Predicting and Monitoring Spontaneous Bacterial Peritonitis in Cirrhotic Patients Using the Mansoura Scoring System
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Spontaneous Bacterial Peritonitis. Basic parameters: 18 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The aim of this prospective study was to examine predictors of SBP in order to develop a noninvasive method to identify or exclude an episode of SBP, for starting early treatment with antibiotics, so decrease morbidity and mortality in these patients.
Detailed description
Spontaneous bacterial peritonitis (SBP) is a bacterial infection of ascitic fluid without any intra-abdominal, surgically treatable cause.
SBP is the most common bacterial infection in patients with cirrhosis, with a mortality rate exceeding 90% in untreated cases. However, inpatient mortality has been reduced to about 20% with early diagnosis and effective treatment.
Delayed diagnosis increases in-hospital mortality; with each hour of delay in performing paracentesis for SBP diagnosis, mortality increases by approximately 3.3%.
A study conducted in the United States reported that paracentesis was performed within the first 24 hours of admission in only 66% of cirrhotic patients with ascites.
Another study noted that routine paracentesis cannot be performed in all patients with liver cirrhosis. Therefore, delaying diagnosis increases mortality, and it is necessary to find a non-invasive and accurate method for predicting SBP.
Important risk factors for the development of SBP in cirrhotic patients include a history of SBP, variceal hemorrhage, and the use of proton pump inhibitors Several laboratory parameters have been evaluated as early predictors of SBP, including C-reactive protein (CRP), neutrophil-to-lymphocyte ratio (NLR), mean platelet volume (MPV), platelet count, and serum creatinine level. However, the data remain inconsistent.
Recently, the Mansoura Scoring System was developed at Mansoura University and retrospectively applied to cirrhotic patients with ascites for early SBP diagnosis without waiting for peritoneal fluid analysis.
The Mansoura score includes four components: age, MPV, and NLR (1 point each), and CRP (2 points), yielding a total score of 0 to 5. SBP is diagnosed when the score is equal to or greater than 4.
Primary outcome measures
- Diagnostic Accuracy of the Mansoura Scoring System for Predicting Spontaneous Bacterial Peritonitis (SBP) [Time frame: At hospital admission ( within 24 hours of admission)]
Eligibility criteria
Inclusion criteria
- Adult patients aged >18 years
- Diagnosed liver cirrhosis
- Presence of ascites
- Provided written informed consent
Exclusion criteria
- Use of antibiotics within the previous two weeks
- Prophylactic treatment for spontaneous bacterial peritonitis (SBP) prior to admission
- Ascites not related to portal hypertension, including:
- Peritoneal tuberculosis
- Peritoneal carcinomatosis
- Congestive heart failure
- Renal disease
- Pancreatitis
- Hemorrhagic ascites
- Secondary peritonitis
- Presence of infections other than SBP, including:
- Pneumonia
- Urinary tract infection
- Skin and soft tissue infection
- Presence of malignancy Hematologic diseases
- Use of antiplatelet drugs or non-steroidal anti-inflammatory drugs (NSAIDs)
- Receipt of platelet or blood transfusion prior to admission
- Diseases associated with elevated mean platelet volume (MPV), including:
- Diabetes mellitus
- Cardiovascular disease
- Hyperthyroidism
- Immune thrombocytopenia
- Myeloproliferative disorders
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07024355 · 04-2025-300593