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Showing results for tags 'cross contamination'.
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The Gluten Contamination Study We've Been Waiting For
Jefferson Adams posted an article in Additional Concerns
Celiac.com 10/14/2019 - One of the big debates among people with celiac disease concerns how vigilant celiacs need to be to make sure they avoid gluten. What does science say about gluten contamination in three common scenarios? How careful do you need to be about gluten contamination? For example, how likely are you to get gluten over 20ppm if you share a toaster, pasta water, or slice a cupcake with the same knife used to cut a non-gluten-free cupcake? A team of researchers recently set out to assess three common scenarios where people with celiac disease might reasonably fear gluten contamination. How did the actual risk for each situation measure up? Scenario 1: Water used to cook regular pasta is reused to cook gluten-free penne and fusilli. The gluten-free pasta is then rinsed and served. Scenario 2: Toasting Gluten-Free Bread in an Uncleaned Shared Toaster Gluten-containing bread is toasted in a toaster. Immediately afterward, gluten-free bread is toasted in the same toaster. Scenario 3: Slicing a Gluten-Free and Regular Cupcake with Same Knife The research team included Vanessa M. Weisbrod, BA; Jocelyn A. Silvester, MD PhD; Catherine Raber, MA; Joyana McMahon, MS; Shayna S. Coburn, PhD; and Benny Kerzner, MD. They are variously affiliated with the Celiac Disease Program, Children’s National Health System, Washington, DC, USA; and the Harvard Celiac Disease Program, Boston Children’s Hospital, Boston, MA. Their paper titled, Preparation of Gluten-Free Foods Alongside Gluten-Containing Food May Not Always Be as Risky for Celiac Patients as Diet Guides Suggest, appears in Gasterojournal.org. Control samples of gluten-free pasta, bread, and cupcakes all tested below the limit of detection. Samples were individually packaged in plastic bags with randomized sample numbers. To avoid “hot spots” and ensure even analysis, all items were homogenized for analysis. Gluten content was measured with R5 sandwich ELISA (R7001, R-Biopharm, Darmstadt, Germany) which has a limit of detection of 5 ppm gluten by Bia Diagnostics (Colchester, Vermont). All control samples were similarly tested. The team then quantified gluten samples as under 5ppm, 5-10ppm, 10-20ppm, or over 20ppm, and based their confidence intervals upon binomial distribution. Boiling Gluten-Free Pasta in Regular Pasta Water In the first scenario, the team boiled sixteen-ounce packages of gluten-containing Barilla brand penne and fusilli separately in stainless steel pots in fresh tap water for 12 minutes, then removed with strainers. The water was reused to cook Dr. Schar gluten-free penne and fusilli. The team also tested the effect of rinsing some samples of the cooked and contaminated pasta under cold tap water for 30 seconds. The team found that Gluten was detected in all pasta samples cooked in water used for gluten-containing pasta, ranging from 33.9ppm to 115.7ppm. The rinsed gluten-free pasta samples tested at 5.1 ppm and 17.5 ppm detectable gluten. Interestingly, rinsing pots with water alone after cooking gluten-containing pasta was as effective as scrubbing with soap and water to prevent detectable gluten transfer. Toasting Gluten-Free Bread After Non-Gluten-Free Bread In the second scenario, the team toasted regular gluten-containing bread in two rolling toasters in a busy hospital cafeteria at 20-minute intervals, or in one of three shared pop-up toasters. Immediately after toasting the gluten-containing bread, they toasted Dr. Schar Artisan White Bread. Gluten-containing crumbs were visible in all toasters. They team did not clean the toasters. The team found that toasting in a shared toaster was not associated with gluten transfer above 20ppm; the four samples with detectable gluten had levels ranging only from 5.1 ppm to 8.3 ppm gluten. Slicing a Gluten-Free Cupcake with Knife Used on Gluten Cupcake In the third scenario, the team used a knife to slice frosted gluten-containing cupcakes. The knife was then reused to slice a frosted gluten-free Vanilla Cupcake from Whole Foods Gluten-Free Bake House. The knife was then washed in soap and water, rinsed in running water, or cleaned with an antibacterial hand wipe (Wet Ones) and a new gluten-free cupcake was sliced. Both gluten-free cupcakes were analyzed for gluten content. Although 28/30 cupcake samples had detectable gluten transfer, only 2/28 tested over 20ppm. The team found that cutting cupcakes with a knife used to cut frosted gluten-containing cupcakes was associated with low-level gluten transfer even when crumbs were visible on the icing adhered to the knife. All three knife washing methods tested were effective in removing gluten. The team acknowledges the limitations of their study, including small sample size, etc. They are calling for further study to assess best kitchen practices for people with celiac disease who are trying to avoid gluten contamination in shared kitchens. Main Takeaways 1) Some kitchen activities may pose less of a risk of cross-contact with gluten than is commonly believed. 2) Standard washing effectively removes gluten from shared utensils. 3) Cooking gluten-free pasta in the same water as regular gluten-containing pasta is likely okay, as long as the pasta gets rinsed well. 4) Sharing a toaster is unlikely to result in gluten contamination. Read more in Gastrojournal.org Conflict of Interest Declaration: JAS has served on an advisory board of Takeda Pharmaceuticals and received research support from Cour Pharma, Glutenostics, and the Celiac Disease Foundation. The other authors have no conflicts of interest to disclose. Funding Source: Supported by philanthropic gifts from the Celiac Disease Foundation, Dr. SCHAR USA, and Bia Diagnostics. JAS is supported by the National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health under Award Number K23DK119584.- 70 comments
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https://www.tastingtable.com/1373953/kroger-recall-frozen-corn-veggies-illness-listeria/ Kroger just released this recall of frozen vegetables. I was just now feeling better from what I thought was a celiac reaction. I eat kroger frozen green beans and I’m instantly sick again. I imagine listeria wouldn’t hit me that quickly? I’ve never had a celiac reaction to their frozen vegetables. But I’m thinking if it’s contaminated with listeria, it could be contaminated with gluten too? Because this feels a lot like I was glutened. I appreciate any advice.
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Hello. I am newly diagnosed, 5 weeks post endoscopy, started gluten-free that day. My symptoms were never that severe, just periodic mid-back ache, short term fatigue and D that I couldn't figure out for a couple years. I have a question that I can't seem to find scientific answers to, despite lots of reading. Because my symptoms weren't that severe, I don't expect to be able to sense if I've accidentally taken in a little gluten. However, from what I understand, small amounts could cause a response from my immune system, and even if I don't feel sick, would set me up for increased risk for all the secondary issues (cancer, other auto-immune issues, etc). So, that leaves me needing to avoid small gluten exposures for future health prevention, not for fear of getting notably sick. From my research it appears the daily limit is 10 mg, or 1/250th of a slice of bread. My very scientific husband and I have been using this number to try to figure out how to run our kitchen (family of 4 including two teenagers). To me, this means avoid all crumbs, have my own butter, toaster, cutting board, etc, which I've done. But every post I read recommends to use your own silicone spoons, wooden spatulas, tupperware, etc, even though it's been washed. I cannot imagine the microscopic gluten on a clean wooden spoon would add up to 10mg of exposure per day. I gather there are many people who are much more sensitive than I am. But my question is, given that I'm not that sensitive, from a scientific point of view, is it ok to share clean utensils, tupperware etc and assume I am keeping my exposure to <10mg/day? Thank you for reading!
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After experiencing severe symptoms for six years, I finally was diagnosed with celiac disease two years ago. I went gluten-free and immediately started feeling better. There was a learning curve (including getting rid of wheat-contaminated spices like turmeric). Recently, I had been really healthy, exercising regularly, getting in shape, eating well and feeling amazing. Suddenly I was glutened three days in a row. Then a week later I was glutened again. I believe it was all cross contamination. Normally I feel miserable, body aches, severe migraine for a couple days. This time I had mild cold symptoms, my lymph node was painfully swollen (very hard and poking out of my neck with a lot of tension), chills, extreme migraine 24/7, higher pulse, easily exerted/heart beating out of my chest, fatigue. It was all similar but much more severe (but still not as severe as accidentally eating some soy sauce which leaves me attached to the toilet for 14 days and in pure hell). I feel like the healthier I am, the stricter I need to be. It’s so hard in a world full of gluten. I am posting to vent and also give an updated experience. I had gone so long without any symptoms. I hate my life and hate the existence of gluten when this happens. I am so miserable. I also become very cranky and negative. Another weird thing I noticed is I will start to feel better and suddenly get sick again. I wonder if it has to do with the lymph node. I was feeling better yesterday but the lymph node was still hard as ever. Today it went down and my miserable migraine returned. I wonder if the lymph node released something that would continue my symptoms. I can barely feel the lymph node now but I feel so miserable. Anyway, just say no to cross contamination. 🙏🏼
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Hello, I have been diagnosed with celiac disease only two months ago. After hearing the diagnosis I've replaced almost everything in my kitchen to brand new items beacuse I was scared of cross contamination. I don't have a dish washer and everything has to be cleaned manually with soap and a sponge. Me and my grandfather find it really hard to get the suds off of the cutting board's surface (especially after cutting meat on it) so he came up with an idea that we could wash it with baking powder (I didn't question it, he has a lot of tricks he knows from "the old days"). It didn't even cross my mind that baking soda has wheat flour in it, I'm so new to this and still very, very lost. And so my brand new cutting board was washed two or three times with baking soda and was kept in my own separate cupboard with new, clean utensils, pots and pans. Some wooden/plastic/teflon (porous basically) and after washing of course we would put it on a drying rack (which I also bought brand new, just for me). I am currently terrified. Do I have to replace these items again because they were kept together in the same spot? Will hand washing and cleaning out the cupboard suffice in getting rid of the potential contamination? Of course I will replace the cutting board itself but what about other things in the said cupboard that the board was touching? We are very poor, replacing these items the first time was extremely costly and for some time put me and my grandfather in a very bad financial situation. I feel so stupid becuase I've been so diligent about my diet and messed up on such an obvious thing like baking powder but I'm young and so new to this lifestyle and diagnosis. I'm very scared and very stressed out, please give me some advice. I'm sorry if my explanations are a little jumbled, I'm shook-up and English is not my first language. Thank you.
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Celiac.com 04/09/2020 - Anyone with celiac disease knows how hard it can be to follow a gluten-free diet. Some studies have shown that even celiacs who strive to stay gluten-free are commonly exposed to gluten. How common is gluten-exposure in celiacs who are following a gluten-free diet? A new study takes a deeper look at real world gluten exposure in celiac patients following a gluten-free diet. To do so, the research team set out to measure levels of gluten immunogenic peptides (GIP) in fecal and urine samples from celiac patients on a gluten-free diet. The research team included Juan Pablo Stefanolo, Martín Tálamo, Samanta Dodds, María de la Paz Temprano, Ana Florencia Costa, María Laura Moreno, María Inés Pinto-Sánchez, Edgardo Smecuol, Horacio Vázquez, Andrea Gonzalez, Sonia Isabel Niveloni, Eduardo Mauriño, Elena F. Verdu, Julio César Bai. They are variously affiliated with the Dr. C. Bonorino Udaondo Gastroenterology Hospital, Buenos Aires, Argentina; the Farncombe Family Digestive Health Research Institute, McMaster University Medical Centre, Health Sciences, Hamilton, ON, Canada; and the Research Institutes of Health, Universidad del Salvador, Buenos Aires, Argentina. The team conducted a prospective study of 53 celiac adults in Argentina who had followed a gluten-free diet for more than two years, and an average of eight years. The team used a celiac symptom index questionnaire to assess celiac-related symptoms for each patient at the beginning of the study. Patients in the study collected stool each Friday and Saturday and urine samples each Sunday for one month. The team used a commercial ELISA to measure gluten immunogenic peptides in stool and point-of-care tests to measure gluten immunogenic peptides in urine samples. Among other revelations, the results showed that nearly 40% of stool and urine samples were positive for gluten immunogenic peptides. Nearly 90% patients had at least one fecal or urine sample that was positive for gluten immunogenic peptides (median, 3 excretions). Nearly 70% of urine samples were positive for gluten immunogenic peptides at least once. Positive gluten immunogenic peptides samples correlated with blood levels of deamidated gliadin peptide IgA, but not with levels of tissue transglutaminase. Interestingly, symptomatic patients had more weeks with detectable gluten immunogenic peptides in stool than patients without symptoms. Patients with celiac disease on a long-term gluten-free diet are still frequently exposed to gluten. Tests to measure gluten immunogenic peptides in stool and urine could help dietitians ensure gluten-free diet compliance. In their celiac patients. In this real world study, nearly nine out of ten celiacs who are following a gluten-free diet tested positive for gluten exposure at least once in this study, and nearly two out of five urine tests was positive for gluten exposure. Moreover, these exposures may not have symptoms. This is pretty alarming news, to be honest. People with celiac disease need to avoid gluten, and they need a reliable way to check and see if they need to adjust their diet. Do you have celiac disease? Are you on a gluten-free diet? Do you think you get exposed to gluten regularly? Do you think that regular testing might help you to avoid gluten? Comment below. Read more in the Clinical Gastroenterology and Hepatology
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Cross contamination
Susan K posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
This is my first post, and am looking for advice, please. I was diagnosed with Celiac disease last Dec. via endo and blood tests. I immediately went gluten-free, and tried to rid the house of as many gluten containing items as possible. My husband still insists on eating his favorite foods in the basement, and it’s filled with crumbs on the carpet and coffee table. He also buys gluten treats for my two grandsons, who touch EVERYTHING in the house. I end up sounding like a harpy or a broken record, to no avail. And I have been getting sick. The person who only vomited 4 times in her entire life (TMI, sorry!) has vomited more in the last few months. I do NOT eat anything with gluten. All hair/nails/body/cleaning products are gluten-free. I think I’m getting gluten-ed from hubby and the kids tracking it upstairs on shoes, socks and clothing. He says I’m wrong and the crumbs won't hurt me. My numbers have come down, but still need work. I have a telehealth appointment next week to discuss the test results. I don’t know what else to do, so looking for suggestions. Maybe moving out is an option… Has anyone else experienced this? Thanks in advance! -
Hey Guys! I love this forum, full of really useful information. I am new to the gluten free world and have just been diagnosed with celiac disease. I live in a apartment with 2 other roommates that are not gluten free. We share the kitchen, utensils, and various other pots and pans. I try to keep my dishes, forks, etc as separate as possible but I was recently ‘glutened’ and I’m trying to figure out why. I have a suspicion that it was because my roommates were not careful while cleaning share kitchen supplies, or I’m paranoid, I’m not sure anymore. I can’t figure out if it was more likely from gluten CC from “gluten-free” foods, lack of attention to detail when doing the dishes, or some something else, or are they all likely to happen? I really appreciate any feedback and have been really trying to educate myself by browsing this forum. Thanks for your help!
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I don’t understand how companies can label their product as gluten free and then on the back of the package make a statement about “processed in a facility that uses wheat, dairy, etc. Wheat as we know contains gluten, so how can they get away with the words “Gluten Free”?
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I live with my mother as an adult, and I am Gluten Intolerant to where if I get around wheat, I get sick. I am sick accidentally three times a week because even though I am careful, something keeps happening. So I bought gloves and kept a few plates, silverware and use the same glass, i clean with a separate sponge, i wipe the counters down with bleach, and the handles. My Mother just put pasta in the fridge hot, and the air went up. that frightens me because i have cheese up there in a block, that is semi open. I also had an open avacado. Should I throw those things away, or is there a way to clean the cheese, only part of the pack is open at the top. Its just a concern. I spend so much time stressing about this because i have to share a kitchen. im this close to washing stuff in the bathroom and we all know how dirty that is..its really very sad...
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Hello, This is my first time posting to this board. My daughters were both recently diagnosed with celiac. We are getting used to it. It's so much easier to control on the home front, trickier when we travel. We suspect we've gluttoned our youngest, who seems to have it much more severely, via cross contact a few times. Dish towels, sponges, cutting boards etc. while visiting family. They go to extraordinary lengths to accommodate us food wise, it's the environmental piece that feels insurmountable right now. What are your best travel tips when visiting family or going on vacation when you want to cook in a kitchen? We love to cook, food is a big deal to us. Do you bring your own items? If so, what do you bring? WOuld love to hear how other approach this. Thanks!
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Can I be cross contaminationed by purchasing resale items that have come in contact with gluten? Can I properly sanitize a bedding set without destroying the color/fabric? If so, how? I purchased a bedding set through a virtual yard sale, and my husband brought this question up. I've never thought of it in my 6 years as a diagnosed celiac. I couldn't find information about cleansing cloth (fully) from gluten, and I'd like to feel safe before picking the set up. Any info or direction would be greatly appreciated.
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Traveling with celiac I would like to relate my experience today and then ask for advice on traveling and bringing food along (being prepared). See last paragraph Today we traveled to a new place and meet new people. We had a project to do and then everyone wanted to go to lunch. So I didn’t have an opportunity to research this place before hand - I could’ve used Find Me Gluten Free - but I didn’t. I took a risk. (I know better now) anyways the place we went had gluten-free options so I asked the waitress if I got the gyro without the pita would it be gluten-free. She said yeah. She asked if I wanted fries even though fried in same fryer as other gluten items. I said yes because I’ve done it before without any repercussions. I love fries. So the place seemed pretty knowledgeable about gluten-free food. My food was great! But an hour or so later I was vomiting in the men’s stall at a gas station (all the fries, TMI?) - the woman’s was occupied! I have only recently started vomiting when I have a cc gluten exposure. Ugh! Ok so I know my mistake was getting the fries. Taking a risk. Not double checking the restaurant. Not maybe being more vigilant for my health. I hate being that person at the restaurant who has to make a scene asking all the gluten free questions. Especially in front of new people. So now I know I need to be better prepared. But does that mean not eating out at new places every again? I need advice in how to travel with celiac disease, how to be better prepared for going to a new restaurant. At this point should I just pack my own lunch every time I go somewhere new? My husband (bless his heart) did pack me veggies to eat but I need more than that or I’ll get hangry. Also I am terrible at being that prepared that I could have brought my own lunch along. Also do I eat my own lunch in the restaurant? I can’t do that right plus it would be weird?
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Good afternoon, My 5 year old daughter has just received her diagnosis of celiac's disease after a biopsy. I have not met with the gastroenterologist since the diagnosis (apparently next appointment will only be in a few months) and we have been told that we will be contacted for an appointment with a nutritionist in a few weeks. Until then, I am left with a lot of questions. This is day 2 of going gluten free and I am feeling slightly insane. I see bread crumbs everywhere! I am trying to think of all the ways cross contamination can occur and have designated a small isolated section of my counter as the GLUTEN counter, where anything bread related must happen. As I fiddled around making three different lunches to accommodate my 4 small children's particular dietary needs and preferences (the 5 year old with celiac is the eldest, and one of my twin babies has an egg allergy), I thought I would lose my mind. Bread crumbs would travel on my fingers, I worried about transporting toast to a plate near hers, and of course, the dreaded idea of toasting her first ever slice of gluten free bread in the regular toaster. I must have washed my hands 10 times and I had to restrain myself from making her eat at a separate table lest her twin baby sisters started to toss their crusts around. I am making a list of things to buy to use exclusively for gluten-free stuff: I need new wooden cooking instruments, a new nonstick pan, a new toaster... or do I? There is a part of me that wonders if I am succumbing to some kind of collective gluten paranoia. Please don't get upset at me for feeling that way! I just have trouble wrapping my head around the idea that a tiny trace of gluten left in a pan that has been cleaned could really do any damage. I have tried to think of the gluten as a poison. It's not like I would accept "just a wee bit of arsenic" in my children's food. But then again, I am visualizing gluten like a feral cat clawing away at my daughter's gut, and then thinking about the little speck of gluten leaving a tiny pinprick... which doesn't seem so concerning. So how bad is cross contamination REALLY? In your experience, based on your knowledge, based on your opinion. I'm open to your thoughts. But, please understand that at this time, I am NOT considering turning my home into a gluten-free home. I don't want everyone to be deprived because of one person's diagnosis, and quite frankly I can barely imagine how I will finance one person's gluten-free diet, let alone 6! Thanks for your feedback!
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Hi All, My my family and I just moved to Switzerland from Australia. As an American expat I was very pleased to find out that I could easily order gluten-free Cheerios for my 3 and 5 year old girls for the first time! Well...for the past two weeks my girls have been displaying signs of being glutened. They are now having terrible direahea for the past 2 weeks since I've been feeding them this cereal every other day or so. I've desperately been trying to rule out what is causing this but we are a gluten-free household...Now, I'm just waiting for the poo samples to come back because none of thier kindergarten and play group friends are sick but these test won't reveal gluten poisoning...sadly, I've just stopped the cereal for brekkie. I am am wondering if anyone here has had any problems with the gluten-free Cheerios as of late? Thank you!
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Hello everyone! I am wondering if anyone knows if Essie nail polish is gluten free?? I contacted the company but didn't hear back I have also tried googling it but didn't find anything. I am currently getting cross contamination somewhere and have a breakout of DH but can't figure out what is causing it so this is my next test to see if it could be the nail polish. Thank you for any help you can give me!!!
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In an effort to find out what I have been eating that is causing my symptoms (migraines, joint pain, brain fog, fatigue, gut pain) I have invested in a Nima tester. Peanut M&M's DID NOT pass the gluten free test! I highly suspect cross contamination as Mars have so many M&M's that contain gluten items like pretzels and cookies. Peanut M&M's are off my safe list of something quick to grab. It also helps to shed light on why my tTg is slightly elevated as I have been eating them as of late. Since I am going with whole foods for awhile to see if that helps resolve my symptoms, peanut M&M's are off my list anyway.
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Hi. Either I can't find a good, pure turmeric, or I am cross-reacting with it. Does anyone else have a problem with turmeric? What is a good, pure, not too expensive commercially available brand (in USA)? Thanks.
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