Dracunculiasis

Blister on the foot of a person with dracunculiasis

The first signs of dracunculiasis occur around a year after infection, as the full-grown female worm prepares to leave the infected person's body.[3] As the worm migrates to its exit site – typically the lower leg, though they can emerge anywhere on the body – some people have allergic reactions, including hives, fever, dizziness, nausea, vomiting, and diarrhea.[4] Upon reaching its destination, the worm forms a fluid-filled blister under the skin.[5] Over 1–3 days, the blister grows larger, begins to cause severe burning pain, and eventually bursts leaving a small open wound.[3] The wound remains intensely painful as the worm slowly emerges over several weeks to months.[6] If at any point the infected person submerges the affected body part in water, the worm spews a white substance into the water containing its larvae.[5] As the worm emerges, the open blister often becomes infected with bacteria, resulting in redness and swelling, the formation of abscesses, or in severe cases gangrene, sepsis or lockjaw.[7][2] When the secondary infection is near a joint (typically the ankle), the damage to the joint can result in stiffness, arthritis, or contractures.[2][8]

Infected people commonly harbor multiple worms – with an average 1.8 worms per person;[9] up to 40 at a time – which will emerge from separate blisters at the same time.[4] 90% of worms emerge from the legs or feet. However, worms can emerge from anywhere on the body.[4]

Life cycle of Dracunculus medinensis

Dracunculiasis is caused by infection with the roundworm Dracunculus medinensis.[3] D. medinensis larvae reside within small aquatic crustaceans called copepods or water fleas. When humans drink the water, they can unintentionally ingest infected copepods. During digestion the copepods die, releasing the D. medinensis larvae. The larvae exit the digestive tract by penetrating the stomach and intestine, taking refuge in the abdomen or retroperitoneal space.[10] Over the next two to three months the larvae develop into adult male and female worms. The male remains small at 4 cm (1.6 in) long and 0.4 mm (0.016 in) wide; the female is comparatively large, often over 100 cm (39 in) long and 1.5 mm (0.059 in) wide.[5] Once the worms reach their adult size they mate, and the male dies.[4] Over the ensuing months, the female migrates to connective tissue or along bones, and continues to develop.[4]

About a year after the initial infection, the female migrates to the skin, forms an ulcer, and emerges. When the wound touches freshwater, the female spews a milky-white substance containing hundreds of thousands of larvae into the water.[4][6] Over the next several days as the female emerges from the wound, she can continue to discharge larvae into surrounding water.[6] The larvae are eaten by copepods, and after two to three weeks of development, they are infectious to humans again.[11]

Dracunculiasis is diagnosed by visual examination – the thin white worm emerging from the blister is unique to this disease.[12] Dead worms sometimes calcify and can be seen in the subcutaneous tissue by X-ray.[2][12]

There is no medicine to kill D. medinensis or prevent it from causing disease once within the body.[13] Instead, treatment focuses on slowly and carefully removing the worm from the wound over days to weeks.[14] Once the blister bursts and the worm begins to emerge, the wound is soaked in a bucket of water, allowing the worm to empty itself of larvae away from a source of drinking water.[14] As the first part of the worm emerges, it is typically wrapped around a piece of gauze or a stick to maintain steady tension on the worm, encouraging its exit.[14] Each day, several centimeters of the worm emerge from the blister, and the stick is wound to maintain tension.[4] This is repeated daily until the full worm emerges, typically within a month.[4] If too much pressure is applied at any point, the worm can break and die, leading to severe swelling and pain at the site of the ulcer.[4]

Treatment for dracunculiasis also tends to include regular wound care to avoid infection of the open ulcer while the worm is leaving. The U.S. Centers for Disease Control and Prevention (CDC) recommends cleaning the wound before the worm emerges. Once the worm begins to exit the body, the CDC recommends daily wound care: cleaning the wound, applying antibiotic ointment, and replacing the bandage with fresh gauze.[14] Painkillers like aspirin or ibuprofen can help ease the pain of the worm's exit.[4][14]

Dracunculiasis is a debilitating disease, causing substantial disability in around half of those infected.[2] People with worms emerging can be disabled for the three to ten weeks it takes the worms to fully emerge.[2] When worms emerge near joints, the inflammation around a dead worm, or infection of the open wound can result in permanent stiffness, pain, or destruction of the joint.[2] Some people with dracunculiasis have continuing pain for 12 to 18 months after the worm has emerged.[4] Around 1% of dracunculiasis cases result in death from secondary infections of the wound.[2]

When dracunculiasis was widespread, it would often affect entire villages at once.[8] Outbreaks occurring during planting and harvesting seasons severely impair a community's agricultural operations – earning dracunculiasis the moniker "empty granary disease" in some places.[8] Communities affected by dracunculiasis also see reduced school attendance as children of affected parents must take over farm or household duties, and affected children may be physically prevented from walking to school for weeks.[15]

Infection does not create immunity, so people can repeatedly experience dracunculiasis throughout their lives.[16]

Children in Chad holding filter straws used to prevent D. medinensis infection

There is no vaccine for dracunculiasis, and once infected with D. medinensis there is no way to prevent the disease from running its full course.[13] Consequently, nearly all effort to reduce the burden of dracunculiasis focuses on preventing the transmission of D. medinensis from person to person. This is primarily accomplished by filtering drinking water to physically remove copepods. Nylon filters, finely woven cloth, or specialized filter straws are all effective means of copepod removal.[4][17] Sources of drinking water can be treated with the larvicide temephos, which kills copepods.[18] Where possible, open sources of drinking water are replaced by deep wells that can serve as new sources of clean water.[18] Public education campaigns inform people in affected areas how dracunculiasis spreads and encourage those with the disease to avoid soaking their wounds in bodies of water that are used for drinking.[4]

Dracunculiasis is nearly eradicated, with just 15 cases reported worldwide in 2021.[19] This is down from 27 cases in 2020, and dramatically less than the estimated 3.5 million annual cases in 20 countries in 1986 – the year the World Health Assembly called for dracunculiasis' eradication.[19][20] Dracunculiasis remains endemic in just four countries: Chad, Ethiopia, Mali, and South Sudan.[21]

Dracunculiasis is a disease of extreme poverty, occurring in places where there is poor access to clean drinking water.[22] Cases tend to be split roughly equally between males and females, and can occur in all age groups.[23] Within a given place, dracunculiasis risk is linked to occupation; people who farm or fetch drinking water are most likely to be infected.[23]

Cases of dracunculiasis have a seasonal cycle, though the timing varies by location. Along the Sahara desert's southern edge, cases peak during the mid-year rainy season (May–October) when stagnant water sources are more abundant.[23] Along the Gulf of Guinea, cases are more common during the dry season (October–March) when flowing water sources dry up.[23]

Rod of Asclepius

Dracunculiasis has been with humans for at least 3,000 years, as the remnants of a guinea worm infection have been found in the mummy of a girl entombed in Egypt around 1,000 BCE.[24] Diseases consistent with the effects of dracunculiasis are referenced by writers throughout antiquity. The disease of "fiery serpents" that plagues the Hebrews in the Old Testament (around 1250 BCE) is often attributed to dracunculiasis.[22][24][note 1] Plutarch's Symposiacon refers to a (now lost) description of a similar disease by the 2nd century BCE writer Agatharchides concerning a "hitherto unheard of disease" in which "small worms issue from [people's] arms and legs... insinuating themselves between the muscles [to] give rise to horrible sufferings".[24] Many of antiquity's famous physicians also write of diseases consistent with dracunculiasis, including Galen, Rhazes, and Avicenna; though there was some disagreement as to the nature of the disease, with some attributing it to a worm, while others considered it to be a corrupted part of the body emerging.[24] In his 1674 treatise on dracunculiasis, Georg Hieronymous Velschius first proposed that the Rod of Asclepius, a common symbol of the medical profession, depicts a recently extracted guinea worm.[24]

Carl Linnaeus included the guinea worm in his 1758 edition of Systema Naturae, naming it Gordius medinensis.[24] In Johann Friedrich Gmelin's 13th edition of Systema Naturae (1788), he renamed the worm Filaria medinensis, leaving Gordius for free-living worms.[24] Henry Bastian authored the first detailed description of the worm itself, published in 1863.[24][25] The following year, in his book Entozoa, Thomas Spencer Cobbold used the name Dracunculus medinensis, which was enshrined as the official name by the International Commission on Zoological Nomenclature in 1915.[24] Despite longstanding knowledge that the worm was associated with water, the lifecycle of D. medinensis was the topic of protracted debate.[26] Alexei Pavlovich Fedchenko filled a major gap with his 1870 publication describing that D. medinensis larvae can infect and develop inside Cyclops crustaceans.[27][28][note 2] The next step was shown by Robert Thomson Leiper, who described in a 1907 paper that monkeys fed D. medinensis-infected Cyclops developed mature guinea worms, while monkeys directly fed D. medinensis larvae did not.[27]

In the 19th and 20th centuries, dracunculiasis was widespread across nearly all of Africa and South Asia, though we lack exact case counts from the pre-eradication era.[23] In a 1947 article in the Journal of Parasitology, Norman R. Stoll used rough estimates of populations in endemic areas to suggest that there could be as many as 48 million cases of dracunculiasis per year.[29][30] In 1976, the WHO estimated the global burden at 10 million cases per year.[30] Ten years later, as the eradication effort was beginning, the WHO estimated 3.5 million cases per year worldwide.[31]

Global dracunculiasis cases according to the World Health Organization, 1989–2021, displayed on a logarithmic scale.

The campaign to eradicate dracunculiasis began at the urging of the CDC in 1980.[34] Following smallpox eradication (last case in 1977; eradication certified in 1981), dracunculiasis was considered an achievable eradication target since it was relatively uncommon and preventable with only behavioral changes.[35] In 1981, the steering committee for the United Nations International Drinking Water Supply and Sanitation Decade (a program to improve global drinking water during the decade from 1981 to 1990) adopted the goal of eradicating dracunculiasis as part of their efforts.[36] The following June, an international meeting termed "Workshop on Opportunities for Control of Dracunculiasis" concluded that dracunculiasis could be eradicated through public education, drinking water improvement, and larvicide treatments.[36] In response, India began its national eradication program in 1983.[36] In 1986, the 39th World Health Assembly issued a statement endorsing dracunculiasis eradication and calling on member states to craft eradication plans.[35] The same year, The Carter Center began collaborating with the government of Pakistan to initiate its national program, which then launched in 1988.[36] By 1996, national eradication programs had been launched in every country with endemic dracunculiasis: Ghana and Nigeria in 1989; Cameroon in 1991; Togo, Burkina Faso, Senegal, and Uganda in 1992; Benin, Mauritania, Niger, Mali, and Côte d'Ivoire in 1993; Sudan, Kenya, Chad, and Ethiopia in 1994; Yemen and the Central African Republic in 1995.[35][37]

Each national eradication program had three phases. The first phase consisted of a nationwide search to identify the extent of dracunculiasis transmission and develop national and regional plans of action. The second phase involved the training and distribution of staff and volunteers to provide public education village-by-village, surveil for cases, and deliver water filters. This continued and evolved as needed until the national burden of disease was very low. Then in a third phase, programs intensified surveillance efforts with the goal of identifying each case within 24 hours of the worm emerging and preventing the person from contaminating drinking water supplies. Most national programs offered voluntary in-patient centers, where those affected could stay and receive food and care until their worms were removed.[38]

In May 1991, the 44th World Health Assembly called for an international certification system to verify dracunculiasis eradication country-by-country.[36] To this end, in 1995 the WHO established the International Commission for the Certification of Dracunculiasis Eradication (ICCDE).[39] Once a country reports zero cases of dracunculiasis for a calendar year, the ICCDE considers that country to have interrupted guinea worm transmission, and is then in the "precertification phase".[40] If the country repeats this feat with zero cases in each of the next three calendar years, the ICCDE sends a team to the country to assess the country's disease surveillance systems and to verify the country's reports.[40] The ICCDE can then formally recommend the WHO Director-General certify a country as free of dracunculiasis.[39]

Since the initiation of the global eradication program, the ICCDE has certified 15 of the original endemic countries as having eradicated dracunculiasis: Pakistan in 1997; India in 2000; Senegal and Yemen in 2004; the Central African Republic and Cameroon in 2007; Benin, Mauritania, and Uganda in 2009; Burkina Faso and Togo in 2011; Côte d'Ivoire, Niger, and Nigeria in 2013; and Ghana in 2015.[21]

Date	South Sudan	Mali	Ethiopia	Chad	Angola	Cameroon	Total
2011	1,028[41]	12[41]	8[41]	10[41]	0	0	1,058
2012	521[42]	7[42]	4[42]	10[42]	0	0	542
2013	113[43]	11[43]	7[43]	14[43]	0	0	148[N 1]
2014	70[44]	40[44]	3[44]	13[44]	0	0	126
2015	5[45]	5[45]	3[45]	9[45]	0	0	22
2016	6[46]	0[46]	3[46]	16[46]	0	0	25
2017	0[47]	0[47]	15[47]	15[47]	0	0	30
2018	10[48]	0[48]	0[48]	17[48]	1[48]	0	28
2019	4[49]	0[49]	0[49]	48[49]	1[49]	1[49]	54
2020	1[50]	1[50]	11[50]	12[50]	1[50]	1[50]	27
2021	4[51]	2[51]	1[51]	8[51]	0[51]	0[51]	15
2022 (through September)	1[52]	0[52]	0[52]	5[52]	0[52]	0[52]	6

In addition to humans, D. medinensis can infect dogs.[53] Infections of domestic dogs have been particularly common in Chad, where they helped reignite dracunculiasis transmission in 2010.[54] Dogs are thought to be infected by eating a paratenic host, likely a fish or amphibian.[55] As with humans, prevention efforts have focused on preventing infection by encouraging people in affected areas to bury fish entrails as well as to identify and tie up dogs with emerging worms so that they cannot access drinking water sources until after the worms have emerged.[55] Domestic ferrets can be infected with D. medinensis in laboratory settings, and have been used as an animal disease model for human dracunculiasis.[56]

Different Dracunculus species can infect snakes, turtles, and other mammals. Animal infections are most widespread in snakes, with nine different species of Dracunculus described in snakes in the United States, Brazil, India, Vietnam, Australia, Papua New Guinea, Benin, Madagascar, and Italy.[53][57] The only other reptile affected is the snapping turtle with infected common snapping turtles described in several U.S. states, and a single infected South American snapping turtle described in Costa Rica.[58] Infections of other mammals are limited to the Americas. Raccoons in the U.S. and Canada are most widely impacted, particularly by D. insignis; however, Dracunculus worms have also been reported in American skunks, coyotes, foxes, opossums, domestic dogs, domestic cats, and (rarely) muskrats and beavers.[59][60]

Wikimedia Commons has media related to Dracunculiasis.

• "Guinea Worm Disease Eradication Program". Carter Center.
• Nicholas D. Kristof from the New York Times follows a young Sudanese boy with a Guinea Worm parasite infection who is quarantined for treatment as part of the Carter program
• Tropical Medicine Central Resource: "Guinea Worm Infection (Dracunculiasis)"
• World Health Organization on Dracunculiasis