Ingest

By PCSG

Dr Charlie Andrews, a GP from Bath and PCSG Committee Member, explores a range of gastroenterology topics from a GPs perspective. The focus of the series covers when to suspect, how to diagnose, when ... more

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FAQs about Ingest:

How many episodes does Ingest have?

The podcast currently has 33 episodes available.

Ingest episodes:

August 09, 2024High Iron Levels (hyperferritinaemia)
Dr Charlie Andrews speaks to Dr Jeremy Shearman about everything related to high iron levels (hyperferritinaemia). We discuss how iron is regulated within the body, causes of raised iron levels, and then we dive into hereditary haemochromatosis - when to suspect, how to test, who to refer (and to whom!), and how the condition is managed.
Useful links to accompany this episode include:
Welcome > Haemochromatosis: genetic iron overload disease (exeter.ac.uk)
Haemochromatosis - British Liver Trust
Key Learnings for Primary Care from the Ingest Podcast on Hyperferritinaemia
Key Learnings
Understanding Iron Regulation and Ferritin
Ferritin is an acute-phase reactant and a marker of total body iron stores, but can be elevated in a range of conditions beyond iron overload, including inflammation, liver disease, and malignancy[2].
Understanding the physiological regulation of iron is crucial for interpreting ferritin results in context.
Causes of Hyperferritinaemia
Raised ferritin can result from:
Hereditary haemochromatosis (genetic iron overload)
Chronic inflammatory states (e.g., infection, autoimmune disease)
Liver disease (e.g., alcoholic liver disease, hepatitis)
Malignancy
Metabolic syndrome
It is important to consider these differential diagnoses when encountering an elevated ferritin[2].
Hereditary Haemochromatosis: When to Suspect
Primary care clinicians should suspect hereditary haemochromatosis in patients with persistently raised ferritin and transferrin saturation, especially with suggestive symptoms (e.g., fatigue, arthralgia, diabetes, liver dysfunction) or family history[2].
Early recognition is key, as treatment can prevent complications.
How to Test
Initial investigations should include:
Repeat ferritin measurement to confirm persistence
Transferrin saturation (TSAT): TSAT >45% is suggestive of iron overload
Liver function tests and assessment for other causes of raised ferritin[2]
If hereditary haemochromatosis is suspected, genetic testing (HFE gene) should be considered.
Who to Refer (and to Whom)
Refer patients with confirmed iron overload (high ferritin and TSAT) or positive HFE mutation to hepatology or a relevant specialist for further assessment and management[2].
Referral is also warranted if there are signs of organ involvement (e.g., abnormal LFTs, diabetes, cardiac symptoms).
Management Principles
For hereditary haemochromatosis, mainstay of treatment is venesection (therapeutic phlebotomy) to reduce iron stores.
Primary care plays a role in monitoring, supporting adherence, and managing comorbidities.
For other causes, management is directed at the underlying condition.
Practical Tips for Primary Care
Do not ignore isolated raised ferritin-always interpret in clinical context.
Exclude common secondary causes (infection, inflammation, liver disease) before pursuing rare diagnoses.
Family screening may be appropriate in hereditary haemochromatosis cases[2].
Use local guidelines and specialist advice where available.
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40min
June 27, 2024 Diverticular disease and diverticulitis
In this episode, Charlie Andrews speaks to Melanie Orchard, a consultant surgeon, about diverticular disease and diverticulitis. This is something that we encounter frequently in primary care, and understanding how to approach this condition is extremely important.
Melanie discusses a really pragmatic approach to patients with symptoms suggestive of diverticulitis. We discuss risk factors, presenting features, and how to assess the patient with suspected diverticulitis. We also discuss the difference between diverticulosis, diverticular disease and diverticulitis, and give you useful tips on what advice to give to patients who has just had a colonoscopy showing that they have diverticulosis.
For a useful visual summary of the management of patients with diverticulosis and diverticulitis, please follow this link: visual-summary-pdf-6968965213 (nice.org.uk)
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23min
May 10, 2024 Hepatitis C
Join Charlie Andrews as he discusses Hepatitis C with hepatologist Dr Kosh Agarwal and GP and clinical champion for Hepatitis C Dr Rik Fijten. They discuss the prevalence and presentation of Hepatitis C, as well as how to test for the condition along with an overview of the treatment options available.
Hepatitis C is a chronic liver disease which carries significant morbidity and mortality if left untreated. Fortunately, it is both easy to test for and the treatments available offer a fantastic cure rate of in excess of 95% with simple and relatively short tablet regimens.
NHS England has set itself the target of eradicating the disease by 2025 through active case finding, simplifying the diagnostic process, and ensuring pathways are in place to provide rapid and effective treatments for the condition.
Resources:
For more information on Hepatitis C, the British Liver Trust offers useful patient-friendly leaflets and further information about the condition: Hepatitis C - British Liver Trust
The self-testing portal mentioned by Rik during the episode can be found here: Home - HepC (hepctest.nhs.uk)
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33min
March 10, 2024 Neuroendocrine tumours (NETs) of the gastrointestinal tract
In this episode, Dr Charlie Andrews speaks to Professor Mark Pritchard about neuroendocrine tumours (NETs) of the gastrointestinal tract. You may be asking yourself: 'Do I really need to know about NETs in primary care, aren't they extremely rare?' The answer to that is a resounding yes, you do need to know about NETs and Mark will tell you why in this episode!
Neuroendocrine cancer is the 10th most prevalent cancer in England, and the second most prevalent cancer of the GI tract, with a rapidly rising incidence (371%) over the last 20 years. NETs are commonly diagnosed at a more advanced stage due to late diagnosis as the signs and symptoms can be vague, or mimic other more common conditions such as IBS. Mark provides lots of useful, practical advice about when to suspect this form of cancer in primary care, which patients may be a higher risk, and what to do if you are suspicious about this form of cancer in your patient.
Listen on to find out more.
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32min
December 28, 2023 Ingest Trailer
Dr Charlie Andrews, a committee member of the Primary Care Society for Gastroenterology (PCSG), introduces Ingest, the podcast for primary care that focuses on when to suspect, how to diagnose and how to manage common gastrointestinal presentations and conditions.
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3min
December 22, 2023 Highlights from Ingest 2023
In this episode Dr Charlie Andrews looks back at 2023 and highlights some key takeaways from Ingest in 2023.
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32min
November 09, 2023 Barrett’s oesophagus
In this episode, Charlie Andrews speaks to Dr Andrew Moore about this condition, which affects up to 1.5% of the population, with a risk of progression to cancer of 3-13% over the patient's lifetime (Cancer Research UK). They discuss the typical presenting features, who needs an endoscopy to look for Barrett's, and how the condition is managed both in primary and secondary care. The BSG guidelines mentioned by Dr Moore in the episode can be found here: https://www.bsg.org.uk/clinical-resource/bsg-guidelines-on-the-diagnosis-and-management-of-barretts-oesophagus/
For more episodes about the oesophagus, you may find the following episodes of Ingest useful: Dyspepsia, Eosinophilic oesophagitis, Dysphagia and Achalasia.
BSG guidelines on the diagnosis and management of Barrett's oesophagus - The British Society of GastroenterologyFitzgerald RC, di Pietro M, Ragunath K et al. Abstract These guidelines provide a practical and evidence-based resource for the management of patients with Barrett’s oesophagus and related early neoplasia. The Appraisal of Guidelines for Research and Evaluation (AGREE II) […]www.bsg.org.uk
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29min
August 14, 2023Bile acid diarrhoea
In this episode, Charlie Andrews speaks to Professor Julian Walters about bile acid malabsorption and diarrhoea. With up to a third of patients with diarrhoea-predominant IBS having underlying bile acid diarrhoea, and with diagnosis rates for this condition being low, this episode is an important one for anyone working in primary care. We explore the role and physiology of bile acids, the causes and symptoms of bile acid malabsorption, the diagnostic tests used to make the diagnosis and the treatment of this common but underdiagnosed condition. Should we use 'trial of treatment' in primary care to support the diagnosis? Are people who have had their gall bladder removed at greater risk of bile acid diarrhoea? Can bile acid sequestrants impact the absorption of other medications? These questions, and lots more, will be discussed in this episode.
Key Learnings for Primary Care from this Ingest Podcast on Bile Acid Diarrhoea
Overview and Prevalence
Bile acid diarrhoea (BAD), also known as bile acid malabsorption, is a significant but under-recognized cause of chronic diarrhoea in primary care. It is more common than Crohn’s disease and ulcerative colitis combined, with a prevalence of about 1% in the general population-comparable to coeliac disease[1].
BAD is often misdiagnosed as IBS with diarrhoea (IBS-D); about one third of patients with IBS-D may actually have BAD[1].
Causes and Classification
BAD is classified into three types:
Type 1: Secondary to ileal disease or resection (e.g., Crohn’s disease, surgical removal of terminal ileum)
Type 2: Primary or idiopathic (often confused with IBS-D; thought to be due to overproduction of bile acids)
Type 3: Other causes affecting absorption, such as cholecystectomy, small intestinal bacterial overgrowth, or radiation[1].
Post-cholecystectomy BAD is relatively common, affecting about 1 in 10 patients after gallbladder removal[1].
Clinical Presentation
Patients typically present with chronic, watery diarrhoea (Bristol stool types 6–7), often frequent (4–12 times daily), sometimes nocturnal, and can be long-standing (sometimes decades)[1].
There is often a long delay in diagnosis; nearly half of patients wait over five years for a correct diagnosis[1].
BAD is frequently overlooked in differential diagnosis, with clinicians more likely to investigate for IBD, coeliac disease, or cancer[1].
Diagnosis in Primary Care
The key is to think about BAD as a possible diagnosis, especially in patients with chronic diarrhoea where other causes have been excluded[1].
The gold standard diagnostic test is the SeHCAT (selenium homocholic acid taurine) scan, which is widely available in the UK but not in all countries[1].
A retention value below 15% at seven days is diagnostic; lower values indicate more severe disease[1].
There is no simple blood test for BAD, unlike coeliac disease[1].
Empirical trials of bile acid sequestrants may be considered if SeHCAT is unavailable or in specific cases (e.g., pregnancy), but a confirmed diagnosis is preferred to guide treatment and improve adherence[1].
Before considering BAD, it is essential to exclude other causes of diarrhoea (negative coeliac serology, faecal calprotectin, and, depending on age, appropriate cancer screening)[1].
Treatment
First-line treatment is with bile acid sequestrants:
Cholestyramine: A powder taken in 4g sachets, usually started at night on an empty stomach for best effec
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28min
July 13, 2023 Faecal calprotectin
In this episode, Charlie Andrews speaks to Dr James Turvill about faecal calprotectin use in primary care. Dr Turvill is a gastroenterologist based in York, who was instrumental in developing the NICE-approved and widely adopted York Faecal Calprotectin Care Pathway. What is calprotectin? When should we use it in primary care? How should we interpret the result? Can any medications or conditions affect the result? Listen on to find the answers to these questions!
The care pathway can be found here: https://www.yorkhospitals.nhs.uk/seecmsfile/?id=941. It is recommended that you have a look at this either before, after or during this episode to enhance your learning. Enjoy!
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38min
May 25, 2023 IBS – dietary management and the 10-minute consultation…
Marianne Williams is an extremely experienced dietician, innovator, digital technology advocate and winner of the NHS England Allied Health Professional of the Year prize for 2018.
In this episode, Marianne shares her wealth of knowledge around all things IBS to discuss initial dietary management, the low FODMAPs diet, the role of probiotics, and gives us some great advice about how we can maximise our (often short) patient consultations with newly diagnosed IBS patients. Marianne also discusses her innovative dietetic-led gastroenterology clinic for IBS patients with us.
There is so much food for thought here, and so many useful nuggets of information throughout this episode. Sit back and tuck into this feast of information!
Useful links/websites discussed in the episode:
Patient Webinars website: https://patientwebinars.co.uk/
Monash university IBS grand tour: https://www.youtube.com/watch?v=Z_1Hzl9o5ic
Monash university app: https://www.monashfodmap.com/ibs-central/i-have-ibs/get-the-app/
IBS symptoms, the low FODMAP diet and the Monash app that can help See updated video for Irritable Bowel Syndrome (IBS) relief: Take the Monash University Low FODMAP grand tour down under! at https://www.youtube.com/watch?v=stdYoA4G9Dg
See more: IBS patient course: https://www.monashfodmap.com/online-training/patients-course/
Website: https://www.monashfodmap.com/
Monash FODMAP blog: https://www.monashfodmap ...www.youtube.com
BSG guidelines on the management of IBS: https://gut.bmj.com/content/gutjnl/early/2021/04/27/gutjnl-2021-324598.full.pdf
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39min

FAQs about Ingest:

How many episodes does Ingest have?

The podcast currently has 33 episodes available.