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W3109911042 abstract "The scope, purpose and guideline topics were agreed by the writing group. The search (population, intervention, comparator and outcome [PICO]) questions were set and an independent systematic literature review carried out. The PubMed, Medline, Embase and Cochrane Library databases were searched and the literature reviewed to address each question. The PICO questions and search strategies are outlined in Appendix 1. Further details of the methodology can be found on the British HIV Association (BHIVA) website (https://www.bhiva.org/file/5d514ec9b503d/OI-guidelines-methods-general.pdf), including the use of the Grading of Recommendations Assessment, Development and Evaluation (GRADE) system to assess and grade the evidence. Gastrointestinal (GI) symptoms occur frequently in people living with HIV (PLWH). Dysphagia and diarrhoea (Table 1) may be caused by a wide variety of infections. Symptoms may arise from any part of the GI tract including the mouth, throat, oesophagus, stomach, small and large intestine, liver, gall bladder, rectum and anus. The incidence of opportunistic infections has fallen as most PLWH take combination antiretroviral therapy (cART), however there remain some differences in type of pathology seen compared to non-HIV-positive populations, and opportunistic infections may still occur in those with higher CD4 counts [1]. If a cause of persisting GI symptoms is not apparent, consultation with a gastroenterologist is indicated because PLWH are also susceptible to many of the same conditions as the non-HIV-infected population. Co-infection with hepatitis B or C virus is not discussed in these guidelines as it is the subject of separate guidelines [2]. The organisms that most commonly cause oropharyngeal infections and oesophagitis are Candida spp. Persistent or recurrent oesophageal candidiasis has decreased in the cART era and most often indicates poor HIV viral control [3]. Candidiasis of the upper GI tract is discussed in detail in a separate chapter of the BHIVA guidelines on the management of opportunistic infection in people living with HIV: The clinical management of Candidiasis 2019 [4]. Oesophagitis should be suspected in patients who experience pain on swallowing with or without symptoms of reflux or dysphagia. The other major HIV-related infectious causes of oesophagitis include herpes simplex virus (HSV) and cytomegalovirus (CMV) infections, which cause ulceration and may coexist with candidiasis, especially in PLWH with CD4 counts <100 cells/mm3. Tuberculosis is a rare cause of oesophageal or oropharyngeal disease. Idiopathic ulcers are also common. Primary syphilis can present with oral ulcers as well as causing genital and perianal ulceration. Individuals at risk should be screened in line with national guidelines. Other non-infectious causes of dysphagia include pill-associated ulcers. These have been associated with a number of medications, most commonly in the mid-oesophagus. Doxycycline and related antimicrobials, non-steroidal anti-inflammatory drugs, potassium supplementation and iron tablets are the commonest causes that are likely to be encountered in PLWH [5]. The results of a randomised trial demonstrated that initial empirical therapy for candidiasis is a reasonable first approach in uncomplicated oesophagitis [6]. Endoscopy should be performed if symptoms have failed to resolve after an empirical trial of azoles, with appropriate swab and/or biopsy if abnormalities are seen. Adequate and appropriate specimens must be collected to enable histological and virological diagnoses, together with cultures and anti-fungal susceptibility testing for the identification of azole-resistant Candida strains. For mouth ulcers, HSV polymerase chain reaction (PCR) or culture tests should be used for diagnosis. Further discussion of the treatment of candidiasis can be found in the candidiasis chapter of the BHIVA guidelines on the management of opportunistic infection in PLWH [4]. Foscarnet 90 mg/kg bd iv may be used in cases of ganciclovir-resistant CMV or 40 mg/kg bd or tds for aciclovir-resistant HSV [10]. Systemic cidofovir 5 mg/kg once weekly for 2 weeks is an alternative treatment for CMV or HSV where there is intolerance of or resistance to other drugs. Diarrhoea is common among PLWH, even in the era of cART. A meta-analysis of post-2008 clinical trials demonstrated that the prevalence of diarrhoea was 18% among PLWH on treatment [11]. Diarrhoea is normally defined as having more than two bowel movements per day, with acute diarrhoea occurring for less than 4 weeks and chronic diarrhoea for more than 4 weeks. Chronic diarrhoea may be more likely to be associated with opportunistic infections in PLWH than in the general population, particularly those with lower CD4 counts. A range of bacteria commonly cause gastroenteritis in PLWH (Table 2). Clostridioides difficile was the most common cause of diarrhoea among PLWH in a US cohort study [12]. However, this has not been replicated in other studies in high-income countries. C. difficile is prevalent in high-income and low-/middle-income countries (LMICs) [13-15] and spans the pre- and post-cART eras [16]. Invasive non-typhoidal salmonellosis (iNTS) was recognised early in the HIV epidemic to be strongly associated with immunosuppression in both high-income countries [17-19] and LMICs [20-22]. As in HIV-negative individuals, other bacterial pathogens causing diarrhoea include Escherichia coli, Campylobacter spp. and Shigella spp. [23-25]. The prevalence of Shigella spp. was higher among HIV-positive men who have sex with men (MSM) compared to HIV-negative MSM in the UK [26] and other pathogens such as Campylobacter spp. are increasingly identified among HIV-positive MSM [27]. Lymphogranuloma venereum (LGV), caused by Chlamydia trachomatis, can be associated with diarrhoea as part of proctocolitis or enteritis syndromes and is increasingly common among MSM in Europe [28, 29]. Older age and lower CD4 count increase the likelihood of diarrhoea in PLWH [30]. Residence in or travel to LMICs increases the risk of diarrhoea due to greater pathogen exposure. In addition, MSM are at risk of sexually acquired diarrhoeal disease. Hospitalisation, gastric acid suppression, lower CD4 count and antibiotic use are risk factors for C. difficile infection in PLWH [13, 16]. The spectrum of clinical presentation ranges from asymptomatic infection to severe dehydration and death. Bacterial gastroenteritis may cause bloody diarrhoea and abdominal pain. Bacteraemia is more likely in PLWH, but remains uncommon overall [31, 32]. In PLWH, iNTS infections present with febrile illness or sepsis syndromes, and diarrhoea may be absent or a less prominent feature [22]. Presenting symptoms of C. difficile infection in PLWH are similar to those in HIV-negative individuals [33, 34]. Data from case series suggest that C. difficile infection is no more severe in PLWH [35, 36]. Recent outbreaks of LGV were associated more with anorectal symptoms than with inguinal lymphadenopathy or ulceration; these symptoms may include tenesmus, constipation, diarrhoea and anal discharge [26]. If a bacterial cause is suspected from the history, antimicrobial therapy may be indicated. Principles of therapy are as for HIV-negative individuals. We suggest that acute bacterial diarrhoea in individuals with preserved CD4 counts (≥200 cells/mm3) does not usually require treatment. In general, when individuals present with acute bacterial diarrhoea and a CD4 count <200 cells/mm3, therapy will be indicated. When indicated, the choice should be guided by sensitivity testing. In cases where the patient presents with signs of sepsis or severe symptoms, the benefits of empirical treatment may outweigh the potential risks and empirical treatment should be commenced. There have been increasing numbers of reports of ciprofloxacin resistance in Campylobacter spp., Shigella spp. and Salmonella spp. [41-43] and choice of empirical agent should be consistent with local guidance. For treatment of C. difficile diarrhoea, as with the management of HIV-negative cases, the first step is to stop the aetiological antibiotic where possible and isolate the patient. Principles of therapy for C. difficile infection are as for HIV-negative individuals and therapy is indicated regardless of the CD4 count. C. difficile infection should be treated according to Public Health England guidelines [37]: for non-severe C. difficile infection metronidazole is currently indicated, and severe infection should be treated with vancomycin or fidaxomicin considered in those who are at high risk of recurrence [37, 44]. There is no evidence for the use of probiotics for C. difficile treatment [45]. The treatment response for PLWH and HIV-negative people appears similar and complications do not appear to be more or less common in PLWH. For recurrent C. difficile infection, treat with fidaxomicin or vancomycin; a tapering therapy may be considered [37]. Faecal transplant may be considered and can be effective in the general population [46-48]. Based on data from case reports and case series, donor stool transplant appears to be safe and effective in PLWH, including those with a low CD4 count [47]. A Cochrane review of antibiotic treatment for C. difficile in the general population demonstrated that vancomycin was more effective than metronidazole for achieving symptomatic cure, but the quality of the evidence was very low [44]. The review also found moderate-quality evidence that fidaxomicin was more effective than vancomycin at achieving symptomatic cure, however only two papers were included in this analysis and both were non-inferiority trials and neither reported intention-to-treat data. Therefore, there is insufficient evidence to change the current recommendations. Trimethoprim-sulphamethoxazole (co-trimoxazole) reduced the incidence of infectious diarrhoea in the pre-cART era [49]. The introduction of cART has been more effective than antimicrobial prophylaxis in preventing recurrence of non-typhoidal salmonella [50, 51]. If given, the duration of antimicrobial prophylaxis, with agents such as fluoroquinolones, need not exceed 30 days in patients established on cART [52]. The incidence of bacterial diarrhoea has declined steadily since the introduction of cART, therefore cART is the mainstay of preventing bacterial diarrhoea [53, 54]. Co-trimoxazole is no longer recommended for prevention of bacterial diarrhoea. A variety of viruses can cause gastroenteritis in PLWH (Table 3), of which CMV is the most important pathogen. CMV is a member of the herpes family of viruses. Primary CMV infection can occur at any stage throughout life, and the virus then remains dormant unless reactivated in the immunocompromised host. Globally, the seroprevalence of CMV varies widely between different risk groups and countries, but there is evidence of past CMV exposure in the majority of PLWH, especially among MSM. CMV is still the most common opportunistic pathogen causing viral enteritis in PLWH although the incidence has decreased substantially in the cART era [55]. Most cases of CMV disease occur in people with prior CMV infection and a CD4 cell count <50 cells/mm3 [56]. PLWH often present with non-specific GI symptoms. Although it can affect the entire GI tract, CMV infection frequently involves the oesophagus or the colon [57, 58]. The most common complications of CMV colitis are weight loss, anorexia, abdominal pain, chronic unremitting diarrhoea and fatigue. There may also be systemic features of CMV infection such as fevers and cytopaenias. Toxic dilatation, haemorrhage and perforation are recognised serious complications. In terms of the impact of cART, all patients with CMV of the GI tract should be assessed for the presence of retinitis. If present, CMV treatment should be initiated and cART initiation delayed – typically by 2 weeks – to reduce the risk of immune reconstitution inflammatory syndrome [59, 60]. If initial examination is negative, direct fundoscopy and ophthalmology review should be repeated if any visual symptoms occur. A delay of more than 2 weeks before starting cART after CMV colitis treatment has begun is not recommended. The presence of CMV-associated GI disease alone is not an indication to delay cART. Therapeutic drug monitoring to ensure adequate cART absorption is advised if the patient’s HIV viral load does not become undetectable within a reasonable, expected time frame. The diagnosis of CMV-associated GI disease is based on the clinical symptoms of GI disease, characteristic mucosal ulceration seen on endoscopy and intracellular and intracytoplasmic ‘owl’s eye’ inclusions seen on pathology, with positive immunohistochemical staining for CMV. CMV viraemia as detected by PCR, antigen assays or culture is non-specific for the presence of colitis in patients with a low CD4 count [61-63]. With respect to serological tests, CMV antibody is not useful in diagnosing CMV enteritis in PLWH, however this diagnosis is unlikely if the patient is CMV IgG seronegative. Opportunistic infection of the GI tract with CMV in PLWH is best prevented by maintaining the CD4 count >100 cells/mm3 with cART. Ganciclovir is the preferred treatment for induction therapy for CMV colitis [65]. Foscarnet is also effective but ganciclovir is the preferred agent because of fewer side effects [66]. Systemic cidofovir 5 mg/kg once weekly for 2 weeks is an alternative treatment for CMV where there is intolerance to other antiviral therapies. Oral valganciclovir may be used for induction therapy in patients who can tolerate and absorb oral medication and where there is evidence of mild or resolving infection. However the evidence base for this is predominantly from treatment of CMV retinitis [67]. Chronic maintenance therapy following treatment of acute CMV disease is not recommended unless clinical relapse occurs. Failure of therapy for CMV-related GI disease may be due to lack of immune reconstitution, inadequate anti-viral levels as a result of poor absorption or antiviral medication resistance. An alternative diagnosis or concurrent GI infection should also be considered. Antiviral-resistant, HIV-related CMV colitis is rare. Prolonged CMV treatment (>6 weeks) and very high initial CMV viral load in blood (>106 IU/mL) are risk factors for resistance. In cases of relapsed CMV retinitis, treatment options include ganciclovir plus foscarnet [69] but there are limited data on this combination in treating relapsed CMV-associated colitis and the treatment is associated with considerable toxicity. CMV resistance to ganciclovir can be confirmed by detection of mutations in the UL97 gene sequence [70]. Resistance to foscarnet or cidofovir occurs through mutations in the CMV UL54 gene. High-level resistance to ganciclovir is associated with resistance to cidofovir (and occasionally foscarnet) [71-73]. Genotypic assays can be completed in a few days; phenotypic resistance testing is not routinely available. There are anecdotal reports supporting the use of other agents, such as cidofovir, in GI antiviral-resistant CMV disease as well as high-dose ganciclovir or high-dose valganciclovir [74]. Novel anti-CMV therapies are becoming available including marabavir, which has a potential role in refractory or resistant CMV infection in haematopoietic cell or solid organ transplant recipients [75], and letermovir, which has a role in CMV prophylaxis after transplantation in CMV-seropositive recipients [76]. These agents could be acquired on a named patient basis, but currently there is a lack of evidence for clinical use in PLWH. Monitoring of ganciclovir/valganciclovir levels is not routinely recommended but should be considered in cases of inadequate response where there is concern about inadequate oral absorption, or where dose adjustment has been made due to renal impairment. Awareness of drug interactions between cART agents and anti-CMV drugs is important. Risk factors for these interactions include advanced age, certain comorbidities and concomitant nephrotoxic medications [77]. Reports of renal toxicity associated with concurrent use of ganciclovir/valganclovir and tenofovir have been published [78]. HSV, adenovirus, norovirus, astrovirus and rotavirus have also been implicated in the causation of viral enteritis in PLWH and there is some suggestion of increased severity in this population [79-81]. Only HSV, which more commonly affects the oesophagus, has established treatment options (see treatment of HSV oesophagitis above). Cidofovir shows activity against adenovirus although cases of clinically significant colitis caused by this virus are rarely reported [82]. There have been reports implicating coronavirus, which may coexist with bacterial pathogens [83] in acute diarrhoea, and adenovirus, which may coexist with CMV in patients with chronic diarrhoea [84]. HSVs (HSV-1 and HSV-2) can cause diarrhoea due to proctocolitis. Older age, lower CD4 count and travel to LMICs increase the risk of diarrhoea among PLWH. MSM and others who have anal sex are at risk of sexually acquired diarrhoeal disease [26]. The spectrum of clinical presentation ranges from asymptomatic infection to severe dehydration and death. Viral gastroenteritis typically presents with a short prodrome with mild fever and vomiting, followed by 1–4 days of non-bloody, watery diarrhoea. Viral gastroenteritis is usually self-limiting. Supportive measures are the mainstay for viral gastroenteritis, primarily ensuring adequate hydration through oral or iv fluids. Treatment of CMV- and HSV-related disease is discussed in depth in other chapters of the BHIVA opportunistic infection guidelines. The incidence of viral opportunistic infections has declined following the introduction of cART [54], and cART is the mainstay of preventing viral diarrhoea. A number of parasites and helminths can cause GI pathology in PLWH (Table 4), and their diagnosis and treatment are summarised below. Metronidazole 400 mg tds po for 7 days or 1 g daily for 3 days. Alternative: tinidazole 500 mg bd po for 7 days or 2 g once only Co-trimoxazole 960 mg bd po for 7 days. Alternative: co-trimoxazole 960 mg qds for 10 days or ciprofloxacin 500 mg bd followed by the same antibiotic as prophylaxis Ivermectin 200 μg/kg od po for 1 or 2 days. Alternative: albendazole 400 mg bd po for 3 days Cryptosporidium is a ubiquitous protozoan parasite, which can cause diarrhoeal disease in humans. Infection is spread by the ingestion of as few as 10–100 Cryptosporidium oocysts following contamination of the water supply by the faeces of infected animals or humans [85]. Sexual transmission can also occur, particularly via the faecal–oral route [86]. Cryptosporidium is a significant cause of chronic diarrhoea in patients with advanced HIV, of diarrhoea in children and of zoonotic and waterborne outbreaks [87]. PLWH are at greatest risk when their CD4 count is <100 cells/mm3 [88]. Cryptosporidium predominately infects the small bowel mucosa, but the large bowel and extraintestinal sites may be involved in the immunocompromised patient. Routine typing of isolates from cryptosporidiosis cases between 2000 and 2008 in England and Wales identified C. hominis in 51% of cases, C. parvum in 44%, mixed infection with C. hominis and C. parvum in 0.4% and the remainder either non-typable or other species [89]. Cryptosporidiosis should be considered in any individual with an acute or subacute history of profuse, non-bloody, watery diarrhoea. Fever is present in approximately one-third of patients and malabsorption is common. Nausea, vomiting and lower abdominal pain may also occur. Cryptosporidiosis is usually self-limiting within 14 days in immunocompetent individuals. In PLWH with a CD4 count <50 cells/mm3, symptoms are more severe and stool volumes of up to 24 L/day have been described, although 2–3 L/day are more commonly passed [90]. As the epithelium of both the pancreatic duct and biliary tract can be infected, cholangitis and pancreatitis may occur in individuals with prolonged infection [91]. Sclerosing cholangitis presents with right upper quadrant pain, vomiting and raised alkaline phosphatase levels. Cases of pulmonary cryptosporidiosis in those with advanced HIV have also been reported [92, 93] and raise the possibility of respiratory transmission of cryptosporidiosis [94]. Cryptosporidiosis can be diagnosed by the detection of oocysts in fresh, unconcentrated stools by microscopy of smears stained with either auramine phenol or modified Ziehl-Neelsen stain. In cases of profuse diarrhoea, cryptosporidiosis may be detected in a single stool sample, but in mild disease repeat samples may be required due to intermittent oocyst excretion. Concentration methods are not required where stool samples are collected fresh without preservatives but may be helpful in very watery samples. Immunofluorescence microscopy can improve diagnostic sensitivity but requires additional resources and costs are increased [93]. Increasingly UK laboratories are using enzyme immunoassays that have a similar sensitivity and specificity to microscopy with auramine phenol [95, 96]. PCR can also be used for the detection and speciation of Cryptosporidium with excellent sensitivity and specificity [97]. Small bowel and rectal histology may be useful although the latter has a low sensitivity for diagnosis. In individuals with abdominal pain, endoscopic retrograde pancreatography may reveal ampullary stenosis and sclerosing cholangitis with associated thickening of the gallbladder wall. In advanced HIV, restoration of the immune system with effective cART is associated with full resolution of Cryptosporidium infection [98, 99]. Although a number of drugs have shown activity in vitro, in animal models and in immunocompetent patients, their use in PLWH has been disappointing. Nitazoxanide has shown efficacy in healthy hosts but has not been shown to be superior to placebo in those who are severely immunocompromised [100-102]. If used, nitazoxanide is given at a dose of 500 mg bd for 3 days, but may be required for up to 12 weeks. Paromomycin has shown little effect on symptoms and oocyst shedding in two randomised placebo-controlled trials [103, 104]. The results of a study combining paromomycin with azithromycin demonstrated substantial reduction in stool frequency and volume [105]. Additional supportive measures such as rehydration, electrolyte replacement, anti-motility agents and referral to a dietician for nutritional support may be required. The use of optimised cART should be continued to prevent relapse. Initiation of cART prior to advanced immunosuppression should prevent the development of cryptosporidiosis. Patients with CD4 counts <200 cells/mm3 should avoid drinking unfiltered water and ensure careful hand hygiene. Standard drinking water chlorination techniques are not sufficient to eradicate the parasite. Specific filtration employing an ‘absolute’ 1-μm filter is required [106]. Bottled water is not necessarily a safer option and boiling of water should be advocated. The Microsporidia are a group of over 1200 small, spore-forming parasitic fungi. They infect a wide range of vertebrate and invertebrate hosts with at least 14 species recognised as human pathogens [107]. Clinical microsporidiosis is most frequently seen in individuals who are severely immunosuppressed, particularly in PLWH with a CD4 count <100 cells/mm3 [108, 109]. Cases have also been reported in transplant recipients, those undergoing chemotherapy, diabetics, children, the elderly, travellers and wearers of contact lenses [107]. GI infection occurs following ingestion of microsporidial spores in contaminated water or via contact with infected faeces or urine. The Microsporidia most commonly linked to GI illness are Enterocytozoon bieneusi and Encephalitozoon (formerly Septata) intestinalis. These species both infect villus epithelial cells of the small intestine but E. intestinalis has a propensity to disseminate elsewhere in the body, particularly the kidneys, skin, nasal mucosa, eyes and gallbladder [110]. Watery, non-bloody diarrhoea, with associated malabsorption, is the most common presentation of GI infection with Microsporidia. Sclerosing cholangitis may occur. Dissemination can lead to encephalitis, sinusitis, myositis and renal and ocular infection. Standard stool microscopy will often not detect Microsporidia. Examination of three stool samples with chromotrope and chemofluorescent stains for microsporidial spores is often sufficient for diagnosis. Stool microscopy does not allow for speciation and electron microscopy remains the gold standard for confirmation and speciation. Where available, PCR is a highly sensitive and specific tool for diagnosis and speciation [111]. If stool samples are consistently negative a small bowel biopsy may be considered [112]. Early initiation of cART is the mainstay of treatment for microsporidiosis and is associated with complete resolution of GI symptoms following restoration of immune function [97, 113]. There is no specific therapeutic agent for the treatment of E. bieneusi. There may be a response to oral fumagillin (20 mg tds for 14 days) but with significant haematological toxicity [114, 115]. Encephalitozoon spp. including E. intestinalis are susceptible to albendazole (400 mg bd for 21 days) and this drug is recommended for initial therapy in addition to cART. Longer therapy may be required for involvement of sites outside the GI tract or in severe disease until immune reconstitution occurs. Nitazoxanide and itraconazole have also been used with variable effectiveness. Thalidomide may be effective for symptom control in some patients [116]. Additional supportive measures such as rehydration, electrolyte replacement, nutritional support and anti-motility agents may be required. The use of optimised cART should be continued to prevent relapse. Initiation of cART prior to advanced immunosuppression should prevent the development of microsporidiosis. Patients with CD4 counts <200 cells/mm3 should avoid drinking untreated water and ensure careful hand hygiene. A number of parasites and helminths are found more frequently in PLWH due to overlapping global distribution and the possibility of sexual transmission in MSM. Giardiasis is caused by the flagellate parasite Giardia lamblia. Infection can be asymptomatic or present with chronic diarrhoea and constitutional symptoms. GI symptoms include nausea, bloating, cramp-like abdominal pain, indigestion and belching. Prolonged diarrhoea may result in a malabsorptive state. Giardiasis is treated with metronidazole (400 mg tds po for 7 days or 1 g od for 3 days) or tinidazole (500 mg bd po for 7 days or a single dose of 2 g). The patient should be given advice regarding the need for stringent personal hygiene to prevent person-to-person spread. If symptoms persist after initial treatment a repeated course of first-line therapy is recommended. Household and sexual contacts should be investigated as a possible source of reinfection and treated if appropriate. Secondary lactose intolerance should also be considered. If symptoms persist in travellers to Asia, specialist advice should be sought, given that there is an increasing incidence of treatment failure in this population [117]. Some studies in countries where G. lamblia is endemic have shown a decline in incidence of giardiasis with the use of cART [118]. Entamoeba histolytica is a protozoan parasite that causes infection following ingestion of cysts in contaminated human faeces. Sexual transmission also occurs, including in PLWH; among the latter, entamoeba infection is most commonly seen in MSM [119]. Following ingestion, E. histolytica trophozoites adhere to colonic epithelial cells. Invasion through the mucosa and into the submucosal tissue results in amoebic colitis. Occasionally haematogenous spread occurs once the trophozoites have breached the colonic mucosa resulting in extra-intestinal disease, most commonly amoebic liver abscess. E. histolytica infection can be asymptomatic and resolve without intervention, although up to 10% of those with asymptomatic infection will develop disease within a year [120]. Fever, abdominal pain and either watery or bloody diarrhoea are the most common symptoms of amoebic colitis. It occurs in PLWH with a range of CD4 counts and is not limited to those with advanced immunosuppression. Liver abscess can present with fever, right upper quadrant pain and tenderness, usually over a number of days although a chronic presentation with fever and anorexia may also be seen [121]. At least three stool samples should be examined for cysts and trophozoites. However the cysts of E. histolytica cannot be differentiated from non-pathogenic E. dispar by microscopy and diagnosis is difficult unless erythrophagocytosis (ingestion of red blood cells) by motile trophozoites is seen. Antigen-based enzyme-linked immunosorbent assays may also be used but PCR is the method of choice in the UK for the diagnosis of both symptomatic and asymptomatic infection [122]. Serology remains positive for years after exposure but can be valuable in the diagnosis of extra-intestinal lesions when combined with imaging. Metronidazole 800 mg tds po for 5–10 days is the regimen of choice for treating amoebic colitis and amoebic liver abscess. Tinidazole 2 g od po for 3 days is an alternative treatment option. Metronidazole and tinidazole are relatively ineffective against E. histolytic cysts within the gut, therefore patients should receive paromomycin 25–35 mg/kg/day in three divided doses for 5–10 days or diloxanide furoate 500 mg tds po for 10 days following treatment with metronidazole to eliminate luminal infection. Cyclospora cayetanensis is an intestinal coccidian protozoan parasite of the small bowel. It is a cause of watery diarrhoea throughout the tropics and sub-tropics and in returning travellers. In PLWH, diarrhoea may be prolonged and biliary involvement has also been reported [123, 124]. Diagnosis is made by the microscopic detection of oocysts in stool specimens. A wet preparation and concentration technique should be used followed by examination under ultraviolet light for parasite autofluorescence or confirmed using modified Ziehl-Neelsen staining and accurate measurement. PCR can aid in diagnosis and specimens should be referred to the Public Health England National Reference Laboratory, Hospital for Tropical Diseases, for confirmation and typing [125]. The clinical and parasitological response to co-trimoxazole 960 mg bd is rapid and 7 days of treatment is usually sufficient [126]. Relapse is common and secondary prophylaxis with co-trimoxazole 960 mg three times a week may be needed while cART is commenced. Cystoisospora belli (formerly known as Isospora belli) has no known animal host but is widespread geographically and causes self-limiting diarrhoea in HIV-seronegative individuals. In PLWH it can cause chronic diarrhoea and is an occasional cause of biliary disease. It is diagnosed by identification of oocysts in stool specimens using microscopy with modified Ziehl-Neelsen staining [127]. The traditional treatment has been co-trimoxazole 960 mg four times daily po for 10 days although 960 mg bd also appears to be effective [126]. Secondary prophylaxis with co-trimoxazole 960 mg three times a week is essential as relapse is common. Ciprofloxacin is a less effective alternative for both treatment and prophylaxis [128]. Strongyloides stercoralis is a gut nematode that causes chronic GI and skin disorders due to its autoinfective lifecycle and can disseminate to cause life-threatening hyperinfection syndromes in immunosuppressed individuals [129-132]. Despite anecdotal reports, there is no conclusive evidence that infection or hyperinfection is more common in PLWH, although it may be implicated in immune reconstitution syndrome [133]. Corticosteroid use appears to be a causative factor in case reports of hyperinfection syndrome in PLWH [134]. Eosinophilia is common and infection is diagnosed by identification of larvae in stool specimens following culture. Serology may also be useful although there may be cross-reaction with other parasitic nematode infections. Discussion with a specialist is recommended prior to treatment of suspected strongyloidiasis due to the potential for complications if alternative nematode infections are present. First-line treatment of choice is ivermectin 200 μg/kg od po for 1 or 2 days, which is more effective than the alternative treatment of albendazole 400 mg bd po for 3 days [135]. Caution should be taken in treating with ivermectin when infection is diagnosed by serology, as cross-reaction with filaria is possible, with the risk of encephalopathy. Examination of stool samples should be repeated at 2–4 weeks to confirm clearance of infection with a further course of ivermectin if there is any concern of residual infection. Hyperinfection requires the course of ivermectin to be continued for at least 14 days, with the Centers for Disease Control and Prevention recommending continuation for 2 weeks after negative stool and/or sputum examination results [136]. Serology and stool examination should be repeated at intervals of 6–12 months over the first 2 years after treatment, as autoinfective migrating larvae may not be eradicated by initial treatment. Schistosomiasis is a chronic inflammatory disease caused by a parasitic blood fluke. There are three main species that cause human disease: Schistosoma haematobium, found throughout Africa, parts of the Middle East and Mauritius, S. mansoni, found in Africa, parts of South America and the Caribbean, and S. japonicum, found in China and parts of South East Asia. Infection occurs following contact with contaminated freshwater bodies. Some people experience a short, self-limiting febrile illness 3–8 weeks following initial infection; many with chronic schistosomiasis are asymptomatic. Those with heavy or repeated infection can experience disease as a consequence of inflammation triggered by eggs produced by the adult worms. S. mansoni, S. japonicum and occasionally S. haematobium occupy the lower mesenteric veins resulting in intestinal or hepatosplenic disease, whereas S. haematobium usually inhabits the venous plexus resulting in urogenital disease. Infection with schistosomiasis is not believed to occur more frequently in PLWH although urogenital schistosomiasis is thought to increase HIV acquisition in women. Accelerated progression of HIV has also been observed in those co-infected with schistosomiasis [137, 138]. Examination of the faeces and urine for eggs is the primary method for diagnosis. Serology can be useful in those with potential exposure who have not previously been treated. However, serology cannot distinguish between past or current infection and has a window period of 8–12 weeks following exposure before a test may be positive. Schistosomiasis can be effectively treated with praziquantel, with dosing determined by species. Candidiasis, histoplasmosis, cryptococcosis, aspergillosis, paracoccidioidomycosis, pneumocystis and talaromycosis (formerly penicilliosis) have been reported as rare causes of lower GI tract infection in PLWH. These mycoses have usually been described in PLWH with low CD4 counts and as disseminated infections. Diagnosis may be established using specific tests such as blood culture or antigen tests, however colonoscopic biopsy may be necessary to establish the diagnosis. Treatment for these mycoses is described in other chapters of the BHIVA opportunistic infection guidelines. The writing group thanks the BHIVA Guidelines Subcommittee for review of the guidelines and helpful comments: N Gupta (Chair), C van Halsema (Vice-Chair), A Bailey, T Barber, D Churchill, Y Gilleece, A Grant, S Khoo, A Maxwell, S Parry, A Pozniak, M Rattue, I Reeves, H Taha, J Thornhill, L Waters, A Winston. The PubMed, Medline, Embase and Cochrane Library databases were searched using the following terms: (HIV OR AIDS) AND (diarrh* OR gastroenteritis OR gastrointestinal disease OR loose stool* OR oropharyng* OR (o)esophag*) (HIV OR AIDS) AND (diarrh* OR gastroenteritis OR gastrointestinal disease OR loose stool* OR oropharyng* OR (o)esophag*) AND (CMV OR cytomegalovirus OR CMV colitis OR human herpesvirus 5 or herpes simplex virus) (HIV OR AIDS) AND (diarrh* OR gastroenteritis OR gastrointestinal disease OR loose stool* OR oropharyng* OR (o)esophag*) AND (campylobacter OR clostridium difficile OR C. difficile OR Escherichia coli OR E coli OR salmonella OR shigella OR candida OR candidiasis OR cryptosporidi* OR microsporidi* OR giardia* OR am(o)ebiasis OR isosporiasis or cystoisospor* or strongyloid* or schistosom* or bilharzia) The literature searches were based on the following PICO questions: What is the best method for diagnosing oropharyngeal candidiasis? When should endoscopy be considered in PLWH with oesophageal disease? What are the best diagnostic tests for CMV and HSV infection in PLWH? Which is the best treatment for CMV oesophagitis or colitis in PLWH? What is the best treatment for oropharyngeal or oesophageal HSV infection? What are the clinical presentations of CMV infection in PLWH? Which virological method is used to diagnose GI infection secondary to CMV infection in PLWH? Is CMV prophylaxis beneficial in PLWH with CD4 counts <100 cells/mm3? What is the best treatment for CMV colitis in PLWH? What is the best treatment for ganciclovir-resistant CMV colitis in PLWH? How does cryptosporidiosis present in PLWH? What is the best diagnostic test for cryptosporidiosis in PLWH? How should cryptosporidiosis be treated in PLWH? How does microsporidiosis present in PLWH? What is the best diagnostic test for microsporidiosis in PLWH? How should microsporidiosis be treated in PLWH? How does Giardia infection present in PLWH? How should Giardia infection be treated in PLWH? Is Giardia infection seen more commonly in PLWH? How does amoebiasis present in PLWH? What is the best diagnostic test for amoebiasis in PLWH? How should amoebiasis be treated in PLWH? How does isosporiasis present in PLWH? How should isosporiasis be diagnosed in PLWH? How should isosporiasis be treated in PLWH? Is HIV a cause of hyperinfection in strongyloidiasis? What is the best diagnostic test for strongyloidiasis in PLWH? How should strongyloidiasis be treated in PLWH? Is schistosomiasis more common in PLWH? What is the best diagnostic test for schistosomiasis? How should schistosomiasis be treated? What causes diarrhoea in PLWH? Which bacteria cause diarrhoea in PLWH? Which viruses cause diarrhoea in PLWH? How does C. difficile infection present in PLWH? What are the risk factors for C. difficile infection in PLWH? How is C. difficile infection treated in PLWH? How does Campylobacter infection present in PLWH? What are the risk factors for Campylobacter infection in PLWH? How is Campylobacter infection treated in PLWH? How does E. coli infection present in PLWH? What are the risk factors for E. coli infection in PLWH? How is E. coli infection treated in PLWH? How does Salmonella infection present in PLWH? What are the risk factors for Salmonella infection in PLWH? How is Salmonella infection treated in PLWH? How does Shigella infection present in PLWH? What are the risk factors for Shigella infection in PLWH? How is Shigella infection treated in PLWH? How does viral gastroenteritis present in PLWH? What are the risk factors for viral gastroenteritis in PLWH? How is viral gastroenteritis treated in PLWH?" @default.
W3109911042 created "2020-12-07" @default.
W3109911042 creator A5009149558 @default.
W3109911042 creator A5017998192 @default.
W3109911042 creator A5072739448 @default.
W3109911042 creator A5073128317 @default.
W3109911042 creator A5086514781 @default.
W3109911042 date "2020-12-01" @default.
W3109911042 modified "2023-09-26" @default.
W3109911042 title "British HIV Association guidelines on the management of opportunistic infection in people living with HIV: the clinical management of gastrointestinal opportunistic infections 2020" @default.
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