Abstract
The sexually transmitted enteric infections topic is one of the chapters of the Clinical Protocol and Therapeutic Guidelines for Comprehensive Care for People with Sexually Transmitted Infections, published by the Brazilian Ministry of Health in 2020. The document was developed based on scientific evidence and validated in discussions with specialists. This article presents epidemiological and clinical aspects of these infections and guidance for service managers on their programmatic and operational management. The aim is to assist health professionals with screening, diagnosis, and treatment of people with sexually transmitted enteric infections and their sexual partners, in addition to supporting strategies for their surveillance, prevention, and control.
Keywords:
Sexually transmitted diseases; Diarrhea; Sexual behavior; Drug therapy
Highlighted excerpt:
The incidence of anorectal sexually transmitted infections has increased over the last years, mainly due to the increase in the practice of unprotected receptive anal sexual intercourse
FOREWORD
This article addresses sexually transmitted enteric infections, a topic that comprises the Clinical Protocol and Therapeutic Guidelines (PDCT) for Comprehensive Care for People with Sexually Transmitted Infections (STI), published by the Health Surveillance Department of the Brazilian Ministry of Health. For elaborating the PDCT, a selection and analysis of the evidence available in the literature were performed, and a panel of specialists discussed it. The document was approved by the National Committee for the Incorporation of Technologies in the Brazilian National Health System (Conitec) and updated by the panel of specialists in STI in 20201.
EPIDEMIOLOGICAL ASPECTS
Enteric pathogens and anorectal infections can be transmitted through different sexual practices without barrier protection in receptive anal or oroanal sex2. The transmission of diverse agents occurs naturally through the fecal-oral route, generally caused by consumption of contaminated food or water. Sexual transmission is well described, and it can happen through direct oroanal practice or indirectly through oral sex after anal penetration or through the use of fingers or fomites3.
Anorectal STI incidence has augmented over the last years, mainly due to the increased frequency of unprotected receptive anal sexual intercourse4. Anorectal intercourse is common, although its exact frequency stays unknown due to asymptomatic infections and the lack of accurate epidemiological data. People with symptoms or anorectal lesions are usually referred to coloproctologists for assessment and management5.
Risks to health arising from anal sex seem to be significantly underestimated by sexually active men and women in North America, Latin America, Asia, Africa, and other regions. Among heterosexual people, the reported prevalence of using condoms are almost universally lower in anal sex than in vaginal sex6.
Outbreaks of sexually transmitted enteric infections in men with sex with men (MSM) show very similar characteristics. Generally, men report having multiple sexual partners7-10, attending places specifically for sexual encounters11-12or particular sexual parties and using recreational drugs, including chemsex, or "chemical sex", sexual practice using crystal methamphetamine, gamma hydroxybutyrate, gamma-butyrolactone, or mephedrone immediately before or during sex8,10. Using the internet7 or geospatial network applications9-10 for finding casual partners that facilitate riskier behaviors is also commonly described13.
Among the p enteric infections related to sexual transmission in MSM, hepatitis A, shigellosis, intestinal protozoan infections, such as amoebiasis and giardiasis, and bacterial gastroenteritis caused by Campylobacter spp. can be cited14. Herpes simplex virus, HSV, and Neisseria gonorrhea are also etiological agents of anorectal infections transmitted through anal sexual intercourse14.
Hepatitis A is a generally self-limited acute infectious disease caused by the hepatitis A virus, transmitted through the fecal-oral route by ingesting contaminated food and water or intimate contact with an infected person15. Outbreaks associated with sexual transmission in MSM are described since 2016 by the European Centre for Disease Prevention and Control16,17. Symptoms after a four-week average incubation period are more common in adults and include fever, discomfort, nausea, anorexia, abdominal pain, and jaundice. Recurring hepatitis and acute hepatic insufficiency can also occur18. Shigellosis caused by the Gram-negative bacterium Shigella spp. is characterized by severe bacillary dysentery19,20. Regular sexual transmission outbreaks of Shigella sonnei and Shigella flexneri among MSM are reported since the 1970s21,22. Sexually transmitted shigellosis is linked to different behaviors, including using douche, recreational drug use, and fisting, a practice consisting of forearm or hand introduction in the partner's vagina or anus8-10,11.
Proctocolitis is associated with food or water-transmitted diseases, including Shigella spp.23. It is characterized by watery or bleeding diarrhea, abdominal pain, tenesmus, and, sometimes, fever and discomfort from four to seven days24,25. Dissemination of multiresistant Shigella spp. infections through the sexual route have been reported26-28. Shigella spp. strains among MSM show increasing resistance to multiple drugs, mostly azithromycin and ciprofloxacin29-33.
The foremost intestinal protozoan infections of interest within STI scope are giardiasis and amoebiasis. Annually millions of people develop these infections, but only 10% to 20% of the infected individuals become symptomatic. The risk of death is more remarkable for amoebiasis due to its invasive nature34. Such protozoan infections characteristically present higher prevalences in areas where sanitary conditions are inadequate, especially in Africa, in the Indian subcontinent, and parts of Central and South America. People who have traveled to developing countries are possible vectors35. Such infections are generally contracted through the fecal-oral route by ingesting contaminated water or food36. The higher incidence of Entamoeba histolytica enteritis among homosexual men seems attributed to direct oral-anal sexual practice37,38 or through sex toys or fellatio. It can denote high-risk behavior and multiple exposures11. Giardiasis underdiagnosis in this context is frequent due to the low suspicion of such transmission routes39,40.
In giardiasis, the most common symptoms include diarrhea, oily stool, flatulence, and abdominal swelling41,42. There can be proctitis43. The average incubation period for giardiasis is one to two weeks, and the symptoms average three to ten weeks44. For amoebiasis, the wide specter of intestinal infection varies from asymptomatic to transitory intestinal inflammation up to fulminant colitis, including megacolon, peritonitis, and hepatic abscess35,45. The incubation period of intestinal amoebiasis is one to four weeks46.
Campylobacter spp. is one of the most worldwide common causes of bacterial gastroenteritis47,48. Many outbreaks have been reported, including resistance to antimicrobial drugs such as ciprofloxacin and macrolides49, Extra-intestinal infection is rare. Still, it can lead to complications, including bacteremia, lung infection, meningitis, or reactive arthritis, mainly in immunocompromised people47,48. Ingestion of contaminated food and water and contact with pets are among the principal forms of transmission. There are reports of fecal-oral sexual transmission in places of sexual encounters with recreational drug use50,51.
HSV infections are characterized by chronicity and recurrence, with variable latency periods. There are two different strains: HSV-2, responsible for genital lesions, and HSV-1, for extragenital ones, specially orolabial52. However, it is possible to find inversions in such order, without clinical specter differences. HSV-1 is commonly acquired in childhood and adolescence, while HSV-2 is linked to sexual activity. The infection risk increases with the number of sexual partners throughout life53.
Gonorrhea is a common bacterial infection, transmitted almost exclusively through sexual or perinatal contact, affecting mainly the urethral and cervical mucous membranes and, less frequently, those in the rectum, oropharynx, and conjunctive54. Rectal N. gonorrhoeae infection is acquired through receptive anal intercourse and perineal contamination with cervicovaginal secretions. Around 35% of women with gonococcal cervicitis will present a concurrent rectal infection through infection contiguous dissemination55.
CLINICAL ASPECTS
The presence of rectal bleeding and wounds or lesions in the anal and perianal area, possibly with pruritus and pain, producing secretions, indicate STI23.
Enteric pathogens cause gastroenteritis, which can have low (rectum) symptoms, such as pain, mucopurulent anal discharge, tenesmus and hematochezia, and high symptomatology (colon), such as diarrhea with a sudden start. When evolved with rectal distensibility loss, diarrhea becomes intense, and when the duodenum is compromised, vomits, and abdominal pains associated with colic occur56,57.
In severe cases, significant morbidity and mortality can be associated with diarrhea, dehydration, bacteremia, hemolytic uremia, and Guillain-Barré syndrome58-59.
The most significant complications encompass inflammation of the rectal mucosa extending to the colon, with bleeding as a substantial sign, in addition to diarrhea, which leads to symptom intensification due to rectal distensibility loss. When the duodenum is compromised, vomits and abdominal pains associated with colic occur56.
DIAGNOSIS
Diagnosis based only on clinical aspects lacks specificity, requiring laboratory examination to identify the enteric infection etiological agent and define its sexual transmission.
Serological markers - IgM and anti-HAV IgG antibodies - are specific examinations for hepatitis A laboratory diagnosis. Leukopenia, aminotransferase, and high bilirubin findings are unspecific60.
For identifying Shigella spp., bacteria insulation is conducted in cultures, mainly in hemoculture and coproculture, in addition to sensitivity tests to antimicrobial drugs for following resistance and drug interaction possible cases61.
Amoebiasis laboratory diagnosis is usually based on microscopic and serological methods, including enzyme-linked immunosorbent assay, ELISA, and indirect hemagglutination assay, latex agglutination, and tests based on nucleic acid amplification62. Intestinal amoebiasis diagnosis in many countries usually depends on fecal sampling microscopic examination regarding the presence or lack of E. histolytica and Giardia lamblia. The proportion of asymptomatic people infected with this protozoan is not clear62. The diagnosis must be confirmed by detecting E. histolytica-specific antigen in stool to distinguish it from other nonpathogenic amoebae. Serological tests can contribute to the diagnosis of invasive diseases, such as amoebiasis. However, their sensitivity can vary according to the disease's type and stage63. Eliminating cysts of G. lamblia can be intermittent and last for weeks. Therefore, many samples must be collected for diagnosis. Collecting three samples on different days ideally allows identifying cysts in more than 90% of the cases compared with 50% to 70% of those with a single sample. ELISA or antibody direct immunofluorescence can identify the parasite, with 88%-98% sensitivity and 87%-100% specificity64. Endoscopic methods with aspiration and duodenal biopsy may be needed in cases of diagnostic greater difficulty64,65.
Campylobacter spp. diagnosis is performed through isolation of the organism from stool samples or rectal swabs using selective media before starting antibiotic treatment. The culture identifies the subtype and susceptibility to antimicrobial drugs. Rapid tests for such pathogens, including antigen tests and nucleic acid-based tests, are available in Brazil65.
Diagnosis of herpes infection is based on the clinical aspect, especially if the condition is recurrent, and on laboratory examinations, such as viral culture, antigen detection, and polymerase chain reaction53. For diagnosis and laboratory investigation of gonorrhea in symptomatic cases, using a swab for anal culture, antibiogram, and molecular biology detection are recommended. On the other hand, for asymptomatic individuals with receptive anal practice without condom use, the recommendation is biannual follow-up through anal swab for detection through molecular biology, highlighting that culture is less sensitive than molecular biology techniques. Extragenital material samples, particularly anal and pharyngeal, and molecular biology tests must necessarily be validated for such collection sites14.
TREATMENT
Treatment of this infection group requires, at first, the identification or suspicion of the etiological agent, and it must start as soon as possible, not only aiming at relieving the symptoms but likewise other STI, also reducing transmission risk to other persons. Treatment includes antibiotics and parasiticide, in addition to hydroelectrolytic and symptomatic support medications.
Unspecific treatment for hepatitis A is conducted with hydration and symptomatic methods. The vaccine is the most efficient way for preventing transmission, which can also be applied after exposure together with immunoglobulin in people presenting high-risk66. For prevention in sexual contact, using an oral condom is the indication67.
The primary treatment for non-complicated Shigella spp. is conducted with ciprofloxacin, including azithromycin and ceftriaxone as alternative therapies. Prevention is accomplished through washing hands and food for consumption, in addition to sexual practices with protective barriers68-71, People living with human immunodeficiency virus, HIV, may have more severe and long-lasting shigellosis, mainly with T-CD4+ lymphocyte counting less than 200 cells/mm³. Antimicrobial therapy may be extended for six weeks72. Meanwhile, changes in mucosae can be gateways for HIV25.
For amoebiasis and giardiasis treatment, using nitroimidazole compounds, such as metronidazole, tinidazole, and secnidazole, is the recommendation, with high cure proportions. Using such drugs is a contraindication for women in the first trimester of pregnancy, breastfeeding women, and people with neurological disorders35. Albendazole and nitazoxanide are antiparasitic medications with efficiency similar to metronidazole against giardiasis and can be used as an alternative, in daily doses, for five to three days, respectively73. For giardiasis, symptoms typically improve within five to seven days after starting treatment. In the case of chronic forms, improvement is slower. In case of diarrhea prolongation, it is possible to request a parasitological stool examination for excluding giardiasis persistence74,75. Complications include hypokalemia, undernutrition, growth delay, cognitive deficits, arthritis, myopathy, irritable bowel syndrome, and chronic fatigue76,77.
Campylobacter spp. infection is self-limited and mild. Treatment is conducted with oral or parenteral hydration, depending on the disease severity and dehydration degree. Avoiding agents inducing intestinal mortality, as they can prevent infection resolution, is needed49. Antibiotics must also be considered for high-risk cases, such as immunocompromised and older people, and in case of more severe cases, with fever, hematochezia, or intense abdominal pain78. Antibiotic resistance, particularly resistance to fluoroquinolone, increased sharply since the 1990s. Different outbreaks were reported, including with resistance to antimicrobial drugs such as ciprofloxacin and macrolides48.
Treatment of HSV infection is based on using aciclovir and its derivatives valaciclovir and famciclovir, which present better absorption through oral route and bioavailability. Topical aciclovir or other antiviral is effective in reducing symptoms, and intravenous use of aciclovir is recommended for special situations, such as disseminated disease, meningoencephalitis pictures, and pneumonitis. In occurrence cases equal to or higher than six episodes per year, suppressive therapy is the recommendation. Suppressive treatment duration varies, but it is generally longer than six months50.
For confirming N. gonorrhoeae as the infectious agent, ceftriaxone associated with azithromycin is recommended14. Treatment can also be conducted with presumptive diagnosis based on anamnesis on the history of receptive anal sexual history without protection79.
SURVEILLANCE, PREVENTION, AND CONTROL
Through Consolidation Ordinance GM/MS no. 4, of September 28, 2017, all viral hepatitis became a compulsory notification matter80. However, hepatitis A has mandatory notification since 200381. The required notification forms are Available from: the Ministry of Health's website82. Other STIs also have a compulsory report. Those that are not compulsory at the federal level can be included in the notification list of the Federal District, states, and municipalities, with free autonomy, surveillance, and control, as long as sanitary standards are observed.
The diseases addressed in this article are transmitted through unprotected sexual intercourse and contaminated water, and food ingestion. Therefore, in addition to condom regular use, the recommendation of not performing sexual actions that may facilitate direct contact with feces, basic prevention measures, and sanitation are crucial.
General basic preventive measures include frequently washing hands, especially when preparing food, before the meals and after going to the toilet; drinking filtrated and chlorinated water; washing fruit and vegetables, and not ingesting food suspected to be contaminated83,84.
Sanitation is comprehended as infrastructure and operational facilities for drinking water provision and sewage and urban cleaning with solid residue management and draining and urban rainwater management, generating better sanitary conditions for the population.
Vaccination against hepatitis A, which, according to the National Immunization Program, is recommended in a single dose for all children between 15 months and five years old, is also effective prevention. Coinfection with hepatitis A virus is frequent among HIV-infected MSM. Studies suggest that early vaccination against hepatitis A in people living with HIV may not provide reliable protection against infection development of such virus. Therefore, post-exposure prophylaxis, immunoglobulin application, and the monovalent vaccine may be considered in hepatitis A virus high-risk recent situations, regardless of prior vaccine situation66.
The cure control of sexually transmitted enteric infections occurs through clinical follow-up after specific treatment.
ACKNOWLEDGMENTS
The authors acknowledge this work's contribution by the members of the technical panel of specialists responsible for developing the 2020 PDCT for Comprehensive Care for People with STI.
Referências
-
1 Brasil. Ministério da Saúde. Portaria MS/SCTIE nº 42, de 5 de outubro de 2018. Torna pública a decisão de aprovar o Protocolo Clínico e Diretrizes Terapêuticas para Atenção Integral às Pessoas com Infecções Sexualmente Transmissíveis (IST), no âmbito do Sistema Único de Saúde - SUS [Internet]. Diário Oficial da União, Brasília (DF), 2018 out 8 [cited 2020 set 21]; Seção I:88. Available from:: http://bvsms.saude.gov.br/bvs/saudelegis/sctie/2018/prt0042_08_10_2018.html
» http://bvsms.saude.gov.br/bvs/saudelegis/sctie/2018/prt0042_08_10_2018.html -
2 Jawale R, Lai KK, Lamps LW. Sexually transmitted infections of the lower gastrointestinal tract. Virchows Arch [Internet]. 2017 Jan [cited 2020 May 31];472(1):149-58. Available from:: https://doi.org/10.1007/s00428-017-2261-5
» https://doi.org/10.1007/s00428-017-2261-5 -
3 Mitchell H, Hughes G. Recent epidemiology of sexually transmissible enteric infections in men who have sex with men. Curr Opin Infect Dis [Internet]. 2018 Feb [cited 2020 May 20]; 31(1):50-6. Available from:: https://doi.org/10.1097/QCO.0000000000000423
» https://doi.org/10.1097/QCO.0000000000000423 -
4 Wexner SD. Sexually transmitted diseases of the colon, rectum, and anus. The challenge of the nineties. Dis Colon Rectum [Internet]. 1990 Dec [cited 2020 May 22]; 33(12):1048-62. Available from:: https://doi.org/10.1007/BF02139224
» https://doi.org/10.1007/BF02139224 -
5 Assi R, Hashim PW, Reddy VB, Einarsdottir H, Longo WE. Sexually transmitted infections of the anus and rectum. World J Gastroenterol [Internet]. 2014 Nov [cited 2020 Jun 12]; 20(41):15262-8. Available from:: https://doi.org/10.3748/wjg.v20.i41.15262
» https://doi.org/10.3748/wjg.v20.i41.15262 -
6 Halperin DT. Heterosexual anal intercourse: prevalence, cultural factors, and HIV infection and other health risks, part I. AIDS Patient Care and STDS [Internet]. 1999 Dec [cited 2020 May 21]; 13(12):717-30. Available from:: https://doi.org/10.1089/apc.1999.13.717
» https://doi.org/10.1089/apc.1999.13.717 -
7 Marcus U, Zucs P, Bremer V, Hamouda O, Prager R, Tschaepe H, et al. Shigellosis - a re-emerging sexually transmitted infection: outbreak in men having sex with men in Berlin. Int J STD AIDS [Internet]. 2004 Aug [cited 2020 May 22]; 15(8):533-7. Available from:: https://doi.org/10.1258/0956462041558221
» https://doi.org/10.1258/0956462041558221 -
8 Mook P, McCormick J, Bains M, Cowley LA, Chattaway MA, Jenkins C, et al. ESBL-Producing and macrolide-resistant shigella sonnei infections among men who have sex with men, England. Emerg Infect Dis [Internet]. 2015 Nov [cited 2020 May 22]; 22(11):1948-52. Available from:: https://doi.org/10.3201/eid2211.160653
» https://doi.org/10.3201/eid2211.160653 -
9 Gilbart VL, Simms I, Jenkins C, Furegato M, Gobin M, Oliver I, et al. Sex, drugs and smart phone applications: findings from semistructured interviews with men who have sex with men diagnosed with Shigella flexneri3a in England and Wales. Sex Transm Infect [Internet]. 2015 Dec [cited 2020 May 22]; 91(8):598-602. Available from:: https://doi.org/10.1136/sextrans-2015-052014
» https://doi.org/10.1136/sextrans-2015-052014 -
10 Simms I, Gilbart VL, Byrne L, Jenkins C, Adak GK, Hughes G, et al. Identification of verocytotoxin-producing Escherichia coli O117:H7 in men who have sex with men, England, November 2013 to August 2014. Euro Surveill [Internet]. 2014 Oct [cited 2020 May 21]; 19(43):20946. Available from:: https://doi.org/10.2807/1560-7917.es2014.19.43.20946
» https://doi.org/10.2807/1560-7917.es2014.19.43.20946 -
11 O’Sullivan B, Delpech V, Pontivivo G, Karagiannis T, Marriott D, Harkness J, et al. Shigellosis linked to sex venues, Australia. Emerg Infect Dis [Internet]. 2002 Aug [cited 2020 Jun 10]; 8(8):862-4. Available from:: https://doi.org/10.3201/eid0808.010534
» https://doi.org/10.3201/eid0808.010534 -
12 Leentvaar-Kuijpers A, Kool JL, Veugelers PJ, Coutinho RA, van Griensven GJ. An outbreak of hepatitis a among homosexual men in Amsterdam, 1991-1993. Int J Epidemiol [Internet]. 1995 Feb [cited 2020 May 19]; 24(1):218-22. Available from:: https://doi.org/10.1093/ije/24.1.218
» https://doi.org/10.1093/ije/24.1.218 -
13 McKenna KYA, Green AS, Smith PK. Demarginalizing the sexual self. J Sex Res [Internet]. 2001 Jan [cited 2020 May 19]; 38(4):302-11. Available from:: https://doi.org/10.1080/00224490109552101
» https://doi.org/10.1080/00224490109552101 -
14 Ministério da Saúde (BR). Secretaria de Vigilância em Saúde. Departamento de Doenças de Condições Crônicas e Infecções Sexualmente Transmissíveis. Protocolo clínico e diretrizes terapêuticas para atenção integral às pessoas com infecções sexualmente transmissíveis (IST) [Internet]. Brasília: Ministério da Saúde; 2020 [cited 2020 ago 28]. Available from:: http://www.aids.gov.br/pt-br/pub/2015/protocolo-clinico-e-diretrizes-terapeuticas-para-atencao-integral-pessoas-com-infeccoes
» http://www.aids.gov.br/pt-br/pub/2015/protocolo-clinico-e-diretrizes-terapeuticas-para-atencao-integral-pessoas-com-infeccoes -
15 Ndumbi P, Freidl GS, Williams CJ, Mardh O, Varela C, Avellón A, et al. European Centre for Disease Prevention and Control. Hepatitis A outbreaks in the EU/EEA mostly affecting men who have sex with men: third update, 28 June 2017. Stockholm, 2017. Euro Surveill [Internet]. 2018 Aug [cited 2020 Jun 13]; 23(33):1700641. Available from:: https://doi.org/10.2807/1560-7917.ES.2018.23.33.1700641
» https://doi.org/10.2807/1560-7917.ES.2018.23.33.1700641 -
16 Stene-Johansen K, Tjon G, Schreier E, Bremer V, Bruisten S, Ngui SL, et al. Molecular epidemiological studies show that hepatitis A virus is endemic among active homosexual men in Europe. J Med Virol [Internet]. 2007 Apr [cited 2020 Jun 20]; 79(4):356-65. Available from:: https://doi.org/10.1002/jmv.20781.
» https://doi.org/10.1002/jmv.20781 -
17 São Paulo (Estado). Secretaria de Estado da Saúde. Coordenadoria de Controle de Doenças. Centro de Vigilância Epidemiológica “Prof. Alexandre Vranjac”. Informe técnico: aumento de casos de hepatite A no Estado de São Paulo [Internet]. São Paulo: SES; 2017 [cited 2020 ago 29]. Available from:: http://nhe.fmrp.usp.br/wp-content/uploads/2017/07/informe_tecnico_hepatite_a.pdf
» http://nhe.fmrp.usp.br/wp-content/uploads/2017/07/informe_tecnico_hepatite_a.pdf -
18 Koff RS. Clinical manifestations and diagnosis of hepatitis A virus infection. Vaccine [Internet]. 1992 [cited 2020 Jun 20]; 10(Suppl 1):S15-7. Available from:: https://doi.org/10.1016/0264-410x(92)90533-p
» https://doi.org/10.1016/0264-410x(92)90533-p -
19 Wilmer A, Romney MG, Gustafson R, Sandhu J, Chu T, Ng C, et al. Shigella flexneri serotype 1 infections in men who have sex with men in Vancouver, Canada. HIV Med. 2015 Feb [cited 2020 Jun 20]; 16(3):168-75. Available from:: https://doi.org/10.1111/hiv.12191
» https://doi.org/10.1111/hiv.12191 -
20 Cresswell FV, Ross S, Booth T, Nicolas OS, Eliza A, Jasmine B, et al. Shigella flexneri: a cause of significant morbidity and associated with sexually transmitted infections in men who have sex with men. Sex Transm Dis [Internet]. 2015 Jun [cited 2020 Jun 22]; 42(6):344. Available from:: https://doi.org/10.1097/OLQ.0000000000000295
» https://doi.org/10.1097/OLQ.0000000000000295 -
21 Aragón TJ, Vugia DJ, Shallow S, Samuel MC, Reingold A, Ângulo FJ, et al. Case-control study of shigellosis in San Francisco: the role of sexual transmission and HIV infection. Clin Infect Dis [Internet]. 2007 Feb [cited 2020 Jun 22]; 44(3):327-34. Available from:: https://doi.org/10.1086/510593
» https://doi.org/10.1086/510593 -
22 Wu HH, Shen YT, Chiou CS, Fang CT, Lo YC. Shigellosis outbreak among MSM living with HIV: a case-control study in Taiwan, 2015-2016. Sex Transm Infect [Internet]. 2019 Feb [cited 2020 Jun 24]; 95(1):67-70. Available from:: https://doi.org/10.1136/sextrans-2017-053410
» https://doi.org/10.1136/sextrans-2017-053410 -
23 Felt-Bersma RJ, Bartelsman JF. Haemorrhoids, rectal prolapse, anal fissure, peri-anal fistulae and sexually transmitted diseases. Best Pract Res Clin Gastroenterol [Internet]. 2009 Aug [cited 2020 Jun 22]; 23(4):575-92. Available from:: https://doi.org/10.1016/j.bpg.2009.04.010
» https://doi.org/10.1016/j.bpg.2009.04.010 -
24 Scallan E, Hoekstra RM, Angulo FJ, Tauxe RV, Widdowson MA, Roy SL, et al. Foodborne illness acquired in the United States--major pathogens. Emerg Infect Dis [Internet]. 2011 Jan [cited 2020 Jun 22]; 17(1):7-15. Available from:: https://doi.org/10.3201/eid1701.p11101
» https://doi.org/10.3201/eid1701.p11101 -
25 Surawicz, CM. Shigella: a sexually transmitted infection in men who have sex with men. Gastroenterology [Internet]. 2007 Nov [cited 2020 Jun 22]; 133(5):1737-8. Available from:: https://doi.org/10.1053/j.gastro.2007.09.044
» https://doi.org/10.1053/j.gastro.2007.09.044 - 26 Borg ML, Modi A, Tostmann A, Gobin M, Cartwright J, Quigley C, et al. Ongoing outbreak of Shigella flexneri serotype 3a in men who have sex with men in England and Wales, data from 2009-2011. Euro Surveill [Internet]. 2012 Mar [cited 2020 Jun 21]; 17(13):20137. Available from:: https://pubmed.ncbi.nlm.nih.gov/22490381
- 27 Bowen A, Eikmeier D, Talley P, Siston A, Smith S, Hud J, et al. Notes from the field: outbreaks of shigella sonnei infection with decreased susceptibility to azithromycin among men who have sex with Men - Chicago and Metropolitan Minneapolis - St. Paul, 2014. MMWR Morb Mortal Wkly Rep [Internet]. 2015 Jun [cited 2020 Jun 21]; 64(21):597-8. Available from:: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4584772
-
28 Hines JZ, Pinsent T, Rees K, Vines J, Bown A, Hurd J, et al. Notes from the field: shigellosis outbreak among men who have sex with men and homeless persons -Oregon, 2015-2016. MMWR Morb Mortal Wkly Rep [Internet]. 2016 Aug [cited 2020 Jun 21]; 65(31):812-3. Available from:: https://www.cdc.gov/mmwr/volumes/65/wr/mm6531a5.htm
» https://www.cdc.gov/mmwr/volumes/65/wr/mm6531a5.htm -
29 Bernstein K, Bowen VB, Kim CR, Counotte MJ, Kirkcaldy RD, Kara E, et al. Infecções sexualmente transmissíveis reemergentes e recentemente reconhecidas: as experiências anteriores podem esclarecer a identificação e o controle futuros? PLoS Med [Internet]. 2017 dez [cited 2020 jun 21]; 14(12):e1002474. Available from:: https://doi.org/10.1371/journal.pmed.1002474
» https://doi.org/10.1371/journal.pmed.1002474 -
30 Ingle DJ, Easton M, Valcanis M, Seemann T, Kwong JC, Stephens N, et al. Co-circulation of multidrug-resistant Shigella among men who have sex with men in Australia. Clin Infect Dis [Internet]. 2019 Nov [cited 2020 Jun 21]; 69(9):1535-44. Available from:: https://doi.org/10.1093/cid/ciz005
» https://doi.org/10.1093/cid/ciz005 -
31 Murray K, Reddy V, Kornblum JS, Waechter H, Chicaiz LF, Rubinstein I, et al. Increasing antibiotic resistance in Shigella spp. from Infected New York City residents, New York, USA. Emerg Infect Dis [Internet]. 2017 Feb [cited 2020 Jun 18]; 23(2):332-5. Available from:: https://doi.org/10.3201/eid2302.161203
» https://doi.org/10.3201/eid2302.161203 -
32 Chiou CS, Izumiya H, Kawamura M, Liao YS, Su YS, Wu HH, et al. The worldwide spread of ciprofloxacin-resistant Shigella sonnei among HIV-infected men who have sex with men, Taiwan. Clin Microbiol Infect [Internet]. 2016 Apr [cited 2020 Jun 18]; 22(4):383.e11-383.e16. Available from:: https://doi.org/10.1016/j.cmi.2015.12.021
» https://doi.org/10.1016/j.cmi.2015.12.021 -
33 Williamson D, Ingle D, Howden B. Extensively drug-resistant Shigellosis in Australia among men who have sex with men. N Engl J Med [Internet]. 2019 Dec [cited 2020 Jun 15]; 381(25):2477-9. Available from:: https://doi.org/10.1056/NEJMc1910648
» https://doi.org/10.1056/NEJMc1910648 - 34 Van Hal SJ, Stark DJ, Fotedar R, Marriott D, Ellis JT, Harkness JL. Amoebiasis: current status in Australia. Med J Aust [Internet]. 2007 Apr [cited 2020 Jul 23]; 186(8):412-6. Available from:: https://pubmed.ncbi.nlm.nih.gov/17437396
-
35 Haque R, Huston CD, Hughes M, Houpt E, Petri WA Jr. Amebiasis. N Engl J Med [Internet]. 2003 Apr [cited 2020 Jul 23]; 348(16):1565-73. Available from:: https://doi.org/10.1056/NEJMra022710
» https://doi.org/10.1056/NEJMra022710 -
36 Escolà-Vergé L, Arando M, Vall M, Rovira R, Espasa M, Sulleiro E, et al. Outbreak of intestinal amoebiasis among men who have sex with men, Barcelona (Spain). Euro Surveill [Internet]. 2017 Jul [cited 2020 Jul 23]; 22(30):30581. Available from:: https://doi.org/10.2807/1560-7917.ES.2017.22.30.30581
» https://doi.org/10.2807/1560-7917.ES.2017.22.30.30581 - 37 Morán P, Ramos F, Ramiro M, Curiel O, González E, Valadez A, et al. Infection by human immunodeficiency virus-1 is not a risk factor for amebiasis. Am J Trop Med Hyg [Internet]. 2005 Aug [cited 2020 Jul 23]; 73(2):296-300. Available from:: https://pubmed.ncbi.nlm.nih.gov/16103593
-
38 Ortega HB, Borchardt KA, Hamilton R, Ortega P, Mahood J. Enteric pathogenic protozoa in homosexual men from San Francisco. Sex Transm Dis [Internet]. 1984 Apr [cited 2020 Jul 12]; 11(2):59-63. Available from:: https://doi.org/10.1097/00007435-198404000-00001
» https://doi.org/10.1097/00007435-198404000-00001 -
39 Escobedo AA, Almirall P, Alfonso M, Cimerman S, Chacín-Bonilla L. Sexual transmission of giardiasis: a neglected route of spread? Acta Tropica [Internet]. 2014 Apr [cited 2020 Jul 13]; 132:106-11. Available from:: https://doi.org/10.1016/j.actatropica.2013.12.025
» https://doi.org/10.1016/j.actatropica.2013.12.025 -
40 Kean BH, William DC, Luminais SK. Epidemic of amoebiasis and giardiasis in a biased population. Br J Vener Dis [Internet]. 1979 Oct [cited 2020 Jul 13]; 55(5):375-8. Available from:: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1045685/pdf/brjvendis00035-0063.pdf
» https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1045685/pdf/brjvendis00035-0063.pdf -
41 Zylberberg HM, Green PH, Turner KO, Genta RM, Lebwohl B. Prevalence and predictors of giardia in the United States. Dig Dis Sci [Internet]. 2017 Jan [cited 2020 Jul 10]; 62(2):432-40. Available from:: https://doi.org/10.1007/s10620-016-4447-0
» https://doi.org/10.1007/s10620-016-4447-0 -
42 Feng Y, Xiao L. Zoonotic potential and molecular epidemiology of Giardia species and giardiasis. Clin Microbiol Rev [Internet]. 2011 Jan [cited 2020 Jul 15]; 24(1):110-40. Available from:: https://doi.org/10.1128/CMR.00033-10
» https://doi.org/10.1128/CMR.00033-10 -
43 Kacker PP. A case of Giardia lamblia proctitis presenting in a V.D. clinic. Brit J Vener Dis [Internet]. 1973 [cited 2020 Jul 15]; 49(3):318-9. Available from:: https://doi.org/10.1136/sti.49.3.318
» https://doi.org/10.1136/sti.49.3.318 -
44 Rosenthal PJ. Giardiasis. In: Papadakis MA, McPhee SJ, Rabow MW. Current medical diagnosis & treatment [Internet]. 56th ed. [S.l.]:McGraw-Hill Education; 2017 [cited 2020 Jul 18]. Available from:: http://accessmedicine.mhmedical.com/book.aspx?bookid=2683
» http://accessmedicine.mhmedical.com/book.aspx?bookid=2683 -
45 Reed SL. Clinical manifestations and diagnosis. In: Ravdin JI, editor. Amebiasis [Internet]. London: Imperial College Press; 2000 [cited 2020 Jul 13]. p. 113-26. Available from:: https://www.worldscientific.com/doi/abs/10.1142/9781848160583_0005
» https://www.worldscientific.com/doi/abs/10.1142/9781848160583_0005 -
46 Healy GR, Garcia LS. Intestinal and urogenital protozoa. In: Murray PR, Baron EJ, Pfaller MA, Tenover FC, Yolken RH, editors. Manual of clinical microbiology [Internet]. 6th ed. Washington, D.C.: ASM Press; 1995 [cited 2020 Jul 23]. p. 1204-28. Available from:: https://www.asmscience.org/content/book/10.1128/9781555817381
» https://www.asmscience.org/content/book/10.1128/9781555817381 -
47 Kaakoush NO, Castaño-Rodríguez N, Mitchell HM, Man SM. Global epidemiology of campylobacter infection. Clin Microbiol Rev [Internet]. 2015 Jun [cited 2020 Jul 20]; 28(3):687-720. Available from:: https://doi.org/10.1128/CMR.00006-15
» https://doi.org/10.1128/CMR.00006-15 -
48 Man SM. The clinical importance of emerging campylobacter species. Nat Ver Gastroenterol Hepatol [Internet]. 2011 Oct [cited 2020 Jun 23]; 8(12):669-85. Available from:: https://doi.org/10.1038/nrgastro.2011.191
» https://doi.org/10.1038/nrgastro.2011.191 -
49 Gaudreau C, Helferty M, Sylvestre JL, Allard R, Pilon PA, Poisson M, et al. Campylobacter coli outbreak in men who have sex with men, Quebec, Canada, 2010-2011. Emerg Infect Dis [Internet]. 2013 May [cited 2020 Jul 14]; 19(5): 764-7. Available from:: https://doi.org/10.3201/eid1905.121344
» https://doi.org/10.3201/eid1905.121344 -
50 Centers for Disease Control and Prevention - CDC. Sexually transmitted diseases treatment guidelines, 2015. MMWR [Internet]. 2015 Jun [cited 2020 Jul 15]; 64(3). Available from:: https://www.cdc.gov/std/tg2015/tg-2015-print.pdf
» https://www.cdc.gov/std/tg2015/tg-2015-print.pdf -
51 Marchand-Senécal X, Bekal S, Pilon PA, Sylvestre JL, Gaudreau C. Campylobacter fetus cluster among men who have sex with men, Montreal, Quebec, Canada, 2014-2016. Clin Infect Dis [Internet]. 2017 Nov [cited 2020 Jul 14]; 65(10):1751-3. Available from:: https://doi.org/10.1093/cid/cix610
» https://doi.org/10.1093/cid/cix610 - 52 Lupi O. Herpes simples, em rotinas de diagnóstico e tratamento das doenças infecciosas e parasitárias. In: Tavares W, Marinho LAC. Rotinas de diagnóstico e tratamento das doenças. São Paulo: Atheneu; 2005.
-
53 Jin SS. Herpes simplex virus. In: Kuritzkes DR, Eron Jr J, editors. Practice hepatology and HIV. Physician continuing medical education (for Point of Care CME activities) [Internet]. [S.l.]: inPractice; 2016 [cited 2020 Aug 28]. Available from:: https://www.inpractice.com/textbooks/hiv/management_of_specific_disease_states/ch29_pt1_viral/chapter-pages/page-2.aspx?origin=2
» https://www.inpractice.com/textbooks/hiv/management_of_specific_disease_states/ch29_pt1_viral/chapter-pages/page-2.aspx?origin=2 - 54 Marrazzo JM, Apicella MA. Neisseria gonorrhoeae (Gonorrhea). In: Bennett JE, editors. Mandell, Douglas and Bennett’s principles and practice of infectious diseases. 9th ed. Philadelphia: Elsevier; 2020. p. 2608.
- 55 Beck D. Sexually transmitted diseases. In: Steele SR, Hull TL, Read TR, Saclarides TJ, Senagore AJ, Whitlow CB, editors. The ASCRS textbook of colon and rectal surgery. 2nd ed. New York: Springer; 2011. p. 295-307.
-
56 Quinn TC. Sexually transmitted enteric infections. In: Schlossberg D, editors. Clinical infectious disease [Internet]. Cambridge: Cambridge University Press; 2017 [cited 2020 Jul 14] p. 352-6. Available from:: https://doi.org/10.1017/CBO9781139855952.060
» https://doi.org/10.1017/CBO9781139855952.060 -
57 Clutterbuck D, Asboe D, Barber T, Emerson C, Field N, Gibson S, et al. 2016 United Kingdom national guideline on the sexual health care of men who have sex with men. Int J STD AIDS [Internet]. 2018 Jan [cited 2020 Aug 10]. Available from:: https://doi.org/10.1177/0956462417746897
» https://doi.org/10.1177/0956462417746897 -
58 Farthing M, Feldman R, Finch R, Fox R, Leen C, Mandal B, et al. The management of infective gastroenteritis in adults. A consensus statement by an expert panel convened by the British Society for the Study of Infection. J Infect [Internet]. 1996 Nov [cited 2020 Jul 14]; 33(3):143-52. Available from:: https://doi.org/10.1016/s0163-4453(96)92057-5
» https://doi.org/10.1016/s0163-4453(96)92057-5 -
59 DuPont HL. Acute infectious diarrhea in immunocompetent adults. N Engl J Med [Internet]. 2014 Apr [cited 2020 Jul 14]; 370(16):1532-40. Available from:: https://doi.org/10.1056/NEJMra1301069
» https://doi.org/10.1056/NEJMra1301069 - 60 Bensabath G, Conde SRSS, Dias Junior LB, Demachki S. Hepatites virais. In: Leão RNQ, coordenador. Medicina tropical e infectologia da Amazônia. Belém: Samauma Editorial; 2013. p 675-739.
-
61 Clinical and Laboratory Standards Institute. M100-S26: Performance standards for antimicrobial susceptibility testing. 30th ed. [S.l]: CLSI; 2016 [cited 2020 Jul 15]. Available from:: http://clsi.org/m100 /
» http://clsi.org/m100 -
62 Krogstad DJ, Spencer HC Jr, Healy GR, Gleason NN, Sexton DJ, Herron CA. Amebiasis: epidemiologic studies in the United States, 1971-1974. Ann Intern Med [Internet]. 1978 Jan [cited 2020 Jun 27]; 88(1):89-97. Available from:: https://doi.org/10.7326/0003-4819-88-1-89
» https://doi.org/10.7326/0003-4819-88-1-89 -
63 Abd-Alla MD, Jackson TG, Ravdin JI. Serum IgM antibody response to the galactose-inhibitable adherence lectin of Entameoba histolytica. Am J Trop Med Hyg [Internet]. 1998 Sep [cited 2020 Jul 17]; 59(3):431-4. Available from:: https://doi.org/10.4269/ajtmh.1998.59.431
» https://doi.org/10.4269/ajtmh.1998.59.431 -
64 Nagaty IM, Hegazi MM. Dot-ELISA copro-antigen and direct stool examination in diagnosis of giardiasis patients. J Egypt Soc Parasitol [Internet]. 2007 Aug [cited 2020 Jul 13]; 37(2):641-8. Available from:: https://emedicine.medscape.com/article/176718-workup
» https://emedicine.medscape.com/article/176718-workup -
65 Centers for Disease Control and Prevention - CDC. Yellow book 2020: health information for international travel. Washington, D.C.: CDC; 2020 [cited 2020 Jun 29]. Available from:: https://wwwnc.cdc.gov/travel/yellowbook/2020/travel-related-infectious-diseases/campylobacteriosis
» https://wwwnc.cdc.gov/travel/yellowbook/2020/travel-related-infectious-diseases/campylobacteriosis -
66 Brennan J, Moore K, Sizemore L, Mathieson AS, Wester C, Dunn JR, et al. Notes from the field: acute hepatitis A virus infection among previously vaccinated persons with HIV infection - Tennessee, 2018. MMWR Morb Mortal Wkly Rep [Internet]. 2019 Apr [cited 2020 Jun 20]; 68(14):328-9. Available from:: https://doi.org/10.15585/mmwr.mm6814a3
» https://doi.org/10.15585/mmwr.mm6814a3 -
67 Ruscher C, Werber D, Thoulass J, Zimmermann R, Eckardt M, Winter C, et al. Dating apps and websites as tools to reach anonymous sexual contacts during an outbreak of hepatitis A among men who have sex with men, Berlin, 2017. Euro Surveill [Internet]. 2019 May [cited 2020 Jun 21]; 24(21):1800460. Available from:: https://doi.org/10.2807/1560-7917.ES.2019.24.21.1800460
» https://doi.org/10.2807/1560-7917.ES.2019.24.21.1800460 -
68 World Health Organization - WHO. Guidelines for the control of shigellosis, including epidemics due to Shigella dysenteriae type 1 [Internet]. Geneva: World Health Organization; 2005 [cited 2020 Sep 22]. Available from:: https://www.who.int/cholera/publications/shigellosis/en /
» https://www.who.int/cholera/publications/shigellosis/en -
69 Bowen A, Grass J, Bicknese A, Campbell D, Hurd J, Kirkcaldy RD. Elevated risk for antimicrobial drug-resistant Shigella infection among men who have sex with men, United States, 2011-2015. Emerg Infect Dis [Internet]. 2016 Sep [cited 2020 Jun 21]; 22(9):1613-6. Available from:: https://doi.org/10.3201/eid2209.160624
» https://doi.org/10.3201/eid2209.160624 -
70 Baker KS, Dallman TJ, Ashton PM, Day M, Hughes G, Crok PD, et al. Intercontinental dissemination of azithromycin-resistant shigellosis through sexual transmission: a cross-sectional study. Lancet Infect Dis [Internet]. 2015 Apr [cited 2020 Jul 13]; 15(8):913-21. Available from:: https://doi.org/10.1016/S1473-3099(15)00002-X
» https://doi.org/10.1016/S1473-3099(15)00002-X -
71 Wong MR, Reddy V, Hanson H, Johnson KM, Tsoi B, Cokes C, et al. Antimicrobial resistance trends of Shigella serotypes in New York City, 2006-2009. Microb Drug Resist [Internet]. 2010 [cited 2020 Jun 29]; 16(2):155-16. Available from:: https://doi.org/10.1089/mdr.2009.0130
» https://doi.org/10.1089/mdr.2009.0130 -
72 Centers for Disease Control and Prevention - CDC. National Institutes of Health. HIV Medicine Association of the Infectious Diseases Society of America. US Department of Health and Human Services. Panel on opportunistic infections in HIV-infected adults and adolescents. Guidelines for the prevention and treatment of opportunistic infections in HIV-infected adults and adolescents [Internet]. Washington, D.C.: CDC ; 2020 [cited 2020 Jul 10]. Available from:: https://aidsinfo.nih.gov/contentfiles/lvguidelines/adult_oi.pdf
» https://aidsinfo.nih.gov/contentfiles/lvguidelines/adult_oi.pdf -
73 Cimerman S, Cimerman B. Parasitoses intestinais: protozooses intestinais. In: Cimerman S, Cimerman B. Conduta em infectologia [Internet]. São Paulo: Atheneu ; 2004 [cited 2020 jun 29]. p. 329-342. Available from:: https://pesquisa.bvsalud.org/portal/resource/pt/lil-407428
» https://pesquisa.bvsalud.org/portal/resource/pt/lil-407428 - 74 Hooshyar H, Rostamkhani P, Arbabi M, Delavari M. Giardia lamblia infection: review of current diagnostic strategies. Gastroenterol Hepatol Bed Bench [Internet]. 2019 Winter [cited 2020 Sep 22]; 12(1):3-12. Available from:: https://pubmed.ncbi.nlm.nih.gov/30949313/
- 75 Busatti HG, Santos JF, Gomes MA. The old and new therapeutic approaches to the treatment of giardiasis: where are we? Biologics [Internet]. 2009 [cited 2020 Jun 30]; 3:273-287. Available from:: https://pubmed.ncbi.nlm.nih.gov/19707415
-
76 Halliez MC, Buret AG. Extra-intestinal and long-term consequences of Giardia duodenalis infections. World J Gastroenterol [Internet]. 2013 Dec [cited 2020 Jun 29]; 19(47):8974-85. Available from:: https://doi.org/10.3748/wjg.v19.i47.8974
» https://doi.org/10.3748/wjg.v19.i47.8974 -
77 Munoz FM. Treatment and prevention of giardiasis. Waltham (MA): UpToDate; 2015 [cited 2020 Jun 29]. Available from:: http://www.uptodate.com/contents/treatment-and-prevention-of-giardiasis
» http://www.uptodate.com/contents/treatment-and-prevention-of-giardiasis -
78 Ruiz-Palacios GM. The health burden of campylobacter infection and the impact of antimicrobial resistance: playing chicken. Clin Infec Dis [Internet]. 2007 Mar [cited 2020 Jun 22]; 44(5):701-3. Available from:: https://doi.org/10.1086/509936
» https://doi.org/10.1086/509936 -
79 Shover CL, Beymer MR, Unger EM, Javanbakht M, Bolan RK. Accuracy of presumptive gonorrhea treatment for gay, bisexual, and other men who have sex with men: results from a large sexual health clinic in Los Angeles, California. LGBT Health. 2018 Mar [cited 2020 Jun 22]; 5(2):139-44. Available from:: https://doi.org/10.1089/lgbt.2017.0115
» https://doi.org/10.1089/lgbt.2017.0115 -
80 Ministério da Saúde (BR). Nota Informativa nº 55/2019-CGAE/. DIAHV/SVS/MS. Orientações acerca dos critérios de definição de casos para notificação de hepatites virais [Internet]. Brasília: Ministério da Saúde ; 2019 [cited 2020 jun 20]. Available from:: http://portalsinan.saude.gov.br/images/documentos/Agravos/Hepatites_Virais/Nota_Informativa_Hepatites_Virais.pdf
» http://portalsinan.saude.gov.br/images/documentos/Agravos/Hepatites_Virais/Nota_Informativa_Hepatites_Virais.pdf -
81 Brasil. Ministério da Saúde. Gabinete do Ministro. Portaria MS/GM nº 2.325, de 8 de dezembro de 2003. Define a relação de doenças de notificação compulsória para todo território nacional [Internet]. Diário Oficial da União , Brasília (DF), 2003 dez 10 [cited 2020 jul 20]; Seção I:81. Available from:: http://bvsms.saude.gov.br/bvs/saudelegis/gm/2003/prt2325_08_12_2003.html
» http://bvsms.saude.gov.br/bvs/saudelegis/gm/2003/prt2325_08_12_2003.html -
82 Ministério da Saúde (BR). Sistema de Informação de Agravos de Notificação. Sinan-Net [Internet]. Brasília: Ministério da Saúde ; 2020 [cited 2020 jul 31]. Available from:: http://portalsinan.saude.gov.br
» http://portalsinan.saude.gov.br -
83 Erickson MC, Ortega YR. Inactivation of protozoan parasites in food, water, and environmental systems. J Food Prot [Internet]. 2006 Nov [cited 2020 Jun 29]; 69(11):2786-808. Available from:: https://doi.org/10.4315/0362-028x-69.11.2786
» https://doi.org/10.4315/0362-028x-69.11.2786 -
84 Shirley DAT, Farr L, Watanabe K, Moonah S. A Review of the global burden, new diagnostics, and current therapeutics for amebiasis. Open Forum Infec Dis [Internet]. 2018 Jul [cited 2020 Jun 29]; 5(7):ofy161. Available from:: https://doi.org/10.1093/ofid/ofy161
» https://doi.org/10.1093/ofid/ofy161
