Peritonitis

Inflammation of abdominal organ lining

This article is about the human condition. For peritonitis in cats, see Feline infectious peritonitis.

Not to be confused with Periodontal disease.

Medical condition

Peritonitis

Other names| Surgical abdomen, acute abdomen[1]
Peritonitis from tuberculosis
Pronunciation|

* /pɛrɪtəˈnaɪtɪs/

Specialty| Emergency medicine, general surgery
Symptoms| Severe pain, swelling of the abdomen, fever[2][3]
Complications| Sepsis (sepsis is likely if not quickly treated), shock, acute respiratory distress syndrome[4][5]
Usual onset| Sudden[1]
Types| Primary, secondary, tertiary, generalized, localized[1]
Causes| Perforation of the intestinal tract, pancreatitis, pelvic inflammatory disease, cirrhosis, ruptured appendix[3]
Risk factors| Ascites, peritoneal dialysis[4]
Diagnostic method| Examination, blood tests, medical imaging[6]
Treatment| Antibiotics, intravenous fluids, pain medication, surgery[3][4]
Frequency| Relatively common[1]

Peritonitis is inflammation of the localized or generalized peritoneum, the lining of the inner wall of the abdomen and covering of the abdominal organs.[2] Symptoms may include severe pain, swelling of the abdomen, fever, or weight loss.[2][3] One part or the entire abdomen may be tender.[1] Complications may include shock and acute respiratory distress syndrome.[4][5]

Causes include perforation of the intestinal tract, pancreatitis, pelvic inflammatory disease, stomach ulcer, cirrhosis, a ruptured appendix or even a perforated gallbladder.[3] Risk factors include ascites (the abnormal build-up of fluid in the abdomen) and peritoneal dialysis.[4] Diagnosis is generally based on examination, blood tests, and medical imaging.[6]

Treatment often includes antibiotics, intravenous fluids, pain medication, and surgery.[3][4] Other measures may include a nasogastric tube or blood transfusion.[4] Without treatment death may occur within a few days.[4] About 20% of people with cirrhosis who are hospitalized have peritonitis.[1]

## Signs and symptoms

[edit]

### Abdominal pain

[edit]

The main manifestations of peritonitis are acute abdominal pain, abdominal tenderness, abdominal guarding, rigidity, which are exacerbated by moving the peritoneum, e.g., coughing (forced cough may be used as a test), flexing one's hips, or eliciting the Blumberg's sign (meaning that pressing a hand on the abdomen elicits less pain than releasing the hand abruptly, which will aggravate the pain, as the peritoneum snaps back into place). Rigidity is highly specific for diagnosing peritonitis (specificity: 76–100%).[7] The presence of these signs in a person is sometimes referred to as peritonism.[8] The localization of these manifestations depends on whether peritonitis is localized (e.g., appendicitis or diverticulitis before perforation), or generalized to the whole abdomen. In either case, pain typically starts as a generalized abdominal pain (with involvement of poorly localizing visceral innervation of the visceral peritoneal layer), and may become localized later (with involvement of the somatic innervation of the parietal peritoneal layer). Peritonitis is an example of an acute abdomen.[9]

### Other symptoms

[edit]

* Diffuse abdominal rigidity (abdominal guarding) is often present, especially in generalized peritonitis
* Fever
* Sinus tachycardia
* Development of ileus paralyticus (i.e., intestinal paralysis), which also causes nausea, vomiting and bloating
* Reduced or no passage of abdominal gas and bowel sound[10]

### Complications

[edit]

* Sequestration of fluid and electrolytes, as revealed by decreased central venous pressure, may cause electrolyte disturbances, as well as significant hypovolemia, possibly leading to shock and acute kidney failure.
* A peritoneal abscess may form (e.g., above or below the liver, or in the lesser omentum)
* Sepsis may develop, so blood cultures should be obtained.
* Complicated peritonitis typically involves multiple organs.

## Causes

[edit]

### Infection

[edit]

* Perforation of part of the gastrointestinal tract is the most common cause of peritonitis. Examples include perforation of the distal esophagus (Boerhaave syndrome), of the stomach (peptic ulcer, gastric carcinoma), of the duodenum (peptic ulcer), of the remaining intestine (e.g., appendicitis, diverticulitis, Meckel diverticulum, inflammatory bowel disease (IBD), intestinal infarction, intestinal strangulation, colorectal carcinoma, meconium peritonitis), or of the gallbladder (cholecystitis). Other possible reasons for perforation include abdominal trauma, ingestion of a sharp foreign body (such as a fish bone, toothpick or glass shard), perforation by an endoscope or catheter, and anastomotic leakage. The latter occurrence is particularly difficult to diagnose early, as abdominal pain and ileus paralyticus are considered normal in people who have just undergone abdominal surgery. In most cases of perforation of a hollow viscus, mixed bacteria are isolated; the most common agents include Gram-negative bacilli (e.g., Escherichia coli) and anaerobic bacteria (e.g., Bacteroides fragilis). Faecal peritonitis results from the presence of faeces in the peritoneal cavity. It can result from abdominal trauma and occurs if the large bowel is perforated during surgery.[11]
* Disruption of the peritoneum, even in the absence of perforation of a hollow viscus, may also cause infection simply by letting micro-organisms into the peritoneal cavity. Examples include trauma, surgical wound, continuous ambulatory peritoneal dialysis, and intra-peritoneal chemotherapy. Again, in most cases, mixed bacteria are isolated; the most common agents include cutaneous species such as Staphylococcus aureus, and coagulase-negative staphylococci, but many others are possible, including fungi such as Candida.[12]
* Spontaneous bacterial peritonitis (SBP) is a peculiar form of peritonitis occurring in the absence of an obvious source of contamination. It occurs in people with ascites, including children.
* Intra-peritoneal dialysis predisposes to peritoneal infection (sometimes named "primary peritonitis" in this context).
* Systemic infections (such as tuberculosis) may rarely have a peritoneal localisation.
* Pelvic inflammatory disease[13]

### Non-infection

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* Leakage of sterile body fluids into the peritoneum, such as blood (e.g., endometriosis, blunt abdominal trauma), gastric juice (e.g., peptic ulcer, gastric carcinoma), bile (e.g., liver biopsy), urine (pelvic trauma), menstruum (e.g., salpingitis), pancreatic juice (pancreatitis), or even the contents of a ruptured dermoid cyst. While these body fluids are sterile at first, they frequently become infected once they leak out of their organ, leading to infectious peritonitis within 24 to 48 hours.
* Sterile abdominal surgery, under normal circumstances, causes localised or minimal generalised peritonitis, which may leave behind a foreign body reaction or fibrotic adhesions. However, peritonitis may also be caused by the rare case of a sterile foreign body inadvertently left in the abdomen after surgery (e.g., gauze, sponge).
* Much rarer non-infectious causes may include familial Mediterranean fever, TNF receptor associated periodic syndrome, porphyria, and systemic lupus erythematosus.

### Risk factors

[edit]

* Previous history of peritonitis
* History of alcoholism
* Liver disease
* Fluid accumulation in the abdomen
* Weakened immune system
* Pelvic inflammatory disease

## Diagnosis

[edit]

A diagnosis of peritonitis is based primarily on the clinical manifestations described above. Rigidity (involuntary contraction of the abdominal muscles) is the most specific exam finding for diagnosing peritonitis.[14] If focal peritonitis is detected, further work-up should be done. If diffuse peritonitis is detected, then urgent surgical consultation should be obtained, and may warrant surgery without further investigations. Leukocytosis, hypokalemia, hypernatremia, and acidosis may be present, but they are not specific findings. Abdominal X-rays may reveal dilated, edematous intestines, although such X-rays are mainly useful to look for pneumoperitoneum, an indicator of gastrointestinal perforation. The role of whole-abdomen ultrasound examination is under study and is likely to expand in the future. Computed tomography (CT or CAT scanning) may be useful in differentiating causes of abdominal pain. If reasonable doubt still persists, an exploratory peritoneal lavage or laparoscopy may be performed. In people with ascites, a diagnosis of peritonitis is made via paracentesis (abdominal tap): More than 250 polymorphonuclear cells per μL is considered diagnostic. In addition, Gram stain is almost always negative, whereas culture of the peritoneal fluid can determine the microorganism responsible and determine their sensitivity to antimicrobial agents.[15][16]

### Pathology

[edit]

In normal conditions, the peritoneum appears greyish and glistening; it becomes dull 2–4 hours after the onset of peritonitis, initially with scarce serous or slightly turbid fluid. Later on, the exudate becomes creamy and evidently suppurative; in people who are dehydrated, it also becomes very inspissated. The quantity of accumulated exudate varies widely. It may be spread to the whole peritoneum, or be walled off by the omentum and viscera. Inflammation features infiltration by neutrophils with fibrino-purulent exudation.[17]

## Treatment

[edit]

Depending on the severity of the person's state, the management of peritonitis may include:

* Antibiotics are usually administered intravenously, but they may also be infused directly into the peritoneum. The empiric choice of broad-spectrum antibiotics often consist of multiple drugs, and should be targeted against the most likely agents, depending on the cause of peritonitis (see above); once one or more agents grow in cultures isolated, therapy will be targeted against them.[18]
* Gram-positive and Gram-negative organisms must be covered. Out of the cephalosporins, cefoxitin and cefotetan can be used to cover Gram-positive bacteria, Gram-negative bacteria, and anaerobic bacteria. Beta-lactams with beta-lactamase inhibitors can also be used; examples include ampicillin/sulbactam, piperacillin/tazobactam, and ticarcillin/clavulanate.[19] Carbapenems are also an option when treating primary peritonitis as all of the carbapenems cover Gram-positives, Gram-negatives, and anaerobes except for ertapenem. The only fluoroquinolone that can be used is moxifloxacin because this is the only fluoroquinolone that covers anaerobes. Tigecycline is a tetracycline that can be used due to its coverage of Gram-positives and Gram-negatives. Empiric therapy will often require multiple drugs from different classes.[20]
* Surgery (laparotomy) is needed to perform a full exploration and lavage of the peritoneum, as well as to correct any gross anatomical damage that may have caused peritonitis.[21] The exception is spontaneous bacterial peritonitis, which does not always benefit from surgery and may be treated with antibiotics in the first instance.

## Prognosis

[edit]

If properly treated, typical cases of surgically correctable peritonitis (e.g., perforated peptic ulcer, appendicitis, and diverticulitis) have a mortality rate of about <10% in otherwise healthy people. The mortality rate rises to 35% in peritonitis patients who develop sepsis, and patients who have underlying renal insufficiency and complications have a higher mortality rate.[22]

## Etymology

[edit]

The term "peritonitis" comes from Greek περιτόναιον peritonaion "peritoneum, abdominal membrane" and -itis "inflammation".[23]

## References

[edit]

1. ^ a b c d e f Ferri, Fred F. (2017). Ferri's Clinical Advisor 2018 E-Book: 5 Books in 1. Elsevier Health Sciences. pp. 979–980\. ISBN 9780323529570. Archived from the original on 2020-10-08. Retrieved 2020-08-24.
2. ^ a b c "Peritonitis - National Library of Medicine". PubMed Health. Archived from the original on 2016-01-24. Retrieved 22 December 2017.
3. ^ a b c d e f "Peritonitis". NHS. 28 September 2017. Archived from the original on 31 December 2017. Retrieved 31 December 2017.
4. ^ a b c d e f g h "Acute Abdominal Pain". Merck Manuals Professional Edition. Archived from the original on 13 July 2018. Retrieved 31 December 2017.
5. ^ a b "Acute Abdominal Pain". Merck Manuals Consumer Version. Archived from the original on 13 July 2018. Retrieved 31 December 2017.
6. ^ a b "Encyclopaedia : Peritonitis". NHS Direct Wales. 25 April 2015. Archived from the original on 31 December 2017. Retrieved 31 December 2017.
7. ^ McGee, Steven R. (2018). "Abdominal Pain and Tenderness". Evidence-based physical diagnosis (4th ed.). Philadelphia, PA: Elsevier. ISBN 9780323508711. OCLC 959371826.
8. ^ "Biology Online's definition of peritonism". Archived from the original on 2018-06-12. Retrieved 2008-08-14.
9. ^ Okamoto, Koh; Hatakeyama, Shuji (2018-09-20). "Tuberculous Peritonitis". New England Journal of Medicine. 379 (12): e20. doi:10.1056/NEJMicm1713168. ISSN 0028-4793. PMID 30231225. S2CID 205088395.
10. ^ Ragetly, G. R.; Bennett, R. A.; Ragetly, C. A. (2012). "Therapie und Prognose der septischen Peritonitis". Tierärztliche Praxis Ausgabe K: Kleintiere / Heimtiere. 40 (5): 372–378\. doi:10.1055/s-0038-1623666. ISSN 1434-1239. S2CID 73133175.
11. ^ "Peritonitis - Symptoms and causes". Mayo Clinic. Archived from the original on September 22, 2017. Retrieved July 2, 2016.
12. ^ Arfania D, Everett ED, Nolph KD, Rubin J (1981). "Uncommon causes of peritonitis in patients undergoing peritoneal dialysis". Archives of Internal Medicine. 141 (1): 61–64\. doi:10.1001/archinte.141.1.61. PMID 7004371.
13. ^ Ljubin-Sternak, Suncanica; Mestrovic, Tomislav (2014). "Review: Chlamydia trachonmatis and Genital Mycoplasmias: Pathogens with an Impact on Human Reproductive Health". Journal of Pathogens. 2014 (183167): 183167. doi:10.1155/2014/183167. PMC 4295611. PMID 25614838.
14. ^ Nishijima, D. K., Simel, D. L., Wisner, D. H., & Holmes, J. F. (2012). Does this adult patient have a blunt intra-abdominal injury?. JAMA, 307(14), 1517–1527. https://doi.org/10.1001/jama.2012.422
15. ^ Spalding, Drc; Williamson, Rcn (January 2008). "Peritonitis". British Journal of Hospital Medicine. 69 (Sup1): M12 – M15. doi:10.12968/hmed.2008.69.Sup1.28050. ISSN 1750-8460. PMID 18293728.
16. ^ Ludlam, H A; Price, T N; Berry, A J; Phillips, I (September 1988). "Laboratory diagnosis of peritonitis in patients on continuous ambulatory peritoneal dialysis". Journal of Clinical Microbiology. 26 (9): 1757–1762\. doi:10.1128/jcm.26.9.1757-1762.1988. ISSN 0095-1137. PMC 266711. PMID 3183023.
17. ^ Arvind, Sharda; Raje, Shweta; Rao, Gayatri; Chawla, Latika (February 2019). "Laparoscopic Diagnosis of Peritoneal Tuberculosis". Journal of Minimally Invasive Gynecology. 26 (2): 346–347\. doi:10.1016/j.jmig.2018.04.006. PMID 29680232. S2CID 5041460.
18. ^ "Peritoneal Dialysis". Brenner and Rector's The Kidney (11th ed.). Philadelphia, PA: Elsevier. 2020. pp. 2094–2118\. ISBN 9780323759335.
19. ^ Holten, Keith B.; Onusko, Edward M. (August 1, 2000). "Appropriate Prescribing of Oral Beta-Lactam Antibiotics". American Family Physician. 62 (3): 611–620\. PMID 10950216. Archived from the original on June 22, 2018. Retrieved July 22, 2019.
20. ^ Li, Philip Kam-Tao; Szeto, Cheuk Chun; Piraino, Beth; de Arteaga, Javier; Fan, Stanley; Figueiredo, Ana E.; Fish, Douglas N.; Goffin, Eric; Kim, Yong-Lim; Salzer, William; Struijk, Dirk G. (September 2016). "ISPD Peritonitis Recommendations: 2016 Update on Prevention and Treatment". Peritoneal Dialysis International. 36 (5): 481–508\. doi:10.3747/pdi.2016.00078. ISSN 0896-8608. PMC 5033625. PMID 27282851.
21. ^ "Peritonitis: Emergencies: Merck Manual Home Edition". Archived from the original on 2010-10-18. Retrieved 2007-11-25.
22. ^ Daley, Brian J (2019-07-23). "Peritonitis and Abdominal Sepsis: Background, Anatomy, Pathophysiology". Medscape Reference. Retrieved 2024-08-08.
23. ^ "peritonitis - Online Etymology Dictionary". Archived from the original on 2011-09-16. Retrieved 2017-05-09.

## External links

[edit]

Classification|

* ICD-10: K65
* ICD-9-CM: 567
* MeSH: D010538
* DiseasesDB: 9860

|

External resources|

* MedlinePlus: 001335
* eMedicine: med/2737
* Patient UK: Peritonitis

* v
* t
* e

Diseases of the human digestive system

Upper GI tract|

| Esophagus|

* Esophagitis
* Candidal
* Eosinophilic
* Herpetiform
* Rupture
* Boerhaave syndrome
* Mallory–Weiss syndrome
* Zenker's diverticulum
* Barrett's esophagus
* Esophageal motility disorder
* Nutcracker esophagus
* Achalasia
* Esophagogastric junction outflow obstruction
* Diffuse esophageal spasm
* Gastroesophageal reflux disease (GERD)
* Laryngopharyngeal reflux (LPR)
* Esophageal stricture
* Inlet patch
* Megaesophagus
* Esophageal intramural pseudodiverticulosis
* Acute esophageal necrosis

|

Stomach|

* Gastritis
* Atrophic
* Ménétrier's disease
* Gastroenteritis
* Peptic (gastric) ulcer
* Cushing ulcer
* Dieulafoy's lesion
* Dyspepsia
* Functional dyspepsia
* Pyloric stenosis
* Achlorhydria
* Gastroparesis
* Gastroptosis
* Portal hypertensive gastropathy
* Gastric antral vascular ectasia
* Gastric dumping syndrome
* Gastric volvulus
* Buried bumper syndrome
* Gastrinoma
* Zollinger–Ellison syndrome

Lower GI tract
Enteropathy|

| Small intestine
(Duodenum/Jejunum/Ileum)|

* Enteritis
* Duodenitis
* Jejunitis
* Ileitis
* Peptic (duodenal) ulcer
* Curling's ulcer
* Malabsorption: Coeliac
* Tropical sprue
* Blind loop syndrome
* Small intestinal bacterial overgrowth
* Whipple's
* Short bowel syndrome
* Steatorrhea
* Milroy disease
* Bile acid malabsorption

|

Large intestine
(Appendix/Colon)|

* Appendicitis
* Colitis
* Pseudomembranous
* Ulcerative
* Ischemic
* Microscopic
* Collagenous
* Lymphocytic
* Dysentery
* Functional colonic disease
* IBS
* Intestinal pseudoobstruction / Ogilvie syndrome
* Megacolon / Toxic megacolon
* Diverticulitis/Diverticulosis/SCAD

Large and/or small|

* Enterocolitis
* Necrotizing
* Gastroenterocolitis
* IBD
* Crohn's disease
* Vascular: Abdominal angina
* Mesenteric ischemia
* Angiodysplasia
* Bowel obstruction: Ileus
* Intussusception
* Volvulus
* Fecal impaction
* Constipation
* Functional
* Diarrhea
* Infectious
* Intestinal adhesions

Rectum|

* Proctitis
* Radiation proctitis
* Proctalgia fugax
* Rectal prolapse (Internal rectal prolapse)
* Anismus
* Solitary rectal ulcer syndrome
* Rectal stricture

Anal canal|

* Anal fissure/Anal fistula
* Anal abscess
* Hemorrhoid
* Anal dysplasia
* Pruritus ani
* Anal stricture

GI bleeding|

* Blood in stool
* Upper
* Hematemesis
* Melena
* Lower
* Hematochezia

Accessory|

| Liver|

* Hepatitis
* Viral hepatitis
* Autoimmune hepatitis
* Alcoholic hepatitis
* Cirrhosis
* PBC
* Fatty liver
* MASLD
* Vascular
* Budd–Chiari syndrome
* Hepatic veno-occlusive disease
* Portal hypertension
* Nutmeg liver
* Alcoholic liver disease
* Liver failure
* Hepatic encephalopathy
* Acute liver failure
* Liver abscess
* Pyogenic
* Amoebic
* Hepatorenal syndrome
* Peliosis hepatis
* Metabolic disorders
* Wilson's disease
* Hemochromatosis

|

Gallbladder|

* Cholecystitis
* Gallstone / Cholelithiasis
* Cholesterolosis
* Adenomyomatosis
* Postcholecystectomy syndrome
* Porcelain gallbladder

Bile duct/
Other biliary tree|

* Cholangitis
* Primary sclerosing cholangitis
* Secondary sclerosing cholangitis
* Ascending
* Cholestasis/Mirizzi's syndrome
* Biliary fistula
* Haemobilia

* Common bile duct
* Choledocholithiasis
* Biliary dyskinesia
* Sphincter of Oddi dysfunction

Pancreatic|

* Pancreatitis
* Acute
* Chronic
* Hereditary
* Pancreatic abscess
* Pancreatic pseudocyst
* Exocrine pancreatic insufficiency
* Pancreatic fistula

Other|

| Hernia|

* Diaphragmatic
* Congenital
* Hiatus

* Inguinal
* Indirect
* Direct
* Umbilical
* Paraumbilical
* Femoral
* Obturator
* Spigelian

* Lumbar
* Petit's
* Grynfeltt–Lesshaft

* Undefined location
* Incisional
* Internal hernia
* Richter's

|

Peritoneal|

* Peritonitis
* Spontaneous bacterial peritonitis
* Hemoperitoneum
* Pneumoperitoneum

Authority control databases

National|

* United States
* France
* BnF data
* Japan
* Czech Republic
* Israel

Other|

* Yale LUX

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