Aug. 25, 2025
To diagnose indigestion, your healthcare professional asks you about your symptoms, recent meals, eating habits, medical history, life stresses, exposure to anyone who's ill and other questions. Your answers help your health professional understand the possible factors linked to your symptoms.
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You also have a thorough medical exam. This includes tapping or pressing on your abdomen and listening to your abdomen with a stethoscope.
Your healthcare professional may be able to diagnose functional indigestion based on your symptoms, medical history and exam.
Your healthcare professional may order a test for H. pylori bacteria. This may be done with a tissue sample from the stomach, breath test or stool sample.
Other tests may be needed if your healthcare professional is concerned about particular symptoms or findings from your exam. You also may need more tests if the first line of treatment for indigestion does not help with symptoms. These tests may include:
Our caring team of Mayo Clinic experts can help you with your indigestion-related health concerns.
A variety of treatments may improve symptoms of indigestion.
Changes to the diet and possible changes in medicines are the first steps in lessening symptoms. These include the following:
Talk therapy with a psychotherapist can help you manage depression, anxiety and related factors that may be contributing to indigestion. Prescription medicines also may help lessen symptoms of depression and anxiety.
Your healthcare professional may prescribe medicines or recommend medicines you can buy without a prescription to lessen indigestion symptoms. These may include:
Explore Mayo Clinic studies testing new treatments, interventions and tests as a means to prevent, detect, treat or manage this condition.
Lifestyle changes that can be part of your routine may help lessen symptoms or prevent the return of symptoms:
Alternative and complementary treatments that may improve symptoms of indigestion include:
Check with your healthcare professional before you take any supplements. Your health professional can help make sure the dose is safe for you. It's also important to make sure the supplement won't react with any other medicines you take.
You're likely to start by seeing your primary healthcare professional. You may be referred to a doctor who specializes in digestive diseases, called a gastroenterologist. Here's some information to help you get ready for your appointment and know what to expect.
Some basic questions you may wish to ask include:
In addition to the questions that you've prepared, don't hesitate to ask other questions during your appointment.
Be ready to answer questions your healthcare professional may ask, such as:
Indigestion care at Mayo Clinic
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Five Key Factors That Affect Acidity
Today we’ll talk about what’s behind the trends in acidity for different molecules and discuss the most important factors that determine these values.
I’ve written in schoolmarmish tones before about how pKa is one of the most important measures you can learn in organic chemistry, and not knowing some basic pKa values before an exam is a lot like walking up to a poker table without knowing the values of the hands: you’re going to lose your shirt. (See article: Know Your pKas)
Let’s quickly review the basics of acidity and basicity. Here’s the condensed version:
With that out of the way, let’s get started.
Table of Contents
Removal of a proton, H+ , decreases the formal charge on an atom or molecule by one unit. This is, of course, easiest to do when an atom bears a charge of +1 in the first place, and becomes progressively more difficult as the overall charge becomes negative. The acidity trends reflect this:
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Note that once a conjugate base (B-) is negative, a second deprotonation will make the dianion (B 2-). While far from impossible, forming the dianion can be difficult due to the buildup of negative charge and the corresponding electronic repulsions that result.
This point causes a lot of confusion due to the presence of two seemingly conflicting trends.
Here’s the first point: acidity increases as we go across a row in the periodic table. This makes sense, right? It makes sense that HF is more electronegative than H2O, NH3, and CH4 due to the greater electronegativity of fluorine versus oxygen, nitrogen, and carbon. A fluorine bearing a negative charge is a happy fluorine.
But here’s the seemingly strange thing. HF itself is not a “strong” acid, at least not in the sense that it ionizes completely in water. HF is a weaker acid than HCl, HBr, and HI. What’s going on here?
You could make two arguments for why this is. The first reason has to do with the shorter (and stronger) H-F bond as compared to the larger hydrogen halides.
The second has to do with the stability of the conjugate base. The fluoride anion, F(–) is a tiny and vicious little beast, with the smallest ionic radius of any other ion bearing a single negative charge. Its charge is therefore spread over a smaller volume than those of the larger halides, which is energetically unfavorable: for one thing, F(–) begs for solvation, which will lead to a lower entropy term in the ΔG.
Note that this trend also holds for H2O and H2S, with H2S being about 10 million times more acidic.
A huge stabilizing factor for a conjugate base is if the negative charge can be delocalized through resonance. The classic examples are with phenol (C6H5OH) which is about a million times more acidic than water, and with acetic acid (pKa of ~4).
Watch out though – it isn’t enough for a π system to simply be adjacent to a proton – the electrons of the conjugate base have to be in an orbital which allows for effective overlap.
Electronegative atoms can draw negative charge toward themselves, which can lead to considerable stabilization of conjugate bases. Check out these examples:
Predictably, this effect is going to be related to two major factors: 1) the electronegativity of the element (the more electronegative, the more acidic) and the distance between the electronegative element and the negative charge.
Again, the acidity relates nicely to the stability of the conjugate base. And the stability of the conjugate base depends on how well it can accomodate its newfound pair of electrons. In an effect akin to electronegativity, the more s character in the orbital, the closer the electrons will be to the nucleus, and the lower in energy (= stable! ) they will be.
Look at the difference between the pKa of acetylene and alkanes: 25! That’s 10 to the power of 25, as in, “100 times bigger than Avogadro’s number”.
Just to give you an idea of scale. That’s the amazing thing about chemistry – the sheer range in the power of different phenomena is awe-inspiring. (See article: pKa Values Span 60 Orders Of Magnitude)
There’s actually a mnemonic I’ve found that can help you remember these effects. This is credited to Dr. Christine Pruis, Senior Lecturer at Arizona State University Tempe.
Charge
Atom
Resonance
Dipole Induction
Orbitals
= CARDIO.
Tread carefully with mnemonics, but there you go.
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Become a MOC member to see the clickable quiz with answers on the back.
Become a MOC member to see the clickable quiz with answers on the back.
Become a MOC member to see the clickable quiz with answers on the back.
Become a MOC member to see the clickable quiz with answers on the back.
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