Hay Fever: Fact or Fiction

You can almost set your clock to it – winter ticks over into spring, plants start to bloom, and people’s noses start to act up – runny nose, stuffy nose, or even post-nasal drainage. The condition commonly called “seasonal allergies” or “hay fever,” which goes by the medical name of “Allergic Rhinitis,” affects up to 60 million people in the United States and can make life a snotty mess. Read below to learn more about this condition, including some common misconceptions.

Fact or Fiction: Seasonal allergies are called that because they only occur in the spring and the fall

FICTION. “Seasonal allergies” can be a bit of a misnomer. While it is certainly common to have flares of symptoms in the spring and fall, many people suffer from perennial (year-round) symptoms. This can occur because of allergies to indoor allergens like dogs, cats, cockroaches, and dust mites. Allergy testing can evaluate for the commonly known allergens like trees, grasses, weeds, and molds and tests for indoor allergens. Unfortunately, many people can’t count on the time of the year to provide relief.

Fact or Fiction: Eating local honey helps prevent or treat nasal allergy symptoms.

FICTION. This commonly suggested remedy offers to provide allergy relief with a tasty treat. Sadly, it is not effective. The thought process is that local honey contains pollen, and eating the honey will allow for exposure to the pollen – similar to an allergy shot. While there can be small amounts of pollen in local (unprocessed) honey, this tends to be from flowering plants, which are less likely to cause allergy symptoms. Pollen allergy is most commonly caused by wind spread pollens like those from grasses, trees, and weeds. 

Fact or Fiction: Allergies aren’t the only cause of this type of nasal symptom.

FACT. Though ⅓ of patients with persistent nasal symptoms have allergic triggers, another ⅓ have non-allergic triggers. These triggers can include perfumes/fragrances, smoke, or even temperature/humidity changes; the latter two can mimic the seasonal pattern seen in seasonal allergies. Thus, the final ⅓ of patients with nasal symptoms have a combination of allergic and non-allergic triggers, which we call “mixed rhinitis.”

Fact or Fiction: Allergic (or non-allergic) nasal symptoms are just a normal part of life that has to be dealt with – there’s nothing to be done about them.

FICTION. Thorough evaluation of symptoms, combined with allergy testing, helps guide specific treatment for your nose symptoms. At Allergy, Asthma & Food Allergy Centers, we are experts in diagnosing and treating allergic, non-allergic, and mixed nasal symptoms. A combination of environmental control measures (to reduce exposure to allergens), treatment with oral or nasal medications, and possibly the addition of allergen immunotherapy (allergy shots) can provide lasting symptom relief.

Allergists are uniquely qualified to help you get the relief you need when it comes to this troublesome condition. You can learn more about this condition in our blog, or by making an appointment to be seen by one of our providers.


Welcome Dr. Waterhouse

We are also excited to welcome Dr. Waterhouse to our AAFAC team! After graduating from medical school at UMKC, Dr. Waterhouse returned to St. Louis and did a pediatric residency at Cardinal Glennon Children’s Hospital.

She completed her allergy and immunology fellowship at SLU, and after finishing her fellowship, she started the allergy department at SSM Medical Group, where she has worked for the past 10 years. Dr. Borts and Dr. Warrier were Dr. Waterhouse’s mentors during her fellowship, and she is honored to practice and work with them again. She’s also excited to offer her patients OIT for those suffering from food allergies. Dr. Waterhouse will mainly be seeing patients in west county in the Chesterfield office at Clarkson and Baxter.


Welcome Dr. Dixit

We are pleased to welcome Dr. Dixit to our team of providers! 

He grew up on the Mississippi Gulf Coast and went to Millsaps College in Jackson, MS. Dr. Dixit stayed in Jackson for medical school at the University of Mississippi School of Medicine and completed his internal medicine training at the University of Mississippi Medical Center. He decided to pursue allergy and immunology and completed his fellowship at Saint Louis University.

Dr. Dixit is excited to be joining the team, and will mainly be seeing patients in the Swansea, Illinois office.


Q & A with Laura Kahle, PA-C

Q: How long have you worked at AAFA Centers?

A: I have worked at AAFA Centers for 4 years- and a lot has changed over that time! Three new offices and many new medical services. It’s been an amazing experience to be part of the growth.

Q: What inspired you to be a physician assistant? 

A: I am also a Registered Dietitian and previously worked in pediatrics (particularly Cystic Fibrosis). I wanted to be able to provide complete medical care and not only nutrition therapy. One of the pulmonologists I worked with encouraged me to pursue Physician Assistant studies. I wanted to work in a field where I could utilize my nutrition and PA background, so here I am!

Q: What do you like to do in your free time? 

A: Pre-COVID, we traveled all over the country to see friends and family and explore the outdoors. Now, my husband and I have gotten a little more creative to keep exploring the local outdoors with our 2 little girls.

 


Biologic Treatments for Asthma

Many people who live with asthma manage their symptoms by identifying and avoiding triggers, taking daily oral and inhaled medications, and using a quick-relief inhaler. Recently, many new drugs known as biologics have been approved for treating moderate-to-severe asthma. Biologic therapies are antibodies (immune proteins) that target specific molecules that contribute to poorly controlled asthma.

There are many new biologic therapy options available to treat severe asthma. They work by disrupting the pathways that lead to inflammation in the body that causes asthma symptoms. Xolair and Nucala are approved for patients as young as six years old, while Dupixent and Fasenra are approved for patients as young as 12 years old. Cinqair is approved for adults 18 years and over. 

Biologic therapy may not work for everyone and it may require the use of other treatments as well, but the vast majority of patients on biologic therapy have significant improvement in their asthma symptoms and also require far less if any oral steroids. It is important to see an asthma specialist in order to learn if biologic treatment is right for you. Our experts at AAFAC can help you identify what triggers your asthma and find the treatment that is unique to you and your needs.

 

Source: verywellhealth.com/biologics-for-severe-asthma-4788216

 


What are USP 797 Guidelines?

Our practice is compliant with USP 797 guidelines – what does that mean, and what is USP?

In the early 1800s, when people needed medicine, they went to their local apothecary, where the druggist would mix together a medical preparation derived from hand-collected plants and minerals. But the potential consequences of inconsistent or poor-quality medicinal ingredients or a mistake by the person behind the counter could be serious. Two hundred years ago, the types and quantities of the drug ingredients varied widely. Patients were sometimes given too little or too much. There were often multiple names for the same medicine, and medicines with the same name didn’t always share the same properties. Medical professionals did their best, but in some instances, the treatment could be more dangerous than the ailment. 

In the years following the American Revolution, as poverty increased and America’s water and air became more polluted, people grew sicker. Mainstream medicine became increasingly ineffective. Americans began to seek out non-conventional medicine and people who embraced these methods. Tensions grew between trained doctors and the American public looking for more effective cures. This growing distrust of traditional medicine was one factor that drove one of the most groundbreaking periods for medical inventions in the 19th century, along with the development of modern medicine in general.

Rising from this tension, Lyman Spalding, a physician and professor from New York, became alarmed when he observed inconsistent and poor-quality medicines threatening the health of his patients. He, with the help of Samuel Mitchill, an American physician, naturalist, and politician from New York, convinced other physicians to meet in January 1820 at the United States Capitol to form the United States Pharmacopeia (USP). They put in place standards for the quality of medicines that would protect the public’s health. Reflecting the spirit of the young nation, the group would not be part of the government but instead would remain an independent organization that relied on the latest science to build trust in medicines. 

They created a well-defined and clearly described roster of the best understood medicinal substances and preparations of the day that could be used by medical professionals across the newly established United States of America to prepare medicines consistently and to establish independence from Britain. This first edition of the U.S. Pharmacopeia was written in both English and Latin, making it broadly accessible, and was printed at a low cost to make it easily affordable. 

Move forward almost 100 years.  In 1911 immunotherapy for grass pollen-induced hay fever was used by collecting grass pollen, creating an extract, and injecting it into patients.  Over the ensuing decades, companies took on the role of collecting and purifying pollens and other allergens and making them available to Allergists in practice worldwide.  Most Allergists used these commercial materials to compound allergy extracts to administer to their patients, although there was often a lack of agreement on what and how much to use for treatment.  

Fast forward to today and the modern practice of Allergy.  The USP has regularly met and revised guidelines and recently has established a set of standards that apply to the practice of Allergy and compounding of allergy extracts used in allergen immunotherapy.  

The current USP Chapter 797 provides standards unique to allergen extract compounding for individual patients.  Under the new standards, to continue in-office compounding of individual treatment for allergen immunotherapy, allergy practices need to comply with personnel qualifications, facilities requirements, and documentation.  

How has Allergy Asthma & Food Allergy Centers addressed and met these requirements? 

  • Our allergen extract mixing is overseen by Dr. Michael Borts who has over 30 years of experience in allergen extract compounding.  
  • Our Clinical Staff, Ashley Crowden, RN and Jessica Tharp, RN have completed training and standardized testing on principles and procedures for sterile compounding, garbing, hygiene, gloved fingertip, and thumb sampling and media fill tests.
  • Our compounding occurs in a dedicated Allergenic Extracts Compounding Area located in our South County office location. 
  • Our allergen extracts are labeled with patient name, type, and fractional dilution with corresponding vial number, beyond use date, and required storage conditions.
  • Training, assessment results, evaluations, and qualification records for all compounding personnel, including any corrective actions following assessments and evaluations are kept on file. 

In addition, we use Rosch Immunotherapy in order to provide additional efficiency and safety with rapid patient check-in (to reduce pre-injection waiting times), bar-coding of vials (to promote patient safety with the right extract for the right patient), and efficient documentation of injections.  

While the lack of any reported cases of an infectious adverse event might make these guidelines seem unnecessary, our practice is willing to comply with the USP Expert Compounding Committee’s guidelines to reflect our dedication to patient safety.

 


Q & A with Lauren Davis PA-C

Q: What inspired you to become a Physician Assistant in the field of allergies, asthma, and immunodeficiencies?

A: Actually, I came across this specialty by accident. My physician assistant program provided a general education across a variety of specialties. I knew I wanted a career where I had an opportunity to work with children. I got really lucky to find this specialty (and this office). Not only do I get to treat children, but I get to treat families. I really enjoy getting to see patients frequently, and I feel that our work makes a difference in allowing kids and adults to live more normal lives.

Q: What do you love most about your job?

A: I love the opportunity to see people over and over again. It allows me to form relationships with the families and to get insight into how they are truly doing. I really like being there for milestones for families. Whether that is watching them eat their first peanut, or getting them through a winter without terrible asthma exacerbations, I like being there for these families and doing things to improve their quality of life.

Q: What are your hobbies outside of work?

A: Anything outside! I love playing tennis, skiing, and hiking. I can’t wait for the nicer weather.


Personalized & Caring Approach to Phlebotomy

To identify what airborne allergens or food substances you are allergic to, we generally perform a prick skin test. Allergy testing can be done by a blood test, or phlebotomy, as well. While in some cases, skin testing can identify an allergy that is missed by blood testing, the latter can be useful for evaluating and managing food allergies. Skin testing allows us to obtain results and to develop a treatment plan at the time of your visit, but sometimes it may be helpful to prepare children for blood testing as well, especially if food allergy is a concern. Our phlebotomist, Emily Alexander, is wonderful and takes a personalized and caring approach to her patients.

Emily shares her story below:

I started my lab career at the age of 18 as a lab assistant, learning all the ins and outs of how a laboratory works. My mom had previously worked in that same lab, so it was easy for me to get started on the right foot from coworkers that knew of me. My interest was piqued at a young age, I got to ask a lot of questions about why and how a lab works. Microscopes, tubes, beakers, needles, and the importance to remember that behind each tube being a person.  

My next step was learning phlebotomy from a team of people that instilled the motto of “lab work is the gateway of going home.” Treating each child as if they were our own and the importance of collecting lab tests properly. That journey started in 2007 at a high-ranking local pediatric hospital where the patients and co-workers treated each other as family. The understanding that patients could be scared and apprehensive when I walk into the room was not to be taken lightly. The parents are often nervous and children can sense it and feed off of it. Taking a caring and gentle approach to each baby, toddler, child, and teenager means as much to the patient and parents as it does to me.   

After years of building trust and confidence with families and their physicians (and getting their sometimes complex laboratory orders completed) is how I met the providers, Dr. Warrier, Dr. Borts, and Dr. Vitale. 

I switched gears to private practice in 2016 at Allergy Asthma & Food Allergy Centers, and I continue to take pride in comforting a wide range of ages from babies to adults. I listen to their concerns and their previous experiences. Children like to hear that everyone gets their blood collected at one point in their life and that they’ll be okay before/after the labs are collected.

Whether the families have driven for hours or minutes to get lab work done, I like for them to feel at ease with me. When it comes down to the actual process of blood collection, it’s always best and helpful for the patient to be hydrated and to try to keep from drinking sodas or anything with caffeine. I use a comforting tone while I speak to the children while making eye contact. I like to give the children my honest step-by-step instructions of how it’ll be done and with a few countdowns of 1-2-3’s so there aren’t any surprises. 

One thing I make sure to do is always put the tourniquet on top of the sleeve and not too tight to cause much discomfort or possible pinching. With that being done at the beginning, I believe that it sets the stage for a more peaceful collection. I always ask how they’re doing and love having conversations about their favorite things, like activities, games, shows, or whatever is on their mind. These hidden gems are the best part of my day. Keeping their minds off of whatever is happening has a great calming effect. 

As parents, we don’t ever want to feel like we’re putting our kids in scary situations. Blood draws can be hard on parents, so be mindful of that. Your little ones feel your energy. For them, manage your fear, anxiety, or apprehension as best you can. I would refrain from telling your child too far ahead of time that it will hurt or making a big deal of it. For some families, it may be helpful that the less nervous parent or caregiver is with the child during this appointment. When the patients and families leave with a smile on their faces and the peace of mind of having accurate results, I’ve done my job.

 


Meet Our Team: Dani Loftus

We are pleased to introduce you to Dani Loftus! She is a Certified Family Nurse Practitioner (FNP-BC) & Certified Pediatric Nurse (CPN) who treats people of all ages at the Allergy, Asthma & Food Allergy Centers (AAFAC). Learn more about her in the Q&A below:

Q: How long have you worked at AAFA centers?

A: I joined AAFAC in November 2019. This is my first position after graduating with my Doctor of Nursing Practice (DNP) Degree in May 2019. Prior to joining AAFAC, I worked at St. Louis Children’s Hospital, Shriners Hospitals for Children, and Southern Illinois University Edwardsville.

Q: What inspired you to be a nurse practitioner? 

A: I was inspired to become a nurse from growing up taking care of my grandmother who had diabetes. She was an inspiration and I miss her dearly. 

I wanted to become a nurse practitioner after experiencing the health care system from the perspective of the patient. In 2014 I had two tumors removed from my tongue, and I was hospitalized twice. I had to relearn to eat and how to talk. It was through that experience that I wanted to become a nurse practitioner. I chose to pursue my education through SIUE as I had excellent experiences attending the school for both my bachelor’s and master’s degrees.

Q: What do you love most about your job?

A: I love that I am in an environment where I can continue to learn something new every day. I enjoy working with a physician team that is passionate about teaching!

Q: What are your hobbies outside of work?

A: Outside of work, I spend a lot of time with my family and our rescue pets. I enjoy playing board games and exploring new places. Travel is a passion of mine, and I have been fortunate to see many beautiful places including the Eiffel Tower and the Great Wall of China!

 


COVID-19 Vaccine

We have received numerous questions over the past several weeks regarding the Covid vaccines, and we will try to address most of them in this post. We have compiled this information from different sources which are listed at the end of this piece. Please note, the Pfizer and Moderna COVID-19 vaccines are some of the safest and most effective vaccines for an infectious disease. These vaccines will end this pandemic if almost every human around the world is inoculated.

 

Will our practice (Allergy, Asthma & Food Allergy Centers) receive vaccines to immunize our patients?

As of 4/28/21, we will NOT as the mRNA approved vaccines require extremely cold temperatures (-70°C or -94°F for Pfizer; -20°C or -4°F for Moderna) for storage, and there is now good access for the general population (except most kids) to receive all 3 approved vaccines.

 

I have allergies (to foods, drugs, pollens, etc.). Am I at risk for a severe allergic reaction to the vaccine?

If you have an allergy to polyethylene glycol or some injectable medications, you may be at risk, but food allergies, drug allergies to oral medications, and environmental allergies do not put you at any significant risk over the general population. You will also be monitored for at least 15-30 minutes after vaccination, and vaccination sites should have epinephrine on hand on the off chance you have a reaction. Remember, no one has died from Covid vaccination despite millions of doses and as of this post, over 400,000 people have died due to COVID in the US.

There was a recent CDC  report with 71% of anaphylaxis cases being in the first 15 min. Anyone with an anaphylactic history can and should wait 30 mins. 

There is currently no validated testing for suspected allergy to polyethylene glycol or for other components of the vaccine. You can find more information here: American College of Allergy, Asthma & Immunology (ACAAI) Guidance on Risk of Allergic Reactions to mRNA COVID-19 Vaccines.

Remember, allergic reactions to the vaccine are relatively infrequent; roughly one in every hundred thousand injections — more than 100 times less common than allergic reactions to penicillin. Reactions are being observed because so many people are being immunized. Importantly, everyone who has had a reaction has been effectively treated and stabilized without any long-term problems.

Large local reactions have been reported, especially after Moderna vaccines, including:

  • Itching, redness, and swallowing are not uncommon. This comes on late (>5 days from vaccination) and can last for weeks. Treatment is symptomatic: antihistamine, NSAIDs (like ibuprofen)/Tylenol, ice. You CAN still get the second dose! In the Moderna vaccine trial, delayed large locals like these occurred 4 times less with the 2nd dose than the 1st dose.
  • Consider switching to the other arm for the second dose if you had a local reaction to the first dose.
  • These large local rxns are all very delayed in onset (often after day 8) so mechanistically they are different from immediate reactions.

 

I’ve heard that the vaccines are made from fetal tissue. Is this true?

NO, the Pfizer and Moderna vaccines are synthetic- made from chemicals. The AstraZeneca (AZ) vaccine (not approved as of 1/25/21) does use an immortalized cell line (HEK 293) derived from an abortive fetus from the 1960s for vaccine production. Here is a commentary that discusses this.

 

Where can I get information on how to get the Covid vaccination?

 

How do the Covid vaccines work?

COVID-19 vaccines help boost the immune system against the pandemic-causing SARS-CoV-2 virus. As of 1/25/21, two COVID-19 vaccines are available in the U.S. One by Pfizer/BioNTech and the other by Moderna.  Both of these utilize messenger RNA (mRNA) to make the spike protein found in the SARS-CoV-2 virus, which attaches to human cells leading to infection. The spike protein stimulates the immune system to make antibodies against this virus, making a person less susceptible to contracting it. Having antibodies against the spike protein can prevent the virus from attaching and infecting human cells.  Both vaccines require two doses, three or four weeks apart in order to achieve an optimal immune response.

 

Are there any safety concerns with the new technologies (mRNA and nanotechnology) being used in the development of COVID-19 vaccines?

There are no known additional risks of mRNA vaccines or lipid nanoparticles. Live attenuated viral vaccines, such as the measles vaccine, induce an immune response that is similar to natural infection. mRNA vaccines, on the other hand, simply give the body instructions to produce one very specific part of a virus – in this case the spike protein – to then induce an immune response.  Because mRNA is broken down very quickly in the human body, it is wrapped in a lipid nanoparticle to be able to get into our cells to do its work. Once it gets into the cells to deliver the instructions, the mRNA breaks down very quickly. There are rumors that mRNA vaccines will alter DNA because the RNA molecule can convert information stored in DNA into proteins. That is not true. It is important to note that the mRNA vaccines never enter the nucleus of the cell, where DNA is stored. After injection, the mRNA from the vaccine is released into the cytoplasm of the cells. Once the viral protein is made and on the surface of the cell, mRNA is broken down and the body permanently gets rid of it, making it impossible to change DNA.

This is a nice set of tweets from Andrew Nowalk, MD, Ph.D., a pediatric infectious disease specialist in Pittsburgh. He presents some information on the vaccines that may alleviate some concerns people have about the speed at which the vaccines were developed. They are presented below (but here is a link to his tweets).

  • This is NOT a vaccine created in 9 months. The origin goes back many years.
  • The first reports of an mRNA vector in a lipid particle used as a transfer vehicle go back to 1989 at the Salk Institute. Vaccines were considered using this in the 1990s. Kariko and Weissman made a big leap forward in 2005.
  • They modified the nucleosides of the mRNA, the building blocks that encode the viral protein so that they would be recognized as host RNA and properly translated.
  • Moderna (ever notice the last 3 letters) started in 2010 to expressly use this technology.
  • The first vaccines of this variety are NOT against #COVID it was MERS and OG SARS. Those trials are more than 3 years old.
  • The real analog here is 2009. That’s when we took the pandemic H1N1 strain and made a vaccine with it in 6 months. That’s a good analogy.
  • When this vaccine technology and development started, REM and Nirvana were the big bands, Clinton was president, and an i-anything from Apple was more than half a decade away.

Risk of Covid vaccine in context by Aaron E. Carrol, M.D., who is a professor of pediatrics at Indiana University.

 

What about Covid-19 vaccination in pregnancy?

Please contact your OBGYN to see what his/her current recommendations are.  Most OBs are recommending it for pregnant and nursing mothers.  The Centers for Disease Control and Prevention (CDC), the American College of Obstetrics and Gynecology (ACOG), and the Society for Maternal-Fetal Medicine agree that the new mRNA COVID-19 vaccines should be offered to pregnant and breastfeeding individuals who are eligible for the vaccine. Here is a piece on the Covid vaccine in pregnancy.

More recently, preliminary findings of a study published in the New England Journal of Medicine on 4/21/21 find COVID-19 mRNA vaccines made by Pfizer and Moderna are safe for pregnant women. A study in JAMA Pediatrics found pregnant women who became infected with the virus were at increased risk for maternal mortality, preeclampsia and preterm birth. Therefore, it is particularly important for those who are pregnant to receive the COVID vaccine, and the CDC now recommends that all pregnant women be vaccinated.

 

What if I have already had COVID, do I still need the vaccine?

Yes, you should still receive the vaccine. Due to the severe health risks associated with COVID-19 and the fact that reinfection with COVID-19 is possible, you should still be vaccinated.

 

How soon after being infected from COVID should I get the vaccine?

 Current CDC guidelines state you can receive the vaccine as soon as you are fully recovered from symptoms and out of the quarantine period.  However, reinfection within 90 days of illness is uncommon, so it may be less critical to get the dose right away.  They can wait until closer to the end of the 90 days if they want.

If you were treated for COVID-19 symptoms with monoclonal antibodies or convalescent plasma, you should wait 90 days before getting a COVID-19 vaccine. 

 

The vaccines are not 100% effective, so why should I take them? 

The mRNA vaccines are nearly 100% effective against severe illness from COVID-19. Of the 32,000 people in the Pfizer trial, only one developed COVID-19 severe enough to require hospitalization. Beyond the 95% prevention of any clinical COVID-19 infection, the 5% that got the illness had a very minimal illness. So these vaccines are almost totally effective in preventing COVID-19 illness in all qualifying age groups.

 

If I can still spread the disease after I’ve received the vaccines, why should I take them? 

Disease spread was not a specific endpoint in the clinical trials, but if the clinical illness is reduced by 95%, the spread of the virus should also be reduced by 95%. In the Moderna trial, the asymptomatic disease appeared to be as reduced as significantly as symptomatic diseases.

 

Will the vaccines protect me against the new variants of Covid?

The current data suggest that the vaccines offer varying amounts of protection against the known mutant strains of Covid. While the protection may not reach 95%, it is still very significant.

 

There are (or will be) different Covid vaccines approved. Which one should I get?

The simplest answer is take whatever vaccine you can get as soon as you can get it since all of the approved (or likely to be approved) vaccines essentially eliminate the risk of a severe Covid infection that will lead to death.

 

Does the vaccine contain toxic chemicals that will make me sterile?

NO! There are no toxic chemicals in the vaccine. The lipid component is in many foods and cosmetics. The amount of this material you are exposed to every day is hundreds of times more than in the vaccine. All these substances have been shown to be safe in large studies because they are in food and cosmetics. Therefore, it is unlikely that anything in the vaccine would cause a toxic effect.

There are many false rumors about the Covid vaccines, specifically targeting women. Some of them are debunked here.

 

The information above was compiled from different sources, including:

Here are more links to frequently asked questions: