pages=839-42 |year=1998 |pmid=9598181 |doi=}}</ref>
***sweetbreads, [[kidney]]s, [[liver]], [[brain]]s, or other offal meats.<ref>{{cite journal |author=Robinson CH |title=The low purine diet |journal=Am. J. Clin. Nutr. |volume=2 |issue=4 |pages=276-7 |year=1954 |pmid=13188851 |doi= |url=http://www.ajcn.org/cgi/reprint/2/4/276}}</ref><ref>{{cite journal |author=Chou P, Soong LN, Lin HY |title=Community-based epidemiological study on hyperuricemia in Pu-Li, Taiwan |journal=J. Formos. Med. Assoc. |volume=92 |issue=7 |pages=597-602 |year=1993 |pmid=7904493 |doi=}}</ref>
***sardines and anchovies <ref>{{cite journal |author=Robinson CH |title=The low purine diet |journal=Am. J. Clin. Nutr. |volume=2 |issue=4 |pages=276-7 |year=1954 |pmid=13188851 |doi= |url=http://www.ajcn.org/cgi/reprint/2/4/276}}</ref>
***[[seafood]] <ref>{{cite journal |author=Choi HK, Atkinson K, Karlson EW, Willett W, Curhan G |title=Purine-rich foods, dairy and protein intake, and the risk of gout in men |journal=N. Engl. J. Med. |volume=350 |issue=11 |pages=1093-103 |year=2004 |pmid=15014182 |doi=10.1056/NEJMoa035700}}</ref>
***[[alcohol]].<ref>{{cite journal |author=Choi HK, Atkinson K, Karlson EW, Willett W, Curhan G |title=Alcohol intake and risk of incident gout in men: a prospective study |journal=Lancet |volume=363 |issue=9417 |pages=1277-81 |year=2004 |pmid=15094272 |doi=10.1016/S0140-6736(04)16000-5}}</ref> Some claim that this applies especially to beer, on the basis that brewer's yeasts are very rich in purine. Since most modern commercial beer contains only trace amounts of yeast, this claim requires further substantiation. Formerly, port wine was sweetened with litharge, causing [[lead poisoning]], of which gout is a complication. Ironically, red wines, particularly those produced by traditional methods,<ref>{{cite journal |author=Corder R, Mullen W, Khan NQ, ''et al'' |title=Oenology: red wine procyanidins and vascular health |journal=Nature |volume=444 |issue=7119 |pages=566 |year=2006 |pmid=17136085 |doi=10.1038/444566a}}</ref> contain procyanidins released from grape seeds during wine making, which have been reported to lower serum uric acid levels by an indirect mechanism.<ref>{{cite journal |author=Wang Y, Zhu JX, Kong LD, Yang C, Cheng CH, Zhang X |title=Administration of procyanidins from grape seeds reduces serum uric acid levels and decreases hepatic xanthine dehydrogenase/oxidase activities in oxonate-treated mice |journal=Basic Clin. Pharmacol. Toxicol. |volume=94 |issue=5 |pages=232-7 |year=2004 |pmid=15125693 |doi=10.1111/j.1742-7843.2004.pto940506.x}}</ref> However, withdrawal of urate-lowering therapy is associated with recurrence of acute gouty arthritis.<ref>{{cite journal |author=Perez-Ruiz F, Atxotegi J, Hernando I, Calabozo M, Nolla JM |title=Using serum urate levels to determine the period free of gouty symptoms after withdrawal of long-term urate-lowering therapy: a prospective study |journal=Arthritis Rheum. |volume=55 |issue=5 |pages=786-90 |year=2006 |pmid=17013833 |doi=10.1002/art.22232}}</ref>
***meat extracts, consommés, and gravies<ref>{{cite journal |author=Robinson CH |title=The low purine diet |journal=Am. J. Clin. Nutr. |volume=2 |issue=4 |pages=276-7 |year=1954 |pmid=13188851 |doi= |url=http://www.ajcn.org/cgi/reprint/2/4/276}}</ref>
 
* To avoid [[dehydration]]:
** Drink plenty of liquids, especially [[water]], to dilute and assist excretion of urates;
** Avoid [[diuretic]] foods or medicines like [[aspirin]](aspirin should be avoided from those suffering from gout, unless specified by a trained physician), [[vitamin C]], [[tea]] and alcohol.  The role of diuretics in triggering gout has been disputed.<ref>{{cite journal |author=Janssens HJ, van de Lisdonk EH, Janssen M, van den Hoogen HJ, Verbeek AL |title=Gout, not induced by diuretics? A case-control study from primary care |journal=Ann. Rheum. Dis. |volume=65 |issue=8 |pages=1080-3 |year=2006 |pmid=16291814 |doi=10.1136/ard.2005.040360}}</ref>
 
* Moderate intake of purine-rich vegetables is not associated with increased gout.<!--
  --><ref name="Choi et al 2004"/>


== References ==
== References ==
{{reflist|2}}
{{Reflist|2}}


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[[Category:Arthritis]]
[[Category:Rheumatology]]
[[Category:Disease]]

Latest revision as of 20:32, 24 June 2022

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Secondary Prevention strategies for Gout include dietary and life style modifications. Dietary and life style modifications are indicated for preventing gout flares. Consuming less purine rich food, fructose rich foods, cherries, vitamin C, increasing low fat dairy product consumption, avoiding red meat go in favour of reducing acute gout flares. Decreasing alcohol consumption, smoking cessation, weight loss, controlling underlying chronic conditions like Diabetes mellitus, Hypertension favour decrease in gout flares.

Secondary prevention

Clinical practice guidelines are available:

  • American College of Physicians (ACP)[1]

Life style modifications[edit | edit source]

  • weight reduction reduces serum uric acid levels.
  • Limiting alcohol intake and abstinence from alcohol in acute flares.
  • All general lifestyle changes( like smoking cessation, increased physical activity, limiting telivision watching, eating healthy, etc.) that play role in control of chronic diseases are found to be more beneficial in gout
  • Prevention and optimal management of chronic diseases and metabolic syndromes, cardiovascular events
Dietary changes[edit | edit source]
  • Decreased levels of meat and sea food consumption and increased intake of low fat or non fat containing dairy products decreases gout attacks, where as foods rich in purine should be limited to moderate amounts.
  • Increased dietary consumption of cherries decreases gout attacks.
  • Limiting high Fructose corn syrup intake reduces attacks of gout.

Urate-lowering protocols

A nurse-driven protocol led to 95% of patients ( versus 30% in usual care) having a target serum uric acid level <360 μmol/L (6 mg/dL) within one year[2]. The protocol was:

  • Allopurinol: "started at 100 mg once per day and titrated upwards in 100 mg increments every 3–4 weeks according to serum urate concentrations, to a maximum of 900 mg once per day"
  • Flare prophylaxis: colchicine prophylaxis was optional
  • Results: more flares in the first year in the treatment group; less flares in treatment group during the second year

A pharmacist-driven protocol led to 35% of patients ( versus 13% in usual care) having a target serum uric acid level <360 μmol/L (6 mg/dL) within 30 weeks[3]. The protocol was:

  • Allopurinol: "100 mg/day (if the estimated glomerular filtration rate was less than 30 mL/min, the starting dose was 50 mg/day), unless there was a known allergy or other contraindication to allopurinol. After any change in ULT, subjects were instructed to return for laboratory assessment (sUA, alanine aminotransferase, complete blood cell count, and estimated glomerular filtration rate) in 2 weeks to 3 weeks, and report any adverse drug reactions or gout flares. Dose titration was in increments of 100 mg/day. The titration process was continued in an iterative fashion until a target sUA level was achieved and maintained"
  • After each dose change: "sUA, alanine aminotransferase, complete blood cell count, and estimated glomerular filtration rate"
  • Flare prophylaxis: "in most cases consisted of daily oral colchicine or any nonsteroidal anti-inflammatory drug"


A target serum uric acid level of '<0.20 mmoles/liter (3.3 mg/dl)' for erosive gout achieved no clear benefit:[4]

  • Allopurinol: "in those in whom allopurinol was well tolerated, the allopurinol dose was increased every month by 50–100 mg daily (increment dependent on the eGFR), to a maximum dose of 900 mg daily"
  • Flare prophylaxis: "antiinflammatory prophylaxis against gout flares using colchicine (0.5 mg once daily) or naproxen (250 mg twice daily) was used for those who had experienced gout flares in the preceding 3 months"

References

  1. ↑ Qaseem A, Harris RP, Forciea MA, Clinical Guidelines Committee of the American College of Physicians. Denberg TD, Barry MJ; et al. (2017). "Management of Acute and Recurrent Gout: A Clinical Practice Guideline From the American College of Physicians". Ann Intern Med. 166 (1): 58–68. doi:10.7326/M16-0570. PMID 27802508. Review in: Ann Intern Med. 2017 Feb 21;166(4):JC14
  2. ↑ Doherty M, Jenkins W, Richardson H, Sarmanova A, Abhishek A, Ashton D; et al. (2018). "Efficacy and cost-effectiveness of nurse-led care involving education and engagement of patients and a treat-to-target urate-lowering strategy versus usual care for gout: a randomised controlled trial". Lancet. 392 (10156): 1403–1412. doi:10.1016/S0140-6736(18)32158-5. PMC 6196879. PMID 30343856.
  3. ↑ Goldfien R, Pressman A, Jacobson A, Ng M, Avins A (2016). "A Pharmacist-Staffed, Virtual Gout Management Clinic for Achieving Target Serum Uric Acid Levels: A Randomized Clinical Trial". Perm J. 20 (3): 15–234. doi:10.7812/TPP/15-234. PMC 4991910. PMID 27352414.
  4. ↑ Dalbeth N, Doyle AJ, Billington K, Gamble GD, Tan P, Latto K; et al. (2022). "Intensive Serum Urate Lowering With Oral Urate-Lowering Therapy for Erosive Gout: A Randomized Double-Blind Controlled Trial". Arthritis Rheumatol. 74 (6): 1059–1069. doi:10.1002/art.42055. PMID 34927391 Check |pmid= value (help).

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