intestinal pseudo-obstruction

{{Infobox medical condition (new)

| name = Intestinal pseudo-obstruction

| synonyms =

| image = Ogilvie ct coronal.jpg

| caption =

| pronounce = soo·doe/uhb·struhk·shn

| field = Gastroenterology

| symptoms = Abdominal pain, nausea, distention, vomiting, dysphagia, and constipation

| complications = Intestinal failure, malabsorption, nutrient deficiencies, small intestinal bacterial overgrowth

| onset =

| duration = Varies according to etiology of disease.

< 6 months is considered acute

| types =

| causes = Idiopathic, Kawasaki disease, Parkinson's disease, Chagas disease, Hirschsprung's disease, intestinal hypogangliosis, collagen vascular disease, mitochondrial disease, endocrine disorders, medication side effects

| risks =

| diagnosis = Signs and symptoms consistent with a mechanical intestinal obstruction with no identifying lesion.

| differential = Intestinal obstruction, Crohn's disease, ovarian torsion, ovarian cyst, neoplasm, infection (parasitic)

| prevention =

| treatment = Aimed at management of complications (e.g. nutrition, hydration, pain relief).

| medication =

| prognosis = 10–25% mortality rate in chronic cases

| frequency = Unknown

| deaths =

}}

Intestinal pseudo-obstruction (IPO) is a clinical syndrome caused by severe impairment in the ability of the intestines to push food through. It is characterized by the signs and symptoms of intestinal obstruction without any lesion in the intestinal lumen.{{cite journal |vauthors=Stanghellini V, Cogliandro RF, De Giorgio R, etal |title=Natural history of chronic idiopathic intestinal pseudo-obstruction in adults: a single center study |journal=Clinical Gastroenterology and Hepatology |volume=3 |issue=5 |pages=449–58 |date=May 2005 |pmid=15880314 |doi=10.1016/S1542-3565(04)00675-5|s2cid=32605317 }} Clinical features mimic those seen with mechanical intestinal obstructions and can include abdominal pain, nausea, abdominal distension, vomiting, dysphagia and constipation{{cite journal|vauthors=De Giorgio R, Sarnelli G, Corinaldesi R, Stanghellini V|date=November 2004|title=Advances in our understanding of the pathology of chronic intestinal pseudo-obstruction|journal=Gut|volume=53|issue=11|pages=1549–52|doi=10.1136/gut.2004.043968|pmc=1774265|pmid=15479666}}{{Cite book|url=https://www.worldcat.org/oclc/972900144|title=Robbins basic pathology|publisher=Elsevier|others=Vinay Kumar, Abul K. Abbas, Jon C. Aster, James A. Perkins|year=2018|isbn=978-0-323-39413-0|edition=10th|location=Philadelphia, Pa.|pages=Chapter 5: intestinal obstruction|oclc=972900144}} depending upon the part of the gastrointestinal tract involved.

It is a difficult condition to diagnose, requiring exclusion of any other mechanical cause of obstruction.{{Cite journal|last1=El-Chammas|first1=Khalil|last2=Sood|first2=Manu R.|date=March 2018|title=Chronic Intestinal Pseudo-obstruction|journal=Clinics in Colon and Rectal Surgery|volume=31|issue=2|pages=99–107|doi=10.1055/s-0037-1609024|issn=1531-0043|pmc=5825855|pmid=29487492}} Many patients are diagnosed late in the course of disease after additional symptoms are seen. Mortality is also difficult to accurately determine. One retrospective study estimated mortality to be between 10 and 25% for chronic intestinal pseudo-obstruction (CIPO) and to vary greatly depending on the etiology of the condition.{{Cite journal|last1=Ko|first1=Dayoung|last2=Yang|first2=Hee-Beom|last3=Youn|first3=Joong|last4=Kim|first4=Hyun-Young|date=2021-05-28|title=Clinical Outcomes of Pediatric Chronic Intestinal Pseudo-Obstruction|journal=Journal of Clinical Medicine|volume=10|issue=11|pages=2376|doi=10.3390/jcm10112376|issn=2077-0383|pmc=8198288|pmid=34071279|doi-access=free}} When present for less than six months, it is diagnosed as acute IPO{{cite journal|author=Saunders MD|date=October 2004|title=Acute colonic pseudoobstruction|journal=Current Gastroenterology Reports|volume=6|issue=5|pages=410–6|doi=10.1007/s11894-004-0059-5|pmid=15341719|s2cid=27281556}} or Ogilvie syndrome. Longer than this is considered chronic.{{cite journal|vauthors=Sutton DH, Harrell SP, Wo JM|date=February 2006|title=Diagnosis and management of adult patients with chronic intestinal pseudoobstruction|url=http://ncp.sagepub.com/cgi/pmidlookup?view=long&pmid=16439766|journal=Nutrition in Clinical Practice|volume=21|issue=1|pages=16–22|doi=10.1177/011542650602100116|pmid=16439766|url-access=subscription}} Owing to the difficulty of diagnosis, few studies are available which have attempted to estimate its prevalence.{{Cite journal|last1=Iida|first1=Hiroshi|last2=Ohkubo|first2=Hidenori|last3=Inamori|first3=Masahiko|last4=Nakajima|first4=Atsushi|last5=Sato|first5=Hajime|date=2013|title=Epidemiology and clinical experience of chronic intestinal pseudo-obstruction in Japan: a nationwide epidemiologic survey|journal=Journal of Epidemiology|volume=23|issue=4|pages=288–294|doi=10.2188/jea.je20120173|issn=1349-9092|pmc=3709546|pmid=23831693}}

The condition can begin at any age. Most studies describing CIPO are in pediatric populations.{{Cite journal|last1=Zenzeri|first1=Letizia|last2=Tambucci|first2=Renato|last3=Quitadamo|first3=Paolo|last4=Giorgio|first4=Valentina|last5=De Giorgio|first5=Roberto|last6=Di Nardo|first6=Giovanni|date=May 2020|title=Update on chronic intestinal pseudo-obstruction|url=https://pubmed.ncbi.nlm.nih.gov/32073506|journal=Current Opinion in Gastroenterology|volume=36|issue=3|pages=230–237|doi=10.1097/MOG.0000000000000630|issn=1531-7056|pmid=32073506|s2cid=211193582}}{{Cite journal|last1=Downes|first1=Thomas J.|last2=Cheruvu|first2=Manikandar S.|last3=Karunaratne|first3=Tennekoon B.|last4=De Giorgio|first4=Roberto|last5=Farmer|first5=Adam D.|date=July 2018|title=Pathophysiology, Diagnosis, and Management of Chronic Intestinal Pseudo-Obstruction|url=https://pubmed.ncbi.nlm.nih.gov/29877952|journal=Journal of Clinical Gastroenterology|volume=52|issue=6|pages=477–489|doi=10.1097/MCG.0000000000001047|issn=1539-2031|pmid=29877952|s2cid=46960493}} It can be a primary condition (idiopathic or inherited) or caused by another disease (secondary).{{cite journal |vauthors=Antonucci A, Fronzoni L, Cogliandro L, etal |title=Chronic intestinal pseudo-obstruction |journal=World Journal of Gastroenterology |volume=14 |issue=19 |pages=2953–61 |date=May 2008 |pmid=18494042 |pmc=2712158 |doi=10.3748/wjg.14.2953 |doi-access=free }} It can be a result of myriad of etiologies including infectious, parasitic, autoimmune, genetic, congenital, neurologic, toxic, endocrinological, or anatomical pathology.

Treatment targets nutritional support, improving intestinal motility, and minimizing surgical intervention. Bacterial overgrowth of the small intestine can occur in chronic cases – presenting as malabsorption, diarrhea, and nutrient deficiencies{{Cite journal|last1=Cucchiara|first1=Salvatore|last2=Borrelli|first2=Osvaldo|date=April 2009|title=Nutritional challenge in pseudo-obstruction: the bridge between motility and nutrition|url=https://pubmed.ncbi.nlm.nih.gov/19300134|journal=Journal of Pediatric Gastroenterology and Nutrition|volume=48|issue=Suppl 2 |pages=S83–85|doi=10.1097/MPG.0b013e3181a15bfe|issn=1536-4801|pmid=19300134|hdl=11573/406753 |s2cid=11393186|doi-access=free}} – which may require the use of antibiotics.

Presentation

Clinical features of IPO can include abdominal pain, nausea, abdominal distension, vomiting, dysphagia, and constipation. Symptoms depend on the portion of the gastrointestinal tract involved and the duration of symptoms. Symptoms may occur intermittently and over a prolonged period of time. It is not unusual for patients to present several times owing to the nonspecific nature of the symptoms. Conditions and onset will vary if the disease is primary vs secondary and the underlying disease (if a secondary manifestation) and its management.

Symptoms indicative of advanced disease and possible intestinal failure include diarrhea, loss of appetite, sepsis, bloating, fatigue, signs of low volume status, and malabsorption including nutritional deficiencies and foul-smelling stools.{{Cite web|title=Pediatric Intestinal Failure|url=https://childrensnational.org/visit/conditions-and-treatments/stomach-digestion-gi/intestinal-failure|accessdate=8 November 2021|website=Children's National}}{{Cite web|title=Intestinal Failure|url=https://www.topdoctors.co.uk/medical-dictionary/intestinal-failure|access-date=8 November 2021|website=Top Doctors United Kingdom}}

Causes

In primary CIPO (the majority of chronic cases) the condition results from disruption of the intestine's ability to move food. These can be broadly classified as myopathic (affecting the smooth muscle), mesenchymopathic (affecting the interstitial cells of Cajal), or neuropathic (of the nervous system) of the gastrointestinal tract.{{cite journal |vauthors=Gabbard SL, Lacy BE |title=Chronic intestinal pseudo-obstruction |journal=Nutrition in Clinical Practice |volume=28 |issue=3 |pages=307–16 |date=June 2013 |pmid=23612903 |doi=10.1177/0884533613485904|s2cid=8288714 }}

In some cases there appears to be a genetic association.{{cite journal |vauthors=Guzé CD, Hyman PE, Payne VJ |title=Family studies of infantile visceral myopathy: a congenital myopathic pseudo-obstruction syndrome |journal=American Journal of Medical Genetics |volume=82 |issue=2 |pages=114–22 |date=January 1999 |pmid=9934973 |doi=10.1002/(SICI)1096-8628(19990115)82:2<114::AID-AJMG3>3.0.CO;2-H}} One form has been associated with DXYS154, some associated with defective ACTG2 gene{{cite journal |vauthors=Auricchio A, Brancolini V, Casari G, etal |title=The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28 |journal=American Journal of Human Genetics |volume=58 |issue=4 |pages=743–8 |date=April 1996 |pmid=8644737 |pmc=1914695}}

Secondary chronic intestinal pseudo-obstruction can occur as a consequence of a number of other conditions including:

  • Hirschsprung's disease{{Cite web|date=4 September 2017|title=Hirschsprung disease|url=https://rarediseases.info.nih.gov/diseases/6660/hirschsprungs-disease|url-status=dead|access-date=8 November 2021|website=GARD: Genetic and Rare Diseases Information Center|archive-date=24 November 2018|archive-url=https://web.archive.org/web/20181124032305/https://rarediseases.info.nih.gov/diseases/6660/hirschsprungs-disease}} – the absence of colonic nerve cells
  • Chagas' disease{{cite needed|date=February 2025}} – a chronic parasitic infection of the colon leading to loss of nerve endings
  • Kawasaki disease{{cite journal |vauthors=Akikusa JD, Laxer RM, Friedman JN |title=Intestinal pseudoobstruction in Kawasaki disease |journal=Pediatrics |volume=113 |issue=5 |pages=e504–6 |date=May 2004 |pmid=15121996 |doi=10.1542/peds.113.5.e504|doi-access=free }}{{Cite journal|last1=Colomba|first1=Claudia|last2=La Placa|first2=Simona|last3=Saporito|first3=Laura|last4=Corsello|first4=Giovanni|last5=Ciccia|first5=Francesco|last6=Medaglia|first6=Alice|last7=Romanin|first7=Benedetta|last8=Serra|first8=Nicola|last9=Di Carlo|first9=Paola|last10=Cascio|first10=Antonio|date=November 2018|title=Intestinal Involvement in Kawasaki Disease|journal=The Journal of Pediatrics|volume=202|pages=186–193|doi=10.1016/j.jpeds.2018.06.034|issn=1097-6833|pmid=30029859|s2cid=51704336|doi-access=free|hdl=10447/350574|hdl-access=free}} - a rare presentation for this particular autoimmune disorder of the vasculature
  • Parkinson's disease{{cite needed|date=February 2025}} - related to the neurodegeneration of gastrointestinal tract
  • Autoimmune conditions — conditions including systemic lupus erythematosus and scleroderma lead to collagen vascular deposition{{Cite journal|last1=Takahashi|first1=Hiroki|last2=Ohara|first2=Mikiko|last3=Imai|first3=Kohzoh|date=June 2004|title=[Collagen diseases with gastrointestinal manifestations]|journal=Nihon Rinsho Men'eki Gakkai Kaishi = Japanese Journal of Clinical Immunology|volume=27|issue=3|pages=145–155|doi=10.2177/jsci.27.145|issn=0911-4300|pmid=15291251|doi-access=free}} and gastrointestinal motility disruption
  • Mitochondrial disease{{Cite journal|last1=Finsterer|first1=Josef|last2=Frank|first2=Marlies|date=January 2017|title=Gastrointestinal manifestations of mitochondrial disorders: a systematic review|journal=Therapeutic Advances in Gastroenterology|volume=10|issue=1|pages=142–154|doi=10.1177/1756283X16666806|issn=1756-283X|pmc=5330602|pmid=28286566}} - IPO is a known presentation for mitochondrial disease
  • Endocrine disorders
  • Certain medications.

The term may be used synonymously with enteric neuropathy if a neurological cause is suspected.

Diagnosis

File:Ogilvie ct coronal.jpg

The symptoms of IPO are nonspecific. It is not unusual for patients to present repeatedly and to undergo numerous tests. Mechanical causes of intestinal obstruction must be excluded to reach a diagnosis of pseudo-obstruction. Attempts must also be made to determine whether the IPO is the result of a primary or secondary condition. A diagnostic work-up may include:

= Classification =

Pseudo-obstruction syndromes are classified as acute or chronic based on their clinical appearance. Acute colonic pseudo-obstruction (ACPO; sometimes known as Ogilvie syndrome) causes the colon to become grossly dilated; if not decompressed, the individual risks perforation, peritonitis, and death. Chronic intestinal pseudo-obstruction is a chronic disorder.{{cite web | last=Cagir | first=Burt | title=Intestinal Pseudo-Obstruction: Background, Anatomy, Pathophysiology | website=Medscape Reference | date=2018-07-23 | url=https://emedicine.medscape.com/article/2162306-overview#showall | access-date=2024-04-15}}

Treatment

Treatment for IPO (acute or chronic) is aimed at removing the disease process and/or managing the complications present. Focus is placed on management of pain, gastrointestinal symptoms, nutritional deficiencies, fluid status, infection control, and improving quality of life. When CIPO is secondary to another disease, treatment is addressed towards the underlying condition. Surgery is sometimes required in severe cases of CIPO.

=Medical treatment=

Prucalopride,{{cite journal |vauthors=Briejer MR, Prins NH, Schuurkes JA |title=Effects of the enterokinetic prucalopride (R093877) on colonic motility in fasted dogs |journal=Neurogastroenterology and Motility |volume=13 |issue=5 |pages=465–72 |date=October 2001 |pmid=11696108 |doi=10.1046/j.1365-2982.2001.00280.x|s2cid=13610558 }}{{cite journal |vauthors=Oustamanolakis P, Tack J |title=Prucalopride for chronic intestinal pseudo-obstruction |journal=Alimentary Pharmacology & Therapeutics |volume=35 |issue=3 |pages=398–9 |date=February 2012 |pmid=22221087 |doi=10.1111/j.1365-2036.2011.04947.x|doi-access=free }} pyridostigmine, metoclopramide, cisapride, erythromycin, and octreotide{{cite journal|vauthors=Sharma S, Ghoshal UC, Bhat G, Choudhuri G|date=November 2006|title=Gastric adenocarcinoma presenting with intestinal pseudoobstruction, successfully treated with octreotide|journal=Indian Journal of Medical Sciences|volume=60|issue=11|pages=467–70|doi=10.4103/0019-5359.27974|pmid=17090868 |doi-access=free }}{{cite journal|vauthors=Sørhaug S, Steinshamn SL, Waldum HL|date=April 2005|title=Octreotide treatment for paraneoplastic intestinal pseudo-obstruction complicating SCLC|journal=Lung Cancer|volume=48|issue=1|pages=137–40|doi=10.1016/j.lungcan.2004.09.008|pmid=15777981}} are medications that aim to enhance intestinal motility.

Intestinal stasis, which may lead to bacterial overgrowth and subsequently, diarrhea or malabsorption, is treated with antibiotics.

Nutritional deficiencies are treated by encouraging patients to avoid foods that increase distention and are difficult to digest (e.g. those high in fat and fibre), consuming small frequent meals (5–6 per day), focusing on liquids and soft food. Reducing intake of poorly absorbed sugar alcohols may be of benefit. Referral to an accredited dietitian is recommended. If dietary changes are unsuccessful in meeting nutritional requirements and energy needs, enteral nutrition is used. Many patients eventually require parenteral nutrition.

Total parenteral nutrition (TPN) is a form of long-term nutritional treatment reserved for patients that have severe pseudo-obstruction. TPN dependent patients require frequent checkups to monitor catheter function, check liver enzyme levels, and evaluate for signs of blood infections. TPN format is typically changed depending on loss/gain of weight and bloodwork results, and is specially formulated to meet each individual patient's needs.{{cite journal |vauthors=Heneyke S, Smith VV, Spitz L, Milla PJ |title=Chronic intestinal pseudo-obstruction: treatment and long term follow up of 44 patients |journal=Archives of Disease in Childhood |volume=81 |issue=1 |pages=21–7 |date=July 1999 |pmid=10373127 |pmc=1717974 |doi=10.1136/adc.81.1.21}}

=Procedures=

Intestinal decompression by tube placement in a small stoma can also be used to reduce distension and pressure within the gut. The stoma may be a gastrostomy, jejunostomy, ileostomy, or cecostomy. These may be used for feed (e.g. gastrostomy and jejunostomy) or to flush the intestines.

Colostomy or ileostomy can bypass affected parts if they are distal to (come after) the stoma. For instance, if only the colon is affected, an ileostomy may be helpful. Either of these ostomies are typically placed at or a few centimeters below the patient's navel per doctor recommendation based on the affected area of the intestines as well as concerns for patient comfort and future physical growth for children.

The total removal of the colon, called a colectomy or resection of affected parts of the colon may be needed if part of the gut dies (for instance toxic megacolon), or if there is a localized area of dysmotility.

Gastric and colonic pacemakers have been tried. These are strips placed along the colon or stomach which create an electric discharge intended to cause the muscle to contract in a controlled manner.

A potential solution, albeit radical, is intestinal transplantation. This is only appropriate in the case of intestinal failure. These procedures are most frequently described in pediatric cases of CIPO.{{Cite journal|last1=Mousa|first1=Hayat|last2=Hyman|first2=Paul E.|last3=Cocjin|first3=Jose|last4=Flores|first4=Alejandro F.|last5=Di Lorenzo|first5=Carlo|date=October 2002|title=Long-term outcome of congenital intestinal pseudoobstruction|url=https://pubmed.ncbi.nlm.nih.gov/12395903|journal=Digestive Diseases and Sciences|volume=47|issue=10|pages=2298–2305|doi=10.1023/a:1020199614102|issn=0163-2116|pmid=12395903|s2cid=25029477}}{{Cite journal|last1=Bond|first1=Geoffrey J.|last2=Reyes|first2=Jorge D.|date=November 2004|title=Intestinal transplantation for total/near-total aganglionosis and intestinal pseudo-obstruction|url=https://pubmed.ncbi.nlm.nih.gov/15660322|journal=Seminars in Pediatric Surgery|volume=13|issue=4|pages=286–292|doi=10.1053/j.sempedsurg.2004.10.016|issn=1055-8586|pmid=15660322}} One operation involving multi-organ transplant of the pancreas, stomach, duodenum, small intestine, and liver, and was performed by Doctor Kareem Abu-Elmagd on Gretchen Miller.[http://dsc.discovery.com/fansites/surgery/follow-up/six-organ/gretchen.html Discovery Channel – Multiorgan transplant]

=Potential treatments=

Further research is necessary into other treatments which may alleviate symptoms. These include stem-cell transplantation{{Cite journal|last1=Westfal|first1=Maggie L.|last2=Goldstein|first2=Allan M.|date=June 2017|title=Pediatric enteric neuropathies: diagnosis and current management|journal=Current Opinion in Pediatrics|volume=29|issue=3|pages=347–353|doi=10.1097/MOP.0000000000000486|issn=1531-698X|pmc=5475271|pmid=28319561}}{{Cite journal|last1=Halter|first1=Joerg P.|last2=Michael|first2=W.|last3=Schüpbach|first3=M.|last4=Mandel|first4=Hanna|last5=Casali|first5=Carlo|last6=Orchard|first6=Kim|last7=Collin|first7=Matthew|last8=Valcarcel|first8=David|last9=Rovelli|first9=Attilio|last10=Filosto|first10=Massimiliano|last11=Dotti|first11=Maria T.|date=October 2015|title=Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy|journal=Brain: A Journal of Neurology|volume=138|issue=Pt 10|pages=2847–2858|doi=10.1093/brain/awv226|issn=1460-2156|pmc=4836400|pmid=26264513}} and fecal microbiota transplantation. Cannabis{{cite journal|vauthors=Lin XH, Wang YQ, Wang HC, Ren XQ, Li YY|date=August 2013|title=Role of endogenous cannabinoid system in the gut|url=http://www.actaps.com.cn/qikan/manage/wenzhang/2013-4-12.pdf|journal=Sheng Li Xue Bao|volume=65|issue=4|pages=451–60|pmid=23963077}} has not been studied with regards to CIPO. Any claims to its efficacy for use in CIPO are speculative.

Related disorders

See also

  • Gastroparesis: ineffective neuromuscular contractions (peristalsis) of the stomach, resulting in food and liquid remaining in the stomach for a prolonged period of time before entering the intestine.

References

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