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Clin Microbiol Rev. Jan 2001; 14(1): 114–128.
PMCID: PMC88965

Treatment of Giardiasis

Abstract

Giardia lamblia is both the most common intestinal parasite in the United States and a frequent cause of diarrheal illness throughout the world. In spite of its recognition as an important human pathogen, there have been relatively few agents used in therapy. This paper discusses each class of drugs used in treatment, along with their mechanism of action, in vitro and clinical efficacy, and side effects and contraindications. Recommendations are made for the preferred treatment in different clinical situations. The greatest clinical experience is with the nitroimidazole drugs, i.e., metronidazole, tinidazole, and ornidazole, which are highly effective. A 5- to 7-day course of metronidazole can be expected to cure over 90% of individuals, and a single dose of tinidazole or ornidazole will cure a similar number. Quinacrine, which is no longer produced in the United States, has excellent efficacy but may be poorly tolerated, especially in children. Furazolidone is an effective alternative but must be administered four times a day for 7 to 10 days. Paromomycin may be used during early pregnancy, because it is not systematically absorbed, but it is not always effective. Patients who have resistant infection can usually be cured by a prolonged course of treatment with a combination of a nitroimidazole with quinacrine.

Giardia lamblia, also called Giardia duodenalis or Giardia intestinalis, is a protozoan parasite of the small intestine that causes extensive morbidity worldwide. It was first described in the late 17th century by the Dutch microscopist Antonie van Leeuwenhoek 62, and research into its epidemiology, pathogenesis, and treatment has intensified since G. lamblia waterborne outbreaks were reported in Europe and the United States during the 1960s and 1970s 53, 81, 123, 128, 174. Giardia infects approximately 2% of the adults and 6 to 8% of the children in developed countries worldwide and is currently responsible for the largest number of waterborne outbreaks of diarrhea in the United States 54, 139.

Despite the recognition of G. lamblia clinical illness for the last 40 years, the nearly 5,000 people hospitalized with giardiasis annually in the United States 149, and the millions infected worldwide, there have been few reviews of therapy for this infection and no definitive treatment protocols have been published 58, 113, 150, 165, 261. In addition, only a handful of agents have been used in therapy, and the agents which are available may have adverse effects or be contraindicated in certain clinical situations. Also, resistance may play a role in some infections. This paper will review the agents currently used for the treatment of giardiasis. The history, mechanism of action, in vitro and clinical studies, and adverse effects are detailed for each drug class. In addition, special clinical situations are discussed and recommendations for therapy are made.

BACKGROUND

The life cycle of G. lamblia has two forms: the trophozoite (Fig. (Fig.1)1) and the cyst. The cyst is the infectious form and is ingested in contaminated water or food or directly from fecal-oral contact. As few as 10 cysts may establish infection 206. After ingestion, excystation occurs. Excystation is thought to be initiated by contact with acidic gastric contents, followed by a highly coordinated sequence of events leading to the release of one or two trophozoites 27, 109, 210. A parasite-derived protease may be activated during the excystation process 252. The trophozoite infects the duodenum and upper intestine, which have a favorable alkaline pH, and gives rise to the clinical sequelae. As trophozoites pass through the small intestine to the colon, encystation occurs. Encystation can be initiated in vitro by culture of parasites in a reduced concentration of bile salts and cholesterol followed by culture in an increased concentration of bile at an alkaline pH 156. Cyst wall proteins are then transcribed, secreted into encystment-specific vesicles, and transported to the newly forming cell wall over 14 to 16 h 75.

FIG. 1
Ventral surface of a Giardia lamblia trophozoite imaged by scanning electron microscopy. It demonstrates the disk and flagella. A second trophozoite is seen behind it. Magnification, ×8,100. Photo courtesy of David Dorward, Rocky Mountain Laboratory, ...

The wide variety of clinical presentations, from severe disease to an asymptomatic carrier state, makes the definitive determination of pathogenesis difficult. However, several theories have been put forward 83, 115. Some of the most likely include the ability of the protozoan to cause direct damage to the intestinal mucosa via adherence with the disk, disaccharidase enzyme reduction following brush border damage, the release from Giardia of cytopathic substances such as thiol proteinases and lectins, and the stimulation of a host immune response with release of cytokines and mucosal inflammation 41, 48, 61, 78, 83, 106, 110, 157, 259. Additionally, it is likely that there are genetic differences between Giardia isolates which may confer virulence 115, 173, 182, 190. The surface of Giardia may also undergo antigenic variation in the human host and thus evade immune detection 181. Given these multiple potential mechanisms, a multifactoral process is likely.

G. lamblia is found primarily in mammals including humans, cats, dogs, beavers, and cattle 40, 74, 77, 257. Transmission of the G. lamblia cyst to humans occurs most commonly following ingestion of contaminated water 139. Transmission via surface water is facilitated by the relative resistance of the cyst to chlorination and its ability to survive in cold water for weeks 59, 122. Transmission by food 22, 152, 187, by direct fecal-oral contact among children in day care 28, 224, 237 or in developing-world settings 96, 159, and by sexual practices which include oral-anal contact 168 represent other common modes of transmission 113. G. lamblia is also seen as a cause of prolonged diarrhea in travelers 37, 66, 125, 136, 205; N. Fiumara, Letter, N. Engl. J. Med. 288:1410–1411, 1973).

Worldwide, the majority of patients infected with G. lamblia are asymptomatic. However, typical clinical symptoms of giardiasis usually begin 1 to 3 weeks after ingestion of cysts and are marked by diarrhea, malaise, flatulence, greasy stools, and abdominal cramps 113, 256. Other symptoms commonly include bloating, weight loss 174, and anorexia. Vomiting and fever are less common, and blood- or mucus-tinged feces are rare. Illness can last several months if untreated and can be characterized by continued exacerbations of diarrheal symptoms. With chronic illness, malabsorption of fat, lactose, vitamin A, and vitamin B12 are reported, and failure of children to thrive has been noted 86, 112, 149, 184, 227.

Giardiasis should be considered in the differential diagnosis of many diarrheal syndromes. A careful history, which notes any risk factors such as recent travel, wilderness exposure, or situations involving poor fecal-oral hygiene, and a physical examination are essential. Infection with G. lamblia can often be distinguished from bacterial and viral infections because of the longer duration of illness, 7 to 10 days by the time of presentation, and the presence of weight loss 113. Parasitic diarrhea with Cryptosporidium or Cyclospora can have similar features in the immunologically normal host and would need to be distinguished by specific diagnostic testing 50, 99.

Several methods exist for detection of the parasite. Demonstration of trophozoites or cysts in the stool, called the ova and parasite (O&P) examination, is the traditional means of diagnosis 167. One stool sample will allow the detection of 60 to 80% of infections, 2 stool samples will allow the detection of 80 to 90%, and three stool samples will allow the detection of over 90% 97, 111. However, in some instances, because of intermittent or low levels of shedding, it is necessary to examine more than three stool samples. The desire for more sensitive and specific, as well as faster and reproducible, diagnostic testing has led to the development of immunoassays. Fecal antigen detection using enzyme-linked immunosorbent assays, nonenzymatic immunoassays, or fluorescein-tagged monoclonal antibodies can be superior diagnostic methods to the O&P examination 7, 89, 90, 161, 262. It is particularly helpful in assessing cure or in screening for Giardia infection. However, when other parasites are in the differential diagnosis, a stool sample for O&P examination should still be ordered. In the unusual patient for whom a diagnosis cannot be made by O&P examination of stool, endoscopy with duodenal fluid sampling and biopsy may be performed 82, 113, 185, 256. An instance in which this may be helpful is the human immunodeficiency virus-infected patient with diarrhea, whose illness has multiple potential etiologies. Culture and sensitivity testing is available only in research settings 120, 138. DNA probes have been generally limited to detection of parasites in water samples 134, 158, and serologic testing is most useful in epidemiologic surveys 118, 119, 170. Figure Figure22 outlines an approach to the diagnosis and management of suspected cases of giardiasis and is discussed further below (see “Recommendations”).

FIG. 2
Outline of the diagnosis and management of suspected cases of giardiasis.

THERAPY OF GIARDIASIS

When evaluating the clinical efficacy of agents used against Giardia, it is difficult to compare studies. They vary as to entry methodology (whether randomization was done and if treatment was blinded or open), population studied (children, adults, symptomatic and/or asymptomatic patients), outcome measures (clinical efficacy and/or stool negativity), and duration of follow-up. Nevertheless, conclusions may be drawn from the studies when viewed as a whole, and statements can be made about the relative efficacy of the agents.

Classes of Agents and Clinical Properties

Nitroimidazoles.

The nitroimidazoles class of agents used to treat G. lamblia infection includes metronidazole, tinidazole, ornidazole, and secnidazole. This class was discovered in 1955 and was found to be highly effective against several protozoan infections 240. Metronidazole [1-(β-hydroxyethyl)-2-methyl-5-nitroimidazole; Flagyl] was determined to be therapeutic against Trichomonas vaginalis and Entamoeba histolytica following its discovery in the late 1950s 67, and in 1962 Darbon et al. reported that it could be used to treat giardiasis 57. Since this discovery, metronidazole and other nitroimidazoles have been used by clinicians as the mainstay of therapy of giardiasis.

Of the nitroimidazoles, the mechanism of killing of Giardia by metronidazole has been the most thoroughly studied. Metronidazole utilizes the anaerobic metabolic pathways present in Giardia. The drug enters the trophozoite, and once it is within the cell, electron transport protein ferredoxins from the parasite donate electrons to the nitro group of the drug 223, 238, 244. The drug becomes “activated” by reduction of this nitro group 223, 238, 240, and a gradient favoring the intracellular transport of metronidazole is established by this reduction reaction. Reduced metronidazole serves as a terminal electron acceptor which binds covalently to DNA macromolecules 72, 177. This results in DNA damage in the form of loss of helical structure, impaired template function, and strand breakage, with subsequent trophozoite death 95. In addition to this effect, metronidazole inhibits trophozoite respiration 81, 189. The reductive activation of metronidazole may also lead to toxic radicals, which react with essential cellular components 244. Trophozoites within cysts may be less affected by nitroimidazoles, possibly because of poor penetration of drug through the cyst wall 236. Resistance to metronidazole has been induced in vitro 29. It correlates with decreased activity of parasite pyruvate:ferredoxin oxidoreductase, which is required for reductive activation of nitroimidazoles 239, 247.

Metronidazole is quickly and completely absorbed after oral administration and penetrates body tissues and secretions such as saliva, breast milk, semen, and vaginal secretions 240. The drug is metabolized mainly in the liver and is excreted in the urine 147.

In vitro assays for nitroimidazole drug susceptibility have been performed with G. lamblia since 1980 112. Using microscopic evaluation of parasite morphology and mobility, Jokipii and Jokipii first demonstrated that metronidazole and tinidazole were effective 129. Subsequently, morphology 13, 166, 175, growth inhibition 56, 69, 94, 116, 160, 225, [3H]thymidine incorporation 32, 117, 164, serum killing 114, vital-dye exclusion 114, 235, inhibition of adherence 21, 55, 79, 166, 192, metabolic 228, and colorimetric 133 assays have been employed to measure the in vitro response of the drug to many therapeutic agents. However, as indicated by the variety of assays used, there is no standard for in vitro testing, making it difficult to compare results and apply in vitro findings to the clinical setting.

Of the nitroimidazoles, tinidazole and metronidazole have consistently demonstrated the greatest in vitro activity; tinidazole possesses a slight advantage 30, 32, 55, 101. More highly substituted nitroimidazoles, such as miconazole, clotrimazole, itraconazole, and ketoconazole, were developed for their antifungal activity and are not effective agents against G. lamblia 55. Sensitivity to nitroimidazoles can vary depending on the stocks and clones of G. lamblia used in testing 29, 31, 79, 160.

In the United States, metronidazole is the only member of the nitroimidazole class available to treat giardiasis; it is also the most common drug used for treatment worldwide. In spite of its widespread and accepted use against Giardia, the U.S. Food and Drug Administration has never approved it for this indication. Clinical trials have employed dosing two and three times daily (usually 250 mg/dose) for 5 to 10 days and short-course (1 to 3 days), daily single-dose therapy (2.0 or 2.4 g/dose) 261. In the 5- to 10-day schedules the efficacy ranges from 60 to 100% in adult and pediatric patients, with a median efficacy in both groups of 92% (Table (Table1)1) 20, 49, 68, 91, 92, 100, 127, 132, 135, 150, 151, 191, 201, 202, 232, 256. In general, this schedule is well tolerated, with most side effects involving gastrointestinal upset and metallic taste (Table (Table2).2).

TABLE 1
Efficacy of anti-Giardia drugs in adult and pediatric infectiona
TABLE 2
Recommended dosing and adverse effects of anti-Giardia drugs

The single-dose, short-course treatments (one high dose given daily) were designed to improve compliance without sacrificing efficacy. They have been used in both adults and children. These regimens are generally less efficacious, particularly if only one dose of metronidazole is given. The efficacy of single-dose therapy ranges from 36 to 60% if the drug is given for 1 day 16, 93, 127, 130, 220, 229 and rises to 67 to 80% if the drug is given for 2 days (Table (Table1)1) 127, 130, 146; E. Green, D. M. Lynch, J. A. McFadzean, and I. M. Pugh, Letter, Br. Med. J. 2:411–412, 1974). Continuing single-dose treatment for 3 days increases efficacy to the range seen with lower-dose, longer-course therapies 229; Green et al., Letter). The high-dose regimens may also carry more side effects 127.

Children have been included in many of the trials of both long- and short-course therapy, with outcomes similar to those in adults and 80 to 100% efficacy (median, 94%) in the 5- to 10-day regimens 91, 100, 132, 135, 186, 201, 232; A. Rastegar-Lari and A. Salek-Moghaddam, Letter, J. Trop. Pediatr. 42:184–185, 1996). Although metronidazole does not come in a standard liquid form, a suspension can be prepared by thoroughly crushing metronidazole tablets, using a drop of glycerin as a lubricant, and suspending the mixture in Cherry Syrup NF 150.

The most common side effects of metronidazole treatment include headache, vertigo, nausea, and a metallic taste in the mouth (Table (Table2).2). Nausea occurs in 5 to 15% of patients given standard multiday courses 135, 151. In addition, pancreatitis, central nervous system toxicity at high doses 144, 212, and transient, reversible neutropenia have been attributed to metronidazole 147. Patients should be warned to avoid alcohol while taking metronidazole. The inhibition of aldehyde dehydrogenase by metronidazole can cause severe vomiting, flushing, headache, and gastrointestinal pain following alcohol ingestion.

Metronidazole is mutagenic in bacteria and carcinogenic in mice and rats at high doses over long periods 34, 153, 240, 251. However, mutagenicity has never been documented in humans, suggesting that the use of metronidazole is safe in this regard 23, 78, 98, 212. This may, however, mitigate against the short-course high-dose regimens in children.

The finding of therapeutic efficacy with metronidazole spurred investigators to develop and test other nitroimidazole derivatives. The other agents, tinidazole, ornidazole, and secnidazole, each have longer half-lives, making them suitable for single daily-dose therapies 217. One dose of tinidazole (Fasigyn) was successfully used in 1971 in a group of Swedish students who acquired giardiasis during a visit to Russia 11. This single, 2-g dose (or equivalent in children) has consistently proven to have a clinical efficacy of 80 to 100% with a median efficacy of 92% (Table (Table1)1) 16, 126, 130, 131, 146, 151, 193, 222, 229, 261; Z. Farid, N. A. El Masry, W. F. Miner, and A. Hassan, Letter, Lancet ii:721, 1974; T. Pettersson, Letter, Br. Med. J. 1:395, 1975) and is far superior to metronidazole when single-dose regimens are directly compared 93, 130, 229, 261. There is also improved compliance with this dosing schedule. The recommended dosing for pediatric populations is usually 50 mg/kg for a single dose (Table (Table2)2) 82, 193, 232, 256, and the drug is available in a liquid suspension.

Adverse effects reported with tinidazole are not as common as with metronidazole but do include bitter taste, vertigo, and gastrointestinal upset (Table (Table2)2) 130, 131; Pettersson, Letter). Tinidazole is not available in the United States, but travel health providers recommend that some travelers, particularly long-term travelers or overland trekkers in Asia, purchase the drug upon arrival at their country of destination and take it in the event of acquiring giardiasis 113.

Another nitroimidazole derivative which is also not available in the United States is ornidazole. There have been fewer studies with ornidazole, but it has excellent efficacy when given over several days and efficacy similar to tinidazole (92 to 100%) when given as a single dose 19, 131, 145, 220, 232, 261. Single-dose ornidazole (40 mg/kg) has also been given to children, with obvious benefits regarding compliance and cost 39, 186. In one study the drug was given intravenously and was associated with increased side effects, making the investigators reluctant to recommend routine use of this drug in children until large-scale studies of recurrence, carcinogenicity and side effects are completed 39.

Secnidazole, a long-acting 5-nitroimidazole derivative, has been used but is not available in the United States. Similar to tinidazole and ornidazole, secnidazole is usually given as a single dose. The most common regimen is 2 g in adults and 30 mg/kg in children 95. Clinical studies demonstrate efficacy rates of over 85% with the single dose in adults 49; R. Baqai, H. Qureshi, and S. J. Zuberi; Letter, J. Pak. Med. Assoc. 45:288, 1995), and in children, this dosing is as effective as a 7- to 10-day course of metronidazole 100; Rastegar-Lari and Salek-Moghaddam, Letter). The drug is rapidly and completely absorbed, has a half-life of 17 to 29 hours, and is metabolized via oxidation in the liver 95. Adverse effects have been reported, most notably gastrointestinal disturbance (nausea, anorexia, and abdominal pain) and dizziness, but usually do not require discontinuation of the drug.

Quinacrine.

Quinacrine (Atabrine) was first introduced as an antimalarial agent in 1930, following the work of Kikuth, and became the antimalarial of choice for allied troops in World War II because of its greater availability and better tolerance compared with quinine 240. After the war, it soon became an important agent against G. lamblia, with a clinical efficacy of 90% or more 20, 52, 105, 255. However, with a U.S. market limited to the treatment of Giardia, the use of quinacrine declined, and its production in the United States was discontinued in 1992, although it may still be obtained through alternative sources (Table (Table22).

The antiprotozoal mechanism of quinacrine is not fully elucidated. The drug intercalates readily with G. lamblia DNA, and it is this interaction which is thought to cause an inhibition of nucleic acid synthesis 240. The differing relative quinacrine uptake rate between human and G. lamblia cells may be responsible for the selective toxicity of the drug 236. In vitro, quinacrine reduces cyst viability and excystation rates 179, 189. Resistance has been induced in vitro, and in one study it was correlated with decreased uptake of the drug 246. Quinacrine is rapidly absorbed from the intestinal tract and is widely distributed in body tissues.

Although results differ, depending on the in vitro sensitivity testing assay used, metronidazole and furazolidone have been shown to be slightly more potent than quinacrine 30, 32, 55, 94. However, in other studies the in vitro efficacies of quinacrine and metronidazole are the same 21, 117, 164. Some of this difference may be related to the greater variation in sensitivity to quinacrine than to metronidazole or furazolidone between clones of Giardia 31.

Clinically, quinacrine is very effective, with studies establishing its efficacy over 5 to 10 days at about 95% (Table (Table1)1) 20, 135, 220, 255. Some researchers consider the drug to be the most efficacious of any of the anti-Giardia therapeutics 256. Dosing is usually 100 mg three times a day over 5 to 7 days for adults and 6 mg/kg/day in three divided doses over 5 to 7 days for children (Table (Table2)2) 150.

Side effects have precluded many clinicians from using quinacrine, particularly in children (Table (Table2).2). A bitter taste, along with vomiting, has been reported in up to 28% of study participants 20, 52, and led to a lower efficacy in children younger than 5 years 52, probably due to low compliance. Yellow/orange discoloration of the skin, sclerae, and urine affects 4 to 5% of those taking quinacrine, beginning about 1 week after starting treatment, and can last up to 4 months after discontinuation of therapy. Other common side effects include nausea, vomiting, headache, and dizziness 254. Drug-induced psychosis is uncommon, and exfoliative dermatitis and quinacrine-induced retinopathy are rare 82. Quinacrine can exacerbate psoriasis, and in glucose-6-phosphate dehydrogenase (G6PDH)-deficient individuals, it can precipitate hemolysis. It is contraindicated in pregnancy due to a possible link with spina bifida and renal agenesis. It has never been demonstrated to be carcinogenic, even though it has a mechanism of action of binding to DNA.

Furazolidone.

Furazolidone (Furoxone) is one of the thousands of nitrofuran compounds created since the class was discovered in the 1940s 143. It is effective against many bacteria including Klebsiella spp., Clostridium spp., Escherichia coli, Campylobacter spp., and Staphylococcus aureus. As early as the 1950s, furazolidone was being used in the treatment of giardiasis 253. It is approved for use in the United States and remains an important therapeutic agent worldwide. Of the common anti-Giardia therapeutics, it is the only one available in a liquid suspension in the United States; therefore, its use has been advocated in pediatric populations 150.

The mechanism of action of furazolidone against G. lamblia, like many of the antiparasitics, is not completely explained. The drug undergoes reductive activation in the G. lamblia trophozoite, but, unlike metronidazole, reduction possibly occurs via an NADH oxidase 38, 244. Its killing effect correlates with the toxicity of reduced products, which can damage important cellular components including DNA. Resistance to furazolidone may be correlated with decreased entry of drug 246 or with increased levels of thiol-cycling enzymes, which can defend against toxic radicals 249. The drug is readily absorbed via the gastrointestinal tract and is metabolized rapidly in tissues, leading to low concentrations in serum and urine 143.

In in vitro susceptibility testing, furazolidone performs comparably to metronidazole and has consistently demonstrated the highest activity of the nonimidazoles 32, 55, 101; it is more active than quinacrine 30.

Clinical studies using furazolidone are numerous and have been completed with a wide range of subjects, doses, and administration schedules. Although its efficacy has generally been considered to be slightly lower than those of metronidazole and quinacrine, curative rates between 80 and 96% have been reported for 7- to 10-day courses (Table (Table1)1) 20, 52, 91, 151, 178, 191, 201, 255. It is when the drug is given for only 5 days that efficacy falls off considerably 151, 178. It is given as four doses per day in both adults (100 mg per dose) and children (1.5 mg/kg) (Table (Table2).2). In the pediatric suspension, two tablespoonfuls substitute for a 100-mg tablet.

About 10% of patients report gastrointestinal symptoms such as nausea, vomiting, and diarrhea (Table (Table2)2) 150, 256. Other adverse effects can include a brown discoloration of the urine; hemolysis can occur in G6PDH-deficient patients. The drug has a monoamine oxidase (MAO) inhibitory effect and should never be given concurrently to individuals already taking MAO inhibitors. There have been rare reports of disulfiram-like reactions when it is taken with alcohol 164b. A furazolidone-induced manic episode in a patient infected with human immunodeficiency virus has been reported 73. Furazolidone is also contraindicated in infants younger than 1 month of age, who could develop hemolytic anemia because of their normally unstable glutathione. Finally, the drug is mutagenic in bacteria and has been demonstrated to cause mammary tumors in rats and pulmonary tumors in mice when given in chronic high doses. However, the implication of this finding for humans is not known and has not been adequately addressed 143, 164b, 236. When treating pediatric populations, the advantages of its minimal adverse effects and the availability of a liquid suspension must be weighed against the need for frequent dosing over a 10-day treatment period.

Benzimidazoles.

Two members of the benzimidazole class of therapeutics, albendazole (Albenza) and mebendazole (Vermox), have been used to treat G. lamblia infection 155. Clinical and in vitro efficacy studies have produced different results as to their effectiveness. However, a comparatively benign side effect profile, combined with proven efficacy against many helminths, renders them promising for treatment 208, 250.

The benzimidazoles exert their toxic effect on Giardia in part by binding to the G. lamblia β-tubulin cytoskeleton 71, 175, 209. This binding causes both inhibition of cytoskeleton polymerization and impaired glucose uptake 250. Although the exact binding site on the cytoskeleton has not been determined, it is postulated that a benzimidazole-colchicine site interaction may play a role 51, 166, 236. The benzimidazoles are poorly absorbed from the gastrointestinal tract, although this can be improved with the coingestion of a fatty meal. The systemic effect of albendazole is due to its primary metabolite, albendazole sulfoxide, which is rapidly formed in the liver following absorption 3. Excretion by the kidneys is negligible.

In vitro susceptibility testing of G. lamblia to the benzimidazoles is limited in comparison to the susceptibility of the parasite to the nitroimidazoles or quinacrine. Nevertheless, studies demonstrate a considerable in vitro effect 79, 175, 208, 209. One report showed that both albendazole and mebendazole were 30- to 50-fold more active than metronidazole and 4- to 40-fold more active than quinacrine in vitro 71. Another demonstrated that the ability of albendazole to affect trophozoite morphology, adherence, and viability was far greater than that of metronidazole or tinidazole 166. However, their variable clinical efficacy demonstrates the discordance between in vitro testing and in vivo activity. Resistance to albendazole can be induced in vitro 154 and correlates with changes in the parasite cytoskeleton 243. Other benzimidazoles such as nocodazole, oxfendazole, thiabendazole, and fenbendazole have also demonstrated some in vitro efficacy 236.

Clinical trials have been limited to albendazole and mebendazole, with mixed results. Hall and Nahar reported equal curative efficacy of albendazole and metronidazole in children when albendazole was given for 5 days but not when it was given in single or 3-day dosing (Table (Table1)1) 104. A decreased efficacy of albendazole when given for 3 days or less was also documented by Kollaritsch et al. in travelers with giardiasis 137, by Pungpak et al. in children and adults 198, and by Pengsaa et al. in children 193. Improved efficacy was seen in other patients when the drug was given for 5 days 171, 207, 214 or 7 days 198. The exception to the need for longer treatment courses was seen in one study in which a single dose was administered 68. An albendazole-metronidazole combination was 100% effective in 20 patients with metronidazole-resistant giardiasis who had failed three to five courses of standard oral metronidazole therapy 44.

Treatment with mebendazole has resulted in widely divergent clinical results. Al-Waili reported over 90% efficacy in two studies in children 8, 9. However, other studies in both pediatric and adult populations have not shown equal success but instead have shown effectiveness in 80% 211 and in 60% or less 39, 92, 132; L. di Martino, A. Nocerino, and M. Pettoello Mantovani, Letter, Trans. R. Soc. Trop. Med. Hyg. 85:557–558, 1991), as well as a failure to decrease the prevalence rates of Giardia when mebendazole was used in mass treatment of helminths 219. Because of this discrepancy, most interest has focused on albendazole.

The dosage in adults is usually 400 mg per day for 5 days for albendazole and 200 to 400 mg per day for 5 to 10 days for mebendazole (Table (Table2).2). The usual dosage in children is 15 mg/kg per day for 5 to 7 days. Both drugs are available in suspension. One advantage of using albendazole in children is its efficacy against many helminths, allowing effective treatment of multiple intestinal parasites 207, 208. Another advantage is its relative lack of side effects. However, with short-term use, it may cause gastrointestinal problems of anorexia and constipation. Long-term, high-dose use of albendazole, such as when it is used for larval cestode infections, has caused reversible neutropenia and elevated hepatic enzyme levels 3, 155, 258. Albendazole is contraindicated in pregnancy, due to possible teratogenicity (pregnancy category C), but animal studies have shown no increase in carcinogenic incidence.

Paromomycin.

Paromomycin (Humatin), a member of the aminoglycoside family, was first isolated in 1956. It is indicated for the treatment of Entamoeba histolytica and Trichomonas and has been proposed as a treatment for G. lamblia in resistant infections and during pregnancy 113, 140. Paromomycin is poorly absorbed from the intestinal lumen; even large-dose oral administrations achieve only minimal concentrations in the blood and urine of patients with normal renal function 140. Paromomycin inhibits G. lamblia protein synthesis by interfering with the 50S and 30S ribosomal subunits (the parasite rRNA has an unusual size and sequence) and causing misreading of mRNA codons 69.

In vitro susceptibility testing demonstrates that paromomycin has activity against G. lamblia, but the activity is generally lower than that of the nitroimidazoles, quinacrine, or furazolidone 30, 101. However, because of poor intestinal absorption, it compensates for its low antiprotozoal activity by achieving high levels in the gut. In a rat model, the drug showed efficacy 15.

Clinical studies are limited, and therapeutic efficacy ranges from 55 to nearly 90% (Table (Table1)1) 47, 63, 140, 191, 218. The usual dose is 500 mg three times per day for 10 days in adults and 25 to 30 mg/kg/day (divided into three doses) in children (Table (Table22).

As with other aminoglycosides, if absorbed systemically paromomycin can cause ototoxicity and nephrotoxicity. However, it may be less ototoxic than other aminoglycosides 142, and with limited systemic absorption, toxicity should not be a concern in persons with normal kidneys. However, it should be used with caution in those with impaired renal function.

Bacitracin zinc.

The search for alternative, effective anti-Giardia therapeutics has led investigators to consider bacitracin. Bacitracin was first isolated in 1945 from a strain of Bacillus and was used systemically against severe staphylococcal infections until 1960, when its toxicity and the availability of other antibiotics restricted it to mainly topical use 141. Zinc was added to the bacitracin complex to promote stability. Bacitracin exerts its effect in bacteria by interfering with a dephosphorylation step in cell membrane synthesis. Following demonstrated in vitro effectiveness against E. histolytica and Trichomonas, bacitracin zinc was tested against Giardia in vitro and found to be active 12, 13.

A clinical trial by Andrews et al. used twice-daily dosing over 10 days and compared the effectiveness of 120,000 U of bacitracin zinc, 120,000 U of bacitracin, 120,000 U of neomycin, and 60,000 U of bacitracin zinc in combination with 60,000 U of neomycin 14. Cure rates of 95% for bacitracin zinc, 88% for either bacitracin or the bacitracin zinc-neomycin combination, and 86% for neomycin were demonstrated. Adverse effects were limited to a small number of patients who experienced diarrhea, abdominal discomfort, constipation, and nausea. Children younger than 10 years were excluded from the study.

The disadvantages of using bacitracin zinc include a potential for nephrotoxicity with prolonged oral dosing and gastrointestinal disturbance. Furthermore, compliance can be affected by the 10-day dosing period, and the formulations used by Andrews in their study are not readily available. Although bacitracin zinc is promising, more investigation is needed before it can gain wide acceptance as an agent against G. lamblia.

Emerging and experimental therapeutics.

A wide variety of chemotherapeutic agents including rifampin, bithionol, dichlorophene, hexachlorophene, pyrimethamine, sodium fusidate, chloroquine, and mefloquine have demonstrated in vitro activity against Giardia 81, 84, 233. Lipophilic tetracyclines, such as doxycycline, are highly active in vitro; however, their clinical efficacy is limited, perhaps because of their rapid absorption from the intestine 70. Certain pentamidine analogs, as well as azithromycin, have in vitro activity comparable to that of metronidazole 25, 33.

Nitazoxanide, a 5-nitrothiazole derivative with broad-spectrum activity against protozoa, helminths, and some bacteria has shown limited efficacy in adults and children in Mexico (71% [213] and 78% [211] effectiveness, respectively) and in a few AIDS patients in Mali 64. It has been given in a dose of 100 to 500 mg twice daily for 3 to 7 days.

Studies using a rat model have demonstrated the efficacy of ivermectin under specific conditions 260. Disulfiram, a zinc finger-active compound used for the treatment of alcoholism in humans, shows significant cure rates and decreased parasitic burdens in a mouse model of giardiasis 180.

In an ethnobotanical survey of the anti-Giardia gastrointestinal remedies employed by the Luo tribes of East Africa, methanolic extracts of 21 of the 36 taxa studied were lethal to or inhibited the growth of G. lamblia in vitro 124. Geranium nivem extracts have also shown in vitro activity 45. The immunomodulatory herbal drug Pippali rasayana, often prescribed for the treatment of worm infections and chronic dysentery in India, achieved a 98% cure of murine infection with G. lamblia 6. Extracts of Piper longum fruit were effective in a mouse model of infection 241.

Proposlina, a bee glue preparation, demonstrated a 60% parasitologic cure rate 1 week after treatment was completed among 48 adults in Cuba 172, 261. In a patient with metronidazole-resistant Giardia infection, the β-adrenergic antagonist dl-propranolol, given in a dose of 40 mg three times a day with 400 mg of metronidazole three times a day for 10 days, cleared infection, demonstrating clinical efficacy in humans 197. In vitro studies demonstrate that propranolol exerts its effect by inhibiting the motility and growth of the protozoan, most probably due to the membrane-stabilizing activity of the drug 85. However, further studies with dl-propranolol and the related compound d-propranolol are needed before they can be recommended as anti-Giardia agents.

Immunoprophylactic strategies to prevent or treat giardiasis have generally not been effective 87. Passive transfer of anti-Giardia immune serum did not facilitate parasite clearance in murine giardiasis 76, 242. Although patients with common variable immunodeficiency do have symptomatic and prolonged infection with Giardia antiparasitic therapy is required to control their infection 106, 216. Breast milk can be cytotoxic to Giardia via free fatty acids which are generated from milk triglycerides by the action of a bile salt-stimulated lipase 204. Also, breast feeding may confer some protection to suckling infants 176, 183; however the approach of providing enteral anti-Giardia antibody has not been studied.

Special Situations

Pregnancy and lactation.

The management of symptomatic G. lamblia infection during pregnancy is a challenge for the clinician because no therapeutic agent combines optimal efficacy and safety. Women who are asymptomatic, have mild disease, or are in their first trimester should usually avoid being treated. However, women in whom adequate hydration and nutritional status cannot be maintained should be treated, even in the first trimester.

Metronidazole, which rapidly enters the fetal circulation after absorption by the mother, has demonstrated mutagenicity in bacteria and carcinogenicity in mice and rats 34, 36, 153, 240, 251. While this information raises concern about the use of the drug during pregnancy, carcinogenicity has not been demonstration in humans 23, 24, 78, 98, 212, nor has there been teratogenicity in rodents 164a. Metronidazole has been used extensively during pregnancy (pregnancy category B), primarily for therapy of trichomoniasis in 7- to 10-day courses 42. The results regarding safety to the fetus are conflicting 36, 42, 107, 212, 215, 218. One retrospective study of 1,469 women who took metronidazole in pregnancy, with 206 using the drug in the first trimester, found no evidence of congenital abnormality 26. However, the Collaborative Perinatal Project, including over 50,000 mother-child pairs, demonstrated that first-trimester exposure to metronidazole in 31 women showed a possible association with malformations 107. A meta-analysis of seven studies, prospectively monitoring 253 mother-infant pairs and retrospectively monitoring 1,083 pairs, found no increased risk of fetal malformation in association with first-trimester use of metronidazole 42, with one report estimating a relative risk of 0.92 for birth defects 215. On balance, there may be a slightly increased risk when using metronidazole during the first trimester, and thus its use should be avoided during this period. High-dose (≥2.0 g), short-course regimens should not be given during pregnancy.

Metronidazole is actively excreted in breast milk in concentrations similar to those in plasma. The American Academy of Pediatrics (AAP) recommends giving a single 2-g dose in nursing mothers, followed by discontinuation of nursing for 12 to 24 h 10, 36. The AAP also recommends that mothers taking tinidazole discontinue nursing for the same time period as those taking metronidazole 10. However, metronidazole is approved for use in children for therapy of amebiasis and is used in children for therapy of anaerobic infections, so it would seem that the small amount secreted in breast milk would not be deleterious. Also, since single, high-dose regimens of metronidazole have poor efficacy and would be expected to lead to higher levels in breast milk, these findings favor traditional treatment with lower doses over 5 to 7 days.

Paromomycin is generally considered safe because it is poorly absorbed from the intestine and excreted almost 100% unchanged in the feces. Therefore, little if any of the drug will reach the fetus. However, it is not as effective as metronidazole or quinacrine. In addition, no clinical trials have addressed the effects of high serum concentrations of paromomycin during pregnancy. Nevertheless, paromomycin has been used successfully to eradicate G. lamblia infection in the gravid patient and is an important agent to consider during the first trimester, when metronidazole should not be used 140, 218. Paromomycin should also be safe in nursing mothers. A study in ewes showed only a 0.018% drug recovery rate in breast milk for the 12 h following parenteral administration 36, 263. The AAP does designate streptomycin and kanamycin, aminoglycoside relatives of paromomycin, to be compatible with breast feeding 10.

One expert on giardiasis has espoused quinacrine treatment in pregnant patients due to its high cure rate 256. While the drug is very effective, its slow excretion from the body and proven teratogenicity in rats make it a suboptimal choice for treatment in pregnancy. Although quinidine and quinine are compatible with breast-feeding, no information regarding the safety of quinacrine for the breast-fed child was available 10.

Furazolidone is not recommended for the pregnant patient. Although it is efficacious, its has caused mammary tumors in mice and mutations in bacteria, which should deter the physician from using it in this setting 164b. Its safety for breast-fed children is not known. Albendazole is considered a pregnancy category C agent, and has been teratogenic in rats and rabbits, although there is little experience of its effects in pregnant women.

Asymptomatic infection.

On a global basis, most persons infected with G. lamblia are asymptomatic or minimally symptomatic. Treating asymptomatic patients, particularly children, is controversial, and there are several factors to consider before initiating therapy. The setting of the infection plays a key role in the decision. In areas where G. lamblia is endemic, treatment may not be desirable because the children are likely to become rapidly reinfected following treatment 96, 231. If Giardia contributes to failure of growth and development 86, 163, 227, treatment, even though reinfection may occur, might allow catch-up growth 103 and might be worth the cost and effort. A drug such as albendazole, which would also treat nematode infections, might be useful in these settings; however, the requirement for 5-day dosing would make it difficult to complete therapy in many situations.

In conditions in which the child's nutritional baseline is excellent, such as in day care centers in the developed world, asymptomatic carriers may not always need therapy 5, 121, 195, 203, 221, 237. However, it should be noted, that aymptomatically infected children may excrete Giardia for months 195, carry it home to family members and thus initiate infection in the household, and even help maintain high levels of Giardia infection in a community 4, 196, 224; G. D. Overturf, Editorial, Clin. Infect. Dis. 18:764–765, 1994). It is not uncommon for a mother of a young child in day care to become symptomatic with giardiasis, identifying the presence in the household of Giardia which has been introduced by the asymptomatic child. If there is recurrent diarrhea attributed to Giardia in day care which cannot be controlled by improved hygiene and by treatment and exclusion of children who are symptomatic, consideration can be given to screening and treating all the children in the day care setting 5, 18, 230.

If Giardia is detected in the stool and there is little likelihood of reinfection, such as in a returned traveler, treatment can be given. In the household, if one member is symptomatic and there is the possibility that fecal-oral spread has occurred within the family or that there is a common source of infection, all family members should be screened and treated so that reinfection will not occur.

Another factor to consider in deciding whether to treat asymptomatic carriers is the consequences of transmission of infection if the carrier is not treated, e.g., infection in food handlers 169, 199. This group should be treated to prevent food-borne outbreaks.

Resistance and relapse.

Treatment failures have been reported with all of the common anti-Giardia agents including metronidazole, quinacrine, furazolidone, and albendazole. However, it is important for the clinician faced with recurrence of symptoms after therapy to differentiate between actual drug resistance, cure followed by reinfection, and post-Giardia lactose intolerance. Therefore, the first step is to document true, persistent infection by sending a stool sample for O&P examination or Giardia antigen detection. If the sample is positive, a careful exposure history should provide information about the likelihood of reinfection, and reinfected individuals should respond to the original therapeutic agent. Reinfection would be common in regions of endemicity around the world and in situations of poor fecal-oral hygiene. If a patient has become reinfected, risk factors should be identified and the patient should be counseled regarding proper hygiene and prevention measures.

Post-Giardia lactose intolerance is the most common of the disaccharidase deficiencies associated with giardiasis and may occur in 20 to 40% of patients 65. Thus, if the stool is negative for Giardia, a trial of avoiding lactose-containing foods and liquids should be instituted. This syndrome may take several weeks to resolve.

True treatment failure could mean infection with a drug-resistant isolate of Giardia. Resistance to most anti-Giardia agents has been documented or induced in vitro 29, 154, 245247, and multiple, genotypically different clones of G. lamblia with different drug class susceptibilities have been found in the human duodenum 46, 81, 160, 248. However, there has not been a consistent correlation between in vitro resistance or sensitivity and clinical failure or success 43, 160, 164, 225, 249, still leaving open the question of true parasite resistance.

Clinically resistant strains have been treated with longer repeat courses or higher doses of the original agent 91, 165, 178. However, the most efficacious means of eradicating these infections seems to involve using a drug from a different class to avoid potential cross-resistance 52, 92. An initial switch to a drug of a different class may not always be effective as demonstrated in two French patients who failed albendazole treatment following two courses of metronidazole but did respond to quinacrine (P. Brasseur and L. Favennec, Letter, Parasite 2:422, 1995). Combination regimens using metronidazole-albendazole, metronidazole-quinacrine, or other active drugs or giving a nitroimidazole plus quinacrine for courses of at least 2 weeks have proven successful against refractory infection 44, 182a, 197, 225, 234. On occasion, several different combinations or approaches will be necessary to effect cure.

In cases of giardiasis in which alternative therapy is not effective, other possibilities should be considered, such as the presence of immunologic deficiency. Chronic giardiasis in patients with hypogammaglobulinemia is well recorded 106, 108, 216 and can be difficult to treat, often requiring prolonged courses of therapy. Although Giardia is seen in homosexual men who engage in oral-anal sexual practices 162, 200, 226, illness may often be neither severe nor prolonged 148. Nevertheless, in AIDS patients with severe giardiasis, prolonged or combination therapy may be necessary 182a.

RECOMMENDATIONS

An approach to the diagnosis and management of suspected giardiasis is illustrated in Fig. Fig.22 and discussed in more detail above (see “Background”). If stools are negative, an empiric course of therapy can be given; however, an alternative diagnosis should be considered. If there is no response to therapy in stool-negative cases, invasive testing by endoscopy can be performed to help determine the diagnosis, particularly if the patient is immunocompromised.

When treatment is carried out, the agents of choice are listed in Table Table33 and the dosages are given in Table Table2.2. The most effective agents for therapy of giardiasis are single doses of tinidazole or ornidazole, 5 to 7 days of quinacrine, and 5 to 7 days of metronidazole. Tinidazole and ornidazole are not approved or available in the United States. Production of quinacrine has been discontinued, but it still may be obtained on a limited basis; however, it has significant side effects, particularly in children. Therefore, the treatment of choice in the United States for both adults and children is metronidazole. A standard course of 5 to 7 days should effectively treat 90% or more of infected individuals. Although the efficacy of 3 days of 2 to 2.4 g in a single daily dose approaches that of longer regimens, this regimen is not recommended. The drug has not received a Food and Drug Administration indication for giardiasis, and these high doses may have increased side effects. Furazolidone is an effective alternative but requires 7 to 10 days of treatment four times a day, which will probably affect compliance. Of the newer therapeutics, albendazole in a 5-day regimen seems most promising, but additional studies are needed. It has the advantage of having broad antiparasitic effect, which may be beneficial in developing-world settings.

TABLE 3
Recommendations for therapy of giardiasis

In pregnancy, if treatment is required, paromomycin should be tried in the first trimester and paromomycin or metronidazole should be used in the second and third trimesters.

Treatment of all asymptomatic patients calls for careful interpretation of the clinical situation, but they may not always require therapy.

It can be expected that parasites will be cleared from the stool in 3 to 5 days and that symptoms will resolve in 5 to 7 days 91, 100, 131, 171. If the symptoms do not abate, the patient should be evaluated for treatment failure or lactose intolerance. If resistance or relapse has occurred, treatment with a drug of a different class or with a combination of a nitroimidazole and quinacrine for at least 2 weeks should eradicate infection.

ACKNOWLEDGMENT

We thank Theodore Nash for helpful comments and suggestions.

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