Domestic Refugee Health Screening Guidance
Intestinal Parasite Screening
Last updated: September 2022
On this page:
Minnesota intestinal screening recommendations
Microlearning series: Intestinal parasites
Labs
Best practices
Background and epidemiology
Resources
Minnesota intestinal parasite screening recommendations
All refugees
- Evaluate all refugees for eosinophilia by obtaining a CBC with differential.
- Review overseas medical paperwork for documentation of any presumptive anti-helminthic treatment(s) received.
- Screen for giardiasis using stool antigen for those with symptoms. Screening asymptomatic children younger than 5 years of age for Giardia stool antigen and treating those who test positive may be beneficial and is done by some experts in refugee children, although data supporting this approach are lacking.
Refugees from Eastern Europe
- Conduct serology for Strongyloides.
Refugees from Asia, Middle East, North Africa, Latin America, or Caribbean
- If no pre-departure albendazole: Provide presumptive albendazole treatment, or conduct stool ova and parasite examination.
- If no pre-departure ivermectin: Provide presumptive ivermectin therapy or conduct serology for Strongyloides.
Refugees from sub-Saharan Africa
- If no pre-departure albendazole: Provide presumptive albendazole treatment, or conduct stool ova and parasite examination.
- If no pre-departure ivermectin: Provide presumptive ivermectin therapy or conduct serology for Strongyloides.
- Do not provide presumptive ivermectin therapy to refugees from Loa loa-endemic regions of sub-Saharan Africa unless Loa loa infection can be ruled out. In patients with a high microfilarial Loa loa load, treatment with ivermectin has been associated with fatal encephalopathy. Refer to CDC: About Loiasis.
- If no pre-departure praziquantel: Provide presumptive praziquantel therapy or conduct serology for schistosomiasis.
Microlearning series: Intestinal parasites
This video (under 5 minutes) is meant to serve as a summary of intestinal parasite screening guidance and resources for providers completing the refugee health screening and all those serving new arrivals.
Refugee Health Microlearning Series: Intestinal Parasites Transcript (PDF)
Labs
- The recommended threshold for eosinophilia is >450 cells/µL.
- Stool antigen is the preferred test for identifying Giardia infections, as stool ova and parasite testing has low sensitivity.
- A “test and treat” approach for soil-transmitted helminths is generally done with two or more separate stool ova and parasite tests done by concentration technique; samples must be collected 12 to 24 hours apart because shedding may be intermittent.
- A “test and treat” approach for strongyloidiasis should include Strongyloides IgG serology. Stool ova and parasite testing lacks sensitivity for Strongyloides infection and should not be used to rule out infection.
- For refugees who are at significant risk of Strongyloides, have potential past exposure to Loa loa, and have not received pre-departure (or previous) treatment with ivermectin:
- A single thin and thick blood smear collected between 10 a.m. and 2 p.m. can be performed (inform the laboratory there is concern of Loa loa infection).
- If the thin and thick smear is negative: High-burden Loa loa parasitemia has been ruled out, and ivermectin may be offered.
- If the thin and thick smear is positive: Consult CDC for further guidance regarding evaluation and treatment options for Loa loa. Refer to resources below for expert phone consultation.
- Alternatively, these refugees may be offered a Strongyloides serologic test. If negative for Strongyloides, no ivermectin is needed. If positive, a thin and thick blood smear between 10 a.m. and 2 p.m. for Loa loa microfilaria (as above) should be performed before treatment with ivermectin.
- A single thin and thick blood smear collected between 10 a.m. and 2 p.m. can be performed (inform the laboratory there is concern of Loa loa infection).
- A “test and treat” approach for schistosomiasis should include Schistosoma IgG serology. Testing of stool and urine for eggs and urine analysis for red blood cells may also be done in conjunction. However, because of lack of sensitivity, these tests should not be used alone to rule out infection.
Best practices
- If absolute eosinophil count is >450 cells/µL, re-check in 3-6 months.
- Generally, U.S.-granted and derivative asylees, special immigrant visa (SIV) holders, certified victims of human trafficking, and parolees do not receive presumptive pre-departure anti-helminthic treatment.
- As with all medication, it is important to check for contraindications to antiparasitic treatments:
- Presumptive albendazole should not be given to children <1 year of age, pregnant women, or individuals with known neurocysticercosis, evidence of cysticercosis (e.g., subcutaneous nodules), or with a history of unexplained seizures.
- Presumptive ivermectin should not be given to children <15 kg or measuring <90 cm, pregnant women in any trimester, or breastfeeding women within the first week after birth. Presumptive ivermectin should not be given to individuals from, or who have resided in, Loa loa-endemic countries in sub-Saharan Africa unless Loa loa infection can be ruled out.
- Presumptive praziquantel should not be given to children <4 years of age or measuring <94 cm, or individuals with known neurocysticercosis, evidence of cysticercosis (e.g., subcutaneous nodules), or with a history of unexplained seizures.
Background and epidemiology
Strongyloides parasites, other soil-transmitted helminths, and Schistosoma species are some of the most common infections among refugees. Strongyloides and Schistosoma, in particular, can persist for long periods of time in the body of a host, without new environmental exposure. Although frequently asymptomatic or subclinical, some infections may cause significant morbidity and mortality.
Epidemiological studies of the prevalence of Strongyloides among Eastern European refugees are limited. The most common way of becoming infected with Strongyloides is by contacting soil that is contaminated with Strongyloides larvae. Most infections are acquired through environmental exposure. Although the typical duration of infection is unknown, chronic, potentially life-long, infection can occur. The most common clinical presentation in refugees is an elevated eosinophil count, although lack of eosinophilia does not exclude infection. Common clinical symptoms in refugees include abdominal complaints, nausea, diarrhea, constipation, dry cough, and skin manifestations (e.g., larva currens).
Soil-transmitted helminth infections, including Ancylostoma duodenale and Necator americanus (hookworm), Ascaris lumbricoides (ascariasis), and Trichuris trichiura (whipworm) are often found in areas with warm and moist climates where sanitation and hygiene are poor, including in temperate zones during warmer months. Ascaris and Trichuris infections occur through indirect exposure. Hookworm infections require direct contact of skin with contaminated soil, and penetration of the larval worm through skin. Infections are most frequently asymptomatic or subclinical. However, ascariasis, when symptomatic, may be associated with abdominal pain, cough (Löffler syndrome), and if high-burden, intestinal obstruction, appendicitis, or cholecystitis. Trichuriasis (whipworm infection) may cause bloody stools, anemia, and rarely, rectal prolapse. Hookworm may cause anemia, which is of particular concern in young children and pregnant women.
All sub-Saharan African countries (except Lesotho) are considered endemic for schistosomiasis. Infection requires direct skin contact with Schistosoma-contaminated fresh water; larval parasites enter by penetrating the skin. Young infants without direct skin exposure to contaminated fresh water are at low risk of infection. However, babies bathed in basins with contaminated fresh water are at risk of infection. Infections are frequently asymptomatic or subclinical; however, infections may persist for more than 50 years, causing ongoing damage. The most common sign of infection is asymptomatic eosinophilia; however, severe manifestations of chronic Schistosoma infection include bowel wall pathology, liver cirrhosis, portal hypertension, dysuria, hematuria, urinary tract obstruction, renal failure, and bladder cancer.
Starting in 1999, CDC initiated presumptive albendazole pre-departure treatment to refugees just prior to U.S. departure. Currently, refugees from Asia, Africa, the Middle East, North Africa, and Latin America all receive pre-departure albendazole unless there are contraindications. In 2005, CDC initiated pre-departure presumptive ivermectin treatment for Strongyloides for refugees departing from those same regions. Presumptive praziquantel treatment for schistosomiasis was initiated in 2010 for refugees departing from sub-Saharan African. At this time, refugees departing from Eastern Europe do not receive presumptive treatment for intestinal parasites.
Though many of the parasitic infections that refugees are recommended to be screened for are not endemic to Minnesota, Giardia is found worldwide, including in every region of the United States. From 2009 to 2018 there were 6,556 cases of giardiasis reported in Minnesota, with recent immigrants and refugees accounting for 8% of cases.
Many refugees arriving to the United States are treated presumptively for intestinal parasites prior to U.S. arrival. This treatment includes albendazole, ivermectin, and/or praziquantel, depending on the individual’s region of origin. During 2009-2019, 67% of refugee arrivals who received a refugee health assessment were treated presumptively for intestinal parasites overseas. The proportion being treated presumptively overseas has increased in recent years, with 53% of those arriving as primary refugees having received presumptive treatment in 2011 compared to 82% in 2019.
Among those not treated presumptively overseas, CDC recommends screening for intestinal parasites or post-arrival presumptive treatment. Among those who did not receive overseas presumptive treatment during this time period, 91% were screened for intestinal parasites using serology and/or ova and parasite stool exam. Fourteen percent of refugee arrivals tested positive for ≥1 pathogenic parasite; the most common parasite identified was Giardia lamblia.
Prevalence of Intestinal Parasites among Primary Refugees to Minnesota, 2011-2019
Region of Origin* | Received RHA** | Received Presumptive Anti-helminthic Overseas (%)*** | Did Not Receive Presumptive Anti-helminthic Overseas (%) | Screened for Intestinal Parasites (% among those not Treated Overseas) **** | Positive for ≥1 Pathogenic Parasite(s) (%)† |
---|---|---|---|---|---|
East Asia/ Pacific | 24 | 5 (21%) | 19 (79%) | 13 (68%) | 1 (8%) |
Eastern Europe | 619 | 6 (1%) | 613 (99%) | 495 (81%) | 44 (9%) |
Latin America/ Caribbean | 191 | 16 (8%) | 175 (92%) | 158 (90%) | 11 (7%) |
North Africa/ Middle East | 1,025 | 389 (38%) | 636 (62%) | 550 (86%) | 55 (10%) |
South/ Southeast Asia | 6,922 | 5,702 (82%) | 1,220 (18%) | 1,168 (96%) | 245 (21%) |
Sub-Saharan Africa | 7,896 | 5,141 (65%) | 2,755 (35%) | 2,560 (93%) | 359 (14%) |
Total | 16,677 | 11,259 (68%) | 5,418 (32%) | 4,944 (91%) | 715 (14%) |
*Based on MDH's world regions
**Refugee Health Assessment (RHA): health screening done in U.S., usually within 90 days of U.S. arrival
*** Received presumptive, pre-departure anti-helminthic overseas (albendazole, ivermectin, and/or praziquantel); % among those who received RHA
**** Screened for intestinal parasites using serology and/or ova and parasite stool exam; % among those who received RHA and were not presumptively treated overseas
† % among those screened for intestinal parasites who were not treated presumptively overseas
Resources
CDC Hotlines for Parasitic Disease Cases (not including Malaria)
Subject matter experts from the Division of Parasitic Diseases are available to assist health professionals with diagnosis and treatment of parasitic diseases that are potentially life threatening. Learn more at CDC: Clinical Overview of Parasitic Diseases or call:
- Parasitic Diseases Hotline: 404-718-4745
Weekdays: 8 a.m. to 4 p.m. EST - Emergency, after-hours hotline: 770-488-7100