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‘Diagnostic procedures employed currently in laboratories around the UK are not optimal for the detection of D. fragilis and B. hominis’
D. fragilis and B. hominis: neglected human protozoa. J. J. Windsor. The Biomedical Scientist. July 2007. Pages 524-27.

Relatively few laboratories in England and Wales use suitable staining methodologies; consequently, many are likely to encounter B. hominis initially in unstained preparations. In fact, many of the cases of B. hominis seen in our laboratory are found by direct microscopy and confirmed subsequently with a trichrome stain. In view of this, it may be pertinent to address proficiency to detect B. hominis by the ability to report it both in unstained and stained preparations.
British Journal of Biomedical Science, 2001. Windsor, J J, Marfarland, L, Whiteside, T M

It is our impression that the variations in the reporting of D.fragilis reflect more the attention that is paid to the parasite and the technique that is used than to the actual incidence.
The Neglected Amoeba: Dientamoeba fragilis. A Report of 100 "Pure" Infections. Kean & Malloch. American Journal of Digestive Diseases. New Series, Vol.11 No.9. 1966

As B.hominis is the most common faecal parasite seen at both Aberystwyth PHL and Swansea PHL in the UK, we feel that the CDSC figures do not reflect the true incidence of B.hominis in England and Wales. Indeed, all 139 reports of B. hominis reported to CDSC Wales in 2000 were detected by our two laboratories (unpublished data). We believe that this can be attributed to laboratory awareness and the use of suitable ethodologies.
JJ Windsor, et al
British Journal of Biomedical Science 2001; 58: 129-130


"A single stool specimen examination will miss many pathogenic protozoan infections in symptomatic persons
(RA Hiatt et al, 1983)

The higher prevalence of D. fragilis infections than that of G. duodenalis is probably related to the method used, a procedure, which is rarely followed in laboratories for the diagnosis of enteric parasites. These epidemiological data suggest that when faecal samples are examined after a period of time and without Giemsa staining, most D. fragilis infections goes undetected.
Dientamoeba fragilis is more prevalent than Giardia duodenalis in children and adults attending a day care centre in Central Italy.
Crotti D , D'Annibale ML , Fonzo G, Lalle M , Caccio SM , Pozio E .
Parasite. 2005 Jun;12(2):165-70.

Even under ideal circumstances, a single stool specimen is diagnostic only 50% to 60% of the time; three samples increases the sensitivity to 80% and six samples to 95% .
Vol. 18, No. 4 The John Hopkins Microbiology Newsletter.
Monday, January 25, 1999


"Our results suggests that a single stool specimen examination will miss many pathogenic protozoan infections in symptomatic persons"
Hiatt RA, Markell EK, Ng E
American Journal of Gastroenterology 1983 Oct;78(10):634-6


Since the number of organisms are reported to vary daily, a series of stool samples for ova and parasite examination should be collected.
D.fragilis: A Gastroeintestinal Protozoan Infection in Adults
Spencer et al
AMJ., Vol 77, No. 8. 1977 2002


Many laboratory technicians, however, are unfamiliar with the appearance of this parasite, either living or in stained preparations, and it is still frequently misdiagnosed as an amoeba.
Intestinal Parasites of Some Diarrhoeic HIV-Seropositive Individuals in North Brazil
Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 94(5),Sept./Oct. 1999: pp 611-613

The laboratory reports of the Communicable Disease Surveillance Centre show that in 1992, 68 cases of D fragilis infection were reported from seven laboratories and that by 1996 this figure had increased to 231 cases reported from 20 laboratories (unpublished data). These results reflect an increase in the number of laboratories performing faecal stains. It can be assumed, however, that the true incidence of D fragilis infection is many times higher: there are an estimated 450 diagnostic laboratories in the United Kingdom, most of which do not look for this pathogen.
Letter to BMJ 1999; 318:735 (13 March 1999). J J Windsor, Senior biomedical scientist & E H Johnson, Associate professor.

The proper collection and preservation of multiple stool specimens in addition to adequate microscopic examinations by qualified, trained individuals are necessary for the identification of D.fragilis.
Spencer et al: Am.J.of Gastro. 1982

Although DF is thought to be uncommon, surveys indicate that it's occurrence is worldwide. In properly collected and preserved stool specimens examined by lab. personnel trained to recognize this flagellate, the incidence of this organism corresponds to that of Giardia lamblia. It is particularly important that permanently stained slides of stool specimens in addition to adequate microscopic examinations by qualified individuals are necessary for the identification of DF.
Dientamoeba fragilis - an intestinal pathogen in childre? (Am J Dis Child 133:390-393, 1979)


Generally considered rare and either not found in surveys, or recovered in small proportions only, we have, since the adoption of a two bottle collection kit for faecal samples, found it almost as common as Giardia lamblia
D.Fragilis: A Review with Notes on its Epidemiology, pathogenicity, mode of transmission and diagnosis by Yang & Scholten (1976)

...physicians should perhaps be more concerned about the competence of the labs. to which they submit samples and be better informed of techniques used routinely by the laboratory before accepting positive or negative reports at face value. It may well be that many cases of abdo. distress of hitherto unknown etiology are, in fact, due to D.fragilis.
A Yang & Scholten,
Am. Journal of Trop. Med. & Hygiene.
Vol 26, No 1 . 1975

"Because competence to accurately diagnose parasitic infections is not easily obtained, physicians should perhaps be more concerned about the competency of the laboratory to which they submit their samples"
Yang & Scholten, D.fragilis: A review with notes. Am.Journal of Trop. Med. & Hygiene 1977

Our results suggest that a single stool specimen will miss many pathogenic protozoan infections in symptomatic people.
How many stool samples are necessary to detect pathogenic intestinal protozoa? Hiatt RA et al. AJTMH 1995

Because the time during which this organism remains in a recognisable condition in stools is limited, samples must be examined shortly after defecation, or be bulk-preserved in a suitable fixative immediately after a bowel movement.
Yang & Sholten, Am.J. TM&H Vol 26, No.1 1975

D. fragilis is believed to be rare; however, when stool specimens are collected and preserved in polyvinyl alcohol or other fixative, followed by permanently-stained smears, the recovery rate increases markedly, particularly when smears are prepared and examined by well-trained laboratory personnel .
DIENTAMOEBA FRAGILIS; A GASTROINTESTINAL PROTOZOAN INFECTION IN ADULTS. Mary J. Spencer, M.D., Martha R. Chapin, R.N., and Lynne S. Garcia, M.T.(ASCP) Am. Journ. of Gastro. Vol. 77. No. 8, 1982

Diagnosis is best made by finding the characteristic trophozoite on a permanently stained faecal smear as it is not reliably detected on direct wet prep. microscopy or a faecal concentrate ......Patients collect their stool specs. at home into polyvinyl alcohol fixative to ensure that there is minimal degeneration of the protozoan while the spec. is being transferred to the lab. Three specs. are collected on different days to increase the chance of detecting intermittent excretion of the protozoan.
DF: A BOWEL PATHOGEN? Oxner, Paltridge, Chapman, Bramwell Cook, Sheppard. New Zealand Med. Journal. 11 Feb. 1987. p 4-65

Unreliable identification of D.fragilis may explain variations in the results of different studies. Even in stained faecal smears, which must be prepared from fresh material (Ockert, 1990), Dientamoeba may be confused with amoeboid forms of Blastocystis, Endolimax and other organisms, or degenerated polymorphonuclear leucocytes. (Markell et al., 1986; Ash & Orihel, 1990.) Nongyao Sawangjaroen, et al. Trans of the Royal Society of Tropical Medicine and Hygiene (1993) 87, 163-165.

"The prevalence of D. fragilis in most localities is poorly documented, as the methods commonly used in intestinal parasite surveys are unsuitable for detecting trophozoites"
J.Clinical Parasitology 9th Ed. Beaver, Jung & C upp 1984

Eight counties in Washington accounted for 72% of all DF cases. The distribution of reported cases by county in Washington differed significantly from the number of stools submitted for examination from these counties. A possible explanation is that stool specimens from the eight counties are routinely sent to the Washington State Public Health Lab (WSPL) when examination for ova and parasites is indicated and stools from other counties are not. In 1985-86 all reported DF diagnoses occurred at the WSPHL. At this time only a few labs in the state, including the WSPHL, reported using the stool collection and examination techniques necessary to detect DF (unpublished data) . In addition, an increased awareness of DF existed among health care providers in San Juan County due to a cluster of cases there, which probably resulted in increased stool spec. submissions.
Descriptive features of Dientamoeba fragilis infections. J. H. Grendon, R. F. Digiacomo and F. J. Frost. Journal of Tropical Med & Hygiene 1995, 98, 309-315

Diagnosing parasites

"(My) doctor has no experience in treating (Blastocystis hominis). In fact he says it is so rare that he hasn't seen or heard about it in 30 years!". NY, USA. Jan. 2006

"I'm almost crying as I read your story on the site. My doctor has continuously diagnosed me with IBS and is on the verge of telling me I'm wasting his time every time I go in there.  I had one stool sample sent to a lab last year in April and the results showed nothing, so I took their word for it. Last night, my pain was so bad, I almost stuck a knife in my chest to end it. No one listens to me. My family says it's all in my head, my doctor tells me it's IBS. Now that I've read your story, I have some hope."
Canada, August 05

"I asked my doctor for B. hominis and D. fragilis testing, she thought I was crazy and refused."
US woman with chronic digestive symptoms. USA 2003

"The doctor said that parasites do not exist." Northern Queensland, Australia. October 2005

"My gastro. eventually came around to say only in 'rare' cases is df a pathogen and he's never seen it in all his 25 years". US, 2003

"I've been testing Ova & Parasite for 15 years and have never seen anything in the USA." Specialist gastroenterologist's response to patient's request for parasite testing to determine cause of chronic digestive symptoms. (2005)

"The Doctor said to my husband today that he had never heard of this bug."
Canadian diagnosed with Blasto. April 2005.

"The only test that has ever worked for me is the purge" (2001)

"Thanks to the info on your site my doctor has allowed me to get my stool testing done at the local hospital wich apparently has a much better testing facility. He's also let me assist in determining how to do the testing (ie. several seperate screenings over the period of a week) as opposed to the single screenings done in the past. This is great news for me cause I was looking at spending $600 to have it done through Great Smokies. D.fragilis was diagnosed. (USA 2005)

"I have been having parasite tests for 5 years with the national health here in the UK since spending two years in India. I have been unable to work or have any quality of life for nearly all of that time. I have finally been diagnosed with Dientamoeba fragilis as well as some additional bacteria and yeast by Great Smokes Diagostics. As with others I have been misdiagnosed, unbelieved and had numerous "normal" test results whilst living, or rather existing, with chronic fatigue, severe digestive problems, intermittent fever, nausea etc etc.
C., UK. April 05

"My name is C. and I am 18 years old & I need some advice. I have been feeling really bad for many years now, I have fluid-retention, foggy thinking that is so bad it feels like I am constantly on drugs, heavy body and so on. The doctors just couldn´t find out why and finally I did a parasite test with a naturopath. They found Dientamoeba fragilis. I have been to countless doctors these four last years, but no one has ever mentioned anything about parasites. I have gotten diagnoses like depression, adhd, hypothyroidism and so on. We actually once mentioned parasite infection, and the doctor only laughed at us. I have missed years of school work now because my thinking is so foggy.... It's really destroying my life. "
(Sweden. 2005)

"I see what you mean about testing is only a small part of the battle." Canadian diagnosed with D.fragilis searching for medical help. (Dec 2005)

"Your site gave me the courage and place to finally get tested properly."
A young Australian woman, suffering symptoms typical of a chronic bowel infection, submitted three fixed samples to a specialist lab on three separate occasions. Because her samples were negative she was diagnosed with Irritable Bowel Syndrome and depression.
A newer test using PCR finally revealed a likely reason for her symptoms: Cryptosporidium and Giardia. (2008)

Need details of specialist labs? Go here.

1975: "Physicians should be concerned about the competence of the labs to which they submit samples, and be better informed of techniques used routinely by the laboratory before accepting positive or negative reports at face value. It may well be that many cases of abdo. distress of hitherto unknown etiology are, in fact, due to D.fragilis."
(Am. Journal of Trop. Med. & Hygiene. 1975 Vol 26, No 1) .


What is fixative? Why is it important?

Blastocystis hominis produces hardy, thick walled cysts. These cysts, which act as protective vessels for the parasite, can survive at room temperature for up to 19 days (Moe et al 1996) and in water, including water which has been chlorinated.

D.fragilis, on the other hand does not produce cysts and unlike Blasto., does not survive in water.

Researchers have long assumed that the human pinworm Enterobius vermicularis may play a role in helping this parasite survive the journey through the human gut.

Both parasites are fragile, and soon after evacuation begin to break apart and become unrecognisable. Fixative improves the accuracy of stool testing by preserving the structure of the parasite, making it easier for the lab to identify the parasite.

Blasto. can be diagnosed without fixative but it is often the hardy cysts which are identified, not the parasite, as shown in this lab report below. The existence of the cyst form was not confirmed until the early 1990s (Stenzil & Boreham 1991).

Fixative increases the likelihood of diagnosis because it enables all forms of Blasto. to be identififed, not just the cysts.

FAECES FOR EXAMINATION
Specimen Number 1

APPEARANCE: Semi-formed
MICROSCOPY (including concentration and fixed stains)
No leucocytes seen
No erythrocytes seen
Cysts of Blastocystis hominis (+) present
The role of Blastocystis in causing diarrhoea is controversial. If symptoms persist after exclusion of other causes, a trial of metronidazole may be indicated.
CULTURE No bacterial pathogens isolated

Th following Australian study confirms the importance of preserving fecal samples in fixative:

All SAF-fixed stools (from twenty-one patients) were positive for Dientamoeba fragilis, while no Dientamoeba fragilis diagnoses were made using fresh stool specimens.
Eradication of Dientamoeba fragilis can resolve IBS-like symptoms, TJ Borody, et al.
Journal of Gastroenterology and Hepatology (2002) 17 (Suppl.)

Other reasons why a parasite infection might be misdiagnosed:

The examples here show that some labs do not report the presence of Blasto.

A New Zealander discovered how important fixative is to diagnose D.fragilis:

"Finally received a result yesterday from the Auckland lab (SCL). The test was positive for Df. The first 2 samples were negative (without a fixative) - despite me driving into town and dropping them off directly to the lab within the hour. Then I supplied another 3 samples in a PVA fixative and the second sample was positive." (May 05)

Unfortunately not everyone is given a choice of submitting fixed samples:

"My tests came back negative though I am not convinced they were done correctly.  My request for the three day liquid suspension was denied by my naturopath who apparently knew better.  The guy she had do the testing was an independant who apparently is some kind of expert in this and he doesn't believe the liquid suspension necessary.  I fear I wasted $80 odd." (Australia. November 2005)

An Australian pathology lab were unfamiliar with both fixative and it's crucial role in diagnosing parasites:

"We spoke to a pathologist about the liquid fixative that should be in the stool tests but they had not heard of it before. What exactly is it?" (Australia. November 2005).

A Western Australia lab located in Perth had to be educated by a patient about the importance of fixative:

"I went to my doctor today and told him that I wanted the tests. I went to my local path collection centre and spoke to the lovely lady to get the fixative. She rang the microbiologist at the Perth lab and he said that I didn't need a fixative. Because I went armed with the relevant printouts of your website re lab testing she was convinced and told the microbiologist that 'the client has quite a lot of information about this and it all indicates that a fixative is needed'. After she found out that they did actually have the fixative (PVA?) in stock she talked him into couriering it out to her collection centre and I pick it up tomorrow! I hope that my specifying a PVA fixative was correct." (September 2007).

Access to even basic stool testing might be denied if the treating dr considers B.hominis or D.fragilis harmless:

"I've tested positive for Blastocystis Hominis, I even managed to get a treatment with Flagyl but the symptoms remain. When asking for a re-test to confirm if Flagyl worked or not they say that since Blasto probably isn't the cause of my problems, there's no reason for another test. According to them I have already gotten more treatment than they normally give for Blasto, since they almost never treat it... Now I've been prescripted "LuneLax", fibre, since they think I have IBS. Been eating fibre for a month and I can't say it helps...

My symptoms are: Fatigue, diarrhea, abdominal discomfort, flatus, dizziness, light head ache (occasionally), muscle/joint ache (occasionally), rectal itching (occasionally).

So, I'm caught in the middle, can't get tested nor any treatment since "Blasto isn't the cause of my problems". Even though I was treated with Flagyl I'm fairly certain that I still carry Blasto, I still have symptoms anyway... "
(Sweden. Nov. 2005)

The following experience of a New Zealand woman is not unique:

Three and a half years after becoming unwell Y. was diagnosed by a specialist lab with D.fragilis. During that time her symptoms of diarrhoea, bloating, flatulence, dizziness, headaches, extreme fatigue, body aches & pains, dry cough and heart palpatations had left her too incapacitated to continue working.

Not surprisingly one of New Zealand's most high profile pathology labs were unable to diagnose her infection because the stool samples were not collected in fixative, and the lab tested only one sample at a time.

A stool antigen test for Giardia was also negative.

Despite the negative result Flagyl was prescribed in case of undetected Giardia. Although the treatment initially reduced her symptoms, the relief was short lived. The result was the same after taking another round of Flagyl a few weeks later.

Understandably Y. felt "very alone" trying to cope with the symptoms of a seemingly undiagnosable and untreatable illness. She wrote: "Family and friends are tired of hearing about my health problems (and I don't blame them)".

More than three years after becoming unwell Y. stumbled on this site, and discovered that specialised stool collection and testing methods are necessary to diagnose the two most common, but vastly underdiagnosed gut parasites: D.fragilis and B.hominis.

Armed with this new information Y. phoned her doctor's "mainstream, high profile lab" to find out about their testing recommendations for D.fragilis and B.hominis:

"I was told by a microbiologist that Bh was "just a fungus" and Dh was "self limiting". I told him that I had published research that proved otherwise. I said they could cause chronic illness that could last for years. I told him that I suspected I was suffering from one of these bugs because I had been sick for 3 1/2 years and my symptoms matched those of a parasitic infection. He replied "well you can make your symptoms match any disease you want to, can't you?" He told me I was interrupting an important meeting he was in and hung up."

Getting nowhere with conventional doctors, Y. asked her naturopath — who had been treating her condition unsuccessfully for a couple of years — to arrange testing with the specialist lab Great Smokies Diagnostics.

Dientamoeba fragilis was diagnosed in the last two of the three fixed samples.

Y. took the result to her GP:

"My GP had never heard of Df and she asked me to leave the info with her so that she could make a few phone calls and she would get back to me. She phoned me back this morning and told me that GSDL was a "dodgy lab" and not recognised by the medical establishment."

The GPs advice was swayed by the microbiologist view that: "It is most likely not the Df that is causing my symptoms - (he doubted) that I even have it."

Y. found herself in the same situation she had read about on this site: diagnosed with D.fragilis or B.hominis, but unable to overcome her infection because of medical dogma. In other words she had been effectively barred from gaining access to the most effective treatments.

After much searching eventually a more open-minded GP was found, three hours drive away. Y. hoped that this doctor would take her D.fragilis into account when diagnosing her symptoms.

Although the new GP was "very helpful and open-minded", he had never encountered a patient infected with this common parasite. He admitted he was "not an expert", and was therefore unfamiliar with specialised drugs necessary to eradicate D.fragilis.

Y. sensibly declined his offer of doxycycline and metronidazole (Flagyl) combined, based on the fact that she had been diagnosed after taking Flagyl - twice!

In the meantime Y. was determined to prove to her doctor and microbiologist the validity of the stool collection and testing methods recommended in the published medical literature and used by Great Smokies as well as other specialist labs. Eventually a small NZ lab agreed to test two stool samples without fixative, and three with. The fresh, unfixed samples, tested within two hours of evacuation, were negative. The second of the three fixed samples was positive for D.fragilis. The other two were negative.

Y. phoned her "open-minded" doctor with the good news:

"..he was surprised that I was so happy about the result - he didn't really seem to understand why I had gone to the trouble of being re-tested by (the private Auckland lab) after the positive GSD result. I told him I want my medical records to include the positive SCL result because I am so annoyed about all the previous negative results I had had by Auckland's major lab - and I am also annoyed that most of the medical establishment view GSD as being "a dodgy lab" - I wanted to prove that GSD were right and show my doctor how difficult it is to be tested correctly. I wanted to be re-tested by SCL - so that I could be certain that they were using the correct testing techniques so that other people can also be confidant in their parasitology testing methods. However after all that effort, when I asked the SCL lab if they could now test two other people - they said that the specific testing methods required to test for Df had been too time consuming."

Unable to find a doctor to take her diagnosis seriously, Y. was forced to self-treat. She recovered from her infection with a combination of three drugs.

One month after her treatment Y. wrote to tell me that for the first time in over three years she was "FEELING REALLY WELL. All my body aches & pains have gone, the nausea has totally gone, my bowel is returning to normal, I can get through the day without having to lie down, my energy levels are way up and my head feels mostly clear."
May 2003.

The following study evaluates the accuracy of stool testing:

No of consecutive
examinations

 

Infections
revealed %

1

-

50-60

3

-

70-83

6

-

90-95

10

-

90-100

The Neglected Ameba:
D.fragilis A Report of 100 "Pure" Infections
B.H.Kean, M.D., & C.L.Malloch, MD
Am.J.of Dig.Dis. Vol 11, N o.9, 1966

"Even under ideal circumstances, a single stool specimen is diagnostic only 50% to 60% of the time; three samples increases the sensitivity to 80% and six samples to 95% .
Vol. 18, No. 4 The John Hopkins Microbiology Newsletter. Monday, January 25, 1999

"As far as the 3-sample rule is concerned it is not 100% accurate. It has been shown to vary depending on the organism but 3 samples are enough to detect 95+% of infections for most of them. That still leaves some undetected of course. I have heard (anecdotally) of someone who had Giardia diagnosed only after 8 samples!" (Parasitologist, London School of Tropical Hygiene and Medicine. 2002)

Parasites do not always show up in stool samples because:

"A number of patients may intermittently shed protozoa in their stool. Similarly, some protozoa (G. intestinalis and D. fragilis) have been shown to have highly variable and intermittent shedding. (van Gool et al., 2003)".

"There is marked fluctuation in the shedding of the parasite from day to day, varying from as high as 17 to 0 per x40 microscopic field. The cystic stages when estimated in 8 Blastocystis-infected individuals ranged from as high as 7.4x10(5) cysts per gram of stool to 0. (Parasitol Res. Vennila GD, et al . 1999 Feb;85(2):162-4)

The number of organisms excreted daily flucuated markedly in the one case investigated. With regard to the distribution of the parasite within a stool, considerably greater numbers were found in the last portion evacuated than in the first half. Dientamoeba fragilis, a review with notes on its epidemiology, pathogenicity, mode of transmissino and diagnosis. Yang & Scholten, Am J Trop Med Hyg. 1977 Jan;26(1):16-22.

Testing too soon after a drug treatment increases the likelihood of a false-negative result because there may not be enough parasites for the lab to identify:

One month after Flagyl treatment only twenty percent of the B.hominis subjects were positive. Six months later the number of positives rose to fifty-three percent. The researchers considered reinfection could explain some, but not all, of the increased detection of this parasite.
A Placebo Controlled Treatment Trial of Bh Infection with Metro.
Nigro. et al. Journal of Travel Med. Vol. 10, No 2.)

The following examples show the limitations of stool testing, even three fixed samples!

  • M., from the US., suffered from mushy stools, abdominal pain, bloating and cramps. Giardia had been diagnosed in two of three fixed samples, and Flagyl ( 500mg 3 times daily for 7 days) was prescribed. His symptoms returned a few weeks after finishing the treatment, yet the three stool samples were negative.

    His GP advised that
    his "system was rebalancing itself because Giardia combined with Flagyl is hard on the body".

    Another three fixed samples were tested and these to were negative.


    An endoscopy, colonoscopy and CAT scan were also negative.

    His symptoms persisted.

    M. had two choices: either accept the possibility that Giardia had caused permanent damage to his digestive tract; or keep submitting samples to a specialist lab and hope that something would eventually show up to explain his symptoms. He decided on the latter.

    After submitting yet another batch of samples to a specialist lab Giardia was diagnosed.

    Flagyl was prescribed, in the same dosage and duration as before. This time the drug had little effect, probably because the parasite had become resistant. Flagyl was followed by five days of Albendazole at 400mg twice daily, then
    ten days of Ornidazole.

    The treatments failed to relieve M's symptoms, and he was now concerned that his bowel flora had been further compromised by the drugs.

    M's GP advised that he had "
    run out of options". M. consulted a naturopath: "The naturopath thinks that I probably still has some parasites combined with a severely disturbed intestinal tract from giardia and all the anti biotics". 

    Another three fixed samples, tested by the same specialist lab, were now positive for Cryptosporidium parvum and Blastocystis hominis. Giardia had disappeared.
    (US. April '07)
  • The father of a twelve year old US girl contacted because his daughter was refusing to eat. His child complained of stomach pain, gas and an "acid stomach" after meals.

    Three fixed samples tested by a proficient lab, were positive for
    D.fragilis, B.hominis and Cryptosporidium.

    A four week course of Iodoquinol (Yodoxin) failed to relieve the symptoms.

    Post treatment stool testing revealed Crypto., but no
    Blasto. hominis or D.fragilis.

    Extensive blood work, an endoscopy and a barium x-ray were negative.

    Another batch of samples was positive for
    D.fragilis and Blasto. hominis. Cryptosporidium had disappeared.

    The child was prescribed a ten day course of Alinia (Nitazoxanide). When her symptoms returned a few weeks after the treatment she was prescribed ten days of Bactrim.

    Post treatment testing revealed higher levels of B. hominis, but no sign of
    Crypto and D.fragilis.


    Repeat stool tests a few months later diagnosed Blastocystis hominis and Dientamoeba fragilis. Cryptosporidium had disappeared.

    (US, September 2006)
  • S., from the UK, felt "desperate and suicidal" when the results of three fixed samples, tested by the London School of Tropical Medicine and Hygiene, were negative for infection.

    For two decades S. had suffered with "severe constipation, intermittent severe fatigue, knawing hungry feeling not relieved with food, feeling faint and weak, bloating and gassy, feeling of toxicity and general malaise & depression".


    She estimated spending at least £20,000 on various alternative therapies over the past two decades.

    After finding this site, with its emphasis on specialised testing, S. felt hopeful that this may be the key to diagnosing her symptoms.


    S's doctor was sceptical that specialised testing was necessary because S. had not recently travelled overseas, but nevertheless agreed to
    arrange to arrange testing with the LSTH&M. S. was advised of the negative result during a consultation with a consultant at the the Hospital for Tropical Diseases in London:

    "Everything was normal. They said that even if the stool samples missed anything, the blood samples would have shows up anything sinister. I did mention that some parasites attach themselves to the wall of the bowel.  The consultant looked at me as if I was mad/ hypochrondiac. He was making such statements such as "I see from your medical notes that you have suffered from depression in the past". I understood what he was getting at."


    The consultant at the Hospital for Tropical Diseases should have made her aware that false-negatives occur due to the problems of intermittent shedding.

    S. pursued testing with another UK lab who also specialise in parasite testing and both Blastocystis hominis and Dientamoeba fragilis were diagnosed.


    Please note that a negative result does not reflect on the competence of the London School of Tropical Hygiene and Medicine. The reason why the infections were not detected are explained here.
  • Read about B's experience here.
  • A US man contacted me about the triple therapy which cures more than eighty percent of Blasto. infections because a number of drugs treatments, incuding Flagyl, had failed to clear Blasto. from his stool samples or relieve his symptoms.

    He went on the triple therapy, and this made a significant difference to his symptoms, but a few weeks later his symptoms reappeared. Within a few weeks he was as sick as before taking the treatment.

    Three stool samples, tested four weeks after finishing the meds, were negative.

    Determined to find out if Blasto. had survived the treatment he decided to submit three fixed samples to a specialist lab every month. Only the seventh batch was positive for Blasto.

  • In 2005 a Canadian man contacted about two years of persistent stomach pain. which at one point was so severe he was admitted to hospital. The hospital tested three fixed samples, and he was diagnosed with Dientamoeba fragilis.

    The two weeks of Flagyl prescribed by the hospital doctor failed to relieve his symptoms.

    An endoscopy, colonsocopy, barium follow through and a lactose test were all normal.

    The antibiotic Ciproflaxin was prescribed, followed by Flagyl.
    The treatment did not help. Based on the results of negative samples tested a few weeks after this treatment he was diagnosed with Irritable Bowel Syndrome. The acid suppressing drug Pariet was prescribed.

    Based on medical literature that Blasto. colonises the cecum — the pouch-like start of the large intestine that links it to the small intestine — I suggested submitting purged samples, which can help force the parasites out of the cecum.

    Three fixed samples were each submitted to two separate specialist labs with this result:

    One lab diagnosed D.fragilis in one of the three fixed samples.

    The other detected
    "a few Blastocystis Hominis and many Dientamoeba Fragilis".
  • N. from the US., had suffered stomach pain and nausea and loose bowel movements for the past eighteen months. Based entirely on his symptoms, without stool testing, Irritable Bowel Syndrome was diagnosed.

    When N. found this site, with its emphasis on specialised testing, he consulted a naturopath about stool testing with a specialist lab. Dientamoeba fragilis was diagnosed in one of three fixed samples.

    A herbal treatment prescribed by the naturopath did not help his symptoms.

    Another batch of purged samples was tested by the same lab, with this result:

    "I have just got my stool tests back which showed that I am still infected with D.fragilis and interestingly this test also showed B.hominis. I must point out that I took a laxative called picosulphate to do purged samples to enhance the effectiveness of the tests. Seems to have worked." October 2003. USA.
  • D., from Australia, had been diagnosed with Blastocystis hominis and prescribed 500mg of Nitazoxanide twice daily for seven days.

    Fourteen days after finishing the treatment she retested with a specialist lab. The result was negative.

    D. assumed that the result of three fixed samples was definitive, and that she was no longer infected with B.hominis, despite still feeling unwell.

    She felt her only option was to control the worst of her symptoms with severe dietary restrictions.

    Three years after testing negative D. found my site, and realised that three fixed samples was not 100% diagostic. She was retested and discovered that not only had Blasto. survived, but that she was also infected with D.fragilis.

    More examples:

    "Just to let you know, I had the results of my Great Smokies test and I have many D. fragilis bugs. If you remember the London School of Tropical Hygiene & Med. test came back negative." UK. Feb 2004
  • "After taking a 20 day course of Iodoquinol combined with Doxycycline I have had follow up 2 tests and unfortunately after a clear first test the second shows not only D. fragilis but now Blasto. as well. I'm devastated as it was such a battle tracking down the Iodoquinol here and expensive not to mention time consuming."

  • This woman, determined to discover the cause of her chronic health problems, submitted four batches of samples to Great Smokies over as many months. It's not something everyone can afford to do, but luckily this woman could. Her persistence enabled her to find out why she was sick: "Great Smokies Lab tested me, and Giardia did not show up until the 12th stool sample."

  • A US man submitted six stools samples — two batches of three — to a specialist lab, but the samples were negative. Despite this result his GP suspected Giardia, and prescribed Flagyl. When treatment failed to help the symptoms another three samples were tested by the same lab. The result confirmed the doctor's suspicions — the patient was positive for Giardia.

  • A US woman submitted four batches of stool samples to a specialist lab over as many months. Each set consisted of three samples in fixative - for a total of 12 samples. B.hominis showed up in the forth batch.
  • A Sydney physician submitted three fixed samples to a specialist lab. The first batch was negative, but a second batch — tested by the same lab a few weeks later — revealed D.fragilis.
  • Over a period of twelve months a US couple each submitted three batches of samples to a specialist lab. Each batch consisted of three fixed samples. The first two batches were negative. The third batch detected Blasto. in both the husband and wife's samples. Flagyl was prescribed and the wife made a complete recovery. The husand was less fortunate: his symptoms returned some weeks after finishing the treatment and he also tested positive to Blasto. as well as D.fragilis.
  • "I had a course of drugs and tests have now come back negative for D.fragilis but positive for Blasto." (US. 2004)
  • "Stool testing found high levels of D.fragilis. Three courses of Flagyl later I not only still had D.flagilis I also now had the Blastocystis appear." October 2005
  • US woman suffered "extreme fatigue, explosive & very pale colored bowel movements, belching, and a constant bloated feeling". Because she had tested positive to D.fragilis her GP prescribed two courses of doxycline for 10 days, and two 20 day courses of Iodoquinol (Yodoxin). Despite testing negative, she was still unwell. Twelve months later she was referred to an infectious diseases specialist to determine if her symptoms were due to internal damage from the parasite. She was retested and discovered she was still positive for D.fragilis. (December 2005)
  • H. returned to the UK, after working in India, with loose stools/diarhoea, gas, chronic fatigue, intermittent headaches, nausea, skin rashes and bowel discomfort and worsening arthritis. Because his GP was "sceptical of testing for parasites" H. had to consult an alternative therapist to arrange comprehensive stool testing. The therapist suspected H. had parasites because of he had become infected with parasites whilst working in India some years earlier. In lieu of testing H. was prescribed an array of herbal treatments, supplements, and probiotics prescribed by alt. therapist did not end H's suffering.

    Finally H's GP agreed to arrange stool tests with the London School of Tropical Medicine & Hygiene, who diagnosed Blasto. hominis. The GP was not familiar with this common parasite or how to treat it. Desperate for relief from the disabling symptoms, and lacking any real treatment choices, H. continued on with the expensive course of anti-parasitic and Chinese herbs, immune boosters, vitamin supplements accompanied by a low carbohydrate, sugar, dairy, yeast and nightshade free diet.

    "(the treatment) has cost me a fortune, which is all coming out of my savings as I'm unemployed due to my situation, and I'm reluctantly having to accept that it's not having an obvious effect. I just don't seem to be moving forward.".

    N. decided to book an appointment with a clinician at the Tropical Diseases Hospital in London. The hospital arranged stool tests with the London School of Tropical Hygiene & Medicine. Despite testing positive to both B.hominis and D.fragilis H. found himself no closer to finding out if these parasites were the cause of his debilitating health problems:

    "I had quite an open chat with Dr X about the whole "pathogenically controversial" issue of blasto and d fragilis. He said the Professor's view is that it's probably not pathogenic. He admitted that some people do appear to get better after a treatment of anti-biotics (Flagyl) but said that the School's view is that this is a placebo effect."

    (March 2005)

Under reporting of parasites:

Because Blasto. is considered controversial in terms of pathogenicity, many labs do not routinely search for this parasite, or may not include this parasite in their test results even if found.

Under-reporting is less likely to occur in the US because labs are required by law to include Blasto. in their report. However, this is not the situation in the UK, New Zealand, Australian and Canada because labs in these countries are not bound by such restrictions.  The following study found that two out of seven labs did not actively look for Blasto., nor did they report this parasite even if it was found: 

Not all laboratories routinely searched for B. hominis. The provincial reference laboratory for parasites reported all parasites found in the samples. In only two of the seven other laboratories was this also done. The five remaining laboratories (involving samples from seven day-care individuals) later stated that they did not actively search for, or report, B. hominis as a matter of course because it was not believed to be pathogenic.
BLASTOCYSTIS HOMINIS: A NEW PATHOGEN IN DAY-CARE CENTRES? Canada Communicable Disease Report - Volume 27-09, 1 May 2001

This study found that government labs did include Blasto. in their report, but private labs did not:

In March 2000, stool samples were collected from 17 symptomatic patients to test for parasites. All patients had at least one of the following symptoms: nausea, vomiting, diarrhoea, abdominal cramps, bloating. Two stool samples were requested for testing at the Provincial Reference Laboratory (a public laboratory in Canada). A further 10 symptomatic individuals were evaluated by their physicians and 2 stool samples from each were sent to 7 different laboratories:

The govt. lab reported all parasites found in the samples, but 5 private labs DID NOT report all parasites, in particular Blastocystis hominis, as they believed this parasite was non-pathogenic and therefore they did not actively search for it. If it was found they did not report it to the treating physician. B. HOMINIS: A NEW PATHOGEN IN DAY-CARE CENTRES? Canada Communicable Disease Report - Volume 27-09, 1 May 2001

The following people were unwitting victims of this controversy:

A Canadian man contacted to say he was diagnosed with Blasto. after being alerted about the importance of specialised testing after finding my site. After being treated with a combination of Flagyl, Bactrim and Iodoquinol he was rested. His samples were negative but his symptoms persisted.

Three years later he wrote again after reading about the problem of under-reporting on this site. He had decided to recontact the lab who tested his two batches of samples. The lab advised him that just before he submitted his second batch of samples the lab had decided to implement a policy of non-disclosure. In other words, the lab no longer informed the doctor that the patient had Blasto. This man, believing that he was no longer infected, had consulted 45-50 doctors trying to find out why he was still unwell. ( December 05)

C. believed he was giving himself the best chance of finding out if he had parasites when his dr arranged stool testing with a high profile lab in Montreal:

"I specifically asked my doctor if they considered Blastocystis Hominis (the parasite that I suspected) to be a potential pathogen?  He said "no" and that they do not even look for it in the samples." (December 2005)

"A microbiologist at the public lab here in Ontario advised me that they will never report blasto when they find it. however, she talked with her supervisor and told me that if my doctor phoned, they would advise him if Blasto was found in my most recent samples." (2003)



Another Canadian, diagnosed with B. hominis, asked a lab. technician attached to a local hospital how often they detect Blasto:

"she said they probably find more than 10-20% of the stool samples contain this parasite but they have only started to report the results since 2001"
(August 02)



Another Canadian infected with Entamoeba histolytica, contacted me in November 2003:

"I won't bore you with all the flagyl misadventures, which are very similar to the stories already on your site. I was treated with the stuff for entamoeba hystolica three times with no success before I found a new doctor who followed the course with 20 days of yodoxin (diodoquin in Canada). Test results finally came back neg for EH. Much rejoicing, until the nurse mentioned, just by the way, there were some other things found that are not considered pathogenic. Suspicious as I was by this point, I asked him for the names of the other things found. This was the first time I had ever heard of blastocystis, and this was a year into my treatment!"



An example from the UK:

"I went to the hospital of Tropical diseases here in London & they said I had nothing. Last week I went to see a specialist in chronic fatigue (as this is what my GP has diagnosed me as having - with no cure) and the specialist Dr. informs me that the hospital have identified BH, but not informed me as they think it is non-pathogenic."
October 2005

Physicians who consider Blasto. harmless do not always disclose a positive result to their patient, as in this case:

"I found your site after looking up blastocytis hominis on the computer. I searched for info on BH because my husband was diagnosed with giardia this past March, but they never mentioned BH. It was only when I got a copy of the lab report that I was aware of the infection." (USA. December 2005)



An Australian man, who tested positive to B. hominis on five separate occasions, was not treated because his doctor did not believe Blasto. was responsible for his patients bloating, fatigue and nausea. Irritable Bowel Syndrome was diagnosed and anti anti-depressants were prescribed. The lab advised that their "opposition does not even mention Blasto. to the referring doctor when they find it as they class it non important.". (2005)



Denmark:

A Danish dr was not confident in the ability of Danish labs to diagnose parasites in his patients:

"if one tests here in Denmark, the test normally comes back negative, but if he sends tests from the same person to the USA, the test is often positive. He thinks that (results from) Danish labs often are unusable in this area.".



Alternatives to the current method of diagnosing parasites - microscopy - are thin on the ground. Here are a few:

Rectal swabbing
(anoscopy) is another diagnostic technique, and involves scraping inside the rectum area with a small brush, preserving the contents in liquid fixative, and sending the samples for testing to a reputable lab.

The usefulness of this procedure has always been questioned by the wider medical community, yet doctors who use it claim increased detection of parasites because the anoscopy brush dislodges parasites embedded in the bowel wall. Their claims are reflected in the number of people who have written to to tell me they would not been diagnosed if not for anoscopy.
Unfortunately many health insurance companies no longer cover this valuable diagnostic procedure, and the cost can be prohibitively expensive for patients:

"I have yet to find a parasite with a purged stool sample sent to Great Smokies yet the rectal swabs have found it 5 times."

"I have had many many stool tests, and non of them have shown the parasites. The only tests that were positive was a rectal swab which showed the cysts of Blasto. hominis and e.histo., an amoeba" (Feb 02.)

"I'm just wondering why the Great Smokies parasite test I did showed no parasites, yet the rectal swab I had done through the doctor in NYC did show the cysts." (Feb. 2003)

"Found blasto. & giardia with an anoscopy in cyst form. I am convinced this is the only valid test for a parasite. Worked for me twice now, when other tests have shown nothing." (2002)

"Results from 3 (fixed) fecal samples tested by Great Smokies Diagnostics, as well as 3 purged samples submitted to Chelsea Biologics, were negative for parasites. However, the samples of an Anoscopy, examined by a parasitologist, revealed: Blastocystic Hominis Cysts" (April 2003)

G. was diagnosed with E.histolytica & giardia by rectal swab after negative results from local labs:

"I have been suffering for more than 20 years. I was diagnosed by a doctor in New York City, Dr. Louis Parish (since retired). He and another doctor had developed a test called a rectal swab. There was a lab tech in the office that looked at the specimen right then and there. He had found Giardia lambia and E. histolytica. (US Dec 2000)

Purging:

A 1986 study (Sheehan et al. Clinical Microbiology) suggests that:

"parasites lodge in the cecum — Intestinal parasites seldom colonize the lower colon, and
therefore, purged stools appear to be more efficient for finding parasites residing in the cecum. The terminal portions of stool collected from our purged patients yielded the highest number of B. hominis organisms, and this finding suggests that B. hominis has a propensity for cecal colonization, as does E. histolytica."

This may explain why a number of people have reported testing positive only after submitting purged samples.

Purging, which involves drinking a strong laxative, can force parasites out of the bowel and by doing so increase detection. However, some laxatives can intefere with lab techniques and by damaging the parasite alter its shape, making detection less likely.

Safe laxatives are:


Fleets Phospho-Soda*, Golytely, Nulytely (USA and Canada), Picoprep (Australia), Picosulphate (UK), and Klean-prep (Europe, African and Middle, Far Eastern countries and Canada).

Check with your dr before taking any products which cause diarrhoea.

* Read this information about Fleets before using.


Culturing consists of placing a stool specimen in a special media. This media encourages the organism to grow. This method is more time-consuming and therefore more costly for laboratories to perform, and for this reason it is not routinely used:

Although D. fragilis is most commonly identified using permanently stained fecal smears, recent advances in culturing techniques are simplifying as well as improving the ability of investigators to detect this organism. However, there are limitations in the use of cultures since they cannot be performed on fecal samples that have been fixed. Emerging from Obscurity: Biological, Clinical, and Diagnostic Aspects of Dientamoeba fragilis. Eugene H. Johnson, Jeffrey J. Windsor, and C. Graham Clark. Clinical Microbiology Reviews, July 2004, p. 553-570, Vol. 17, No. 3

The following studies also show the value of culturing:

It is important to subculture, even if protozoa are not seen in the primary culture , the first subculture often detects more infections with D. fragilis and Entamoeba species than does the primary culture (Ockert, 1990).

Without culture, we would have overlooked the organism in 2 of 4 infected stool samples. Even so, we probably underdiagnosed the infection by examining only one stool sample from each patient. The number of D. fragilis in faeces can vary widely from day to day. (Desser & Yang, 1976).

Culture contributes even more to the diagnoses of D. fragilis infection . Silard et al (1979) found faecal culture to be more than 5 times as sensitive to microscopy in detecting Dientamoeba and E. histolytica infections, and Ockert (1990) reported still greater i ncreases in sensitivity.
Diagnoses by faecal culture of Dientamoeba fragilis infections in Australian patients with diarrhoea. Nongyao Sawangjaroen, et al. Transactions of the Royal Society of Tropical Medicine and Hygiene (1993) 87, 163-165.

The use of culture techniques may increase detection of D.fragilis signficantly, with reported cases as high as 18.1% in Israel, 36% in Holland and 41.5% in Germany.

Dientamoeba fragilis: the unflagellated human flagellate. Jeffrey J. Windsor and Eugene H. Johnson. British Journal of Biomedical Science 1999; 56: 293-306


ELISA (enzyme-linked immunosorbent assay):

A biochemical test named ELISA (enzyme-linked immunosorbent assay) is available for diagnosing Entamoeba histolytica, Giardia and Cryptosporidium. It is considered much more reliable than microscopy because it depends on detecting parasite antigens, in contrast to microscopy which relies on microscopic identification. Because of the cost involved in antigen testing most labs will only carry out this test when a specific request is made by the dr.

The US Centre for Disease Control website contains useful information about specialised ELISA testing. Antigen testing is usually performed on fresh (unfixed) stool.

Antigen test is not yet available for either D.fragilis or B.hominis.



Antibody testing:

Salivary:

Antibodies are produced by the body in response to an infection. Because antibody testing cannot distinguish current infection from past exposure, most doctors do not consider it useful. My view is that until more sensitive and reliable testing is available to diagnose Blasto. and D.fragilis, and because these parasites can cause so much misery to the sufferer, antibody testing has a role for patients who are symptomatic but who have failed stool testing.

Antibody testing is available from Diagnos-Techs, Inc. Because this test is controversial the results are not always accepted by doctors. Example here.



Optimising your results:

The following products may interfere with test results and should be avoided for three weeks prior to, and during, the testing phase:

tetracyclines, sulfonamides, antiprotozoal agents, certain laxatives (see purging below), antacids, castor oil, magnesium hydroxide, barium sulphate, bismuth kaolin compounds, hypertonic salts, mineral supplements, anti-parasitic herbs, antibiotics, antacids, antidiarrheals, enemas, intestinal & radiocontrast agents. Some toilet papers contain chemicals which can interfere with test results.

Always consult your doctor before stopping any medications.

Submit small random samples from the last half, rather than the first half of the stool, because:

The number of organisms excreted daily flucuated markedly in the one case investigated. With regard to the distribution of the parasite within a stool, considerably greater numbers were found in the last portion evacuated than in the first half.
Dientamoeba fragilis, a review with notes on its epidemiology, pathogenicity, mode of transmissino and diagnosis. Yang & Scholten, Am J Trop Med Hyg. 1977 Jan;26(1):16-22.

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