Bedfont® champions Heart of Kent Hospice auction by winning sponsored sculpture and contributing to the memorial garden.

Bedfont® Scientific Ltd. a local med-tech company with over 47 years of expertise in the design and manufacture of medical breath analysis devices, proudly sponsored a Shaun the Sheep sculpture in this year’s Shaun in the Heart of Kent Art Trail. Organised by Heart of Kent Hospice, the event took place in the summer and saw many Shaun the Sheep sculptures lovingly decorated by local artists and community initiatives. The sculptures were then placed in various locations in and around Maidstone, aiming to raise vital funds for the hospice. The Bedfont® sponsored sculpture ‘Shorn the Return’ was located by the Old Boat Café in Maidstone.

Once the trail finished at the end of August, 60 of the Shaun sculptures went up for auction to raise further funds for Heart of Kent Hospice. The Bedfont team was in attendance, waiting patiently for lot number 33 to come up. The team put in the winning bid for ‘Shorn the Return’ securing his return to the Bedfont offices

One of the sculptures ‘Changing of the season’s’ which was located in Fremlin Walk, was created by Annabelle Hodd with the intention of being brought back to the Heart of Kent Hospice memorial garden. However, as Heart of Kent Hospice is a charity, they were unable to meet the funds to buy it back. Nevertheless, 11 companies, including Bedfont®, donated and it is now happily heading to the Heart of Kent Hospice memorial garden.

Jason Smith, CEO at Bedfont® comments “We are honoured to have been a part of this wonderful initiative supporting such an important cause. Sponsoring a sculpture in the Shaun in the Heart of Kent trail allowed us to contribute to the community, but having the opportunity to bid and win our sponsored piece was truly special. More importantly, coming together with other local companies to donate a sculpture for the hospice’s memorial garden is a testament to the collective commitment of our community to give back”

Over 250 people attended the auction event and every sculpture was sold, raising a staggering £267,250.00 on the night. The event proved to be a massive success and the vital funds raised will allow Heart of Kent Hospice to continue the much-needed care and support to those at the end of their lives, along with their families and friends.

To find out more about the Bedfont® efforts in supporting Heart of Kent Hospice, follow the social channels @bedfontltd.

Bedfont® Scientific Limited hosted an insightful webinar Mastering Gut Health: Understanding SIBO, Carbohydrate Malabsorption, and Accurate Gastrointestinal Investigation. Gastrointestinal Physiologist and Bedfont® Medical Advisory Board member Melissa Dooley, led the discussion and shared valuable information on various gastrointestinal disorders and the importance of not self-diagnosing.

Melissa Dooley began her career as a Gastrointestinal Physiologist at St. James’s’ Hospital Dublin, and developed a keen interest in Small Intestinal Bacterial Overgrowth (SIBO). Melissa is a member of both the Irish Institute of Clinical Measurement Scientists and the British Society of Gastroenterology, as well as the founder and director of Gastrolife Clinic in Ireland.

The webinar covers some important topics:

  • SIBO & dietary malabsorption
  • Finger-prick food intolerance testing. Does it play a supporting role in clinical testing, or is it a costly test without scientific evidence?
  • Food allergies vs food intolerances
  • Home breath testing devices & regulations

Small Intestinal Bacterial Overgrowth (SIBO) What is it?

SIBO occurs when there are higher numbers of bacteria in the small intestine. Too much bacteria here can interfere with the digestion and the absorption process. Bacteria, however, can also provide some benefits, such as:

  • Production of micronutrients
  • Aiding metabolism or activation of medicines
  • Biotransformation of bile salts
  • Fermentation of indigestible polysaccharides

Prevention of luminal colonisation by pathogenic microorganisms

What causes SIBO?

One of the most common causes is a dysfunction of the normal intestinal motility. Slow movement through the intestines allows bacteria to grow, causes of this can be:

  • History of food poisoning
  • Diabetes
  • Certain medications
  • Nerve damage

However, in some cases, the cause can be unknown. Melissa continues to discuss the consequences of SIBO, which include the dampening of villi, protein and carbohydrate malabsorption and B12 deficiency to name a few.

How can we test for SIBO?

The ‘Gold standard’ of SIBO diagnosis, culturing jejunal aspirate, is limited because many bacteria species do not grow in routine culture media, not to mention how invasive and costly this procedure is. The hydrogen breath test was developed due to difficulty accessing the small intestine and is used to detect SIBO and dietary malabsorption.

How can breath samples tell me what is happening in my intestines?

During metabolism, all cells produce carbon dioxide, however, only bacteria produce hydrogen and methane as metabolic by-products. These gases pass through the walls of the intestine into the blood. Once the blood reaches the lungs, a gas exchange occurs, allowing these gases to be detected in exhaled breath.

How to take a SIBO or malabsorption test

A hydrogen and methane breath test (HMBT) device is used. The GastroCH4ECK® Gastrolyzer® measures the amount of hydrogen or methane gases in the exhaled breath. Before the start of the breath test, the patient must follow a strict protocol. This includes a restricted diet followed by a fasting period. Not adhering to the protocol can result in an elevated baseline recording or a false positive result.

Before drinking the relevant substrate, a baseline breath sample is taken. The substrate ingested is mixed with 250ml of water and the type of substrate depends on the test being taken. The substrates can be either:

  • Glucose
  • Lactulose
  • Sucrose
  • Sorbitol

Breath samples are then taken at 15-30-minute intervals, depending on the test and can take up to 4 hours depending on the type of test. Treatment can involve antibiotics or dietary changes, depending on the test type and results.

Fructose malabsorption

Fructose malabsorption is a dietary disability of the small intestine. Most people can absorb between 25g-50g of fructose in one sitting, however, in people who suffer from fructose malabsorption, their small intestine fails to absorb fructose properly, resulting in the fructose travelling to the large intestine where it has to be metabolised by the bacteria there. This then increases the hydrogen and methane gases released by the bacteria. Possible causes of fructose malabsorption are:

  • Inherited or acquired abnormality of the fructose-transporting protein
  • Overuse of high fructose corn syrup or fruit juices in children
  • SIBO
  • Celiac disease
  • Chemotherapy or radiation
  • Dumping syndrome

Symptoms of fructose intolerance can include:

  • Bloating
  • Diarrhoea
  • Constipation
  • Flatulence

Unfortunately, there is no known cure, but an appropriate diet would help. Foods that have a high content of glucose will help absorb fructose.

To test for fructose intolerance, the patient would need to ingest 25g of fructose in 250ml of water. Breath samples would then be taken at 30-minute intervals over 3 hours.

Lactose malabsorption

Lactose is normally hydrolysed into glucose and galactose, which is readily absorbed in the jejunum. Lactose needs to be hydrolysed in the small intestine by lactase. If the lactase enzyme is lacking, the lactose will not be completely hydrolysed and result in lactose malabsorption. Symptoms of lactose malabsorption can include:

  • Distension
  • Cramps
  • Flatulence

Lactose malabsorption is the most common intolerance, affecting almost half the world’s population.

Food allergies vs food intolerances

Often people confuse a food intolerance and a food allergy. A food intolerance can be caused by a change of routine, hormones, and eating out. Symptoms can be quite disruptive to someone’s life and lead them to avoid social activities due to the unpredictability of the symptoms. Because of this, many sufferers will turn to the internet for a quick and easy solution.

An intolerance is where the enzymes in the gut responsible for breaking foods down are deficient, defective, or there is an issue with the mechanism that transports the molecules through the small intestine. Symptoms are:

  • Abdominal pain
  • Discomfort
  • Diarrhoea

Common food intolerances are:

  • Lactose
  • Fructose
  • Sucrose
  • Sorbitol

It’s important not to self-diagnose as many conditions can cause similar symptoms to irritable bowel syndrome (IBS) & SIBO, but they will have different treatments and management. It’s always important to visit your GP or healthcare professional. A food intolerance can be diagnosed by an elimination diet or a breath test.

There is a significant difference between a food intolerance and a food allergy. A food allergy is a reaction involving the immune system, symptoms can be:

  • Rash
  • Itching
  • Breathing difficulties

If you have a food intolerance you may be able to consume a small amount of the food, however, with an allergy you must avoid these foods as food allergies can be fatal. Food allergies can be tested through skin prick allergy testing or an elimination diet.

Tests currently not recommended by healthcare professionals for food intolerances are finger prick tests and hair analysis tests, as these do not have any supportive scientific evidence.

Breath testing is the recommended method for detecting lactose malabsorption for several reasons. If you proceed with an elimination diet and remove milk, you may still ingest lactose which can be found in many unsuspecting foods such as:

  • Hot dogs
  • Breaded chicken
  • Sweets

So even if the patient attempts to remove lactose from their diet, they can un-intentionally ingest lactose.

Other test methods can include:

  • Endoscopic biopsies (invasive & costly)
  • Blood test (repeated every 30 minutes)
  • Stool acidity test (infants, young children)

Home breath testing devices

Home breath testing devices were more widely optimised due to the COVID-19 pandemic, to prevent waiting list delays and people felt safer taking the tests at home. There are several benefits of home testing kits, such as:

  • Living far from the clinic and difficulty getting there
  • Difficulty getting time off work
  • Childcare issues
  • Difficulties leaving the house with symptoms

However, the limitation of a home test could be that the patient doesn’t collect their samples correctly, resulting in the test having to be retaken. Therefore, patients must be provided with very clear and precise instructions to follow.

There are many home testing devices available now, but using one of these devices without the advice or guidance of a healthcare professional could result in self-interpretation, misdiagnosis, and incorrect preparation, leading to unnecessary avoidance of important food groups.

Home testing devices must be sourced from a reputable healthcare professional, who can discuss the results or provide a report for the treating medical professional. This will ensure an appropriate follow-up is conducted to make sure the patient doesn’t end up with a nutritional deficiency due to self-diagnosis.

There are many factors involved in diagnosing and treating gastrointestinal conditions. Melissa has highlighted these conditions and discussed the importance of not self-diagnosing, watch the full webinar now:

Bedfont® named regional winner of the prestigious British Chamber of Commerce Digital Revolution Award.

The British Chamber of Commerce is a network of accredited Chambers of Commerce across the UK and overseas. Representing businesses of all sizes and sectors, the Chamber Business Awards is an annual event that celebrates and recognises the success and contributions of businesses throughout the UK. Bedfont® was nominated for the 2024 Chamber Business Awards by the Kent Invicta Chamber of Commerce.

Bedfont® is an innovative Medtech company, with over 47 years of expertise in designing and manufacturing of medical breath analysis devices. Over the years, Bedfont® has been investing in innovation and has continued to revolutionise the breath analysis market.

In September, Bedfont® was shortlisted in the Digital Revolution Category and was proudly announced as the winner by an independent panel at the British Chambers of Commerce.

Jason Smith, CEO of Bedfont® said “We are truly honoured to be recognised as Business of the Year by the British Chambers of Commerce. This achievement is a testament to the hard work, dedication, and passion of our entire team. It reflects our commitment to innovation, excellence, and customer service. I am incredibly proud of what we have achieved together, and this award motivates us to continue pushing boundaries, growing, and contributing positively to our industry. Thank you to the Chamber and everyone who has supported us on our journey.”

Winning Business of the Year is a significant milestone for Bedfont®. This award not only highlights the commitment to excellence and innovation but also fuels our drive to continue delivering outstanding service to our customers and providing cutting-edge technology to the breath analysis market.

To find out more about Bedfont® and how their breath analysis devices are improving patient care, click here.

Methods of measuring FeNO

Fractional exhaled nitric oxide (FeNO) measurement plays a crucial role in the diagnosis and management of airway inflammation. FeNO testing is recommended by the National Institute for Health and Care Excellence (NICE) to help diagnose asthma1, with the NObreath® device one of three devices recommended by NICE1.

In 2005 the American Thoracic Society (ATS) and the European Respiratory Society (ERS) published recommendations for standardised procedures of FeNO testing highlighting that whilst evidence shows ambient levels of nitric oxide (NO) do not affect the result; it is preferable to avoid doubt by removing it from the breath sample2. This can be done by either ‘partitioning’ the sample; effectively ignoring the potential initial spike caused by ambient NO, or another method is inhaling through an NO scrubber before exhalation.

The NObreath® utilises the partition method. This article explores the partitioning method, how it works, and why Bedfont® Scientific Limited selected this method for the NObreath® device.

What is the partition method?

The partition method essentially ‘parts’ the breath sample, and omits the first few seconds to ensure any potential high ambient levels of NO present in the breath are not measured during sampling.

When performing a breath test with the NObreath®, the user will be prompted to take a deep breath and then instructed to blow gently into the mouthpiece with an onscreen flow meter to guide the patient on their exhalation rate. The NObreath® offers two test modes: A 12-second test mode and a 10-second test mode for those up to 10 years old who cannot complete the 12-second test mode.

As the breath sample enters the NObreath® device, the first few seconds are partitioned and vented through the device bypassing the sensor chamber. After the partition period has elapsed, the pump will draw the remaining viable sample into the sensor chamber, where the breath sample will be analysed. When the patient completes a breath test using the NObreath® a green tick will appear on the screen to indicate a successful test, and the patient’s results will be shown onscreen in parts per billion (ppb) instantly.

The NObreath® applying the partitioning method

The partition method is a user-friendly method designed to measure airway inflammation, providing instant results, and eliminating wait times for both patients and healthcare professionals. The patient does not have to inhale through a device that has been used on multiple prior patients, as even highly effective bacterial viral filters may not be 100% effective and the patient does not have to inhale through an NO scrubber*. Avoiding inhalation means these risks do not arise and this is another reason why Bedfont® chose this technique for NObreath®. The NObreath® also utilises an NO scrubber for accuracy but this does not form any part of the breath pathway.

To learn more about the NObreath® utilising partitioning method, please visit https://www.nobreathfeno.com/measuring-feno-with-the-nobreath/

FeNO testing

The use of FeNO testing, combined with a comprehensive clinical history and additional examinations, enhances the efficiency of asthma diagnosis and improves patient care. This allows for effective monitoring of patients’ responses to asthma interventions. Bedfont® are world leaders in breath analysis, with over 47 years of experience. Bedfont® has been manufacturing the NObreath® portable FeNO device for over 15 years. Used by healthcare professionals to measure airway inflammation to aid in the diagnosis and management of asthma, taking a minimal amount of valuable consultation time with the ability to monitor airway inflammation in both adult and child patients. With annual servicing and minimal consumables, the NObreath® can be used as a functional device for years**.

Visit https://www.nobreathfeno.com to learn how to support your patients with FeNO monitoring using the NObreath® from Bedfont® Scientific Limited.

*NO scrubbing filters typically utilise potassium permanganate (a potentially hazardous substance) which has been referenced in certain conditions, if inhaled, to cause irritation to the nose, throat and lungs causing coughing and/or shortness of breath3,4,5,6.

**The NObreath® has been validated for up to 29,000 tests when used as instructed and properly maintained and serviced. The number of tests can be periodically checked within the settings of the device; when 29,000 tests are reached a service is recommended. Contact your local service centre.

References:

  1. Measuring fractional exhaled nitric oxide concentration in asthma: NIOX MINO, NIOX VERO and NObreath [Internet]. National Institute for Health and Care Excellence. 2014. [Cited Monday 12th August 2024]. Available from: https://www.nice.org.uk/guidance/dg12/chapter/1-Recommendations
  2. American Thoracic Society Documents. ATS/ERS recommendations for standardised procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005. Am J Respir Crit Care Med. 2005;171(8):912-30. DOI: 10.1164/rccm.200406-710ST.
  3. Hazardous substance fact sheet [Internet]. New Jersey Department of Health and Senior Services. 2002. [Cited Monday 12th August 2024]. Available from: https://nj.gov/health/eoh/rtkweb/documents/fs/1578.pdf
  4. Safety data sheet potassium permanganate [Internet]. AquaPhoenix Scientific. 2015. [Cited Monday 12th August 2024]. Available from: https://beta-static.fishersci.com/content/dam/fishersci/en_US/documents/programs/education/regulatory-documents/sds/chemicals/chemicals-p/S25497.pdf
  5. . Potassium permanganate permanganic acid potassium salt [Internet]. Safety International Chemical Cards. 2016. [Cited Monday 12th August 2024]. Available from: https://www.ilo.org/dyn/icsc/showcard.display?p_lang=en&p_card_id=0672&p_version=2
  6. Potassium permanganate safety data sheet [Internet]. LabChem. 2014. [Cited Monday 12th August 2024]. Available from: https://palsusa.com/wp-content/uploads/sites/6/2024/08/POTASSIUM-PERMANGANATE.pdf

A door opens to ensure the gold standard of FeNO testing is available in Latin America.

Bedfont® Scientific Limited, world leaders in breath analysis, with over 47 years of experience in the manufacturing and distribution of breath analysis devices have partnered with worldwide respected medical company Geratherm® Group, to enable them to manufacture a Fractional exhaled Nitric Oxide (FeNO) testing device.

Geratherm® Group predominantly known for their medical glass thermometers are an internationally aligned group that develop and produce medical solutions from respiratory therapy to women’s health at its five locations in Germany. They export 82% of their products to over 60 different countries every year, with many products in use in practices, clinics and rehabilitation facilities worldwide.

Their Latin America sales office, which was founded in May 2002 based in Brazil, is currently the focal point for sales, warehousing and customer service from Mexico to Chile for the entire group. This is where the partnership begins between Bedfont® and Geratherm®.

Marcio Souza, CEO of Geratherm® Medical Latin America visited the Bedfont® premises back in April, for a tour of the company, to oversee production. During the visit, final details were discussed and an agreement was reached.

Marcio Souza, CEO of Geratherm® says “We are excited to announce a new commercial partnership with Bedfont®, a recognised leader in the medical field, focused on respiratory analysis. This collaboration aims to bring the Brazilian market the best FeNO device available in the medical area, which will allow us to offer innovative and quality solutions to Latin American markets. Together, we are committed to delivering all benefits such as improving patient health, increasing efficiency, better costs and faster exam results. We believe that this union will be an important milestone in the advancement of medicine and the transformation of the healthcare experience.”

Adding to their already extensive well established product listing, Bedfont® are supplying the FeNObreath® kit which will allow Geratherm® to manufacture a FeNO testing device. Adding a FeNO device to their listing is a huge step forward in aiding the diagnosis and treatment of asthma in Latin America.

FeNO is a gas that is produced when airways are inflamed, a typical symptom of asthma. By measuring the FeNO on a person’s breath you can differentiate between allergic asthma and non-allergic asthma, as well as monitoring a person’s adherence to medication. A FeNO testing device is a great tool for asthma management and will certainly boost Geratherm’s already impressive catalogue of products.

Jason Smith, Managing Director of Bedfont® says “We are thrilled to announce our strategic partnership with Geratherm® for the manufacturing of our innovative FeNO device. This collaboration marks a significant milestone in our efforts to expand access to FeNO testing in Latin America. By leveraging Geratherm’s manufacturing expertise and our cutting-edge technology, we are poised to make a substantial impact on respiratory health management in the region. This partnership not only strengthens our global footprint but also reaffirms our commitment to improving patient care through advanced diagnostic solutions.”

For more information on how FeNO testing is revolutionising asthma care, visit nobreathfeno.com

FeNO Testing in Asthma Care

Although airway eosinophilic inflammation is a key characteristic of asthma, there are few methods available to measure it. This inflammation can be assessed by measuring eosinophils and eosinophilic cationic protein (ECP) in sputum or by measuring ECP in blood samples1. However, these methods are considered time-consuming, expensive, and not readily available.

For most asthma patients, airway inflammation is driven by an allergen-induced Th2 response2. Evidence from the literature suggests that fractional exhaled nitric oxide (FeNO) is a crucial biomarker for respiratory tract inflammation2. Elevated FeNO levels in asthma are thought to result from inducible NOS2 expression in the inflamed airways2. The NObreath® FeNO device provides a non-invasive and significantly more cost-effective alternative aid to diagnose asthma and assess airway eosinophilic inflammation.

This article delves into the challenges encountered within primary care and how the innovative technology of the NObreath® can assist. Additionally, the article discusses the transition of the use of the NObreath® from primary care environments to secondary care facilities.

Challenges in Primary Care

GPs often face restricted budgets due to resource allocation for population needs, and financial sustainability to stay within healthcare budgets and prevent overspending. Each patient appointment is typically limited to just 10 minutes.

Population needs

In the UK, approximately 5.4 million people, or about 8 in every 100 individuals, suffer from asthma3. The National Review of Asthma Deaths (NRAD) documented 195 asthma-related deaths among adults in 2013, highlighting preventable factors in 89 of the 195 deaths (46%), such as lack of specific asthma expertise (17%) and non-adherence to UK asthma guidelines (25%)4. FeNO testing is valuable in GP settings, as GPs often encounter a spectrum of asthma cases, from mild to severe. The NObreath® device facilitates rapid and reliable FeNO measurements, to allow GPs to make informed decisions and aid in identifying patients who do or do not require ongoing treatment5. This also reduces emergency visits and hospital admissions related to poorly controlled asthma.

Financial sustainability

One of the ongoing challenges in primary care is maintaining financial sustainability. The NObreath® FeNO device is cost-effective, with minimal ongoing costs. The device requires only one consumable- the NObreath® mouthpiece which has a long shelf life and an integrated infection control filter, effectively removes airborne bacteria (>99%) and viruses (>98%)6. The device also incurs low annual servicing costs and imposes no test limits*.

Time with patient

When a GP determines the need for a FeNO test using the NObreath®, there’s no warm-up time, and the device operates through a simple exhale-only technique with on-screen visual guidance. Patients receive instant results, eliminating wait times. Intended for adult and paediatric patients**, the NObreath® offers two test modes: a 10-second test mode for those up to 10 years old who cannot complete the 12-second test mode.  GPs can store up to 25 results in up to 50 patient profiles and view a graph of results. If a GP office possesses only one NObreath®, they benefit from the device size and portability, ensuring that healthcare providers can efficiently utilise the device wherever patient care demands.

Carol Stonham, a member of Bedfont® Scientific Limited Medical Advisory Board and policy lead for Policy Care Respiratory Society (PCRS), comments “The NObreath® is my preferred choice for primary care in managing asthma for many reasons. Primarily it suits the unpredictability of the volume of testing in primary care – none of the consumables or device needs to be used or lost in a short time frame. It is an intuitive machine which is easy to use and teaches patients of all ages.”

Primary Care to Secondary Care

Using the NObreath® device in primary care can reduce the number of inappropriate referrals to secondary care clinics. However, if a patient is referred to an asthma specialist in secondary care, the NObreath® FeNO device can aid in the diagnosis and management of asthma. The NObreath® helps differentiate between allergic (eosinophilic) and non-allergic asthma7. FeNO measurements show the patient’s response to the treatment, enabling accurate prescription of medication and safer, monitored adjustments. This helps patients understand their condition better by demonstrating how their FeNO levels correlate with their symptoms and treatment adherence. Measuring airway inflammation with the NObreath® can help monitor the effectiveness of medication and predict the risk of asthma attacks8***

Gold Standard FeNO Testing

FeNO testing is increasingly recognised as a valuable tool in the management of asthma, but what makes the NObreath® stand out from other FeNO devices on the market? Developed by Bedfont® in 2008, the NObreath® has over 15 years of clinical use and has been featured in numerous studies worldwide, contributing to the advancement of FeNO testing. Conforming to both the American Thoracic Society (ATS) and European Respiratory Society (ERS) guidelines, the NObreath® is also one of three FeNO devices recommended by the National Institute for Health Care Excellence (NICE)9, an independent international organisation providing national guidance and advice to improve health and social care.

To find out how you can support your patients with FeNO testing in asthma care with the NObreath®, please visit: https://www.nobreathfeno.com/

*The NObreath® has been validated for up to 29,000 tests when used as instructed and properly maintained and serviced. The number of tests can be periodically checked within the settings of the device; when 29,000 tests are reached a service is recommended. Contact your local service centre.

**NObreath® can be used on paediatric and adult patients, provided they can follow test protocol. USA only: NObreath® can be used on patients 7+ years old.

***FeNO is not a definitive indication of asthma and should be used in conjunction with (but not limited to) spirometry, patient history, and symptoms.

References:

  1. Pizzichini E, Pizzichini MM, Efthimiadis A, Dolovich J, Hargreave FE. Measuring airway inflammation in asthma: eosinophils and eosinophilic cationic protein in induced sputum compared with peripheral blood. Journal of allergy and clinical immunology. 1997 Apr 1;99(4):539-44. DOI: 10.1016/S0091-6749(97)70082-4.
  2. Keller AC, Rodriguez D, Russo M. Nitric oxide paradox in asthma. Memórias do Instituto Oswaldo Cruz. 2005;100:19-23. PMID: 15962094 DOI: 10.1590/s0074-02762005000900005.
  3. What is Asthma? [Internet]. Asthma+ Lung UK. 2024. [Cited Monday 8th July 2024]. Available from: https://www.asthmaandlung.org.uk/conditions/asthma/what-asthma#:~:text=Asthma%20is%20a%20common%20condition,cough%20or%20a%20tight%20chest.
  4. Royal College of Physicians. Why asthma still kills: the National Review of Asthma Deaths (NRAD) Confidential Report. London, RCP; 2014.
  5. Taylor DR, Pijnenburg MW, Smith AD, Jongste J. Exhaled nitric oxide measurements: clinical application and interpretation. Thorax. 2006 Sep 1;61(9):817-27. PMID: 16936238 PMCID: PMC2117092 DOI: 10.1136/thx.2005.056093.
  6. Public Health England. An Evaluation of Filtration Efficiencies Against Bacterial and Viral Aerosol Challenges. Salisbury: Public Health England; 2020.
  7. Ref: Coumou H, Bel EH. Improving the diagnosis of eosinophilic asthma. Expert review of respiratory medicine. 2016 Oct 2;10(10):1093-103. DOI: 10.1080/17476348.2017.1236688.
  8. Saito J, Gibeon D, Macedo P, Menzies-Gow A, Bhavsar PK, Chung KF. Domiciliary diurnal variation of exhaled nitric oxide fraction for asthma control. European Respiratory Journal. 2014 Feb 1;43(2):474-84. DOI: 10.1183/09031936.00048513.
  9. Measuring fractional exhaled nitric oxide concentration in asthma: NIOX MINO, NIOX VERO and NObreath [Internet]. National Institute for Health and Care Excellence. 2014. [Cited Wednesday 10th July 2024]. Available from: https://www.nice.org.uk/guidance/dg12/chapter/5-Outcomes

A series of events and initiatives culminate in remarkable fundraising achievements by Med-Tech company Bedfont® and NewMed.

Bedfont® Scientific Ltd. world leaders in breath analysis, with over 47 years of expertise in the design and manufacture of medical breath analysis devices, welcomed the roaming Shaun the Sheep sculpture to its offices on Friday, 26th July, for the exciting announcement. Bedfont® teamed up with NewMed Ltd. earlier in the year to sponsor and support Heart of Kent Hospice and its various charity events throughout the year, and are extremely proud to have contributed to raising over £28,000.

Heart of Kent Hospice, based in Aylesford, is a charity with a passion for improving quality of life and provides specialist care and support to adults with terminal illnesses. Bedfont®, along with NewMed, have been actively involved in a variety of fundraising events for Heart of Kent Hospice, and have been engaging employees and the community to support this worthy cause.

In May, Bedfont® participated in the Bluebell Walk, following a picturesque walk through the North Downs and raised substantial funds through sponsorships and raffles. Bedfont® also proudly sponsored a beautiful Shaun the Sheep sculpture for the Hospice’s Shaun in the Heart of Kent art trail, the event not only highlights local artistry but also draws significant attention to the hospice’s mission. Additionally, Bedfont® took part in the Shaun the Sheep Selfie Challenge, capturing joyful moments and sharing them widely to further boost donations and awareness.

Jason Smith, Managing Director at Bedfont® Scientific Ltd., comments “At Bedfont®, we believe in the power of community and the importance of giving back. Our partnership with NewMed Ltd. and our ongoing support for the hospice, reflect our commitment to making a positive impact on the lives of those around us. We look forward to continuing our efforts and exploring new ways to support Heart of Kent Hospice in the future”

David Dadswell, Corporate Partnerships Manager at Heart of Kent Hospice, commented “Collaborating with the local business community plays a pivotal role in the Hospice’s strategy, and allows us to create increased awareness of the services we provide and supports our fundraising events to deliver the best experience for all those who participate. Both Bedfont® Scientific and NewMed fully immersed themselves into the recent Bluebell Walk as headline sponsors, exhibitors, and participants and through their efforts, we raised over £28,000. It’s the perfect partnership between organisations that have strong values around healthcare and a commitment to giving back to their local communities.

To find out more about Bedfont® and the continued efforts in supporting Heart of Kent Hospice, follow us on social media @BedfontLtd

Like any healthcare investment, consideration needs to be given when deciding which fractional exhaled nitric oxide (FeNO) device might best suit the clinical area in which it will be used. So, what would be sensible to consider when including FeNO devices for implementation into the respiratory pathway? And how does the NObreath® measure up?

External approval is an important factor in healthcare device purchase. It acts as an independent validation of quality and reliability. In England, approval from the National Institute of Health and Care Excellence (NICE) demonstrates that a device or medicine has been assessed by independent committees and has made evidence-based recommendations for the health and social care sector1. Technology appraisals2 assess the clinical and cost-effectiveness of health technology, including devices such as the FeNO device. As the technology market increases and additional devices are brought to market, it is important to investigate what external approval a device has received, and that it has undertaken an independent process before approval. The NObreath® has successfully undergone the required NICE technology appraisal.

Reassurance that tests performed are accurate, and repeatedly so, is vital in healthcare. The evidence for individual devices is reviewed as a part of the NICE technology appraisal. A device that is CE-marked also ensures that the manufacturer conforms to European standards for health, safety and environmental requirements.

A vital component in any healthcare system is the cost. As with many healthcare devices, this extends beyond the initial price tag. Is there an ongoing maintenance cost? What is the cost of the consumables such as mouthpieces required? Is there any potential for waste? Will the device offer longevity in a pathway if it is correctly maintained?

When considering cost, it is also worth considering the value of including the test and the potential price of not including FeNO in a respiratory pathway. Is there the potential for other costs to emerge without the test? Incorrect diagnosis resulting in lifelong unnecessary inhaled medication is seen in asthma3,with the associated costs to the patient and the healthcare system along with the additional burden a diagnosis of asthma can bring. Alternately, the cost and burden of a missed diagnosis can also occur leaving patients with untreated symptoms and the associated risk of asthma. Objective tests including FeNO are recommended4,5,6 in making an accurate diagnosis of asthma.

Tests that are simple to perform are more likely to be used in primary care where time is short. Recent research has found many competing priorities for services currently and the pressure on workforce training and capacity7 has impacted primary care’s ability to reinstate spirometry services. Despite funded training for spirometry in England, it has been slow to increase because of the complexity and time taken to achieve the required standard and registration. The requirement for competence in using a FeNO device is not as onerous, does not take long to complete and is free to complete in the UK. New technology should ideally be easy for patients to use, easy for competent healthcare professionals to teach to others who might undertake testing, and suitable for testing on a broad age range. FeNO testing meets all the criteria, it is a quick simple test that is relatively easy for all ages to perform with minimal coaching, and the test procedure is easy to teach to others.  

A device that is portable and can be moved between consulting rooms will increase its use and test availability for patients. This allows a FeNO test to be quickly and easily integrated into relevant primary care consultations.

One of the most impactful things that healthcare professionals are influenced by are guidelines. These may be international, national or local guidelines. FeNO has an identified place in the current guidelines 4,5,6. As guidelines progress to reflect the most current evidence, it is likely that FeNO testing as a part of the diagnostic process, and as a tool to monitor established asthma, will become more prominent.

Comparing the Bedfont® NObreath® FeNO device against these considerations, is it a good choice? The NObreath® has successfully been through the NICE technology appraisal so has demonstrated that it is a clinically effective device offering reliable repeatable testing and is cost-effective. The NObreath® is a non-invasive device with visual incentives to encourage patients of all ages to achieve optimal flow rate for testing. The test settings can be used for adults and children so is an all-age device. It is simple to explain and easy for patients to perform, taking a minimal amount of valuable consultation time. It is small, and easily transported. It requires annual servicing and minimal consumables and can be used as a functional device for many years.

Taking advantage of these features, some practices and primary care networks have taught all clinicians how to perform the test when the patient initially presents with a history and symptoms of asthma, so that treatment can begin without delay and the patient can be reviewed with steroid naive FeNO results as the national and international guidelines recommend.

References:

  1. National Institute for Health and Care Excellence (2024). Available from https://www.nice.org.uk/guidance [Last accessed 19.6.24]
  2. National Institute for Health and Care Excellence (2024). Available from https://www.nice.org.uk/About/What-we-do/Our-Programmes/NICE-guidance/NICE-technology-appraisal-guidance [Last accessed 19.6.24]
  3. Aaron SD, Vandemheem KL, FitzGerald JM, Ainslie M, Gupta S et al.: Canadian Respiratory Research Network. Re-evaluation of diagnosis in adults with physician-diagnosed asthma. JAMA 2017;317:269-279
  4. British Thoracic Society (2019)Guidelines for the management of asthma. Available from https://www.brit-thoracic.org.uk/quality-improvement/guidelines/asthma/ [Last accessed 20.6.24]
  5. National Institute for health and Care Excellence (2017). Asthma: diagnosis, monitoring and chronic asthma management NG80. Available from https://www.nice.org.uk/guidance/ng80 [Last accessed 20.6.24]
  6. Global Initiative for Asthma (2024) Global Strategy for Asthma Management and Prevention. Available from https://ginasthma.org/2024-report/ [Last accessed 20.6.24]
  7. Doe G, JC Taylor SJC, Topalovic M, Russell R, Evans RA et al (2023) Spirometry services in England post-pandemic and the potential role of AI support software: a qualitative study of challenges and opportunities. British Journal of General Practice 2023;  73 (737): e915e923. DOI: https://doi.org/10.3399/BJGP.2022.068

Plastic Free July, a pivotal initiative of the Plastic Free Foundation, was launched in 2011 by Rebecca Prince-Ruiz. This global movement is dedicated to realising a world free of plastic waste. The staggering figure of 20 million metric tons of plastic litter that infiltrates our environment annually1 underscores the urgent need for collective action against this pervasive global issue.

Bedfont®, world leaders in breath analysis, is fully committed to reducing its impact on the environment. By working with employees, customers and suppliers, materials are sustainably sourced and, where possible, recyclable or biodegradable materials are used.

Plastic packaging can take hundreds to thousands of years to decompose, accumulating plastic waste in landfills and natural habitats and creating long-term environmental pollution.

Bedfont® are always taking steps to reduce plastic waste; a couple of examples are:

The iCOquit®: a personal carbon monoxide (CO) device which is used to help people quit smoking. Initially, the iCO™ released in 2015 came in plastic packaging. When the next generation, iCOquit®, was introduced in 2020, Bedfont® changed the packaging to an eco-friendly material that can be recycled.

Another significant stride in this direction is the transformation of the Steribreath™ mouthpiece. Initially made of polypropylene, this component was revamped in 2020 to the more sustainable Steribreath™ Eco version, made from and packaged in sustainably sourced and recyclable materials.

These steps are part of the broader Bedfont® Eco Resolution. By making these changes, Bedfont® is not only reducing plastic waste but also reinforcing its commitment to sustainability.

As we celebrate Plastic Free July, Bedfont® is dedicated to continuing efforts to reduce plastic usage, lower its carbon footprint, and innovate in ways that benefit both its distributors and the environment.

To keep up to date with the Bedfont® Eco Resolution make sure you follow our social channels.

1. ICUN, Issues Brief, Plastic Pollution. [cited on 19/6/24] Available from https://www.iucn.org/resources/issues-brief/plastic-pollution

To mark Love Your Lungs Week, Bedfont® Scientific Ltd. raises awareness of FeNO testing in asthma care.

Love Your Lungs Week is an annual event which takes place from 21st to 27th June. The event aims to raise lung health awareness and promote habits that support respiratory well-being. Bedfont®, world leaders in breath analysis have over 47 years of experience in designing and manufacturing of breath analysis devices. Through innovating breath analysis devices, Bedfont® look to improve patient care with devices like the NObreath®. The NObreath® is a Fractional Exhaled Nitric Oxide (FeNO) device, recommended by NICE for FeNO measurement in asthma care.

Asthma is a chronic respiratory condition where the airways become inflamed and narrowed, making breathing difficult. Sadly 1,261 people lost their lives from asthma in 20201, highlighting that asthma is a serious condition. Asthma is caused by a combination of genetic and environmental factors, and as there is no cure, treating and managing the condition is essential.

FeNO is produced naturally in the lungs and can be found in exhaled breath; measuring FeNO can help assess the level of inflammation in the lungs, aiding in the diagnosis and management of asthma.

Using a FeNO device such as the NObreath® is a quick and easy, non-invasive way to assess a patient’s FeNO level. The NObreath® is especially useful for managing asthma in patients who are known to have allergic triggers, as it specifically measures the type of inflammation most commonly associated with allergic asthma

Elevated FeNO levels can suggest eosinophilic inflammation, a common underlying cause in many asthma patients. By using the NObreath® to monitor these levels, healthcare providers can tailor treatment efficiently.

Jason Smith, Managing Director of Bedfont® says “At Bedfont®, we are committed to supporting initiatives that promote lung health. Love Your Lungs Week is an excellent opportunity to raise awareness about the importance of early diagnosis and proactive management of respiratory conditions. The NObreath® FeNO device not only aids in identifying airway inflammation but also assists in monitoring treatment efficacy, ensuring that patients receive the best possible care.”

The NObreath® is fairly priced and conforms to both ATS and ERS guidelines, allowing a future where everyone has access to instant, non-invasive, simple breath testing to aid in medical diagnosis.

To find out more about FeNO testing in asthma care, please visit our website to watch an insightful webinar hosted by Carol Stonham MBE earlier in the year, ‘How FeNO testing can empower and educate healthcare professionals and patients alike:’ www.bedfont.com

1. Public health profiles. Office for Health Improvement & Disparities. [cited on 1/5/24] Available from https://fingertips.phe.org.uk/search/asthma 

Back to top