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Infectious Disease

What Happens During a River Blindness Skin Snip Test?

At a Glance

A skin snip test for river blindness is a quick, bloodless procedure that takes tiny, shallow skin samples, usually from the hips or buttocks. The sample is placed in saline for up to 24 hours to see if microscopic worms emerge. This test is the best way to confirm an active infection.

A skin snip test is the traditional gold-standard method for diagnosing onchocerciasis (river blindness) by looking for the parasite’s larvae (microfilariae) directly in your skin [1]. While the idea of a “snip” or biopsy might sound intimidating, the procedure is very quick and takes only a tiny, superficial piece of skin [2].

The Procedure: Step-by-Step

When you have a skin snip test, your doctor will collect small skin samples from specific areas of your body where the parasites are most likely to gather. The most common spots are the hips (iliac crests), the buttocks (gluteal folds), or sometimes the shoulders and calves [3] [4]. Usually, doctors will take several snips (often two to four) to ensure the test is as accurate as possible [4].

To take the sample, your doctor will use either a specialized instrument called a scleral punch or a sterile scalpel [5] [6]. A scleral punch works a bit like a tiny hole puncher. If a scalpel is used, the doctor will usually gently lift the top layer of the skin with a needle and carefully slice off the tiny raised piece [7].

Because the sample taken is extremely shallow and bloodless, the procedure is usually done without anesthesia [2]. A numbing shot (like lidocaine) is typically not used because the burning of the injection itself would actually cause more discomfort than the quick, nearly painless pinch of the test itself [3] [8].

It is very important that this snip is bloodless [2]. If blood mixes with the sample, it can obscure the view under the microscope and accidentally introduce other blood-borne parasites (such as Loa loa) that confuse the diagnosis [9] [7]. Because the snips are so superficial, they require minimal aftercare and heal quickly [2].

Analyzing the Sample

Once the skin sample is collected, the doctor or lab technician does not look at it immediately. Instead, the tiny piece of skin is placed in a small dish filled with saline (saltwater) or a similar liquid [1] [10].

The sample sits in this fluid at room temperature [10]. If you are infected with the Onchocerca volvulus parasite, the microscopic worms (microfilariae) will begin to emerge from the skin tissue and swim out into the saline [11]. While the idea of worms swimming out of your skin might sound terrifying, these microfilariae are completely invisible to the naked eye—you will not feel them leaving the sample, and you will not see them in the dish [1] [11].

You will not need to wait in the clinic while this happens. Initial results may be ready in a few hours, but the sample is typically left for up to 24 hours to give the microscopic worms plenty of time to emerge [1] [12]. After this incubation time, the technician examines the fluid under a microscope to count any worms that have appeared [1].

Modern Testing Enhancements and Alternatives

While examining the saline under a microscope is standard, the worms can sometimes be hard to find if you have a mild infection or have recently taken anti-parasitic medication like ivermectin [13]. Because of this, labs sometimes run advanced molecular tests, such as PCR (Polymerase Chain Reaction), on the skin snips [12]. PCR looks directly for the parasite’s DNA and is much more sensitive than relying solely on a microscope [14].

Patients often ask if they can choose a rapid blood test instead of a skin snip to avoid the biopsy altogether. While rapid, less invasive blood tests that look for antibodies are increasingly used, they generally tell doctors if you have ever been exposed to the parasite at some point in your life [15] [16]. The skin snip test, particularly when combined with PCR, remains an important tool to confirm if you have an active, current infection that requires treatment right now [12] [16].

Common questions in this guide

Does a skin snip test for river blindness hurt?
The procedure causes only a quick, nearly painless pinch because the sample taken is extremely shallow. A numbing shot is usually not used because the injection itself would cause more discomfort than the actual test.
Where on the body are skin snips taken?
Doctors typically collect small skin samples from areas where the parasites are most likely to gather. The most common spots are the hips, the buttocks, shoulders, or calves.
How long does it take to get results from a skin snip test?
Initial results may be ready in a few hours, but the sample is typically left in fluid for up to 24 hours to allow any microscopic worms to emerge. If your sample is sent out for advanced DNA testing, results may take longer.
Why can't I just get a blood test for river blindness?
While rapid blood tests are available, they generally only tell doctors if you have ever been exposed to the parasite. A skin snip test is necessary to confirm if you have an active infection that requires treatment right now.
Will I see worms swimming out of my skin during the test?
No, you will not see or feel any worms. The skin sample is placed in fluid away from you, and any emerging parasite larvae are completely invisible to the naked eye.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.Which areas of my body will you be taking the skin snips from?
  2. 2.How many skin samples do you plan to take to ensure the test is accurate?
  3. 3.Does your clinic rely on the microscope method, or will my skin snips also be sent for PCR (DNA) testing to ensure accuracy?
  4. 4.When should I expect to receive a phone call or message with my results?
  5. 5.What specific aftercare steps should I take to keep the biopsy sites clean and avoid infection?
  6. 6.Are there rapid blood tests we could consider alongside the biopsy to get a complete picture of my health?

Questions For You

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References

References (16)
  1. 1

    Detection of Onchocerca volvulus in Skin Snips by Microscopy and Real-Time Polymerase Chain Reaction: Implications for Monitoring and Evaluation Activities.

    Thiele EA, Cama VA, Lakwo T, et al.

    The American journal of tropical medicine and hygiene 2016; (94(4)):906-11 doi:10.4269/ajtmh.15-0695.

    PMID: 26880774
  2. 2

    Response to the Letter to the Editor by Eberhard et al.

    Bottomley C, Isham V, Vivas-Martínez S, et al.

    Parasites & vectors 2017; (10(1)):240 doi:10.1186/s13071-017-2125-5.

    PMID: 28511662
  3. 3

    A community-based cross-sectional study of the epidemiology of onchocerciasis in unmapped villages for community directed treatment with ivermectin in Jimma Zone, southwestern Ethiopia.

    Dana D, Debalke S, Mekonnen Z, et al.

    BMC public health 2015; (15()):595 doi:10.1186/s12889-015-1888-x.

    PMID: 26130117
  4. 4

    Modelling Neglected Tropical Diseases diagnostics: the sensitivity of skin snips for Onchocerca volvulus in near elimination and surveillance settings.

    Bottomley C, Isham V, Vivas-Martínez S, et al.

    Parasites & vectors 2016; (9(1)):343 doi:10.1186/s13071-016-1605-3.

    PMID: 27301567
  5. 5

    First detection of Onchocerca lupi infection in dogs in southern Spain.

    Miró G, Montoya A, Checa R, et al.

    Parasites & vectors 2016; (9(1)):290 doi:10.1186/s13071-016-1587-1.

    PMID: 27193758
  6. 6

    Progress report on the elimination of human onchocerciasis, 2015-2016.

    Releve epidemiologique hebdomadaire 2016; (91(43)):505-14.

    PMID: 27801998
  7. 7

    Unusual Localization of Blood-Borne Loa loa Microfilariae in the Skin Depends on Microfilarial Density in the Blood: Implications for Onchocerciasis Diagnosis in Coendemic Areas.

    Niamsi-Emalio Y, Nana-Djeunga HC, Chesnais CB, et al.

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2021; (72(Suppl 3)):S158-S164 doi:10.1093/cid/ciab255.

    PMID: 33909066
  8. 8

    Feasibility of utilizing the SD BIOLINE Onchocerciasis IgG4 rapid test in onchocerciasis surveillance in Senegal.

    Dieye Y, Storey HL, Barrett KL, et al.

    PLoS neglected tropical diseases 2017; (11(10)):e0005884 doi:10.1371/journal.pntd.0005884.

    PMID: 28972982
  9. 9

    Loa loa Microfilariae in Skin Snips: Consequences for Onchocerciasis Monitoring and Evaluation in L. loa-Endemic Areas.

    Nana-Djeunga HC, Fossuo-Thotchum F, Pion SD, et al.

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2019; (69(9)):1628-1630 doi:10.1093/cid/ciz172.

    PMID: 30861060
  10. 10

    Dermal microfilariae of dogs, jackals and cats in different regions of Iran.

    Sazmand A, Bahiraei Z, Nemati F, et al.

    Parasites & vectors 2022; (15(1)):28 doi:10.1186/s13071-021-05141-2.

    PMID: 35057824
  11. 11

    The Functional Parasitic Worm Secretome: Mapping the Place of Onchocerca volvulus Excretory Secretory Products.

    Vanhamme L, Souopgui J, Ghogomu S, Ngale Njume F

    Pathogens (Basel, Switzerland) 2020; (9(11)) doi:10.3390/pathogens9110975.

    PMID: 33238479
  12. 12

    Comparison of a new visual isothermal nucleic acid amplification test with PCR and skin snip analysis for diagnosis of onchocerciasis in humans.

    Alhassan A, Osei-Atweneboana MY, Kyeremeh KF, et al.

    Molecular and biochemical parasitology 2016; (210(1-2)):10-12 doi:10.1016/j.molbiopara.2016.07.006.

    PMID: 27473357
  13. 13

    Differential susceptibility of Onchocerca volvulus microfilaria to ivermectin in two areas of contrasting history of mass drug administration in Cameroon: relevance of microscopy and molecular techniques for the monitoring of skin microfilarial repopulation within six months of direct observed treatment.

    Abong RA, Amambo GN, Chounna Ndongmo PW, et al.

    BMC infectious diseases 2020; (20(1)):726 doi:10.1186/s12879-020-05444-2.

    PMID: 33008333
  14. 14

    O-5S quantitative real-time PCR: a new diagnostic tool for laboratory confirmation of human onchocerciasis.

    Mekonnen SA, Beissner M, Saar M, et al.

    Parasites & vectors 2017; (10(1)):451 doi:10.1186/s13071-017-2382-3.

    PMID: 28969662
  15. 15

    Surveillance for Onchocerciasis-Associated Epilepsy and OV16 IgG4 Testing of Children 6-10 Years Old Should Be Used to Identify Areas Where Onchocerciasis Elimination Programs Need Strengthening.

    Dusabimana A, Siewe Fodjo JN, Ndahura MM, et al.

    Pathogens (Basel, Switzerland) 2022; (11(3)) doi:10.3390/pathogens11030281.

    PMID: 35335605
  16. 16

    Rapid diagnostic testing for onchocerciasis in Maridi (South Sudan) before and after improving elimination strategies: a repeated cross-sectional survey.

    Hadermann A, Jada SR, Amaral LJ, et al.

    Open research Europe 2023; (3()):206 doi:10.12688/openreseurope.16093.2.

    PMID: 38617116

This page provides educational information about diagnostic testing for river blindness. Always consult an infectious disease specialist or your healthcare provider for medical advice and accurate diagnosis.

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