Peritonitis differential diagnosis: Difference between revisions
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{{Peritonitis}} | {{Peritonitis}} | ||
{{CMG}} {{AE}} {{SCh}} | |||
==Overview== | |||
==Differential Diagnosis== | |||
{| border="2" cellpadding="4" cellspacing="0" style="margin: 1em 1em 1em 0; background: #f9f9f9; border: 1px #aaa solid; border-collapse: collapse; | |||
|+'''Differentiating Secondary peritonitis from other causes of peritonitis''' | |||
! colspan="2" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Disease'''}} | |||
! colspan="1" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Prominent clinical findings'''}} | |||
! colspan="1" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Lab tests'''}} | |||
! colspan="1" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Tratment'''}} | |||
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| rowspan="3" |'''Primary peritonitis''' | |||
|'''[[Primary peritonitis|Spontaneous bacterial peritonitis]]''' | |||
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* Absence of GI [[perforation]], most closely associated with [[cirrhosis]] and [[Liver disease|advanced liver disease]]. | |||
* Presents with abrupt onset of [[fever]], [[abdominal pain]], [[distension]], and [[rebound tenderness]]. | |||
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* Most have clinical and biochemical manifestations of advanced [[cirrhosis]] or [[nephrosis]] like [[leukocytosis]],[[hypoalbuminemia]], | |||
* a prolonged [[prothrombin]] time. SAAG >1.1 g/dL, increased serum [[lactic acid]] level, or a decreased [[Ascites|ascitic fluid]] pH (< 7.31) supports the diagnosis. [[Gram staining]] reveals bacteria in only 25% of cases. | |||
* Diagnosed by analysis of the [[Ascitic|ascitic fluid]] which reveals [[WBC]] > 500/ML, and [[PMN]] >250cells/ml. | |||
* [[Culture medium|Culture]] of ascitic fluid inoculated immediately into [[blood culture]] media at the bedside usually reveals a single [[Enteric Bacilli|enteric organism]], most commonly ''[[Escherichia coli]]'', ''[[Klebsiella]]'', or [[streptococci]]. | |||
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* Once diagnosed,it is treated with [[Ceftriaxone]]. | |||
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|'''[[Tuberculous peritonitis]]''' | |||
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* Seen in 0.5% of new cases of [[tuberculosis]] particularly in young women in endemic areas as a primary infection. | |||
* Presents with [[abdominal pain]] and [[distension]], [[fever]], [[night sweats]], [[weight loss]], and altered bowel habits. | |||
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* [[Ascites]] is present in about half of cases. [[Abdominal mass]] may be felt in a third of cases. The [[peritoneal fluid]] is characterized by a [[protein]] concentration > 3 g/dL with < 1.1 g/dL SAAG and [[Lymphocyte|lymphocyte predominance]] of [[WBC]]. | |||
* Definitive diagnosis in 80% of cases is by culture. Most patients presenting acutely are diagnosed only by [[laparotomy]]. | |||
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* Combination [[Antituberculosis|antituberculosis chemotherapy]] is preferred in chronic cases. | |||
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|'''[[Continuous ambulatory peritoneal dialysis|Continuous Ambulatory Peritoneal Dialysis]]''' [[Continuous ambulatory peritoneal dialysis|('''CAPD peritonitis)''']] | |||
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* [[Peritonitis]] is one of the major complications of [[peritoneal dialysis]] & 72.6% occurred within the first six months of [[peritoneal dialysis]]. | |||
* Historically, [[coagulase-negative staphylococci]] were the most common cause of peritonitis in [[Continuous ambulatory peritoneal dialysis|CAPD]], presumably due to touch contamination or infection via the pericatheter route. | |||
* Treatment for [[peritoneal dialysis]]-associated peritonitis consists of [[Antimicrobial drug|antimicrobial therapy]], in some cases catheter removal is also warranted. | |||
* Additional therapies for [[Peritonitis|relapsing or recurrent peritonitis]] may include [[Fibrinolytic agent|fibrinolytic agents]] and [[peritoneal lavage]]. Most episodes of peritoneal dialysis-associated peritonitis resolve with outpatient [[Antibiotic|antibiotic treatment]]. | |||
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* Majority of [[peritonitis]] cases are caused by [[bacteria]] (50%-due to [[Gram-positive bacteria|gram positive]] organisms, 15% to [[gram negative]] organisms,20% were culture negative.2% of cases are caused by [[fungi]], mostly [[Candida]] species. Polymicrobial infection in 4%.Exit-site infection was present in 13% and a [[peritoneal fluid]] leak in 3 % and [[M.tuberculosis]] 0.1%. | |||
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* [[Antibiotic|Initial empiric antibiotic coverage]] for peritoneal dialysis-associated peritonitis consists of coverage for [[gram-positive]] organisms (by [[vancomycin]] or a [[Cephalosporins|first-generation cephalosporin]]) and [[gram-negative]] organisms (by a [[cephalosporin|third-generation cephalosporin]] or an [[aminoglycoside]]). Subsequently, the regimen should be adjusted based on [[Culture medium|culture]] and [[sensitivity]] data. Cure rates are approximately 75%. | |||
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| rowspan="2" |'''[[Secondary peritonitis]]''' | |||
|'''Acute [[bacterial]] [[secondary peritonitis]]''' | |||
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* Occurs after perforating, penetrating, inflammatory, infectious, or [[ischemic]] injuries of the GI or GU tracts. Most often follows disruption of a hollow viscus→chemical peritonitis→bacterial peritonitis(polymicrobial, includes [[aerobic]] [[gram negative]] {[[E coli]], [[Klebsiella]], [[Enterobacter]], [[Proteus mirabilis]]} and gram positive { [[Enterococcus]], [[Streptococcus]]} and [[anaerobes]] {[[Bacteroides]], [[clostridia]]}). | |||
* Presents with [[abdominal pain]], [[tenderness]], [[guarding]] or rigidity, [[distension]], free peritoneal air, and diminished [[bowel sounds]]. Signs that reflect irritation of the parietal peritoneum resulting [[ileus]]. Systemic findings include [[fever]], [[chills]] or [[rigors]], [[tachycardia]], [[sweating]], [[tachypnea]], [[restlessness]], [[dehydration]], [[oliguria]], [[disorientation]], and, ultimately, refractory [[shock]]. | |||
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* [[Peritoneal lavage]], [[Laparoscopy]] are the treatment of choice. | |||
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|'''[[Biliary]] [[Secondary peritonitis|peritonitis]]''' | |||
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* Most often seen in cases of rupture of pathological [[gallbladder]] or [[bile duct]] or [[Cholangitis|cholangitic abscess]] or secondary to obstruction of the [[biliary tract]]. | |||
* Seen in alcoholic patients with [[ascites]]. | |||
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| colspan="2" |'''[[Peritonitis|Tertiary peritonitis]]''' | |||
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* Persistence or recurrence of [[Infection|intraabdominal infection]] following apparently adequate therapy of [[Peritonitis|primary or secondary peritonitis]]. | |||
* Associated with [[Mortality|high mortality]] due to multi organ dysfunction. It presents in a similar way as other [[peritonitis]] but is recognized as an adverse outcome with poor prognosis. | |||
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* [[Enterococcus]], [[Candida]], [[Staphylococcus epidermidis]], and [[Enterobacter]] being the most common organisms. | |||
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* Characterized by lack of response to appropriate surgical and [[antibiotic therapy]] due to disturbance in the hosts [[immune response]]. | |||
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| colspan="2" |'''[[Familial mediterranean fever|Familial Mediterranean fever (periodic peritonitis, familial paroxysmal polyserositis)]]''' | |||
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* Rare [[Genetic disorder|genetic condition]] which affects individuals of Mediterranean genetic background. | |||
* Etiology is unclear. | |||
* Presents with recurrent bouts of [[abdominal pain]] and [[tenderness]] along with [[pleuritic]] or [[joint pain]]. [[Fever]] and [[leukocytosis]] are common. | |||
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* [[Colchicine]] prevents but does not treat acute attacks. | |||
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| colspan="2" |'''[[Granulomatous peritonitis]]''' | |||
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* A rare condition caused by disposable surgical fabrics or food particles from a [[perforated ulcer]], eliciting a vigorous [[granulomatous]] ([[Hypersensitivity|delayed hypersensitivity]]) response in some patients 2-6 weeks after [[laparotomy]]. | |||
* Presents with [[abdominal pain]], [[fever]], [[nausea and vomiting]], [[ileus]], and systemic complaints, mild and diffuse [[abdominal tenderness]]. | |||
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* Diagnosed by the demonstration of diagnostic Maltese cross pattern of starch particles. | |||
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* The disease is self-limiting. | |||
* Treated with [[corticosteroids]] or [[Anti inflammatory medications|anti-inflammatory agents]]. | |||
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| colspan="2" |'''[[Sclerosing encapsulating peritonitis]]''' | |||
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* Seen in conditions associated with long term [[peritoneal dialysis]], shunts like [[Ventriculoperitoneal shunt|VP shunts]], history of [[Abdominal surgery|abdominal surgeries]], [[liver transplantation]]. | |||
* Symptoms include [[nausea]], [[abdominal pain]], [[diarrhea]], [[anorexia]], bloody [[ascites]]. | |||
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| colspan="2" |'''[[Abscess|Intraperitoneal abscesses]]''' | |||
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* Most common etiologies being [[Perforation|Gastrointestinal perforations]], postoperative complications, and penetrating injuries. | |||
* Signs and symptoms depend on the location of the [[abscess]] within the [[peritoneal cavity]] and the extent of involvement of the surrounding structures. | |||
* Diagnosis is suspected in any patient with a predisposing condition. In a third of cases it occurs as a sequela of [[Peritonitis|generalized peritonitis]]. | |||
* The pathogenic organisms are similar to those responsible for [[peritonitis]], but [[anaerobic]] organisms occupy an important role. | |||
* The [[mortality rate]] of serious [[Abscesses|intra-abdominal abscesses]] is about 30%. | |||
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* Diagnosed best by [[CT-scans|CT]] scan of the abdomen. | |||
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* Treatment consists of prompt and complete [[CT]] or [[Ultrasound|US]] guided drainage of the [[abscess]], control of the primary cause, and adjunctive use of effective [[Antibiotics|antibiotics.]] Open drainage is reserved for [[abscesses]] for which percutaneous drainage is inappropriate or unsuccessful. | |||
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| colspan="2" |'''[[Peritoneal mesothelioma]]''' | |||
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* Arises from the [[mesothelium]] lining the [[peritoneal cavity]]. | |||
* Its incidence is approximately 300-500 new cases being diagnosed in the United States each year. As with [[pleural mesothelioma]], there is an association with an [[Asbestos|asbestos exposure]]. | |||
* Most commonly affects men at the age of 50-69 years. Patients most often present with [[abdominal pain]] and later increased abdominal girth and [[ascites]] along with [[anorexia]], [[weight loss]] and [[abdominal pain]]. | |||
* Mean time from diagnosis to death is less than 1 year without treatment. | |||
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* [[Computed tomography|CT]] with [[Contrast|intravenous contrast]] typically demonstrates the thickening of the [[peritoneum]]. [[Laparoscopy]] with tissue biopsy or CT guided tissue biopsy with [[immunohistochemical staining]] for [[calretinin]], [[cytokeratin|cytokeratin 5/6]], [[mesothelin]], and [[WT1|Wilms tumor 1 antigen]] remain the [[Gold standard (test)|gold standard]] for diagnosis. | |||
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* At [[laparotomy]] the goal is cytoreduction with [[excision]]. Debulking surgery and intraperitoneal [[chemotherapy]] improves survival in some cases. | |||
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| colspan="2" |'''[[peritoneal carcinomatosis]]''' | |||
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* Associated with a history of [[ovarian]] or [[Malignancy|GI tract malignancy]]. | |||
* Symptoms include [[ascites]], [[abdominal pain]], [[nausea]], [[vomiting]]. | |||
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==References== | ==References== | ||
{{ | {{Reflist|2}} | ||
{{WS}} | |||
{{ | {{WH}} | ||
{{ |
Latest revision as of 12:48, 1 May 2017
Peritonitis Main Page |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Shivani Chaparala M.B.B.S [2]
Overview
Differential Diagnosis
Disease | Prominent clinical findings | Lab tests | Tratment | |
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Primary peritonitis | Spontaneous bacterial peritonitis |
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Tuberculous peritonitis |
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Continuous Ambulatory Peritoneal Dialysis (CAPD peritonitis) |
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Secondary peritonitis | Acute bacterial secondary peritonitis |
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Biliary peritonitis |
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Tertiary peritonitis |
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Familial Mediterranean fever (periodic peritonitis, familial paroxysmal polyserositis) |
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Granulomatous peritonitis |
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Sclerosing encapsulating peritonitis |
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Intraperitoneal abscesses |
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Peritoneal mesothelioma |
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peritoneal carcinomatosis |
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