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IMPROVED EFFECTIVENESS IN TREATING PATIENTS WITH
ASCITS PERITONITIS CAN BE ACHIEVED THROUGH THE
CREATION OF AN ERGONOMIC ANTIBOETIC THERAPY PROGRAM.
Sh.T.Urokov
1
D.J.Komilov
2
1
Doctor of Medical Sciences, Associate Professor, Head of the Department;
Department of Surgical Diseases, Bukhara State Medical Institute named after
Abu Ali ibn Sina, Bukhara, Republic of Uzbekistan
2
Bukhara branch of the Republican Scientific Center for Emergency Medical
Care.
https://doi.org/10.5281/zenodo.15797279
Relevance:
A small intestine motility abnormality brought on by cirrhosis
increases the risk of intestinal bacterial overgrowth and translocation.
Furthermore, the fact that these patients use proton pump inhibitors often may
make this problem worse by decreasing stomach acidity and increasing
intestinal permeability, which encourages bacterial translocation and
colonization of mesenteric lymph nodes. The deterioration of the div's
defensive mechanisms also contributes to the subsequent infection of the fluid
in the peritoneal cavity. Additionally, bacteria that cause SBP can enter the
peritoneal cavity through the lymphatic or circulatory systems from extra-
gastrointestinal foci such the lungs, the urinary tract, dermatitis and
subcutaneous tissue, pharyngitis, and frequently disregarded odontogenic foci.
The diagnosis confirms the finding of > 250 polymorphonuclear cells
(PMNs) in a milliliter of ascitic fluid. If additionally the ascitic fluid culture is
positive, as is observed in approximately 40% of SBP cases, we can diagnose a
culture-positive SBP; otherwise the disease is called neutrocytic ascites. When
the ascitic fluid culture is positive and the number of PMNs is < 250 in a milliliter
of ascitic fluid the condition is called bacterascites. As cirrhosis is a condition of
immunosuppression, called cirrhosis-associated immune dysfunction (CAID),
the div’s response to infection may be poorly expressed. Therefore, in all
patients with liver cirrhosis and even mild ascites, in the case of sudden
deterioration of liver function, SBP should always be taken into account, even in
the absence of obvious clinical symptoms or deviations in laboratory tests.
We discuss the pathogenesis, diagnosis, and current clinical management of
ascites, with an emphasis on recent promising developments such as closed
transjugular intrahepatic portosystemic shunt. Spontaneous bacterial peritonitis
occurs in up to 10% of patients with ascites due to bacterial overgrowth with
translocation through increased permeability of the small intestinal wall and
disruption of protective mechanisms. Against the background of AP, liver failure
with nephrotic syndrome increases in 30% of patients.
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Primary ascites-peritonitis, or, according to foreign literature, spontaneous
bacterial peritonitis, causes difficulties in diagnosis. The cause of spontaneous
bacterial AP is the penetration of microorganisms through the intestinal wall
into the mesenteric lymph nodes and the peritoneal cavity.
Secondary AP in patients with cirrhosis occurs due to inflammatory
processes in the abdominal cavity and pelvis, perforation of hollow organs,
strangulated hernias, and surgical interventions. The effectiveness of treatment
for AP largely depends on its early diagnosis. According to the literature, today
diagnostic paracentesis with laboratory testing of AF is of decisive importance.
Determination of the number of polymorphonuclear leukocytes, protein content,
albumin and amylase concentrations is considered mandatory.
Objective Of The Study
— The effectiveness of treatment of patients with
AP can be improved by substantiating the optimal antibiotic therapy program in
combination with complex treatment of patients with cirrhosis.
Materials And Methods
The results of treatment of 23 patients with
cirrhosis complicated by AP were analyzed. There were 10 men (43.5%), 13
women (56.5%). The average age was 57.5 ± 11.4 years. According to the degree
of hepatic decompensation in accordance with the Child – Turcotte – Pugh
criteria, patients were distributed as follows: class B - 3 patients, class C - 20
patients. According to the nature of ascites, 8 patients had transient ascites, and
15 patients had resistant ascites.
Primary ascites-peritonitis was diagnosed in 16 patients. Secondary
bacterial peritonitis was detected in 7 patients: in 2 patients - as a consequence
of gangrenous calculous cholecystitis, in 1 - phlegmonous appendicitis. Four
patients diagnosed with secondary bacterial peritonitis had a history of invasive
manipulations accompanied by a violation of the integrity of the peritoneum:
laparocentesis in 2 patients, mesentericocaval-H anastomosis in one case, and
herneoplasty for an umbilical hernia in one case.
All patients underwent puncture of the peritoneal cavity under ultrasound
guidance. In 11 (52.3%) patients, ultrasound of the abdominal cavity revealed
acoustic heterogeneity of the AF: floating fibrin threads, suspended protein
particles, and fibrinous deposits were visualized. However, their presence was
not strictly pathognomonic for AP.
The diagnosis of ascites-peritonitis was established when the total cytosis
in the AF increased over 800 cells in 1 μl and the number of neutrophil
leukocytes increased over 250 cells in 1 μl. To exclude infection of the AF, in
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each case, its bacteriological control was carried out by inoculating it on
enrichment media.
Results Of The Study
showed that the maximum concentration of
cefoperazone and sulbactam when administered intravenously is detected 1
hour after intravenous administration of the drug and decreases by 37% by 12
hours. The dynamics of drug concentrations in the AF were of a different nature:
Cmax in the AF reached values of 24.097 ± 3.375 μg/ml 1 hour after the start of
intravenous administration and decreased by half by 12 hours from the initial
level.
When comparing the concentrations of the antibacterial drug in the AF, it
was revealed that the concentration of cefoperazone and sulbactam in the
second group after 1 hour was significantly lower, but by 6 and 12 hours it
increased significantly and exceeded by 64% the concentration in the AF of the
first group.
When comparing the concentrations of the antibacterial drug in the AF, it
was revealed that the concentration of cefoperazone and sulbactam in the
second group after 1 hour was significantly lower, but by 6 and 12 hours it
increased significantly and exceeded by 64% the concentration in the AF of the
first group .
With endolymphatic administration of the antibiotic, its bioavailability in
ascitic fluid is significantly higher than with intravenous administration.
However, the effective concentration is achieved only 6 hours after
administration. When administered intravenously, within an hour the
concentration of cefoperazone is significantly higher (24.097 ± 3.375 μg/ml).
Taking into account the obtained data on the bioavailability of cefbactam in
the AF, 3 patients of the third group received combination antibacterial therapy.
After the diagnosis of AP was made, antibacterial therapy was started with
intravenous administration. Then, after inserting a catheter into the inguinal
lymph node, cefbactam at a dose of 1 gram was administered endolymphatically.
A study of the concentration of cefoperazone and sulbactam in AF was carried
out .
With combined antibacterial treatment, the effect of the antibiotic began
from the first hours of the start of therapy and persisted for 12 hours. On the
2nd day after the start of antibacterial therapy, all patients underwent repeated
cytological and microbiological examination of the AF.
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Conclusions
When diagnosing AP, it is necessary to begin timely
combination antibacterial therapy. It should include joint, simultaneous
intravenous and endolymphatic administration of cefbactam.
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