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SeHCAT

SeHCAT, or tauroselcholic [75-selenium] acid (also known as 75-selenium homocholic acid taurine), is a synthetic bile acid analogue radiolabelled with the gamma-emitting isotope selenium-75, serving as a radiopharmaceutical in nuclear medicine scintigraphy to diagnose bile acid malabsorption (BAM).^[1] The test assesses the enterohepatic circulation of bile acids by having the patient ingest a gelatin capsule containing approximately 370 kBq (0.01 mCi) of SeHCAT, which mimics natural bile salts in absorption primarily by the terminal ileum; whole-body retention is then measured via gamma camera scans at baseline (about 3 hours post-ingestion, representing ~100% retention) and after 7 days, with retention ≤15% indicating clinically significant BAM.^[1] Bile acid malabsorption, affecting up to 30% of patients with chronic watery diarrhea (including those with diarrhea-predominant irritable bowel syndrome or post-cholecystectomy), leads to excess bile acids in the colon that stimulate water and electrolyte secretion, causing symptoms often mistaken for other functional disorders.^[1] As the gold standard diagnostic tool for BAM, SeHCAT provides quantitative severity grading (mild: 10–15% retention; moderate: 5–10%; severe: <5%), which correlates with the likelihood of response to bile acid sequestrants like cholestyramine or colestipol, enabling targeted therapy that resolves symptoms in 80–90% of positive cases.^[1] The test's high diagnostic performance includes a sensitivity of 100% and specificity of 91% at the 15% cutoff, outperforming alternative methods like the 23-seleno-25-homotaurocholic acid serum test or fecal bile acid measurement in accuracy and reproducibility.^[1] Despite its clinical value, SeHCAT availability is limited to about 12 European countries and Canada, unavailable in the United States due to regulatory and production challenges with the selenium-75 isotope, which has a 118-day half-life and requires specialized manufacturing.^[1] The procedure involves minimal radiation exposure (effective dose of 0.26 mSv for adults, equivalent to a chest X-ray), with no reported adverse effects beyond rare mild gastrointestinal upset.^[1] In the UK, the National Institute for Health and Care Excellence (NICE) diagnostics guidance DG44 (2021) does not recommend routine SeHCAT use for investigating chronic diarrhea, IBS-D, or Crohn's disease without ileal resection, citing limited high-quality evidence on long-term outcomes and calling for further research on its impact on treatment decisions and patient quality of life.^[2]

Background

Bile Acid Physiology

Bile acids are amphipathic steroid molecules synthesized in the liver from cholesterol through the classical pathway, which accounts for approximately 90% of production in humans and is initiated by the rate-limiting enzyme cholesterol 7α-hydroxylase (CYP7A1).^[3] These molecules possess a hydrophilic α-face and a hydrophobic β-face, enabling them to act as detergents that facilitate the solubilization of lipids.^[4] Prior to secretion, primary bile acids such as cholic acid and chenodeoxycholic acid are conjugated in the liver with glycine (predominantly) or taurine, forming bile salts that enhance aqueous solubility and lower their pKa for more effective ionization in the intestinal environment.^[3] The enterohepatic circulation of bile acids is a highly efficient recycling process that conserves the bile acid pool and supports lipid digestion. Synthesized bile acids are secreted by hepatocytes into bile via the bile salt export pump (BSEP) and stored in the gallbladder, where they are concentrated up to tenfold.^[4] Following a meal, cholecystokinin stimulates gallbladder contraction, releasing bile into the duodenum, where bile acids emulsify dietary fats by forming mixed micelles with phospholipids and cholesterol, thereby aiding the digestion and absorption of lipids and fat-soluble vitamins in the proximal small intestine.^[5] Approximately 95% of bile acids are then reabsorbed in the terminal ileum through active transport mediated by the apical sodium-dependent bile acid transporter (ASBT, or SLC10A2), returning via the portal vein to the liver for reuptake and resecretion.^[3] This circulation recycles bile acids 6-10 times per day, maintaining a total pool size of 2-4 grams in healthy adults, with the majority residing in the enterohepatic system at any given time.^[4] The daily turnover rate is low, with only 0.2-0.6 grams lost in feces, corresponding to a half-life of 3-5 days, which underscores the efficiency of the process in cholesterol homeostasis and nutrient absorption.^[5] The cycle can be visualized as a loop: hepatic synthesis and secretion to the gallbladder, postprandial release to the intestine for micelle-mediated digestion, ileal reabsorption, and hepatic recapture, ensuring sustained bile acid availability without excessive de novo synthesis.^[3]

Bile Acid Malabsorption

Bile acid malabsorption (BAM), also known as bile acid diarrhea, is a condition characterized by the excessive loss of bile acids in the feces due to impaired reabsorption in the terminal ileum, resulting in their accumulation in the colon where they irritate the mucosa and provoke diarrhea.^[6] This leads to a disruption in the enterohepatic circulation of bile acids, which normally recycles about 95% of secreted bile acids back to the liver.^[7] BAM is often underdiagnosed because its symptoms mimic other functional gastrointestinal disorders, contributing to historical delays in recognition and management.^[8] BAM is classified into three main types based on etiology. Type 1 BAM is secondary to ileal pathology, such as Crohn's disease, ileal resection, or radiation enteritis, which directly impairs the active reabsorption of bile acids via the apical sodium-dependent bile acid transporter (ASBT).^[6] Type 2, or primary/idiopathic BAM, arises without evident structural damage and is linked to overproduction of bile acids due to defective negative feedback mechanisms involving fibroblast growth factor 19 (FGF19) and the farnesoid X receptor (FXR) in the ileum.^[7] Type 3 BAM encompasses miscellaneous secondary causes, including cholecystectomy, chronic pancreatitis, celiac disease, or small intestinal bacterial overgrowth, which indirectly affect bile acid handling through altered motility or inflammation.^[8] The primary symptoms of BAM include chronic watery diarrhea, fecal urgency, incontinence, nocturnal defecation, excessive flatulence, and abdominal pain, often persisting despite dietary modifications.^[6] These manifestations frequently overlap with diarrhea-predominant irritable bowel syndrome (IBS-D), where BAM prevalence reaches up to 30% in affected patients.^[7] Pathophysiologically, unabsorbed bile acids in the colon activate Takeda G-protein-coupled receptor 5 (TGR5) and other pathways, stimulating chloride and fluid secretion, enhancing colonic motility, and causing mucosal damage, which collectively drive the diarrheal response.^[8] This condition poses diagnostic challenges owing to its nonspecific presentation and limited awareness, often leading to misattribution to IBS or other entities without targeted testing like SeHCAT scintigraphy.^[6]

Development and Composition

Historical Development

SeHCAT, a synthetic analog of taurocholic acid, was developed in the late 1970s to facilitate the study of enterohepatic circulation of bile acids using gamma scintigraphy.^[9] This radiopharmaceutical was designed to mimic natural bile acid behavior while allowing non-invasive tracking via selenium-75 labeling. Early research focused on its pharmacokinetics and potential for assessing ileal function, with initial human studies demonstrating its enterohepatic cycling and retention patterns in healthy volunteers and patients. A seminal evaluation by Merrick et al. in 1982 confirmed its suitability for clinical investigation, showing effective absorption, recirculation, and fecal excretion comparable to endogenous bile acids.^[10] Commercial development of SeHCAT was undertaken by Amersham International (now part of GE Healthcare) during the 1980s, leading to its approval for clinical use across Europe as a diagnostic tool for bile acid malabsorption (BAM).^[11] This marked a shift toward accessible nuclear medicine-based testing, building on the molecule's chemical similarity to taurocholic acid to ensure physiological relevance in vivo. By the mid-1980s, it was supplied for research and routine applications, with national authorizations following, such as in the Netherlands in 1996.^[12] Key milestones in SeHCAT's history include its role in supplanting earlier diagnostic methods, notably the 14C-glycocholic acid breath test, which was discontinued due to concerns over beta radiation exposure, procedural complexity, and limited specificity.^[12] It also reduced reliance on invasive fecal bile acid measurements, offering a simpler whole-body retention assessment. SeHCAT saw its first widespread clinical adoption in the United Kingdom during the 1980s and 1990s for investigating chronic diarrhea, particularly in cases suspected of BAM. By the 2000s, SeHCAT had become a standard in BAM diagnosis, integrated into clinical guidelines such as those from the British Society of Gastroenterology in 2018, which recommend it for patients with irritable bowel syndrome-diarrhea predominant or unexplained chronic diarrhea.^[13] No significant technological updates have occurred since the early 2000s, though a minor manufacturing change to pre-filled capsules was implemented in 2024 to comply with regulations, without affecting composition or efficacy.^[12] Ongoing validation studies continue to affirm its diagnostic accuracy and utility in diverse patient populations.^[11]

Chemical Structure and Radiolabelling

SeHCAT, chemically known as 23-seleno-25-homotaurocholic acid or tauroselcholic acid, has the molecular formula C₂₆H₄₅NO₇SSe and a molar mass of 594.68 g/mol.^[14]^[15] The molecule is a synthetic homolog of the natural bile acid taurocholic acid, featuring a steroid nucleus with hydroxyl groups at positions 3α, 7α, and 12α, and a side chain extended by one carbon atom compared to taurocholic acid. Selenium replaces the carbon atom at position 23 in the side chain, which enhances chemical stability against bacterial deconjugation in the intestine, with studies showing only 8% deconjugation of SeHCAT after 24 hours compared to 58% for taurocholic acid.^[16] It is conjugated to taurine at the 24-carboxyl group, promoting water solubility similar to endogenous conjugated bile acids.^[14] SeHCAT is radiolabeled with the gamma-emitting isotope selenium-75 (⁷⁵Se), which has a physical half-life of approximately 120 days and primarily emits photons at 136 keV (with a secondary emission at 265 keV).^[17] The standard diagnostic dose contains about 370 kBq of ⁷⁵Se activity, with less than 0.1 mg of carrier compound absorbed onto an inert material within a capsule.^[17] This design enables SeHCAT to mimic the enterohepatic cycling of natural bile acids without significant metabolism or degradation during gastrointestinal transit.^[18] It is classified under the ATC code V09DX01 as a diagnostic radiopharmaceutical.^[19] SeHCAT was developed as a gamma-emitting alternative to carbon-14 labeled bile acid tests to facilitate external detection.^[17]

Diagnostic Procedure

Patient Preparation

Patients undergoing the SeHCAT test are typically advised to fast for 2-4 hours prior to capsule administration to optimize absorption and minimize gastrointestinal interference, although some protocols permit normal eating and drinking on the day of the procedure.^[20]^[1]^[21] Certain medications that affect bile acid absorption or intestinal motility must be withheld to ensure accurate results; bile acid sequestrants such as cholestyramine, colestipol, and colesevelam should be discontinued 2-7 days before the test, while antidiarrheal agents like loperamide require suspension for at least 1-2 days prior.^[1]^[21]^[22] Laxatives and opioids, which can alter bowel motility, are generally withheld for 48 hours before administration to avoid impacting retention measurements.^[21] The test is contraindicated in pregnancy due to fetal radiation exposure risks, and no interruption of breastfeeding is required, as the estimated radiation dose to an infant from excreted activity in breast milk is minimal (17 μSv over 6 months of exclusive feeding).^[23] Recent barium studies or contrast-enhanced bowel imaging within 1-2 months should be disclosed, as residual contrast may interfere with scanning; such procedures are ideally avoided in the weeks surrounding the test.^[21]^[22] Patients receive instructions to maintain hydration, swallow the small capsule with water, and follow no specific dietary restrictions after ingestion, with informed consent obtained regarding the low-level radiation exposure involved. These preparations collectively reduce variables that could skew bile acid retention assessment.^[24]^[25]^[1]

Administration and Scanning

The administration of SeHCAT begins with the patient swallowing a single oral capsule containing 370 kBq of [75Se]tauroselcholic acid, typically taken with water to facilitate passage into the gastrointestinal tract.^[26] Patients are usually fasted for at least 1 hour prior to ingestion to optimize tracer absorption. The procedure is performed in a nuclear medicine department, and no sedation is required. The initial scan occurs 1 to 3 hours after capsule ingestion, with the patient positioned supine on the scanning couch and the gamma camera placed over the abdomen to capture counts from the tracer.^[27] A dual-headed, uncollimated gamma camera is commonly used for this whole-body counting acquisition, often acquiring anterior-posterior and posterior-anterior views either sequentially or simultaneously, with the patient remaining still for the duration. To ensure reproducibility, the exact patient positioning—including supine orientation—is recorded and replicated for subsequent imaging; arms are generally placed alongside the body unless specified otherwise for comfort and consistency. Each scan typically lasts 10 to 15 minutes, during which the patient lies comfortably without needing to undress or remove non-metallic items.^[28] Seven days later, a second scan is performed using the identical setup and positioning to measure tracer retention, allowing the patient to resume normal diet and activities in the interim.^[27] Post-scan voiding is not required, as the procedure focuses on whole-body retention rather than localized excretion.^[1] The total time commitment per visit is minimal, enabling outpatient completion without disruption to daily routines.^[24]

Radiation Exposure

The SeHCAT test delivers a low effective radiation dose of approximately 0.26 mSv to adults when administering the standard activity of 370 kBq of ^{75}Se-labelled tauroselcholic acid.^[1] For children, the same activity is typically used, but the effective dose per MBq is higher than in adults (e.g., up to 3.9 mSv/MBq in 1-year-olds, resulting in approximately 1.4 mSv total), necessitating careful risk-benefit assessment, though overall exposure remains at diagnostic levels.^[29] This dose is equivalent to roughly 1–3 months of natural background radiation in regions like the UK, where annual exposure averages 1–3 mSv.^[1] In comparison, a standard abdominal CT scan exposes patients to 5–10 mSv, making SeHCAT a lower-radiation alternative for bile acid malabsorption assessment.^[30] The long physical half-life of ^{75}Se (approximately 118 days) enables a single capsule administration, as isotopic decay is negligible during the 7-day retention measurement period, minimizing the need for repeated dosing.^[19] Biologically, the tracer follows enterohepatic circulation and is primarily excreted via feces (>95% elimination), resulting in a short biological half-life of about 2.6 days for the majority (97%) of the administered activity in healthy individuals, with a minor retained component having a half-life of around 62 days; this kinetics prevents significant internal accumulation.^[12]^[31] SeHCAT procedures adhere to the ALARA (as low as reasonably achievable) principle to optimize patient safety, with the International Commission on Radiological Protection (ICRP) classifying such diagnostic nuclear medicine tests as low-risk when doses stay below established thresholds.^[32] For breastfeeding individuals, no interruption is required, as the estimated radiation dose to an infant from excreted activity in breast milk is minimal (17 μSv over 6 months of exclusive feeding).^[23]

Interpretation of Results

Retention Calculation

The retention of SeHCAT is calculated from gamma camera scans performed shortly after administration (typically 3 hours post-ingestion on day 0) and again on day 7, using the formula:

\text{Retention (\%)} = \left( \frac{\text{counts on day 7}}{\text{counts on day 0}} \times 100 \right) \times \text{decay correction factor}

where the decay correction factor accounts for the physical decay of ^{75}Se (half-life approximately 120 days) over the 7-day interval and is given by e^{\lambda t}, with \lambda = \ln(2)/120 days^{-1} and t = 7 days, yielding a factor of approximately 1.04.^[33]^[34] This correction compensates for the radionuclide's decay rate of roughly 0.5% per day, ensuring the retention value reflects biological loss rather than physical decay alone.^[33] The calculation involves several preprocessing steps to ensure accuracy. Counts are obtained from anterior and posterior static images of the abdomen, acquired for about 5 minutes each using an uncollimated gamma camera centered on the umbilicus, with a region of interest (ROI) drawn over the whole abdomen to encompass the liver and gut areas. Background counts, measured separately from a 5-minute acquisition at the detector's maximum radius, are subtracted from the anterior and posterior counts. The geometric mean of these corrected counts—\sqrt{(\text{anterior} \times \text{posterior})}—is then computed for both day 0 and day 7 to normalize for photon attenuation and scatter in the body.^[33]^[34] These computations are typically automated within gamma camera software systems, such as those integrated with GE Healthcare or similar vendors, which handle ROI delineation, background subtraction, and geometric mean calculations. Manual verification is recommended to check for positioning errors or patient movement that could affect ROI consistency between scans. The overall precision of the retention measurement is approximately ±5%, influenced by factors like counting statistics and methodological variations between collimated and uncollimated approaches.^[34]^[35]

Diagnostic Thresholds

The diagnostic thresholds for bile acid malabsorption (BAM) using SeHCAT are based on the percentage of isotope retention at 7 days post-administration, with retention greater than 15% indicating normal bile acid absorption and no BAM.^[36] Mild BAM is typically defined as 10-15% retention, moderate BAM as 5-10% retention, and severe BAM as less than 5% retention.^[36] These thresholds allow for grading the severity of BAM and guiding clinical management. These cutoff values are supported by studies correlating SeHCAT retention with fecal bile acid excretion, where levels exceeding 2 mmol/24 hours are indicative of BAM as the gold standard reference.^[37] The SeHCAT test demonstrates high diagnostic accuracy, with an average sensitivity of approximately 87% and specificity of 93% when using a 10% retention threshold for BAM diagnosis.^[36] Thresholds have been established through consensus in clinical practice, such as a 10% cutoff widely adopted since 1991, though some laboratories use 15% for broader sensitivity.^[12] Variations exist due to differences in reference populations and equipment, but false positives are rare overall. Primary bile acid diarrhea diagnosed by SeHCAT is associated with higher body mass index, occurring in approximately 40% of overweight and 60% of obese individuals.^[38]

Clinical Applications

Indications

SeHCAT testing is primarily indicated for evaluating bile acid malabsorption (BAM) in patients presenting with chronic diarrhea lasting more than six months that remains unresponsive to standard antidiarrheal therapies. This includes individuals with suspected type 2 (idiopathic) BAM, particularly those fulfilling Rome IV criteria for diarrhea-predominant irritable bowel syndrome (IBS-D), characterized by recurrent abdominal pain associated with loose or watery stools for at least six months. The British Society of Gastroenterology (BSG) guidelines recommend SeHCAT as a diagnostic tool in such cases to identify BAM, which affects approximately 25-33% of IBS-D patients, with a meta-analysis reporting a prevalence of 28% based on abnormal SeHCAT retention. Testing is typically considered after initial investigations, such as colonoscopy, have ruled out organic causes like inflammatory bowel disease or infection. Secondary indications encompass scenarios where BAM is a likely contributor to persistent diarrhea, including post-cholecystectomy syndrome, where up to 10% of patients develop BAM-related symptoms. It is also recommended for patients with ileal resection or Crohn's disease involving the terminal ileum, as these conditions disrupt bile acid reabsorption and are associated with a high prevalence of type 1 BAM. In cases of radiation proctitis following pelvic radiotherapy, SeHCAT can assess for type 3 BAM, with studies indicating abnormal retention in over 50% of affected individuals. Similarly, for microscopic colitis with ongoing diarrhea despite treatment, SeHCAT helps differentiate BAM as a comorbid factor. The BSG guidelines for investigating chronic diarrhea endorse a targeted "test and treat" approach using SeHCAT for suspected BAM in functional or idiopathic presentations, rather than empirical therapy alone. In contrast, the National Institute for Health and Care Excellence (NICE) diagnostic guidance advises against routine adoption of SeHCAT for chronic diarrhea, IBS-D, or Crohn's disease without ileal resection, but permits continued use in established centers with ongoing data collection to evaluate clinical impact. This targeted application underscores SeHCAT's role in precision diagnosis for specific high-yield patient groups, avoiding broad screening in all diarrhea cases.

Correlation with Treatment Response

SeHCAT retention levels exhibit an inverse correlation with the clinical response to bile acid sequestrants, such as cholestyramine and colesevelam, in patients with bile acid malabsorption (BAM). Lower retention indicates more severe malabsorption and predicts higher rates of symptom improvement, with studies demonstrating response rates exceeding 80% for patients with 7-day retention below 10%. Specifically, pooled data from multiple prospective studies show response rates of 96% for severe BAM (retention <5%), 80% for moderate BAM (retention 5-10%), and 70% for mild BAM (retention 10-15%), highlighting a dose-response relationship where therapy titration—starting with standard doses and escalating based on residual symptoms—optimizes outcomes.^[39] In a retrospective analysis of 377 patients with SeHCAT-confirmed BAM, 50% reported diarrhea improvement after diagnosis and treatment initiation, but 74% continued to experience symptoms, with 62% relying on regular anti-diarrheal medications including sequestrants.^[40] Primary BAM (idiopathic, type 2) often necessitates lifelong therapy with bile acid binders to maintain symptom control, as the underlying enterohepatic circulation defect persists without surgical intervention.^[41] Follow-up SeHCAT testing is rare due to its radiation exposure and the stability of BAM severity, with monitoring typically relying on symptom assessment and fecal bile acid markers like serum 7α-hydroxy-4-cholesten-3-one (C4) or total fecal bile acids to guide therapy adjustments. The test's role in reducing irritable bowel syndrome (IBS) misdiagnosis enhances cost-effectiveness, as early identification averts prolonged investigations and empirical treatments, potentially halving diagnostic costs in affected cohorts.^[42]^[43]

Limitations and Alternatives

Availability and Accessibility

SeHCAT is widely utilized in the United Kingdom and Europe, where it is provided through public health systems such as the National Health Service (NHS), with approximately 10,000 tests conducted annually in the UK.^[44] The test holds marketing authorization in the European Union via the European Medicines Agency (EMA), enabling its availability in at least twelve European countries.^[12]^[1] It is also licensed and accessible in Australia and Canada, reflecting broader adoption in select non-European regions.^[45]^[1] However, as of 2025, SeHCAT remains unapproved by the U.S. Food and Drug Administration (FDA), resulting in its absence from routine clinical practice in the United States.^[1] Access to SeHCAT is constrained by the need for specialized nuclear medicine departments equipped with gamma cameras to administer the oral capsule and perform retention scans.^[1] The radiolabeled component, 75Se-homocholic acid taurine, relies on a cyclotron-based production process involving proton irradiation of arsenic targets, which introduces supply chain vulnerabilities.^[46] Occasional shortages have been reported due to the isotope's half-life of approximately 120 days, which limits stockpiling and requires consistent manufacturing cycles; industry updates from suppliers like GE Healthcare have addressed adaptations to capsule formulations to mitigate such disruptions.^[47] In the UK, the cost of a SeHCAT test typically ranges from £300 to £500, encompassing the £195 capsule price and £186–£282 for administration and scanning, positioning it as a relatively expensive diagnostic option compared to non-nuclear alternatives.^[48] These barriers contribute to geographic disparities, leading to underdiagnosis of bile acid malabsorption in regions outside Europe, Australia, and Canada, where alternative empirical treatments are often employed instead.^[1] Ongoing efforts to expand availability include clinical guideline integrations in Canada to promote wider adoption and preliminary discussions for potential trials or regulatory pathways in North America, though no major approvals have materialized by 2025.^[49] The test's favorable radiation profile, with effective doses under 1 mSv, supports its suitability for outpatient procedures without compromising safety.^[19]

Alternative Diagnostic Methods

Several alternative diagnostic methods exist for bile acid malabsorption (BAM), particularly in regions where the SeHCAT test is unavailable or impractical. These include direct measurement of fecal bile acids, serum biomarkers such as 7α-hydroxy-4-cholesten-3-one (C4), and fibroblast growth factor 19 (FGF19), each offering non-invasive or semi-invasive options with varying accuracy and practicality. While SeHCAT remains the gold standard with a sensitivity of approximately 87% and specificity of 93%, these alternatives are increasingly used for screening or confirmation, especially since 2018 when biomarkers like C4 and FGF19 have gained traction in clinical practice.^[50] The 48-hour fecal bile acid test involves collecting stool after a high-fat diet (typically 100 g fat/day) to quantify total and primary bile acids (cholic acid and chenodeoxycholic acid). A diagnosis of BAM is indicated by total fecal bile acids exceeding 2337 µmol over 48 hours or primary bile acids comprising more than 10% of total bile acids; alternative cutoffs include total bile acids >1000 µmol/48 hours combined with primary bile acids >4%. This method has a sensitivity of 67% and specificity of 79% compared to SeHCAT, providing direct evidence of excess bile acid excretion. However, it is invasive, requires patient compliance for complete collection, and demands specialized laboratory analysis like high-performance liquid chromatography, limiting its routine use.^[51]^[50] Serum 7α-C4, a fasting marker of hepatic bile acid synthesis, is elevated in BAM (threshold >48 ng/mL) and serves as a non-invasive screening tool available in U.S. laboratories such as Mayo Clinic Labs. Levels of C4 correlate moderately with SeHCAT results (r ≈ 0.7), with a sensitivity of 85% and specificity of 71% for detecting BAM. It is particularly useful in patients with irritable bowel syndrome-diarrhea or post-cholecystectomy diarrhea but can be influenced by factors like liver disease or statin use.^[50]^[52] FGF19, an ileal hormone that suppresses bile acid synthesis, is measured via ELISA and typically low in BAM (threshold ≤145 pg/mL). This blood-based test has a sensitivity of 64% and specificity of 72% relative to SeHCAT, with lower validation compared to C4 due to variability from recent meals or assay standardization issues. It is employed as a supplementary biomarker in research settings but less commonly in routine diagnostics.^[50] These alternatives are particularly valuable in areas without SeHCAT access, where SeHCAT is preferred when available due to its superior accuracy. Emerging combination approaches, such as elevated C4 levels combined with an empiric trial of bile acid sequestrants, enhance diagnostic efficiency without relying on a single test.^[50]

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Mar 1, 2021 · The aim of this article is to enable departments to calculate the uncertainty of SeHCAT retention measurements so that the acquisition time can ...
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https://doi.org/10.1186/s12876-019-1102-1
[37]
Alimentary Pharmacology & Therapeutics - Wiley Online Library
Aug 16, 2015 · ... SeHCAT retention aids in predicting clinical response to bile acid sequestrants. Moreover, considering that patient intolerance of ...
[38]
Long-term effect of medical treatment of diarrhoea in 377 patients ...
Long-term effect of medical treatment of diarrhoea in 377 patients with SeHCAT scan diagnosed bile acid malabsorption from 2003 to 2016; a retrospective study.Missing: primary lifelong
[39]
Recent advances in the understanding of bile acid malabsorption
Nov 8, 2009 · The main treatment goal with type 2, idiopathic bile acid diarrhoea, is control of diarrhoea with oral administration of bile acid binders.Missing: therapy | Show results with:therapy
[40]
What is the cost of delayed diagnosis of bile acid malabsorption and ...
If SeHCAT scanning was booked later (n=25), patients reported symptoms for 30 months (median, range 0.5–360) and the cost was £1568.31 (95% CI £1200.55 to £ ...
[41]
A single faecal bile acid stool test demonstrates potential efficacy in ...
May 18, 2022 · This study examines the validity of measuring faecal bile acids (FBA) in a single stool sample as a diagnostic tool for bile acid diarrhoea (BAD)<|control11|><|separator|>
[42]
Background and definition of the decision problem - SeHCAT ... - NCBI
SeHCAT is manufactured by GE Healthcare. The SeHCAT test is used to measure how well the body absorbs bile acids. The radiopharmaceutical capsule contains 75 ...Missing: development | Show results with:development
[43]
The efficacy of a low-fat diet to manage the symptoms of bile acid ...
We evaluated low-fat diets for managing gastrointestinal symptoms in these patients. All patients reporting type 6 or 7 stool were offered a selenium-75 ...
[44]
[PDF] Simultaneous production and quality control of 73Se and 75Se ...
It can be considered as the method of choice for simultaneous production of 73Se and 75Se. Key words: Selenium-75, Selenium-73, cyclotron, simultaneous ...Missing: SeHCAT | Show results with:SeHCAT
[45]
Supply Updates from Industry - British Nuclear Medicine Society
Recent supply updates include a Curium I123 Petten disruption, Terumo Holmium production discontinuation, changes to SeHCAT capsules, and a Technescan HDP ...
[46]
SeHCAT (tauroselcholic [75 selenium] acid) for diagnosing bile acid ...
3.35 The total cost of SeHCAT in the base-case model was £477 per test, the same as in the IBS-D or functional diarrhoea model. 3.36 The costs of treating bile ...Missing: misdiagnosis | Show results with:misdiagnosis
[47]
Canadian Association of Gastroenterology Clinical Practice ...
Sep 14, 2019 · ... SeHCAT scanning in patients with diarrhoea-predominant irritable bowel syndrome ... test to document ileal dysfunction due to late radiation ...Missing: procedure | Show results with:procedure<|control11|><|separator|>
[48]
Scientific summary - SeHCAT [tauroselcholic (selenium-75) acid] for ...
The principal diagnosis/indication for this assessment is chronic diarrhoea due to bile acid malabsorption (BAM). BAM is one of several causes of chronic ...
[49]
Methods for diagnosing bile acid malabsorption: a systematic review
Nov 14, 2019 · Our systematic review indicates that 75 SeHCAT has the highest diagnostic accuracy for BAM, followed by serum C4 assay.Missing: replacement | Show results with:replacement
[50]
Advances in the pathophysiology, diagnosis and management of ...
BAM is classified as severe, moderate, or mild based on the percentage of retained radioactive selenium (<5%, 5–10%, and 10–15%, respectively) [12]. In a ...Missing: consensus | Show results with:consensus
[51]
Measurement of serum 7α‐hydroxy‐4‐cholesten‐3‐one (or 7αC4), a ...
Jun 10, 2009 · ... BAM relative to the 75SeHCAT retention test. Our aim was to develop a serum 7αC4 assay, normal values, and compare results from healthy ...