Giardiasis: Epidemiology, clinical manifestations, and diagnosis

INTRODUCTION — 

Giardia duodenalis (also known as G. lamblia or G. intestinalis) is a protozoan parasite capable of causing sporadic or epidemic diarrheal illness. Giardiasis is an important cause of waterborne and foodborne disease, daycare center outbreaks, and illness in international travelers.

The epidemiology, microbiology, pathogenesis, clinical manifestations, and diagnosis of giardiasis will be reviewed here. The treatment and prevention of giardiasis are discussed separately. (See "Giardiasis: Treatment and prevention".)

EPIDEMIOLOGY

Risk factors — G. duodenalis infection occurs worldwide [1]. High-risk groups include infants, young children, international adoptees, travelers [2,3], immunocompromised individuals, and patients with cystic fibrosis [4].

One case-control study in the United States identified the following risk factors for sporadic giardiasis: male-male sexual behavior (aOR 45.7), international travel (adjusted odds ratio [aOR] 13.9), drinking water from a river, lake, stream, or spring (aOR 6.5), swimming in a natural body of water (aOR 3.3), contact with children in diapers (aOR 1.6), antibiotic use (aOR 2.5), and presence of a chronic gastrointestinal condition (aOR 1.8) [5].  

Incidence — Giardiasis is especially common in areas with poor sanitary conditions and limited water-treatment facilities. Children <10 years have higher rates of giardiasis than older individuals [6]. In some areas with poor sanitation, the prevalence of giardiasis has been reported to be as high as 20 to 40 percent; in such settings, the rate of infection is highest among children <5 years [1]. Worldwide, G. lamblia is a common agent of diarrheal disease in children <5 (after rotavirus and Cryptosporidium spp); >300 million cases are reported annually [7]. Peaks in cases are often observed during spring and summer months with warm, humid climatic conditions [8].

Giardiasis is a well-recognized cause of enteric disease among international travelers in the United States, Canada, and Europe [9-11]. In the United States in 2019, almost 15,000 cases were reported (approximately 6 cases per 100,000 population) [12,13]. In a study including 147 pediatric patients with acute nondysenteric diarrhea in the United States, giardiasis was the cause in 15 percent of cases, second only to rotavirus [14].

TRANSMISSION — 

Transmission of infectious Giardia cysts to humans often occur via three routes: waterborne, foodborne, or fecal-oral transmission [15]. In addition, soil, environmental contamination, and animal exposures can occasionally be sources of infection [16].

●Waterborne transmission – Water is a major source of giardiasis transmission. Giardia cysts survive readily in mountain streams because they can survive in cold water. Water-dwelling mammals, such as beavers, can become infected and may serve as ongoing sources of water contamination. For these reasons, giardiasis is an important cause of diarrheal illness among hikers in wilderness areas who drink water that has not been adequately filtered, treated, or boiled [17].

Deep well water, in contrast with surface well water, is usually safe because filtration of water through soil removes Giardia cysts.

Giardia cysts are resistant to chlorination; therefore, bacterial coliform counts are not a reliable measure of Giardia contamination in chlorinated water sources.

●Foodborne transmission – Foodborne transmission of giardiasis can occur via ingestion of raw or undercooked food (including raw vegetables, salad bars, and fresh fruit) contaminated with cysts and via food that is contaminated after cooking [18]. However, foodborne outbreaks have been difficult to document, likely because of limitations in detection methods [19].

●Person-to-person transmission – Person-to-person transmission can occur in settings in which there is fecal incontinence and poor hygiene, such as childcare centers [20]. The risk of acquisition and transmission is greatest for young children who are not yet toilet trained; such children can also serve as a source for secondary cases within households [21].

Giardiasis can also be transmitted via anal-oral sexual contact [22].

MICROBIOLOGY AND PATHOGENESIS

Microbiology — Species of the genus Giardia infect many hosts ranging from mammals to amphibians and birds [1]. Eight known Giardia species are restricted to nonhuman hosts and are not recognized as causes of human disease [23]. The ninth species, Giardia duodenalis, consists of at least eight genetic groups (or assemblages, genotypes A to H); two assemblages are found in both humans and animals (A and B), and the remaining six are rarely found in humans, instead occurring mainly in nonhuman hosts, including canines, felines, rodents, and seals (assemblages C to H).

Genotypes vary even within assemblages A and B, and it is likely that only some genotypic variants have potential to cause infection in humans. Because of this heterogeneity, the role of animals in the epidemiology of human infection remains poorly understood [1]. Beavers have been clearly implicated in transmission of waterborne infection to humans, although the roles of domestic dogs and cats as sources of human infection remain to be ascertained [24].

The relative roles of Giardia assemblages and the human host responses that contribute to asymptomatic and symptomatic infections have not been fully determined. Additionally, human infections often involve mixed subtypes [25]. Host factors likely influence the clinical presentation of giardiasis since different studies have shown that assemblage A and assemblage B strains lead to variable levels of symptomatic infections [26-28].

Life cycle — Giardia species have two morphological forms: cysts and trophozoites. Cysts are the infectious form of the parasite; they are excreted in stool and can survive in moist environments for prolonged periods (figure 1). Cysts are immediately infectious upon excretion in feces [13], and ingestion of 10 cysts is thought to be sufficient to cause symptomatic giardiasis [18,29]. Following cyst ingestion, excystation occurs in the proximal small bowel with release of trophozoites.

Trophozoites are pear-shaped, binucleate, multi-flagellated parasite forms capable of division by binary fission: they localize principally to the proximal small bowel. An adhesive disk on the ventral surface of the trophozoite facilitates trophozoite attachment to the mucosal surface of the duodenum and jejunum, although the trophozoite does not invade the mucosal epithelium. Trophozoites that do not adhere to the small bowel move forward to the large intestine, where they revert to the infectious cyst form; conjugated bile salts appear to foster encystation. Cysts are passed back into the environment in excreted stool; in the setting of diarrhea, trophozoites can also be found in the stool.

Pathogenesis — Giardia is a noninvasive parasite, and the pathogenesis of symptoms that can occur in giardiasis (including acute diarrhea and longstanding malabsorption) is not fully understood. Trophozoites can attach to epithelial cells lining the intestinal tract (most commonly the proximal small intestine), leading to structural and functional abnormalities. Light microscopy may demonstrate no abnormalities, mild or moderate partial villous atrophy, or subtotal villous atrophy in severe cases. An increase in crypt depth may be seen, and microvilli shortening or disruption may occur. Intestinal epithelial tight junctions may be disrupted leading to increased permeability and altered epithelial cell survival. Consequent deficiencies in small bowel epithelial brush border enzymes, including disaccharidases such as lactase, may develop. Such local epithelial enzyme deficiencies likely contribute to symptoms such as malabsorption seen in acute and chronic giardiasis and are slow to recover even with effective treatment of the infection. Loss of intestinal barrier function and disruption of the commensal intestinal microbiota in the setting of infection are also thought to contribute to symptoms [19,30]. In addition to affecting the composition of the intestinal microbiota, Giardia may also lead to a metabolic shift among the intestinal microbial community, thereby impacting on the virulence of other microbes [31].

Infection with Giardia may also promote colonization or infection by other enteric pathogens [32].

Host immunity — Chronic exposure to G. duodenalis may induce partial immunity; travelers to areas with poor sanitation have higher rates of symptomatic disease than long-term residents [33]. Nevertheless, reinfections among long-term residents can be frequent, so any acquired immunity appears to be limited.

Humoral immunity appears to be important for host defense against giardiasis. Secretory immunoglobulin (Ig)A antibodies are an important humoral response to infection, since trophozoites are localized to the intestinal lumen. Patients with cystic fibrosis or immunoglobulin deficiencies (such as common variable immunodeficiency or X-linked agammaglobulinemia) tend to have more severe disease, perhaps because of deficiencies in secretory IgA and cell-mediated immunity [34].

Non-antibody host responses are also increasingly recognized as contributing to the host response to Giardia infections, in particular interleukin 17, although a range of cytokines are likely involved [31].

Patients with HIV infection have impaired immune response to the parasite but do not seem to develop more severe disease [35]. Asymptomatic infections occur in the presence of HIV, although with progressive immunosuppression, the risk of symptomatic infection increases [36,37].

CLINICAL MANIFESTATIONS

Spectrum of infection — The severity of clinical manifestations associated with giardiasis is variable. In general, about 50 percent of exposed individuals clear the infection in the absence of clinical symptoms, approximately 15 percent of individuals shed cysts asymptomatically, and the remaining 35 percent of individuals have symptomatic infection [15,38]. The nature of clinical manifestations in an individual likely depends on a number of factors including the virulence of the isolate, the parasite load, and the host immune response.

Asymptomatic infection — Asymptomatic infection occurs in both children and adults, and asymptomatic cyst shedding can last six months or more [39,40]. Many individuals with Giardia in stool samples are asymptomatic; in some studies, Giardia has been observed more frequently in the stool of asymptomatic individuals than among individuals with acute diarrhea [41].

It has been observed that in settings with poor sanitation, most children will have encountered Giardia by age two years without it being associated with diarrhea, although infected children may present with impaired growth and development later on [42,43].

Acute giardiasis — Symptoms usually develop after an incubation period of 7 to 14 days. Onset of acute gastrointestinal symptoms within less than a week of exposure is not likely attributable to infection with Giardia. When acute symptoms occur, they generally last one to four weeks.

Symptoms of acute giardiasis include [15]:

●Diarrhea (90 percent)

●Malaise (86 percent)

●Foul-smelling and fatty stools (steatorrhea; 75 percent)

●Flatulence (75 percent)

●Abdominal cramps and bloating (71 percent)

●Nausea (69 percent)

●Weight loss (66 percent)

●Vomiting (23 percent)

●Fever (15 percent)

●Constipation (13 percent)

●Urticaria (10 percent)

Chronic giardiasis — Chronic giardiasis may follow the acute phase of illness or may develop in the absence of an antecedent symptomatic acute illness. Among symptomatic individuals, chronic symptoms can develop in up to half of symptomatic individuals that are not promptly treated after acquiring the infection [44].

Symptoms of chronic giardiasis may include:

●Loose stools but usually not diarrhea

●Steatorrhea

●Profound weight loss (10 to 20 percent of body weight)

●Malabsorption

●Stunted growth

●Malaise

●Fatigue

●Depression

●Abdominal cramping

●Borborygmi

●Flatulence

●Burping

The manifestations may wax and wane over many months. Some patients may have persistent infection after initial treatment, which may be associated with development of malabsorption and weight loss [45]. Even in cases of otherwise asymptomatic infection, malabsorption of fats, sugars, carbohydrates, and vitamins may occur. This can lead to hypoalbuminemia and deficiencies of vitamin A, B12, and folate.

Acquired lactose intolerance occurs in up to 40 percent of patients; clinically, this manifests with exacerbation in intestinal symptoms following ingestion of dairy products. Recovery can take many weeks, even after clearance of the parasite [46,47].

Complications — Complications from giardiasis are common and include growth impairment in children, hypersensitivity phenomena, irritable bowel syndrome, chronic fatigue, and biliary complications.

●Growth impairment – In children, chronic giardiasis may affect growth and development [42,48-50]. A study among Colombian children suggested that giardiasis was a strong predictor of stunted growth [49]. A longitudinal study including 597 children in Brazil found that growth was impeded among children with giardiasis, even among those with asymptomatic infection [50]. Likewise, in Bangladesh, a prospective longitudinal birth cohort study found decreased growth measures among children with giardiasis, even those without diarrhea [42].

●Hypersensitivity phenomena – Hypersensitivity phenomena such as rash, urticaria, aphthous ulceration, and reactive arthritis or synovitis have been described in the setting of giardiasis, although these manifestations are rare [44,51,52].

●Chronic irritable bowel syndrome – Irritable bowel syndrome and chronic fatigue appear to be common following acute (even asymptomatic) infection. As an example, following a large waterborne epidemic of giardiasis in Norway, a cohort study including more than 800 individuals exposed to Giardia noted that the prevalence of irritable bowel syndrome (39 percent) and chronic fatigue (31 percent) were significantly increased six years after exposure (relative to unexposed controls) [53]. Although the frequency of these symptoms declined with time after the initial exposure, at 10 years, those who had developed Giardia infection still had a lower Quality of Life score [54]. Another study in the United States noted individuals diagnosed with giardiasis were more likely to have a subsequent diagnosis of irritable bowel syndrome [55]. Ongoing symptoms of diarrhea and abdominal cramping in the presence of a negative Giardia stool test should prompt suspicion for post-infectious IBS.  

●Biliary and pancreatic complications – Rarely, Giardia can spread from the duodenum to the biliary and pancreatic ducts, leading to cholecystitis, cholangitis, or granulomatous hepatitis as manifestations of chronic giardiasis [56]. Impaired exocrine pancreatic function with diminished secretion of trypsin and lipase has also been described.

Laboratory and radiographic findings — In general, patients with giardiasis do not have peripheral leukocytosis or eosinophilia. Leukocytes in stool specimens are usually absent as well. Fecal fat excretion and other laboratory tests of malabsorption may be abnormal. Upper gastrointestinal series are usually normal but may demonstrate mucosal edema in some cases.

DIAGNOSIS

When to suspect giardiasis — Many cases of giardiasis will present as acute giardiasis. However, it is important to consider chronic giardiasis in certain patients as well.

●Acute giardiasis – Acute giardiasis should be suspected in a patient presenting with foul-smelling and fatty stool diarrhea accompanied by flatulence and abdominal cramping or pain, especially if associated with a recent (>1 week prior to onset of symptoms) presence of an epidemiologic risk factor (eg, residing in or travelling to an area with poor sanitation, hiking in the mountains).  

●Chronic giardiasis – Chronic giardiasis should be suspected in patients presenting with any of the following symptoms, even if there is no apparent history of acute giardiasis or risk factors for Giardia exposure:

•Growth impairment in children

•Evidence of malabsorption or vitamin deficiencies

•Profound weight loss (10 to 20 percent of body weight)

•Presence of loose stools, steatorrhea, abdominal cramping, and flatulence

Approach to diagnosis — The diagnosis of acute and chronic giardiasis should be made via stool microscopy or by sending a Giardia spp PCR or antigen detection assay. If stool microscopy is performed, direct fluorescent antibody (DFA) test can be performed to help visualize Giardia (and Cryptosporidium) cysts under a fluorescent microscope. Ideally, three separate stool specimens should be submitted to optimize the likelihood of visualizing the cysts and/or trophozoites on microscopy, particularly if fluorescent antibody testing is not available. PCR and antigen assays have the advantages of higher sensitivity, however may not be available in resource-limited settings [57].

Detection of Giardia spp on PCR or antigen assays or visualization of Giardia cysts and/or trophozoites on stool microscopy (picture 1 and picture 2 and picture 3) confirms the presence of giardiasis, although particularly if a highly-sensitive multiplex PCR assay is used and multiple pathogens are detected, it may not be the cause of symptoms. Additionally, in patients who have recently been treated for giardiasis, antigen and PCR assays may remain positive for weeks even after treatment due to detection of killed parasites.

Diagnostic tests — Diagnostic tests for giardiasis include antigen detection assays, PCR assays, and stool microscopy [58].

●Antigen detection assays — Antigen detection assays are a preferred diagnostic modality for detection of Giardia spp in stool. Many immunoassays using antibodies against cyst or trophozoite antigens have been developed for stool analysis. Available kits include direct immunofluorescent assays (DFAs) that use fluorescein-tagged monoclonal antibodies, immunochromatographic assays, and enzyme-linked immunosorbent assays (ELISAs). In general, these methods have greater sensitivity and faster turn-around time than conventional stool microscopy methods. Specificity and cost are usually relatively comparable. Many of the commercially available assays can detect both Giardia and Cryptosporidium simultaneously.

One study of 325 stool specimens demonstrated that an ELISA against a specific Giardia antigen (antigen 65) detected 30 percent more cases of Giardia than stool microscopy [59]. Another study that compared stool microscopy, DFA, and three immunodiagnostic techniques for diagnosis of Giardia found that there was agreement among the methods in 76 percent of cases and that immunologic methods detected more positive results than stool microscopy in 12 percent of cases [60].

Antigen detection assays are both sensitive and specific. A systematic review reported the pooled estimate for sensitivity to be 92 percent and for specificity to be 97 percent [61]. In a study of stool samples from patients with abdominal symptoms using different assays for detection of Giardia, the sensitivities obtained by Ridascreen Giardia, Rida Quick Giardia, Rida Quick Combi, and Giardia-Strip were 82, 80, 80, and 44 percent, respectively. The specificity of all tests was ≥98 percent [62]. In another study, the Ridascreen Giardia ELISA was reported to be 100 percent sensitive and 91.5 percent specific, including in children [63]. Test results vary in different geographic regions, likely due to differences in assemblages. (See 'Microbiology' above.)

Immunoassays are of limited use following treatment of infection. Loss of detectable stool antigens is suggestive of effective treatment, but continued stool antigen shedding could reflect shedding of killed parasites.

●Polymerase chain reaction assays — Polymerase chain reaction (PCR) assays are a preferred diagnostic modality for detection of Giardia spp in stool because it is the most sensitive of all techniques [58,64,65]. Many PCR tests are now commercially available, often as part of a panel for organism detection in stool samples [66-69]. However, PCR is of limited use following treatment of infection as residual detection might represent killed or non-viable parasites [65].

PCR-based tools have also been applied to detect Giardia and other pathogens in water and food supplies [70].

Whole-genome sequencing is also emerging as an increasingly used tool for the identification of novel genotypes, mixed infections, and in the setting of outbreak investigations [71].

●Stool microscopy — Giardia cysts are oval in shape, 8 to 12 microns in length, and contain four nuclei. Trophozoites contain two nuclei and have four pairs of flagellae and an adhesive disc for attachment to intestinal epithelial cells. Stool microscopy to detect Giardia is specific and may also be useful for detecting other potential parasitic causes of gastrointestinal symptoms. Limitations include intermittent excretion of Giardia cysts (necessitating up to three stool exams), cumbersome processing procedures, and technician expertise. Use of DFA testing for Giardia can increase the sensitivity of stool microscopy and obviate the need for three serial stool specimens.

Laboratory processing of stool samples consists of a saline suspension to look for trophozoites and cysts (picture 2) and a polyvinyl alcohol and/or formalin preparation for permanent staining. Loose, watery stool is more likely to be positive for trophozoites; a semiformed or formed stool will likely contain cysts only (picture 3 and picture 1).

After treatment, trophozoite and cyst shedding in stool can persist for up to three and six months, respectively [39,40].

In a study among 100 patients with chronic diarrhea, all patients were evaluated by stool microscopy and nested PCR; 30 patients also had upper gastrointestinal endoscopy and duodenal biopsy performed [72]. Among these patients, 48 percent had evidence of Giardia infection; stool microscopy detected 65 percent, stool PCR detected an additional 27 percent, and duodenal biopsy PCR detected an additional 8 percent of cases.

The choice of diagnostic method should be guided by the local availability of microscopy, antigen detection and/or PCR tests; individual laboratories often have their own algorithms for which test is used. The greater sensitivity of PCR and antigen detection assays compared with microscopy means that these tests are preferred to rule out giardiasis, but do not obviate the utility of microscopy which is also helpful to rule out other parasitic infections.

DIFFERENTIAL DIAGNOSIS — 

The differential diagnosis of giardiasis includes:

●Travelers' diarrhea caused by bacteria – Travelers' diarrhea can be caused by a range of pathogens, including enterotoxigenic Escherichia coli and Campylobacter spp; it consists of malaise, anorexia, and abdominal cramps followed by watery diarrhea in the setting of travel to an area with poor sanitation practices and limited access to safe drinking water. The diagnosis is usually established based on clinical history; the illness is generally self-limited. Onset of travelers' diarrhea is usually within days, whereas symptomatic giardiasis develops only after a week or more after infection. Additionally, evaluation for Giardia is warranted in the setting of delayed onset (at least one week following exposure) of upper gastrointestinal manifestations (such as bloating, gas, or nausea) and in the setting of persistent symptoms. (See "Travelers' diarrhea: Treatment and prevention".)

●Cryptosporidiosis – Cryptosporidium is similar to Giardia in that it can cause a diarrheal illness with associated malaise, nausea and anorexia, crampy abdominal pain, and low-grade fever. They may be distinguished via stool antigen testing, nucleic acid amplification/PCR testing, or stool microscopy. (See "Cryptosporidiosis: Epidemiology, clinical manifestations, and diagnosis".)

●Cyclosporiasis – Cyclosporiasis is similar to Giardia in that it can cause a diarrheal illness with associated watery diarrhea, flatulence, abdominal cramping, low grade fever, nausea, anorexia, and malaise/fatigue. They may be distinguished via nucleic acid amplification/PCR testing or stool microscopy. (See "Cyclospora infection", section on 'Diagnosis'.)

●Lactose intolerance – Clinical symptoms of lactose intolerance include diarrhea, abdominal pain, and flatulence after ingestion of milk or milk-containing products. The diagnosis is established by a lactose tolerance test. (See "Lactose intolerance and malabsorption: Clinical manifestations, diagnosis, and management", section on 'Diagnostic evaluation'.)

●Tropical sprue – Tropical sprue is a chronic diarrheal disease that occurs in the tropics and involves the small intestine; it is characterized by nutrient malabsorption. The diagnosis is established by upper endoscopy with biopsy of the small bowel. (See "Tropical sprue".)

●Crohn's ileitis – Crohn's disease is an inflammatory disease that may involve the entire gastrointestinal tract; most patients have small bowel involvement (usually the distal ileum); one-third have ileitis exclusively. The diagnosis is established by endoscopy with biopsy. (See "Clinical manifestations, diagnosis, and prognosis of Crohn disease in adults".)

●Dientamoeba fragilis – The clinical manifestations of Dientamoeba fragilis are similar to those of giardiasis and include abdominal pain, flatulence, and diarrhea. It may be associated with eosinophilia; the diagnosis is established by stool microscopy. (See "Dientamoeba fragilis".)

●Irritable bowel syndrome – Irritable bowel syndrome may present with a wide array of symptoms including chronic abdominal pain, diarrhea, and/or constipation and bloating. It is chronic in nature and the diagnosis is established based on diagnostic criteria (table 1). (See "Clinical manifestations and diagnosis of irritable bowel syndrome in adults".)

SOCIETY GUIDELINE LINKS — 

Links to society and government-sponsored guidelines from selected countries and regions around the world are provided separately. (See "Society guideline links: Acute diarrhea in adults".)

INFORMATION FOR PATIENTS — 

UpToDate offers two types of patient education materials, "The Basics" and "Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5^th to 6^th grade reading level, and they answer the four or five key questions a patient might have about a given condition. These articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written at the 10^th to 12^th grade reading level and are best for patients who want in-depth information and are comfortable with some medical jargon.

Here are the patient education articles that are relevant to this topic. We encourage you to print or email these topics to your patients. (You can also locate patient education articles on a variety of participants by searching on "patient info" and the keyword(s) of interest.)

●Beyond the Basics topic (see "Patient education: Giardia (Beyond the Basics)")

SUMMARY

●Epidemiology – G. duodenalis infection occurs worldwide. High-risk groups include infants, young children, international adoptees, travelers, immunocompromised individuals, and patients with cystic fibrosis. Giardiasis is especially common in areas with poor sanitary conditions and limited water-treatment facilities. (See 'Epidemiology' above.)

●Routes of transmission – Transmission of infectious Giardia cysts to humans may occur via three routes: waterborne (eg, hikers drinking unfiltered water from streams), foodborne (eg, raw/undercooked food contaminated with Giardia cysts), or fecal-oral transmission (eg, poor hygiene in setting of fecal incontinence). (See 'Transmission' above.)

●Clinical manifestations

•The severity of clinical manifestations associated with giardiasis is variable. In general, about half of exposed individuals clear the infection in the absence of clinical symptoms, approximately 15 percent of individuals shed cysts asymptomatically, and the remaining 35 to 45 percent of individuals have symptomatic infection. (See 'Spectrum of infection' above.)

•Symptoms of acute giardiasis include diarrhea, malaise, abdominal cramps, and weight loss. Symptoms of chronic giardiasis includes significant weight loss and malabsorption, impaired growth in children, and loose stools and steatorrhea. (See 'Acute giardiasis' above and 'Chronic giardiasis' above.)

●When to suspect giardiasis

•Acute giardiasis – Acute giardiasis should be suspected in a patient presenting with foul-smelling and fatty stool diarrhea accompanied by flatulence and abdominal cramping or pain, especially if associated with a recent (>1 week prior to onset of symptoms) presence of an epidemiologic risk factor (eg, residing in or travelling to an area with poor sanitation, hiking in the mountains). (See 'When to suspect giardiasis' above.)

•Chronic giardiasis – Chronic giardiasis should be suspected in patients presenting with any of the following symptoms, even if there is no apparent history of acute giardiasis or risk factors for Giardia exposure (See 'When to suspect giardiasis' above.):

-Growth impairment in children

-Evidence of malabsorption or vitamin deficiencies

-Profound weight loss (10 to 20 percent of body weight)

-Presence of loose stools, steatorrhea, abdominal cramping, and flatulence

●Approach to diagnosis – The diagnosis of acute and chronic giardiasis should be made via stool microscopy or by sending a Giardia spp PCR or antigen detection assay. If available, antigen detection assay or PCR are preferred due to their higher sensitivity and faster turn-around time compared with stool microscopy.

If stool microscopy is performed, DFA test can be performed to increase sensitivity. If DFA test is not available, three separate stool specimens must be submitted to optimize the likelihood of visualizing the cysts and/or trophozoites (picture 1 and picture 2 and picture 3).

In patients who have recently been treated for giardiasis, antigen and PCR assays may remain positive for weeks even after treatment due to detection of killed parasites. (See 'Approach to diagnosis' above.)