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Author(s): Rebecca W. Van Dyke, M.D., 2012

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M2 GI Sequence

    Diarrhea and Malabsorption
              Rebecca W. Van Dyke, MD




Winter 2012
Learning Objectives
•   At the end of this lecture on diarrhea, students should be able to:
•
•   1. Identify and characterize the major pathophysiologic causes of
    diarrhea.
•   2. Discuss mechanisms responsible for secretory and osmotic
    diarrheas and be able to differentiate between them.
•   3. Construct a differential diagnosis for a patient with diarrhea in order
    of likelihood.
•   4. Identify a sequence of tests to determine the cause of diarrhea
    depending on the presenting symptoms.
Industry Relationship Disclosures
   Industry Supported Research and
         Outside Relationships

• None
DIARRHEA
• Familiar to all of us
• Increased stool volume
  – Usually to >> 200 ml/24 hours
• Altered stool consistency
  – Increased liquidity
• Increased number of stools (not always)
Intestinal Fluid Movement (water follows solutes)
Diarrhea occurs when SB/colon solute
        loads exceed their absorptive capacities.



Small
bowel




Colon




              NORMAL              DIARRHEA
DIARRHEA - Mechanisms
• Too much input

• Not enough absorption

• Combination of both
Mechanisms of Diarrhea
•   Secretory Diarrhea
•   Osmotic diarrhea/malabsorption
•   Increased bowel motility
•   Decreased bowel surface area
•   Inflammation
Secretory Diarrhea - A problem of excess input of
           SECRETORY DIARRHEA
     electrolytes (NaCl) with water following.



     Cl
                                    Water
     Na
                                    Water
     Cl

     Na                             Water

     Cl




                            Massive volume of
                            plasma-like fluid
Clinical Manifestations of
      Secretory Diarrhea
• Large volume, watery diarrhea
• Little response to fasting
• Stool compositon is similar to plasma
  – (high NaCl)
• Dehydration and plasma electrolyte
  imbalance are common
• No WBC or RBC in stool
Cholera Vibrios
Cholera toxin
                                              affects these
                                        -     transporters        +
Lumen                                         by increases
                                              in cAMP             Cl
                                                                           Na




         Na Glucose
                      Na Amino
                         acids
                                   Na
                                        Cl                cAMP
                                                          increases
                                 cAMP                     transport
                                 decreases                                       2 Cl
            K                    transport                    K
                                                                                Na      K




Tissue                                       Cl
                Na                                                     K
side                      K                                       Na

          Villus Absorptive Cells                       Crypt Secretory Cells
Clues to Secretory Diarrhea from Clinical
    Lab Studies: Fecal Electrolytes
  High Na in stool, blood hypokalemia
                                Secretory
                       Normal   Diarrhea
   Na+ (mEq/l)         ~20-40   ~80-110
   K+                  ~90      ~40
   Cl-                 ~15      ~60
   HCO3-               ~30      ~50
 Anions      (SO4-2,   ~85      ~30
 PO4-3, fatty acids)
  Other (Mg+2)         <15-20   <10
 Volume (liters/day)   <1       5-10
Consequences of Large Volume
 Diarrhea/Secretory Diarrhea
• Dehydration due to massive loss of fluid
  overwhelming homeostatic mechanisms
• Electrolyte abnormalities
  – Hypokalemia (loss of K in stools)
  – Acidosis (loss of bicarbonate in stools)
  – Hyponatremia (loss of Na in stools and oral
    intake of free water)
• Mild malabsorption due to rapid transit
  and dilution of digestive enzymes
Origin of Electrolyte
                Abnormalities
• Dehydration: loss of 1-7 liters per day of liquid
  containing 80-100 mEq/liter Na
• Hyponatremia: loss of sodium and replacement
  orally with hypotonic fluids (water, sodas, fruit
  juices) in the presence of ADH (anti-diuretic
  hormone)
• Hypokalemia: stool K is high – may reach 40-80
  mEq/liter. 2 liters of stool with 45 mEq/liter K in it
  is a daily loss of 90 mEq which is difficult to
  replace. (1 medium banana has 19 mEq)
Patient with cholera surrounded by bottles representing
                  intestinal fluid loss.




     This Ccopyrighted material is used for illustrative purposes, in an effort to advance the instructor’s teaching
     goals. This use is Fair and consistent with the U.S. Copyright Act. (USC 17 § 107)
Causes of Intestinal Secretion – I
    stimulation of NaCl secreation
• Bacterial toxins
  – Cholera, E. coli, Shigella, etc.
• Inflammatory mediators
  – prostaglandins
• Circulating hormones
  – Gastrin (Z-E syndrome), Vasoactive
    intestinal polypeptide (VIP)
Causes of Intestinal Secretion - II
 • Malabsorbed compounds that reach the colon
   and stimulate secretion
    – Bile acids
    – Fatty acids
 • Laxatives (“natural” from plants) that
   stimulate secretion
    – Ricinoleic acid
    – Senokot
 • Lack of mature villus/surface absorptive cells
   reducing absorption
    – viral gastroenteritis/celiac sprue
Osmotic Diarrhea is caused by the presence of
  poorly absorbed luminal osmols
Carbohydrates:
– Lactose (lactase deficiency)
– Sorbitol (chewing gum)
Minerals:
– Magnesium salts (MOM, Mg citrate)
Osmotic Principles
• The driving force of fluid movement is ion or
  solute transport
  – Solutes may be actively transported through cell membranes
  – Solute may move passively through cells following concentration and/or
    electrical gradients

• Water movement follows solute movement by
  osmosis
• Water may move between cells (tight
  junctions) or through cell membrane channels
  (aquaporins)
Pathophysiology of Osmotic Diarrhea
Step 1:
Oral intake of a
concentrated solution                                  0 mV
of a non-absorbable
solute, sorbitol.                        Duodenum
                                                      -7 mV
      150 mmoles of sorbitol
                                                                       Lumen
        250 mls of volume
     = 600 mM concentration
         = 600 mOsms/l                                        H2O



                                      Na=15                           Gut
                                      K=90                            Epithelial
                                      Cl=20                           Cells

                               Interstitial fluid Na=145
                               Blood              K=5           H2O
                                                  Cl=100
                                                  Osmolality ~ 300
Pathophysiology of Osmotic Diarrhea
Step 2:
Sorbitol diluted to
isotonicity by flow
of water across
leaky epithelium.                        Jejunum


 150 mmoles of sorbitol        150 mmoles sorbitol
   250 mls of volume           500 ml volume
= 600 mM concentration                                  H2O
    = 600 mOsms/l
                               =300 mM or mOsms/l

                                 Na=15                           Gut
                                 K=90
                                                                 Epithelial
                                 Cl=20
                                                                 Cells
                          Interstitial fluid Na=145
                          Blood              K=5           H2O
                                             Cl=100
                                             Osmolality ~ 300
Step 3:                       Pathophysiology of Osmotic Diarrhea
Salts move down
concentration gradient
accompanied by water                    Jejunum
to try to equilibrate ion
concentrations.
                                        150 mmoles (150 mM) sorbitol
                                        75 mmoles (75 mM) Na
150 mmoles sorbitol                     75 mmoles (75 mM) Cl

500 ml volume                           1000 ml volume =300 mM
=300 mM
                            Na, Cl   H2O



                                Na=15
                                K=90
                                Cl=20


                                     H2O         Na=145
                                                 K=5
                            Na, Cl
                                                 Cl=100
Step 4:                        Pathophysiology of Osmotic Diarrhea
Ileum (less leaky, better
able to maintain Na
gradient) reduces NaCl
                                             Ileum
concentration and
volume .
                             750 ml volume at 300 mM (mOsms/l):

   150 mmoles sorbitol       150 mmoles (200 mM) sorbitol
   75 mmoles Na              37.5 mmoles (50 mM) Na
   75 mmoles Cl              37.5 mmoles (50 mM) Cl


   1000 ml volume           Na, Cl    H2O
   =300 mM




                                                   Na=145
                                       H2O
                                                   K=5
                            Na, Cl                 Cl=100
Step 5:                     Pathophysiology of Osmotic Diarrhea
Colon (fairly “tight”
and able to maintain
higher Na gradient)
further reduces NaCl              Colon
concentration and
volume .                   600 ml volume at 300 mM (mOsms/l):

  750 ml volume at 300     150 mmoles (250 mM) sorbitol
  mM (mOsms/l):            15 mmoles (25 mM) Na
                           15 mmoles (25 mM) Cl
  150 mmoles (200 mM)
     sorbitol
                         Na, Cl    H2O
  37.5 mmoles (50 mM)
     Na
  37.5 mmoles (50 mM)
     Cl



                                                Na=145
                                    H2O
                                                K=5
                         Na, Cl                 Cl=100
Pathophysiology of Osmotic Diarrhea

Step 6:
Overall Result



    Oral Input:
                                                    Stool Output:
 150 mmoles of sorbitol                             600 ml volume
                                                    150 mmoles sorbitol
   250 mls of volume
                                                    15 mmoles Na
= 600 mM concentration
                                                    15 mmoles Cl
Pathophysiology of Osmotic Diarrhea

• GI epithelia cannot maintain an osmotic gradient
  and cannot generate as high a Na or other ion
  gradient as the kidney can.

• Thus osmotic diarrhea is due to three factors
   – Amount of ingested material containing non-absorbed
     solute.
   – Volume of extra water needed to dilute the ingested
     material to isotonicity
   – Volume of water accompanying the Na, Cl and other
     ions that equilibrate across the gut epithelia.
Clinical Manifestations of
       Osmotic Diarrhea
• Moderate volume of stool
• Improves/disappears when oral intake
  stops
• Moderately watery/soft stool
• Often associated with increased flatus if
  due to carbohydrate malabsorption (see
  malabsorption lecture)
• No WBC or RBC in stool
Examples of Osmotic Diarrhea

• Ingestion of non-absorbable
  compounds
  – Magnesium salts
    • Antacids (Maalox, Mylanta)
    • Laxatives (Milk of Magnesia)
  – Sugars
    • Lactulose, sorbitol, mannitol, fructose, lactose
• Malabsorption of specific carbohydrates
  – Disaccharidase deficiency
• Generalized malabsorption of nutrients
Therapeutic agents that cause osmotic diarrhea:
 lactulose (used medically) and magnesium salts
              Magnesium citrate
                                         Lactulose
Causes of Osmotic
                         Diarrhea
                     Poorly absorbed sugars
                      such as:

                     Sorbitol
                     Fructose


Elsie esq., Flickr
Sources of Sorbitol Leading to Osmotic Diarrhea




      Patricil, Flickr
Clues to Osmotic Diarrhea
   from Clinical Lab Tests

• Fecal electrolytes

• Fecal osmotic gap
Fecal Electrolytes
Solute (mEq/l)           Normal          Secretory       Malabsorption            Osmotic
                                                         (Carbohydrate)           (Mg salt)
Na+                        ~40            ~90               ~40                     ~20
K+                         ~90            ~40               ~40                     ~20
Cl-                        ~15            ~60               ~10                     ~60
     -
HCO3                       ~30            ~50               ~10                     ~20
Anions (SO4-2,             ~85            ~30               ~80                     ~100
 PO4-2, fatty acids)
Other (Mg+2)             <15-20           <10               10                       ~70
Sugars (mM)                  0             0                ~100                      0

Volume (liters/day)        <1              5-10              1-2                     1-2
                                                                   *
Osmolality (mOsm/l)        ~290            ~290            ~290                     ~290

2 (Na+K)                    ~260          ~260             ~160                    ~80
Fecal osmotic gap           ~30           ~30              ~100                    ~200
                       (range ~10-50)
*
 Measured osmolality of stool can be greater than plasma osmolality if unabsorbed
carbohydrates are present and stool sits at room termperature for hours, allowing bacterial
fermentation.
OSMOTIC GAP

Question: Are there osmotically active molecules in stool
                that should not be there?

Cations + anions + neutral molecules = 300 mM

Cations = anions (electroneutrality)

Na and K are the usual stool cations and are easily measured.

Anions are a mixed bag (Cl, bicarbonate, sulfate, phosphate, fatty acids)
     and are NOT easily measured.

Neutral molecules and unmeasured cations are also a mixed bag but
     usually constitute < 30mM.

Equation for measurable ions/molecules in stool:    2(Na+K) ~ 270-290 mM
                                                    (plasma osmolality)

Thus the osmotic gap (osmotically active molecules that cannot be accounted for)
can be calculated as:

     Osmotic gap ~ 300 – 2(Na+K) ~10-50 mM for normal stool

     An osmotic gap of >> 50 is quite abnormal and suggests osmotic diarrhea
Fecal Electrolytes
Solute (mEq/l)         Normal        Secretory   Malabsorption    Osmotic
                                                 (Carbohydrate)   (Mg salt)
Na+                      ~40           ~90          ~40             ~20
K+                       ~90           ~40          ~40             ~20
Cl-                      ~15           ~60          ~10             ~60
     -
HCO3                     ~30           ~50          ~10             ~20
Anions (SO4-2,           ~85           ~30          ~80             ~100
 PO4-2, fatty acids)
Other (Mg+2)           <15-20          <10           10              ~70
Sugars (mM)                0            0            ~100             0

Volume (liters/day)      <1            5-10           1-2            1-2

Osmolality (mOsm/l)     ~290           ~290          ~290           ~290

2 (Na+K)                 ~260         ~260           ~160          ~80
Fecal osmotic gap         ~30         ~30             ~100         ~200
                        (10-50)
Consequences of Osmotic
         Diarrhea
• Major: Diarrhea due to osmotic effects
         of non-absorbed solutes

• Other: Nutritional deficiencies if
         generalized malabsorption is
         the cause
Diarrhea Due to
Increased Bowel
Motility
Rapid intestinal motility
may result in diarrhea
due to reduced contact
time between luminal
contents and bowel
mucosa.

Examples include:
  Anxiety
  Hyperthyroidism
  Irritable bowel syndrome
  Postvagotomy diarrhea
     (dumping syndrome)
   Bowel infection (viral gastroenteritis)
Clues to Increased Bowel
             Motility
• Moderate diarrhea - usually watery
• Often occurs after meals - accentuated
  gastro-colic reflex
• No WBC, RBC in stool
• Recently eaten food visable in stools
• Louder bowel sounds often apparent
• No diagnostic tests- often must rule-out
  secretory/osmotic/inflammatory causes
Consequences of Increased
      Bowel Motility
• Malabsorption
  – Nutrients (if small bowel is involved)
• Diarrhea and urgency
• Increased bowel sounds (if severe)
• Crampy abdominal pain (if severe)
Loss of Bowel Surface Area
• Functionally equivalent to increased
  bowel motility
• Underlying process causing loss of
  surface area may produce additional
  symptoms/signs
• Causes include surgical resection,
  mucosal disease, fistulas
Pig small intestinal villi before (A) and after (B) viral
                        gastroenteritis.
Viral infection temporarily destroys mature villus enterocytes
        and can cause some malabsorption/secretion.
Small bowel x-ray
of Crohn’s disease
showing fistula
(arrow) between
loops of bowel.

This fistula allows
lumenal contents to
bypass considerable
small bowel mucosa.
Inflammation and Diarrhea
   Normal Colon                        Ulcerative
                                 Colitis/Shigella
dysentery
Inflammation-induced diarrhea
        Results from several mechanisms

4. Stimulated secretion and inhibited absorption
5. Stimulation of enteric nerves causing propulsive
   contractions and stimulated secretion
6. Mucosal destruction and increased permeability
7. Nutrient maldigestion malabsorption
Clinical Manifestations of
     Inflammatory Diarrhea
• Fever and systemic signs of inflammation (if
  severe/invasive organism)
• Small to moderate volume of diarrhea
• Bloody diarrhea and/or WBC/RBC in stool
  – except in mild inflammation like viral/microscopic
    colitis
• Often accompanied by rapid
  motility/abdominal cramps
• Urgency/tenesmus if rectum is involved
Differential Diagnosis of
    Inflammatory Diarrhea
• Infectious diarrhea
  – viral, bacterial, parasitic
• Idiopathic inflammatory bowel disease
  – Crohn’s disease, Ulcerative colitis
  – microscopic colitis
• Response to ischemia/injury
Normal
air-contrast
barium enema
Air-contrast barium enema showing mucosal ulcerations and
              inflammation in ulcerative colitis.
            This reduces absorptive surface area.
Crohn’s Disease
 of the Terminal
 Ileum

Inflammation
  damages the
  mucosa,
  reducing the
  surface area
  for absorption.
Clues to Inflammatory Diarrhea on Gram Stain:
            Presence of WBC/RBC;
        Monotonic Bacterial Population

                  PMNs




                                   RBCs
Overview: Differential
    Diagnosis of Diarrhea - I
• Secretory:   bacterial toxins, hormones
                     bile acids, fatty acids,
               idiopathic
• Osmotic      malabsorption
               laxative abuse
               intake of non-
                 absorbable solutes
Differential Diagnosis of Diarrhea - II
• Inflammatory: infections
                inflammatory bowel disease
                microscopic colitis
                lymphoma/ischemia

• Increased motility: hyperthyroidism
                      irritable bowel syndrome

• Decreased surface area:     fistulas
                              post-surgical
Diagnostic Approach to Diarrhea
• Use clinical clues from history, PE and
  basic laboratory studies to determine
  the most likely mechanism present.
• Utilize specific tests to confirm the type
  of diarrhea that is present (secretory,
  osmotic etc.)
• Construct a differential diagnosis and
  select diagnostic tests
• Algorithms are included in textbook and
  syllabus
Treatment of Diarrhea
• Specific
  – Logical approach is to identify and treat the
    underlying disease
• Symptomatic
  – In practice, symptomatic therapy may be
    critical to patient survival and the only
    available approach
Non-specific Treatment Of
          Diarrhea
• Rehydration
  – Often life-saving in severe diarrhea,
    especially in the very young (children) and
    the elderly
  – IV electrolytes and water - high tech,
    expensive
  – Oral rehydration solutions - high concept,
    low tech and very cheap.


• Anti-motility drugs
Options available for management of diarrhea
              especially severe secretory diarrhea


               –   Oral rehydration therapy
               –   Measurement of stool output
               –   Antibiotics
               –   IV fluids and electrolytes




Antimotility
  drugs
World Health Organization Oral Rehydration Solution

                    Rehydration    Fecal Electrolytes
                     Solution          (mEq/l)

   Glucose            110mM               --
     Na+             90 mEq/l             75
      K+             20 mEq/l             20
 HCO3-/citrate       30 mEq/l             50
     Cl-             80 mEq/l             45
Mechanism of Action of Oral Rehydration Solutions
                                in Secretory Diarrhea
 Oral
 Rehydration
 Sodium                                                  Cholera toxin       Cl
                                                                                      Na
 Glucose
 (Amino acids)                                    -      affects these
                                                         transporters
                                                                         +

                 Na Glucose
                              Na Amino
                                 acids
                                           Na
                                                Cl


                                                                                            2 Cl
                    K                                                    K
                                                                                           Na      K

Villus                                                                                                 Crypt
Absorptive                                                                                             Secretory
Cells                                                 Cl                                               Cells
                        Na                                                   Na   K
                                  K
                                         Glucose Amino
                                                 acids

             Even in the presence of cholera toxin/cAMP, sodium (and water and chloride)
             absorption can be driven by coupled uptake of sodium with solutes such
             as glucose or amino acids.
Anti-motility Agents (opiates)
• Increase capacitance of gut and thus time for
  reabsorption
• Useful in many types of diarrhea if specific
  therapy is not available or adequate
• Often need to use large doses and/or potent
  drugs and administer on a regular (rather
  than PRN) basis.
• Do not use in acute bloody diarrhea
  (infectious or inflammatory)
Additional Source Information
                                   for more information see: http://open.umich.edu/wiki/CitationPolicy

Slide 33, Image 1 (left): Elsie esq., "Coca Cola tin," Flickr, http://www.flickr.com/photos/elsie/4023275760/, CC: BY 2.0,
   http://creativecommons.org/licenses/by/2.0/deed.en
Slide 34, Image 1 (left): Patricil, "trident watermelon twist," Flickr, http://www.flickr.com/photos/patricil/3345342836/, CC: BY-NC-SA 2.0.
   http://creativecommons.org/licenses/by-nc-sa/2.0/deed.en

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01.26.12: Diarrhea and Malabsorption

  • 1. Author(s): Rebecca W. Van Dyke, M.D., 2012 License: Unless otherwise noted, this material is made available under the terms of the Creative Commons Attribution – Share Alike 3.0 License: http://creativecommons.org/licenses/by-sa/3.0/ We have reviewed this material in accordance with U.S. Copyright Law and have tried to maximize your ability to use, share, and adapt it. The citation key on the following slide provides information about how you may share and adapt this material. Copyright holders of content included in this material should contact open.michigan@umich.edu with any questions, corrections, or clarification regarding the use of content. For more information about how to cite these materials visit http://open.umich.edu/education/about/terms-of-use. Any medical information in this material is intended to inform and educate and is not a tool for self-diagnosis or a replacement for medical evaluation, advice, diagnosis or treatment by a healthcare professional. Please speak to your physician if you have questions about your medical condition. Viewer discretion is advised: Some medical content is graphic and may not be suitable for all viewers.
  • 2. Attribution Key for more information see: http://open.umich.edu/wiki/AttributionPolicy Use + Share + Adapt { Content the copyright holder, author, or law permits you to use, share and adapt. } Public Domain – Government: Works that are produced by the U.S. Government. (17 USC § 105) Public Domain – Expired: Works that are no longer protected due to an expired copyright term. Public Domain – Self Dedicated: Works that a copyright holder has dedicated to the public domain. Creative Commons – Zero Waiver Creative Commons – Attribution License Creative Commons – Attribution Share Alike License Creative Commons – Attribution Noncommercial License Creative Commons – Attribution Noncommercial Share Alike License GNU – Free Documentation License Make Your Own Assessment { Content Open.Michigan believes can be used, shared, and adapted because it is ineligible for copyright. } Public Domain – Ineligible: Works that are ineligible for copyright protection in the U.S. (17 USC § 102(b)) *laws in your jurisdiction may differ { Content Open.Michigan has used under a Fair Use determination. } Fair Use: Use of works that is determined to be Fair consistent with the U.S. Copyright Act. (17 USC § 107) *laws in your jurisdiction may differ Our determination DOES NOT mean that all uses of this 3rd-party content are Fair Uses and we DO NOT guarantee that your use of the content is Fair. To use this content you should do your own independent analysis to determine whether or not your use will be Fair.
  • 3. M2 GI Sequence Diarrhea and Malabsorption Rebecca W. Van Dyke, MD Winter 2012
  • 4. Learning Objectives • At the end of this lecture on diarrhea, students should be able to: • • 1. Identify and characterize the major pathophysiologic causes of diarrhea. • 2. Discuss mechanisms responsible for secretory and osmotic diarrheas and be able to differentiate between them. • 3. Construct a differential diagnosis for a patient with diarrhea in order of likelihood. • 4. Identify a sequence of tests to determine the cause of diarrhea depending on the presenting symptoms.
  • 5. Industry Relationship Disclosures Industry Supported Research and Outside Relationships • None
  • 6. DIARRHEA • Familiar to all of us • Increased stool volume – Usually to >> 200 ml/24 hours • Altered stool consistency – Increased liquidity • Increased number of stools (not always)
  • 7. Intestinal Fluid Movement (water follows solutes)
  • 8. Diarrhea occurs when SB/colon solute loads exceed their absorptive capacities. Small bowel Colon NORMAL DIARRHEA
  • 9. DIARRHEA - Mechanisms • Too much input • Not enough absorption • Combination of both
  • 10. Mechanisms of Diarrhea • Secretory Diarrhea • Osmotic diarrhea/malabsorption • Increased bowel motility • Decreased bowel surface area • Inflammation
  • 11. Secretory Diarrhea - A problem of excess input of SECRETORY DIARRHEA electrolytes (NaCl) with water following. Cl Water Na Water Cl Na Water Cl Massive volume of plasma-like fluid
  • 12. Clinical Manifestations of Secretory Diarrhea • Large volume, watery diarrhea • Little response to fasting • Stool compositon is similar to plasma – (high NaCl) • Dehydration and plasma electrolyte imbalance are common • No WBC or RBC in stool
  • 14. Cholera toxin affects these - transporters + Lumen by increases in cAMP Cl Na Na Glucose Na Amino acids Na Cl cAMP increases cAMP transport decreases 2 Cl K transport K Na K Tissue Cl Na K side K Na Villus Absorptive Cells Crypt Secretory Cells
  • 15. Clues to Secretory Diarrhea from Clinical Lab Studies: Fecal Electrolytes High Na in stool, blood hypokalemia Secretory Normal Diarrhea Na+ (mEq/l) ~20-40 ~80-110 K+ ~90 ~40 Cl- ~15 ~60 HCO3- ~30 ~50 Anions (SO4-2, ~85 ~30 PO4-3, fatty acids) Other (Mg+2) <15-20 <10 Volume (liters/day) <1 5-10
  • 16. Consequences of Large Volume Diarrhea/Secretory Diarrhea • Dehydration due to massive loss of fluid overwhelming homeostatic mechanisms • Electrolyte abnormalities – Hypokalemia (loss of K in stools) – Acidosis (loss of bicarbonate in stools) – Hyponatremia (loss of Na in stools and oral intake of free water) • Mild malabsorption due to rapid transit and dilution of digestive enzymes
  • 17. Origin of Electrolyte Abnormalities • Dehydration: loss of 1-7 liters per day of liquid containing 80-100 mEq/liter Na • Hyponatremia: loss of sodium and replacement orally with hypotonic fluids (water, sodas, fruit juices) in the presence of ADH (anti-diuretic hormone) • Hypokalemia: stool K is high – may reach 40-80 mEq/liter. 2 liters of stool with 45 mEq/liter K in it is a daily loss of 90 mEq which is difficult to replace. (1 medium banana has 19 mEq)
  • 18. Patient with cholera surrounded by bottles representing intestinal fluid loss. This Ccopyrighted material is used for illustrative purposes, in an effort to advance the instructor’s teaching goals. This use is Fair and consistent with the U.S. Copyright Act. (USC 17 § 107)
  • 19. Causes of Intestinal Secretion – I stimulation of NaCl secreation • Bacterial toxins – Cholera, E. coli, Shigella, etc. • Inflammatory mediators – prostaglandins • Circulating hormones – Gastrin (Z-E syndrome), Vasoactive intestinal polypeptide (VIP)
  • 20. Causes of Intestinal Secretion - II • Malabsorbed compounds that reach the colon and stimulate secretion – Bile acids – Fatty acids • Laxatives (“natural” from plants) that stimulate secretion – Ricinoleic acid – Senokot • Lack of mature villus/surface absorptive cells reducing absorption – viral gastroenteritis/celiac sprue
  • 21. Osmotic Diarrhea is caused by the presence of poorly absorbed luminal osmols Carbohydrates: – Lactose (lactase deficiency) – Sorbitol (chewing gum) Minerals: – Magnesium salts (MOM, Mg citrate)
  • 22. Osmotic Principles • The driving force of fluid movement is ion or solute transport – Solutes may be actively transported through cell membranes – Solute may move passively through cells following concentration and/or electrical gradients • Water movement follows solute movement by osmosis • Water may move between cells (tight junctions) or through cell membrane channels (aquaporins)
  • 23. Pathophysiology of Osmotic Diarrhea Step 1: Oral intake of a concentrated solution 0 mV of a non-absorbable solute, sorbitol. Duodenum -7 mV 150 mmoles of sorbitol Lumen 250 mls of volume = 600 mM concentration = 600 mOsms/l H2O Na=15 Gut K=90 Epithelial Cl=20 Cells Interstitial fluid Na=145 Blood K=5 H2O Cl=100 Osmolality ~ 300
  • 24. Pathophysiology of Osmotic Diarrhea Step 2: Sorbitol diluted to isotonicity by flow of water across leaky epithelium. Jejunum 150 mmoles of sorbitol 150 mmoles sorbitol 250 mls of volume 500 ml volume = 600 mM concentration H2O = 600 mOsms/l =300 mM or mOsms/l Na=15 Gut K=90 Epithelial Cl=20 Cells Interstitial fluid Na=145 Blood K=5 H2O Cl=100 Osmolality ~ 300
  • 25. Step 3: Pathophysiology of Osmotic Diarrhea Salts move down concentration gradient accompanied by water Jejunum to try to equilibrate ion concentrations. 150 mmoles (150 mM) sorbitol 75 mmoles (75 mM) Na 150 mmoles sorbitol 75 mmoles (75 mM) Cl 500 ml volume 1000 ml volume =300 mM =300 mM Na, Cl H2O Na=15 K=90 Cl=20 H2O Na=145 K=5 Na, Cl Cl=100
  • 26. Step 4: Pathophysiology of Osmotic Diarrhea Ileum (less leaky, better able to maintain Na gradient) reduces NaCl Ileum concentration and volume . 750 ml volume at 300 mM (mOsms/l): 150 mmoles sorbitol 150 mmoles (200 mM) sorbitol 75 mmoles Na 37.5 mmoles (50 mM) Na 75 mmoles Cl 37.5 mmoles (50 mM) Cl 1000 ml volume Na, Cl H2O =300 mM Na=145 H2O K=5 Na, Cl Cl=100
  • 27. Step 5: Pathophysiology of Osmotic Diarrhea Colon (fairly “tight” and able to maintain higher Na gradient) further reduces NaCl Colon concentration and volume . 600 ml volume at 300 mM (mOsms/l): 750 ml volume at 300 150 mmoles (250 mM) sorbitol mM (mOsms/l): 15 mmoles (25 mM) Na 15 mmoles (25 mM) Cl 150 mmoles (200 mM) sorbitol Na, Cl H2O 37.5 mmoles (50 mM) Na 37.5 mmoles (50 mM) Cl Na=145 H2O K=5 Na, Cl Cl=100
  • 28. Pathophysiology of Osmotic Diarrhea Step 6: Overall Result Oral Input: Stool Output: 150 mmoles of sorbitol 600 ml volume 150 mmoles sorbitol 250 mls of volume 15 mmoles Na = 600 mM concentration 15 mmoles Cl
  • 29. Pathophysiology of Osmotic Diarrhea • GI epithelia cannot maintain an osmotic gradient and cannot generate as high a Na or other ion gradient as the kidney can. • Thus osmotic diarrhea is due to three factors – Amount of ingested material containing non-absorbed solute. – Volume of extra water needed to dilute the ingested material to isotonicity – Volume of water accompanying the Na, Cl and other ions that equilibrate across the gut epithelia.
  • 30. Clinical Manifestations of Osmotic Diarrhea • Moderate volume of stool • Improves/disappears when oral intake stops • Moderately watery/soft stool • Often associated with increased flatus if due to carbohydrate malabsorption (see malabsorption lecture) • No WBC or RBC in stool
  • 31. Examples of Osmotic Diarrhea • Ingestion of non-absorbable compounds – Magnesium salts • Antacids (Maalox, Mylanta) • Laxatives (Milk of Magnesia) – Sugars • Lactulose, sorbitol, mannitol, fructose, lactose • Malabsorption of specific carbohydrates – Disaccharidase deficiency • Generalized malabsorption of nutrients
  • 32. Therapeutic agents that cause osmotic diarrhea: lactulose (used medically) and magnesium salts Magnesium citrate Lactulose
  • 33. Causes of Osmotic Diarrhea Poorly absorbed sugars such as: Sorbitol Fructose Elsie esq., Flickr
  • 34. Sources of Sorbitol Leading to Osmotic Diarrhea Patricil, Flickr
  • 35. Clues to Osmotic Diarrhea from Clinical Lab Tests • Fecal electrolytes • Fecal osmotic gap
  • 36. Fecal Electrolytes Solute (mEq/l) Normal Secretory Malabsorption Osmotic (Carbohydrate) (Mg salt) Na+ ~40 ~90 ~40 ~20 K+ ~90 ~40 ~40 ~20 Cl- ~15 ~60 ~10 ~60 - HCO3 ~30 ~50 ~10 ~20 Anions (SO4-2, ~85 ~30 ~80 ~100 PO4-2, fatty acids) Other (Mg+2) <15-20 <10 10 ~70 Sugars (mM) 0 0 ~100 0 Volume (liters/day) <1 5-10 1-2 1-2 * Osmolality (mOsm/l) ~290 ~290 ~290 ~290 2 (Na+K) ~260 ~260 ~160 ~80 Fecal osmotic gap ~30 ~30 ~100 ~200 (range ~10-50) * Measured osmolality of stool can be greater than plasma osmolality if unabsorbed carbohydrates are present and stool sits at room termperature for hours, allowing bacterial fermentation.
  • 37. OSMOTIC GAP Question: Are there osmotically active molecules in stool that should not be there? Cations + anions + neutral molecules = 300 mM Cations = anions (electroneutrality) Na and K are the usual stool cations and are easily measured. Anions are a mixed bag (Cl, bicarbonate, sulfate, phosphate, fatty acids) and are NOT easily measured. Neutral molecules and unmeasured cations are also a mixed bag but usually constitute < 30mM. Equation for measurable ions/molecules in stool: 2(Na+K) ~ 270-290 mM (plasma osmolality) Thus the osmotic gap (osmotically active molecules that cannot be accounted for) can be calculated as: Osmotic gap ~ 300 – 2(Na+K) ~10-50 mM for normal stool An osmotic gap of >> 50 is quite abnormal and suggests osmotic diarrhea
  • 38. Fecal Electrolytes Solute (mEq/l) Normal Secretory Malabsorption Osmotic (Carbohydrate) (Mg salt) Na+ ~40 ~90 ~40 ~20 K+ ~90 ~40 ~40 ~20 Cl- ~15 ~60 ~10 ~60 - HCO3 ~30 ~50 ~10 ~20 Anions (SO4-2, ~85 ~30 ~80 ~100 PO4-2, fatty acids) Other (Mg+2) <15-20 <10 10 ~70 Sugars (mM) 0 0 ~100 0 Volume (liters/day) <1 5-10 1-2 1-2 Osmolality (mOsm/l) ~290 ~290 ~290 ~290 2 (Na+K) ~260 ~260 ~160 ~80 Fecal osmotic gap ~30 ~30 ~100 ~200 (10-50)
  • 39. Consequences of Osmotic Diarrhea • Major: Diarrhea due to osmotic effects of non-absorbed solutes • Other: Nutritional deficiencies if generalized malabsorption is the cause
  • 40. Diarrhea Due to Increased Bowel Motility Rapid intestinal motility may result in diarrhea due to reduced contact time between luminal contents and bowel mucosa. Examples include: Anxiety Hyperthyroidism Irritable bowel syndrome Postvagotomy diarrhea (dumping syndrome) Bowel infection (viral gastroenteritis)
  • 41. Clues to Increased Bowel Motility • Moderate diarrhea - usually watery • Often occurs after meals - accentuated gastro-colic reflex • No WBC, RBC in stool • Recently eaten food visable in stools • Louder bowel sounds often apparent • No diagnostic tests- often must rule-out secretory/osmotic/inflammatory causes
  • 42. Consequences of Increased Bowel Motility • Malabsorption – Nutrients (if small bowel is involved) • Diarrhea and urgency • Increased bowel sounds (if severe) • Crampy abdominal pain (if severe)
  • 43. Loss of Bowel Surface Area • Functionally equivalent to increased bowel motility • Underlying process causing loss of surface area may produce additional symptoms/signs • Causes include surgical resection, mucosal disease, fistulas
  • 44. Pig small intestinal villi before (A) and after (B) viral gastroenteritis. Viral infection temporarily destroys mature villus enterocytes and can cause some malabsorption/secretion.
  • 45. Small bowel x-ray of Crohn’s disease showing fistula (arrow) between loops of bowel. This fistula allows lumenal contents to bypass considerable small bowel mucosa.
  • 46. Inflammation and Diarrhea Normal Colon Ulcerative Colitis/Shigella dysentery
  • 47. Inflammation-induced diarrhea Results from several mechanisms 4. Stimulated secretion and inhibited absorption 5. Stimulation of enteric nerves causing propulsive contractions and stimulated secretion 6. Mucosal destruction and increased permeability 7. Nutrient maldigestion malabsorption
  • 48. Clinical Manifestations of Inflammatory Diarrhea • Fever and systemic signs of inflammation (if severe/invasive organism) • Small to moderate volume of diarrhea • Bloody diarrhea and/or WBC/RBC in stool – except in mild inflammation like viral/microscopic colitis • Often accompanied by rapid motility/abdominal cramps • Urgency/tenesmus if rectum is involved
  • 49. Differential Diagnosis of Inflammatory Diarrhea • Infectious diarrhea – viral, bacterial, parasitic • Idiopathic inflammatory bowel disease – Crohn’s disease, Ulcerative colitis – microscopic colitis • Response to ischemia/injury
  • 51. Air-contrast barium enema showing mucosal ulcerations and inflammation in ulcerative colitis. This reduces absorptive surface area.
  • 52. Crohn’s Disease of the Terminal Ileum Inflammation damages the mucosa, reducing the surface area for absorption.
  • 53. Clues to Inflammatory Diarrhea on Gram Stain: Presence of WBC/RBC; Monotonic Bacterial Population PMNs RBCs
  • 54. Overview: Differential Diagnosis of Diarrhea - I • Secretory: bacterial toxins, hormones bile acids, fatty acids, idiopathic • Osmotic malabsorption laxative abuse intake of non- absorbable solutes
  • 55. Differential Diagnosis of Diarrhea - II • Inflammatory: infections inflammatory bowel disease microscopic colitis lymphoma/ischemia • Increased motility: hyperthyroidism irritable bowel syndrome • Decreased surface area: fistulas post-surgical
  • 56. Diagnostic Approach to Diarrhea • Use clinical clues from history, PE and basic laboratory studies to determine the most likely mechanism present. • Utilize specific tests to confirm the type of diarrhea that is present (secretory, osmotic etc.) • Construct a differential diagnosis and select diagnostic tests • Algorithms are included in textbook and syllabus
  • 57. Treatment of Diarrhea • Specific – Logical approach is to identify and treat the underlying disease • Symptomatic – In practice, symptomatic therapy may be critical to patient survival and the only available approach
  • 58. Non-specific Treatment Of Diarrhea • Rehydration – Often life-saving in severe diarrhea, especially in the very young (children) and the elderly – IV electrolytes and water - high tech, expensive – Oral rehydration solutions - high concept, low tech and very cheap. • Anti-motility drugs
  • 59. Options available for management of diarrhea especially severe secretory diarrhea – Oral rehydration therapy – Measurement of stool output – Antibiotics – IV fluids and electrolytes Antimotility drugs
  • 60. World Health Organization Oral Rehydration Solution Rehydration Fecal Electrolytes Solution (mEq/l) Glucose 110mM -- Na+ 90 mEq/l 75 K+ 20 mEq/l 20 HCO3-/citrate 30 mEq/l 50 Cl- 80 mEq/l 45
  • 61. Mechanism of Action of Oral Rehydration Solutions in Secretory Diarrhea Oral Rehydration Sodium Cholera toxin Cl Na Glucose (Amino acids) - affects these transporters + Na Glucose Na Amino acids Na Cl 2 Cl K K Na K Villus Crypt Absorptive Secretory Cells Cl Cells Na Na K K Glucose Amino acids Even in the presence of cholera toxin/cAMP, sodium (and water and chloride) absorption can be driven by coupled uptake of sodium with solutes such as glucose or amino acids.
  • 62. Anti-motility Agents (opiates) • Increase capacitance of gut and thus time for reabsorption • Useful in many types of diarrhea if specific therapy is not available or adequate • Often need to use large doses and/or potent drugs and administer on a regular (rather than PRN) basis. • Do not use in acute bloody diarrhea (infectious or inflammatory)
  • 63. Additional Source Information for more information see: http://open.umich.edu/wiki/CitationPolicy Slide 33, Image 1 (left): Elsie esq., "Coca Cola tin," Flickr, http://www.flickr.com/photos/elsie/4023275760/, CC: BY 2.0, http://creativecommons.org/licenses/by/2.0/deed.en Slide 34, Image 1 (left): Patricil, "trident watermelon twist," Flickr, http://www.flickr.com/photos/patricil/3345342836/, CC: BY-NC-SA 2.0. http://creativecommons.org/licenses/by-nc-sa/2.0/deed.en