Abdominal pain, diarrhea, nausea, vomiting, bloating, weight loss, dyspepsia, oily stool production, iron deficiency, or unexplained malabsorptive symptoms. Those common complaints in a primary care practice may reflect self-limited illness like acute gastroenteritis, food-borne illness, or indigestion. However, they may also signal more serious autoimmune, cancerous, cardiometabolic, infectious, genetic, and inflammatory conditions with meaningful downstream consequences for patients.
In this article:
Clinical challenge | Why it matters | Ordering recommendations | Interpreting test results | Next steps | Supporting resources
Because gut health symptoms frequently overlap in gastrointestinal (GI) conditions—celiac disease, exocrine pancreatic insufficiency (EPI), Helicobacter pylori (H pylori) infection, infectious diarrhea, and inflammatory bowel disease (IBD)—clinical presentation alone is often insufficient for a definitive diagnosis. (see Fig A) The challenge for clinicians is to accurately and promptly differentiate between potential causes to initiate proper management and avoid the detrimental health consequences of a delayed gastrointestinal diagnosis. (see Fig B)
A practical, yet comprehensive, diagnostic approach can clarify etiology, reduce diagnostic delay, and support earlier clinical decisions, whether by primary care physicians or gastroenterologists.
A differential diagnostic approach in this situation is key to ensuring timely and precise clinical management that helps avoid the significant health consequences of a delayed or missed diagnosis.
| Gastrointestinal condition | Abdominal pain | Abdominal burning sensation | Feeling of fullness | Bloating | Diarrhea | Nausea | Vomiting | Weight loss | Iron deficiency | Oily stools | Red, dark, tarry stools | Malabsorption symptoms |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Acute infectious diarrhea | X | X | X | X | X | |||||||
| H pylori infection | X | X | X | X | X | X | X | X | X | |||
| Inflammatory bowel disease | X | X | X | X | X | X | X | X | X | X | X | X |
| Celiac disease | X | X | X | X | X | X | X | X | X | X | ||
| Exocrine pancreatic insufficiency | X | X | X | X | X | X | ||||||
| Hepatitis | X | X | X | X | ||||||||
| Metabolic dysfunction-associated steatotic liver disease (MASLD) | X | X | X | X | X | |||||||
| Metabolic dysfunction-associated steatohepatitis (MASH) | X | X | X | X | ||||||||
| Gallstones (cholelithiasis) | X | X | X | X | X | X | X | X | X |
List not inclusive of all digestive conditions or all associated symptoms.
| Gastrointestinal condition | Potential consequences of delayed diagnosis or misdiagnosis |
|---|---|
| Acute infectious diarrhea | Severe dehydration and shock; toxic megacolon; increased risk for hemolytic uremic syndrome if antibiotics are used when Shiga producing E coli is the root cause for symptoms |
| H pylori infection | Chronic gastritis; peptic ulcers; iron deficiency anemia; idiopathic thrombocytopenic purpura (ITP); gastric cancer; mucosa-assisted lymphoid tissue (MALT) lymphoma |
| Inflammatory bowel disease | Permanent, irreversible damage to digestive tract; abscesses, bowel obstructions, and fistulas that can require surgical intervention; toxic megacolon that can progress to colon rupture; higher risk for pre-cancer and colon cancer |
| Celiac disease1-3 | Chronic, often irreversible damage to multiple organ systems; permanent bone loss; infertility and reproductive issues; increased risk for cancer, additional autoimmune disorders, and neurological damage; cognitive impairment; mental health challenges |
| Exocrine pancreatic insufficiency | Muscle wasting (sarcopenia); higher risk for cardiovascular events; increased mortality risk and poorer cancer outcomes |
| Hepatitis | Cirrhosis; liver cancer; liver failure; higher risk for kidney disease, cardiovascular issues, and type 2 diabetes; cognitive impairment; mental health challenges |
| Metabolic dysfunction-associated steatotic liver disease (MASLD) | Missed opportunity to reverse and avoid progression to irreversible metabolic dysfunction-associated steatohepatitis; cardiovascular disease; increased risk for liver cancer, type 2 diabetes and other non-liver cancers |
| Metabolic dysfunction-associated steatohepatitis (MASH) | Advanced liver fibrosis, scaring, and cirrhosis that can lead to liver failure; liver cancer; type 2 diabetes; cognitive impairment; mental health challenges |
| Gallstones (cholelithiasis) | Chronic gallbladder disease; acute pancreatitis; secondary biliary cirrhosis; gallbladder rupture; increased risk for sepsis and gallbladder cancer |
List not inclusive of all digestive conditions or all potential consequences due to delayed diagnosis or misdiagnosis.
Timely, first-line laboratory testing can help primary care physicians transform patient care on a large scale by screening for common pathologies, narrowing the differential diagnosis earlier, selecting the right next step, and coordinating gastroenterology specialty care more efficiently when needed.
To support the gastroenterology care continuum, Quest Diagnostics offers a spectrum of gut health screening and diagnostic tests that align with the latest clinical guidelines. Primary care providers can help patients stay ahead of serious complications by ordering key tests at the first sign of gut distress.
Celiac disease requires both diagnostic testing to determine the condition as well as ongoing testing to monitor progress and to detect associated conditions.
Components include Tissue Transglutaminase (tTG) Antibody (IgA) [8821], IgA (Immunoglobulin A) [539].
Quest’s noninvasive and highly specific test enables providers to diagnose EPI, an underrecognized but clinically significant gastrointestinal condition.
Quest offers a full H pylori infection testing menu aligned with American College of Gastroenterology (ACG) guidelines.8
The H pylori Urea Breath Test is indicated for diagnosing active infection in individuals older than 3 years to those under 60 years with no alarming symptoms and for confirming eradication of infection 4 weeks post-treatment. The H pylori Stool Antigen Test is indicated for the same use cases but can also be used for children under the age of 3.
From a single specimen, Quest’s qualitative PCR panel can simultaneously detect 9 of the most common pathogens associated with infectious diarrhea.
Includes Campylobacter group, Salmonella species, Shigella species, Vibrio group, Yersinia enterocolitica, Shiga toxin 1, Shiga toxin 2, Norovirus GI/GII, and Rotavirus A.
Using the results of a CBC (6399) and one inflammatory marker—Calprotectin, Stool (test code: 16796), Lactoferrin, Qualitative, Stool (test code: 10156), Lactoferrin, Quantitative, Stool (test code: 17321)—primary care clinicians can utilize Quest’s IBD Differentiation Panel to gain early diagnostic insight. This allows for a more informed, high-priority referral to a gastroenterologist while the patient awaits a definitive endoscopy. The panel also aids gastroenterologists in differentiating between Crohn disease and ulcerative colitis when endoscopic findings are inconclusive.
Components include ANCA Screen with Reflex to ANCA Titer [70171], Myeloperoxidase Antibody (MPO) [8796], Proteinase-3 Antibody [34151], Saccharomyces cerevisiae Antibodies (ASCA) (IgG) [10294], Saccharomyces cerevisiae Antibodies (ASCA) (IgA) [10295].
* CPT code is subject to a Medicare Limited Coverage Policy and may require a signed ABN when ordering.
The CPT® codes provided are based on American Medical Association guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
Components of panels can be ordered separately.
Test result interpretation is highly dependent on the condition and the individual test.
If tTG IgA is detected (≥15.0 U/mL), a positive endomysial antibody (IgA) screen further increases the specificity of the diagnosis. If immunoglobulin A is flagged as low based on the age-appropriate reference range, then tTG IgG and/or gliadin (deamidated) antibody (IgG) should be performed for those with a suspected IgA deficiency. According to best practice guidelines, celiac disease should be confirmed with biopsy of the small intestine.
According to American Gastroenterological Association (AGA) guidance, test result levels <100 μg/g stool are consistent with EPI in the appropriate clinical context, and levels of 100 to 200 μg/g stool are considered indeterminate for EPI.9
Positive results indicate H pylori infection. Clinical guidelines indicate that all patients with positive H pylori results be offered eradication therapy, as well as post-treatment testing to confirm eradication.8
A positive result shows the presence of the pathogens or toxins associated with infectious diarrhea. However, a negative result does not rule out an infection caused by pathogens not included in the panel.
Patients with IBD symptoms should undergo testing to rule out other conditions with similar symptoms. Once differential diagnosis is complete and IBD remains the most likely cause, endoscopy and histology should be used to unequivocally diagnose IBD.
When initial workups are completed and a gastrointestinal condition is confirmed or strongly suspected, primary care providers can refer patients to a gastroenterology specialist for any follow-up tests, appropriate treatment, and ongoing monitoring. Testing performed up to this point will help the specialist streamline next steps for the patient.
Reach out to receive additional information on Quest's infectious disease and immunology lab tests, services, and coverage.
1. Laurikka P, Kivelä L, Kurppa K, Kaukinen K. Review article: Systemic consequences of coeliac disease. Aliment Pharmacol Ther. 2022;56 Suppl 1(Suppl 1):S64-S72. doi:10.1111/apt.16912
2. Özden Y. Impact of delayed diagnosis in celiac disease on long-term complications: osteoporosis, infertility, and lymphoma. Diagnostic and Interventional Endoscopy. 2026;5(1):1-6. doi:10.14744/DiagnintervEndosc.2026.00096
3. Silano M, Volta U, Mecchia AM, et al. Delayed diagnosis of coeliac disease increases cancer risk. BMC Gastroenterol. 2007;7:8. doi:10.1186/1471-230X-7-8
4. CDC. IBD facts and stats. Published June 21, 2024. Accessed March 20, 2026. https://www.cdc.gov/inflammatory-bowel-disease/php/facts-stats/index.html
5. Rubio-Tapia A, Ludvigsson JF, Brantner TL, et al. The prevalence of celiac disease in the United States. Am J Gastroenterol. 2012;107(10):1538-44. doi:10.1038/ajg.2012.219
6. Kobayashi T, Iwaki M, Nakajima A, et al. Current research on the pathogenesis of NAFLD/NASH and the gut–liver axis: gut microbiota, dysbiosis, and leaky-gut syndrome. Int J Mol Sci. 2022;23(19):11689. doi:10.3390/ijms231911689
7. Kolodziejczyk AA, Zheng D, Shibolet O, et al. The role of the microbiome in NAFLD and NASH. EMBO Mol Med. 2019;11(2):e9302. doi:10.15252/emmm.201809302
8. Chey WD, Howden CW, Moss SF, et al. ACG clinical guideline: treatment of Helicobacter pylori infection. Am J Gastroenterol. 2024;119(9):1730-1753. doi:10.14309/ajg.00000000000 02968
9. Whitcomb DC, Buchner AM, Forsmark CE. AGA clinical practice update on the epidemiology, evaluation, and management of exocrine pancreatic insufficiency: expert review. Gastroenterology. 2023;165(5):1292-1301. doi:10.1053/j.gastro.2023.07.007