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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_837_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Foreword
- •Preface
- •Second Edition Clinical Decision Making
- •Acknowledgments
- •Contents
- •Editors and Contributors
- •Editors
- •Contributors
- •Refer to Algorithm in Fig. 1.1
- •Conclusion
- •Suggested Reading
- •1: Anorectal Examination
- •Suggested Reading
- •3: Physiologic Testing
- •Refer to Algorithm in Fig. 3.3
- •Suggested Reading
- •Refer to Algorithm in Fig. 4.1
- •Single Center Studies
- •Special Considerations
- •Low Rectal or Coloanal Anastomosis
- •Multi-center Studies
- •Suggested Reading
- •Summary
- •Suggested Reading
- •Introduction
- •Refer to Algorithm in Fig. 6.1
- •Minimally Invasive Colorectal Surgery
- •Intraoperative Fluid Administration
- •Analgesia
- •Venous Thromboembolism Prophylaxis
- •Surgical Site Infection Prevention
- •Postoperative Analgesia
- •Intravenous Fluid Management
- •Early Oral Feeding
- •Early Ambulation
- •Conclusion
- •Suggested Reading
- •Refer to Algorithm in Fig. 7.1
- •Refer to Algorithm in Fig. 7.2
- •Melena Caused by Upper Gastrointestinal Bleeding
- •Hematochezia Caused by Anorectal Bleeding
- •Severe Hematochezia Causing Hemodynamic Instability
- •Suggested Reading
- •Suggested Reading
- •Suggested Reading
- •10: Anal Conditions: Anal Fissure/Recurrent Anal Fissure
- •Suggested Reading
- •Suggested Reading
- •12: Anorectal Abscess
- •Suggested Reading
- •13: Anal Conditions: Fistula-in-Ano
- •Suggested Reading
- •14: Anal Conditions: Rectovaginal Fistula
- •Refer to Algorithm in Fig. 14.1
- •Background
- •Etiology
- •Evaluation
- •Treatment
- •Ileoanal Pouch-Vaginal Fistulas
- •Vaginal Approaches
- •Conclusion
- •Suggested Reading
- •15: Anal Conditions: Anorectal Crohn’s Disease—Fistula
- •Introduction
- •Conclusion
- •Suggested Reading
- •Suggested Reading
- •Suggested Reading
- •18: Anal Conditions: External Hemorrhoids
- •Introduction
- •Refer to Algorithm in Fig. 18.4
- •Suggested Reading
- •Refer to Algorithm in Fig. 19.1
- •D. Hair Removal
- •Suggested Reading
- •20: Anal Conditions: Pruritus Ani
- •Suggested Reading
- •21: Anal Conditions: Hidradenitis Suppurativa
- •Suggested Reading
- •22: Anal Conditions: Anorectal Trauma
- •Suggested Reading
- •23: Anal Conditions: STDs
- •Refer to Algorithm in Fig. 23.1
- •Anal Conditions: Sexually Transmitted Diseases
- •Suggested Reading
- •24: Anal Considerations: Fournier’s Gangrene
- •Refer to Algorithm in Fig. 24.1
- •Suggested Reading
- •25: Non-healing Perineal Wounds
- •Suggested Reading
- •26: Anal Intraepithelial Neoplasms
- •Diagnoses
- •Suggested Reading
- •27: Anal Conditions: Anal Margin Tumors
- •Suggested Reading
- •28: Invasive Anal Canal Neoplasia
- •Suggested Reading
- •29: Pelvic Floor Conditions: Rectal Prolapse/Recurrence
- •Suggested Reading
- •30: Pelvic Floor Conditions: Rectal Intussusception
- •Suggested Reading
- •31: Pelvic Outlet Obstruction
- •Suggested Reading
- •32: Pelvic Floor Conditions: Biofeedback
- •Background
- •Pelvic Floor Dysfunction
- •Biofeedback Therapy
- •Suggested Reading
- •33: Pelvic Floor Conditions: Fecal Incontinence
- •Fiber Supplementation
- •Medications
- •Biofeedback
- •End-to-End Sphincteroplasty
- •Tibial Nerve Stimulation
- •Graciloplasty
- •Gluteoplasty
- •∗Other Therapies
- •Injectables
- •RF Remodeling
- •Conclusion
- •Suggested Reading
- •34: Pelvic Floor Conditions: Diarrhea
- •Refer to Algorithm in Fig. 34.1
- •Suggested Reading
- •35: Chronic Constipation
- •Introduction
- •Diagnosis
- •Management
- •Suggested Reading
- •36: Retrorectal Tumors
- •Evaluation
- •Risk Assessment
- •Pathology: Four Tissue Types
- •Treatment
- •Suggested Reading
- •37: Rectal Cancer: Local Therapy
- •Suggested Reading
- •38: Rectal Conditions: Rectal Cancer—Proctectomy
- •Suggested Reading
- •39: Rectal Conditions: Rectal Cancer—Adjuvant and Neoadjuvant Therapy
- •Refer to Algorithm in Fig. 39.1
- •Suggested Reading
- •40: Rectal Conditions: Stage IV Rectal Cancer
- •Introduction
- •Refer to Algorithm in Fig. 40.1
- •Suggested Reading
- •Refer to Algorithm in Fig. 41.1
- •Suggested Reading
- •42: Rectal Conditions: Rectal Cancer—Postoperative Surveillance
- •Suggested Reading
- •43: Recurrent Rectal Cancer
- •Introduction
- •Refer to Algorithm in Fig. 43.2
- •A–C.
- •Carbon-Ion Radiation (CIRT)
- •Conclusion
- •Suggested Reading
- •44: Locally Advanced Rectal Cancer
- •Suggested Reading
- •45: Colonic: Diverticulitis
- •Refer to Algorithm in Fig. 45.1
- •Suggested Reading
- •46: Colonic Conditions: Large Bowel Obstruction
- •Suggested Reading
- •47: Colonic Conditions: Volvulus
- •Refer to Algorithm in Fig. 47.1
- •Introduction
- •Suggested Reading
- •48: Colonic Stricture
- •Suggested Reading
- •49: Acute Colonic Pseudo-Obstruction (ACPO): Ogilvie’s Syndrome
- •Suggested Reading
- •50: Colonic Conditions: Irritable Bowel Syndrome (IBS)
- •Introduction
- •Suggested Reading
- •51: Colorectal Trauma
- •Suggested Reading
- •52: Endometriosis
- •Suggested Reading
- •53: Colonic Conditions: Ulcerative Colitis
- •Conclusions
- •Suggested Reading
- •54: Colonic Conditions: Indeterminate Colitis
- •Suggested Reading
- •55: Colonic Conditions: Toxic Colitis
- •Medical Management
- •Risk Assessment
- •Surgical Management
- •Suggested Reading
- •56: Crohn’s Colitis
- •Suggested Reading
- •57: Ischemic Colitis
- •Suggested Reading
- •58: Colonic Conditions: Infectious Colitis
- •Suggested Reading
- •59: Colonic Conditions: Benign Colonic Neoplasia
- •Suggested Reading
- •60: Familial Adenomatous Polyposis
- •Suggested Reading
- •61: Colonic Conditions: Lynch Syndrome
- •Suspected Lynch Syndrome
- •Lynch Syndrome Diagnosis Without Clinical Symptoms or Phenotype
- •Suggested Reading
- •62: Malignant Colon Polyps
- •Suggested Reading
- •63: Colonic Conditions: Adenomatous Polyps
- •Suggested Reading
- •64: Colon Cancer Surgical Therapy
- •Suggested Reading
- •65: Colonic Conditions: Locally Advanced Colon Cancer
- •Conclusion
- •Suggested Reading
- •66: Recurrent Colon Cancer
- •Suggested Reading
- •67: Appendiceal Neoplasms

Acute Colonic Pseudo-Obstruction (ACPO): Ogilvie’s Syndrome
AnatheaC.Powell andDavidA.Etzioni
49
Refer toAlgorithm inFig. 49.1
A. Overview
Acute colonic pseudo-obstruction (ACPO)
was rst described by Sir Heneage Ogilvie in
a 1948 report of two patients who presented
with signs and symptoms of colonic obstruction without evidence of any organic disease.
As both patients were found to have malignant masses invading the celiac plexus, he
hypothesized that the tumors had disrupted
the sympathetic innervation to the intestine.
Since this initial description, many series of
the phenomenon have been published, and
ACPO is now a well-recognized clinical
entity. Currently, ACPO is dened as massive
colonic dilatation in the absence of mechanical obstruction.
The etiology of ACPO is incompletely
characterized but is still thought to be due to
autonomic dysregulation of the colon causing
unopposed parasympathetic stimulation.
Although ACPO is idiopathic in some
patients, the vast majority of patients have
A. C. Powell
Department ofSurgery, Brigham andWomen’s
Hospital, Boston, MA, USA
D. A. Etzioni (*)
Section of Colon and Rectal Surgery,
Dignity Health Cancer Center/St. Joseph’s Hospital
and Medical Center, Phoenix, AZ, USA
e-mail: etzioni.david@mayo.edu
underlying conditions that predispose them to
ACPO.These conditions include trauma, surgery, infection, malignancy, cardiopulmonary
conditions, and others. Electrolyte disturbances and medications can be instigating
factors; familiar precipitators are opioids and
calcium channel blockers. A 2011 study using
the National Inpatient Sample (NIS) found
the incidence of ACPO to be 105 cases per
100,000 hospitalizations.
ACPO affects both men and women, but
there is a small preponderance in men.
Patients present typically in the fth or sixth
decade of life. As described, these patients
usually have a predisposing condition, and
for surgical patients, present on average
between post-operative days 4 and 5. Signs
and symptoms can include nausea and vomiting, abdominal pain, constipation, diarrhea,
fever, abdominal pain and distention.
Abdominal pain and distention are usually
the chief ndings. Ischemia and perforation
are the feared complications of ACPO, and
avoidance of these drives management. Fever
and leukocytosis are worrisome for ischemia
or perforation. Reports of perforation vary
from 3–15%.
B. Evaluation and Diagnosis
The diagnosis of ACPO is made on the
basis of clinical and radiographic ndings.
The evaluation should consist of a complete
history and physical examination. All medica-
© Springer Nature Switzerland AG 2020
S. R. Steele etal. (eds.), Clinical Decision Making in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-65942-8_49
381

382
A. C. Powell and D. A. Etzioni
Fig. 49.1 Algorithm for evaluation and management of ACPO
tions, including non-prescription medications,
should be reviewed. Every attempt should be
made to immediately discontinue all narcotics. Laboratory investigation is obtained to
evaluate for leukocytosis, acidosis, renal
insufciency, and electrolyte disturbances
such as hypokalemia or hypocalcemia.
Leukocytosis and/or acidosis indicate possible perforation and/or ischemia and should
prompt intervention.
Plain radiographs of patients with ACPO
will show gaseous distention of the colon,
either throughout the colon, or sometimes
with a cutoff at the splenic exure with proximal dilatation. It is essential to distinguish
between mechanical obstruction and ACPO;
ACPO should be a diagnosis of exclusion.
This goal can be accomplished with either
abdominal computed tomography (CT) or
water soluble contrast enema. CT is benecial as it provides additional extra-colonic
information. The exam can be performed
without contrast, but enteral contrast is helpful to delineate the bowel lumen; retrograde
is the preference of the authors. Once
mechanical obstruction is excluded and the
diagnosis of ACPO made, plain radiographs
and serial examination can be used to follow
patients.
The cecum is most susceptible to perforation based on LaPlace’s law of wall tension.
Risk factors for perforation can be judged

49 Acute Colonic Pseudo-Obstruction (ACPO): Ogilvie’s Syndrome
383
based on the diameter of the cecum and duration of dilation. In one of the largest reported
series, the rate of perforation was zero when
the cecum was less than 12cm, but rose to
7% at 12 cm, and almost 25% at 14 cm or
greater. Duration of dilation is also a risk factor for perforation; in this same study, the
mortality based on delay in decompression
from time of diagnosis for <4days, 4–7days
and >7days was 15%, 27%, and 73% respectively. Another study showed higher perforation rates when dilation had been present for
more than 2days. Therefore, in the absence
of physiologic or laboratory concern for ischemia or perforation, intervention should typically be undertaken when cecal diameter is
12 cm or greater, and/or dilation has been
present for more than 2–3days.
C. Optimization/Non-operative Management
Once the diagnosis of ACPO has been
established, the management is well established. The vast majority of patients with
ACPO (over 75%) will improve with conservative measures alone directed at decompression and restoration of colonic motility
(Table 49.1). These steps consist rst of
bowel rest and decompression. A large bore
urinary catheter (20 French) with holes cut in
the side in the manner of a chest tube should
be inserted into the rectum and connected to
straight drainage. Nasogastric tube decom-
Table 49.1 Non-operative measures for ACPO
Non-operative measures
• Nothing per mouth
• Nasogastric decompression (minimize swallowed air
reaching colon)
• Rectal decompression with rectal tube (large urinary
catheter with holes cut in side)
• Aggressively correct electrolyte imbalances
• Limit or stop offending medications
– Review medications with pharmacist
– For surgical patients, use non-opioid pain
medication as much as possible
• Mobilize patient out of bed
– Ambulate
– Out of bed to chair if unable to walk
– If unable to be out of bed, turn frequently and use
knee-chest position if possible
• Treat underlying conditions
pression is useful to eliminate swallowed air
as best as possible.
The patient’s medications should be carefully reviewed and medications that alter
bowel motility, such as opioids or calcium
channel blockers, should be stopped or their
doses minimized. Enlisting the help of a
pharmacist can be very useful in these cases.
Opioid pain relievers are common precipitating factors in surgical patients. Again, every
effort should be used to achieve pain control
with non-opioid medication. Options include
acetaminophen (especially now that an intravenous preparation is available), ketorolac if
renal function will permit, regional anesthetics, or transdermal patches.
Electrolytes should be aggressively supplemented to achieve normal levels. Patients
should be mobilized out of bed; ideally to
walking. If walking is not possible, patients
should sit in a chair; failing this, patients
should be turned frequently and the kneechest position may be attempted. Underlying
conditions, such as infection, should be
treated.
While treating patients with ACPO with
conservative measures, daily abdominal
radiographs should be obtained to evaluate
the diameter of the cecum. Additionally, the
duration of distention should be tracked. If
these measures fail to provide clinical and
radiographic improvement within 2–3 days,
or the cecal diameter approaches 12cm, more
aggressive measures should be undertaken.
D. Pharmacologic Stimulation (Neostigmine)
Neostigmine is an acetylcholinesterase
inhibitor administered intravenously as a
stimulatory agent. Neostigmine was shown to
be effective in a small randomized clinical
trial published in 1999. Ten of eleven patients
receiving neostigmine experienced immediate improvement in symptoms and distention
within minutes. Two of the responders
recurred and required further intervention.
None of the ten patients who received placebo had an immediate clinical response.
Other non-randomized studies have been
performed with similar results. The side

384
A. C. Powell and D. A. Etzioni
Table 49.2 Neostigmine for ACPO
Neostigmine administration
• Ensure no contraindication
– Bronchospasm, arrhythmias major
contraindications
• Move patient to monitored setting with telemetry and
frequent vital sign measurement
• Atropine at bedside to treat symptomatic bradycardia
• Give 2mg of neostigmine as infusion over 5min
• If no response within 30min, give second infusion of
2mg
• The patient should remain monitored for at least
30min after infusion(s)
effects of neostigmine include bradycardia,
excessive salivation, abdominal pain and
vomiting.
Neostigmine should be administered in a
monitored setting with telemetry and frequent
vital sign measurement (Table49.2). An infusion of 2 mg of neostigmine is given over
5min and the patient monitored by the physician for improvement. If there is no response
within 30min, a second dose of 2mg of neostigmine may be given. As bradycardia can be
clinically signicant, atropine must be available at the bedside for symptomatic bradycardia. If the patient shows no response after two
doses, endoscopic decompression should be
initiated.
E. Endoscopic Decompression
Endoscopic decompression for ACPO was
rst introduced in 1977. Prior to this, patients
for whom other measures had failed had been
managed operatively. Endoscopic decompression has been reported in many studies to be
safe, although it is technically challenging in
these patients. This technique is the established
next line of management if an experienced
endoscopist is available. Decompression can
be achieved with colonoscopy alone or with
colonoscopy and placement of decompression
tube (Table 49.3). Perforation, the major complication of decompressive colonoscopy, is low
in reported series (as low as 2%).
Benzodiazepines alone should be used for
sedation to avoid opioid exacerbation of colonic
inertia. A bowel prep is unnecessary as the
colonic dilatation facilitates colonoscopic
advancement over feces without difculty in
Table 49.3 Endoscopic decompression in ACPO
Tips Tools
• Should be performed by
experienced endoscopist
• Use benzodiazepines
alone for sedation
• No prep is needed
• Minimize insufation
• Liberal use of suction
• Advance colonoscope
beyond splenic exure
• Leave long rectal
decompression tube
• Stop and proceed to
operation if mucosal
ischemia seen
• Best colonoscopic
options
– Large therapeutic
channel
– Dual channel
• Decompression tubes
– Vary in diameter and
length based on
commercial kit used
almost all cases. The colonoscope should be
advanced using as little insufation as possible
and liberal suction should be used for both stool
and air. Little is known regarding the benet of
carbon dioxide insufation versus air.
Decompression is achieved by advancing the
colonoscope past the splenic exure, but it is not
necessary to advance all the way to the cecum.
In several series, successful decompression
with immediate clinical and radiographic
improvement has been reported in approximately 60–85% of cases. However, recurrence
can be as high as 45% and varies in time to
recurrence. In one study, the mean time to
recurrence was 3.7 days (range 1–8 days).
Placement of a long rectal tube during decompressive colonoscopy has been shown to signicantly decrease recurrence rate versus
colonoscopy alone. If recurrence does occur
and the patient remains non-toxic, colonoscopy may be attempted again. There is debate
regarding what to do if mucosal ischemia is
seen and there are few data to guide decision
making. The authors recommend starting antibiotics and proceeding to surgery if the
patients develop recurrent symptoms after two
colonoscopies or ischemia is seen.
F. Denitive Decompression
Denitive decompression is required in a small
percentage of patients for whom neostigmine
was either contraindicated or failed and endoscopic decompression failed.
For non-toxic patients without evidence for
ischemia or perforation, either percutaneous

49 Acute Colonic Pseudo-Obstruction (ACPO): Ogilvie’s Syndrome
385
or open cecostomy may be considered. These
procedures have been reported to be successful in small series of patients. However, cecostomy is an infrequently performed procedure
and may become a legacy technique.
If laparotomy is planned, factors dictating
management include the length and section of
involved bowel, presence of perforation or
ischemia, and surgeon experience. Mortality
for patients requiring surgery ranged from
12% to 15% in the 2011 NIS study, but has
been reported previously to be as high as
35–60%. In the case of suspected perforation
or ischemia, bowel resection and proximal
diversion is the standard. The distal bowel can
either be managed with a long Hartmann’s
pouch or as part of a Prasad ileostomy; the
Prasad ileostomy technique will assist with
reversal in the future. In the absence of perforation or ischemia, options for management
vary and include partial colectomy, almost
always including the right colon, with or without diversion, total colectomy and ileostomy,
and ileostomy. Given the high mortality rates
associated with laparotomy, diversion is safest.
The ileostomy may be an end, Prasad, or loop,
although little has been written about loop ileostomy in this setting.
Suggested Reading
Geller A, Peterson BT, Gostout CJ. Endoscopic decom-
pression for acute colonic pseudo-obstruction.
Gastrointest Endosc. 1996;44(2):144–50.
Harig JM, Fumo DE, Loo FD, Parker HJ, Soergel KH,
Helm JF, Hogan WJ. Treatment of acute nontoxic
megacolon during colonoscopy: tube placement
versus simple decompression. Gastrointest Endosc.
1988;34(1):23–7.
Johnson CD, Rice RR, Kelvin FM, Foster WL, Williford
ME.The radiologic evaluation of gross cecal distention: emphasis on cecal ileus. AJR Am J Roentgenol.
1985;145(6):1211–7.
Kukora JS, Dent TL. Colonoscopic decompression of
massive nonobstructive cecal dilatation. Arch Surg.
1977;112(4):512–7.
Loftus CG, Harewood GC, Baron TH. Assessment
of predictors of response to neostigmine for acute
colonic pseudo-obstruction. Am J Gastroenterol.
2002;97(12):3118–22.
Maloney N, Vargas HD. Acute intestinal pseudo-
obstruction (Ogilvie’s syndrome). Clin Colon Rectal
Surg. 2005;18(2):96–101.
Ogilvie H.Large-intestine colic due to sympathetic depri-
vation. Br Med J. 1948;2(4579):671–3.
Ponec RJ, Saunders MD, Kimmey MB.Neostigmine for
the treatment of acute colonic pseudo-obstruction. N
Engl J Med. 1999;341(3):137–41.
Ramage JI, Baron TH. Percutaneous endoscopic
cecostomy: a case series. Gastrointest Endosc.
2003;57(6):752–5.
Ross SW, Oommen B, Wormer BA, Walter AL,
Augenstein VA, Heniford BT, Sing RF, Christmas
AB. Acute colonic pseudo-obstruction: dening the
epidemiology, treatment and adverse outcomes of
Ogilvie’s syndrome. Am Surg. 2016;82(2):102–11.
Saunders MD. Acute colonic pseudo-obstruction. Best
Pract Res Clin Gastroenterol. 2007;21(4):671–87.
Saunders MD, Kimmey MB. Systematic review: acute
colonic pseudo-obstruction. Aliment Pharmacol Ther.
2005;22(10):917–25.
Vanek VW, Al-Salti M.Acute pseudo-obstruction of the
colon. Dis Colon Rectum. 1986;29(3):203–10.
Vogel JD, Feingold DL, Stewart DB, Turner JS, Boutros
M, Chun J, Steele SR.Clinical practice guidelines for
colon volvulus and acute colonic pseudo-obstruction.
Dis Colon Rectum. 2016;59(7):589–600.

Colonic Conditions: Irritable Bowel Syndrome (IBS)
CrystalP.Koerner andPatrickS.Sullivan
50
Introduction
Irritable bowel syndrome (IBS) is a chronic functional disorder characterized by abdominal pain
and altered bowel habits in the absence of an
organic cause to explain these symptoms. IBS may
be divided into subtypes, including IBS with diarrhea, IBS with constipation, IBS with mixed bowel
habits, alternating IBS, post infectious IBS, and
unspecied IBS (refer to Table50.1). Various factors are thought to contribute to the pathology of
IBS and include changes to the gut microbiome,
intestinal permeability, gut immune function,
motility, visceral sensation, brain-gut interactions,
and psychosocial state. There appears to be a
genetic component, as genetic polymorphisms
have recently been associated with the development of IBS.Alterations in the innate immune system have been demonstrated in patients with IBS
and are hypothesized to contribute to the development of IBS. IBS is one of the most commonly
encountered medical conditions, with a worldwide
prevalence of 10–15%. It is also one of the costliest medical conditions with an estimated cost of
$21 billion to the United States yearly. Younger
patients and women are more likely to be diagnosed with IBS, with a female to male ratio of 2:1.
The most common age at diagnosis is between 30
C. P. Koerner · P. S. Sullivan (*)
Division of Colon and Rectal Surgery, Department of
Surgery, Emory University School of Medicine,
Atlanta, GA, USA
e-mail: Patrick.s.sullivan@emory.edu
Table 50.1 Classication of IBS subtypes
• IBS with constipation: hard stools ≥25%, loose
stools <25%
• IBS with diarrhea: loose stools ≥25%, hard stools
<25%
• IBS with mixed symptoms: hard stools ≥25%, loose
stools ≥25%
• Undened IBS: absence of sufcient abnormality in
stool consistency
• IBS with alternating symptoms: symptom uctuance
over time
and 50years of age. The prevalence of IBS is equal
among Caucasians and African Americans and
may be lower in Hispanics. Other functional bowel
disorders such as functional dyspepsia, pain disorders including bromyalgia, chronic pain, interstitial cystitis and psychological conditions inclusive
of anxiety, somatization are often seen in patients
with IBS and are more prevalent than in the general population.
Refer toAlgorithm inFig. 50.1
A. Abdominal discomfort or pain with an alter-
ation in bowel habits are the classic symptoms described in patients with IBS. The
abdominal pain is often diffuse, intermittent
and crampy in nature. The alterations in
bowel habits may include diarrhea, constipation or both. Other symptoms that many
patients experience include bloating,
urgency, and relief of pain after defecation.
© Springer Nature Switzerland AG 2020
S. R. Steele etal. (eds.), Clinical Decision Making in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-65942-8_50
387

388
C. P. Koerner and P. S. Sullivan
Fig. 50.1 Algorithm diagnostic workup and treatment of irritable bowel syndrome
It has been demonstrated that patients with
IBS are more likely to have additional comorbid conditions, as high as 50%. In particular, functional dyspepsia and GERD
have a high prevalence among patients with
.−
IBS
associated extra-intestinal complaints
may include fatigue, headache, musculo-
skeletal pain, pelvic pain and impaired
sleep. Alarm symptoms are symptoms that
should alert the clinician that an organic
cause for symptoms should be sought out.
These include weight loss, blood in the
stool, fever, pain that awakens one from
sleep, and age greater than 50.

50 Colonic Conditions: Irritable Bowel Syndrome (IBS)
389
B. The diagnosis of IBS can be challenging and
frustrating for the clinician. Patients with IBS
usually present to a physician with a host of
nonspecic complaints. Performing a thorough
history, physical exam and utilizing selected
tests to exclude various organic causes are
essential to the diagnosis of IBS. Clinicians
should consider the diagnosis of IBS if a patient
reports abdominal pain or discomfort, bloating
and a change in bowel habits for greater than
6months. Targeted questions regarding alarm
symptoms should be asked and an alternative
diagnosis should be sought out if present. Any
of the following physical signs should alert the
clinician to a possible alternative diagnosis,
anemia, blood on rectal exam, palpable abdominal or rectal masses.
C. Many factors are thought to increase the risk
of developing IBS, the most well documented
is post-infectious IBS.Post-infectious IBS is
a subtype that occurs after development of
gastroenteritis, most commonly with salmonella, campylobacter, shigella or giardia. The
risk of developing IBS with exposure to acute
gastroenteritis has been estimated at 5–32%.
IBS has been shown to cluster in families,
with an increased risk of two- to threefold if
a relative is diagnosed with IBS.Other risk
factors include recent antibiotic use, history
of childhood abuse, and having a low birth
weight.
D. The Rome III criteria can be utilized to help
diagnose patients with IBS (Table50.2).
E. The differential diagnosis for irritable bowel
syndrome is broad and varies according to
the subtype. In patients with diarrheapredominant, these include microscopic colitis, infectious colitis, malabsorption, bacterial
Table 50.2 Rome III diagnostic criteria for irritable
bowel syndrome (IBS)
• At least 3months, with onset at least 6months
previously of recurrent abdominal pain or discomfort
associated with two or more of the following:
– Relieved with defecation and/or
– Onset associated with a change in frequency of
stool and/or
– Onset associated with a change in appearance of
stool
overgrowth, lactose intolerance, ulcerative
colitis, Crohn’s disease, and Celiac disease.
The differential for constipation and mixed
type include medication induced, malignancy and endocrinopathies.
F. The role of diagnostic testing in patients with
IBS should be targeted and begin with a careful history and physical examination. Patients
with alarm symptoms, signs or strong family
histories of colorectal cancer, inammatory
bowel disease, or celiac disease should prompt
the clinician to investigate causes other than
IBS.Basic lab work including CBC, ESR, and
CRP can help exclude inammatory bowel
disease. In patients with diarrhea-predominant
IBS, stool studies and fecal fat testing can help
to rule out infectious and malabsorptive etiologies. Tissue Transglutaminase IgA can be
obtained if celiac disease is a concern. The
role of imaging studies is limited in patients
with IBS and should be considered if organic
pathology is in the differential. In patients that
are anemic or older than 50 years of age, a
colonoscopy should be performed to exclude
malignancy. In addition, endoscopy may be
used in IBS diarrhea predominant patients to
exclude microscopic colitis as a cause of the
diarrhea with a mucosal biopsy.
G. It has long been recognized that a signicant
proportion of patients with IBS have associated psychiatric illness and personality
pathology. Multiple standard psychometric
instruments have been utilized to evaluate
anxiety and depression as well as personality
characteristics in patients with IBS, including Hamilton anxiety scale, Beck depression
scale, State-Trait Anxiety Inventory (STAI),
Minnesota Multiphasic Personality Inventory
(MMPI), and Eysenck Personality Inventory.
Recent studies have demonstrated a signicant difference in scores between patients
with IBS compared to healthy controls. In
addition, it has been shown in various randomized clinical trials that dietary, lifestyle,
medical, and behavioral modications are
effective in the treatment of irritable bowel
syndrome. It is clear that a strong patientphysician relationship is an important com-

390
C. P. Koerner and P. S. Sullivan
ponent in the care of patients with IBS and
decreases health care visits.
H. Dietary and lifestyle modications have been
shown to be effective in patients with IBS.In
particular, a high ber diet has been shown to
improve symptoms. Recently, there has been
a growing interest in fermentable oligosaccharides, disaccharides, monosaccharides
and polyols (FODMAPs) as they relate to IBS
symptoms. FODMAPs are poorly absorbed
short chain fatty acids such as fructose and
lactose. Evidence suggests that intake of
FODMAPs increase GI symptoms in patients
with IBS, and studies have shown signicant
symptom reduction with a low FODMAP
diet. Physical activity has also been shown to
reduce symptoms and symptom severity in
patients with IBS.
I. In many patients with IBS the goal of therapy
is symptom reduction. Antispasmodic agents
have been shown to reduce symptom severity
when compared to placebo. Antidepressants
such as Tricyclic antidepressants (TCAs) and
SSRIs, have been shown in some series to
improve symptoms. Although, other studies
have shown no benet between TCAs and
SSRIs when compared to placebo. The benet
of antidepressants remains to be elucidated.
Other therapies such as probiotics and neuropathic agents are often used to treat IBS.
Gabapentin was shown to reduce symptom
thresholds in patients with IBS and studies
have shown that probiotics improve abdominal pain and atulence when compared to
placebo.
J. Specic agents have shown efcacy in the sub-
types of IBS and include antidepressants and
serotonin antagonists. Amitiza
®
(Lubiprostone)
a chloride channel activator and Linzess®
(Linaclotide), a Guanylate cyclase agonist,
have been FDA approved for treatment in
patients with IBS-C subtype. In a recent metaanalysis, Amitiza® was found to decrease the
severity of constipation, improve the consistency of stool, decrease degree of straining and
degree of abdominal bloating compared to placebo in patients with IBS- C.Linzess® has been
shown to decrease abdominal pain, discomfort,
bloating and fullness when compared to placebo in patients with IBS-C. In patients with
IBS-D subtypes, Rifaximin, Loperamide, and
Alosetron have been shown to improve symptoms. In particular, Alosetron was shown to
improve quality of life scores and bowel function, in patients with diarrhea predominant IBS.
Rifaximin improved abdominal pain, bloating
and loose stools when compared to placebo in a
double-blind randomized control trial.
K. Alternative therapies have been utilized for the
treatment of IBS including acupuncture, biofeedback and psychotherapy. Acupuncture has
been shown to be associated with greater symptom improvement than standard pharmacologic
treatment in multiple RCTs. Psychotherapy has
been shown to have an impact in the treatment
of IBS.In one study, psychotherapy was delivered in ten sessions and focused on coping
mechanisms and resolving emotional problems. Psychotherapy was found to relieve
abdominal pain and bowel dysfunction more
than medical therapy alone. Biofeedback has
recently been shown to improve abdominal
pain and bloating in patients with IBS-C, when
delivered consistently.
L. As a functional disease, surgery has had
a limited role in the management of IBS
patients, yet a high surgical rate exists in
these patients. Patients with IBS have a
higher rate of cholecystectomy, appendectomy, hysterectomy, colon resection, and
back surgery than those without IBS.Newer
minimally invasive procedures such as sacral
nerve stimulation (SNS) may be of use in
highly selected patients with IBS refractory
to conservative management. However, IBS
is not an FDA labeled indication for SNS.In
one small randomized, crossover control
trial, sacral nerve stimulation was shown to
improve pain, bloating, diarrhea, constipation, and satiety. In addition, SNS improved
quality of life endpoints including, sleep,
emotional distress, eating habits, fatigue and
impaired daily activity. The mechanism of
symptom improvement with SNS has yet to
be fully explained, but it has been shown that
SNS relaxes the rectal wall, making the rectal

50 Colonic Conditions: Irritable Bowel Syndrome (IBS)
391
wall more sensitive to stretch and less sensitive to cold. Decreased rectal wall stiffness
has been associated with symptomatic relief.
Additional studies are needed to further elucidate the efcacy and safety of sacral nerve
stimulation as a therapy for patients with IBS.
M. IBS is a chronic relapsing disorder that can
greatly affect the quality of life of patients,
but studies have shown no increase in mortality when compared to patients without IBS.
In addition, when followed over the long
term, very few patients are found to have an
organic cause of their symptoms. Patients
with IBS have been shown to have lower
quality of life scores when compared to
healthy subjects, with scores similar to other
chronic disorders such as GERD and diabetes. However, quality of life scores have been
shown to increase when proper therapeutic
treatments were initiated.
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