Mogu li probiotici poboljšati efikasnost i bezbednosni profil trostruke eradikacione terapije za Helicobacter pylori? Prospektivna randomizirana studija

  • Saša Petar Grgov Department of Gastroenterology and Hepatology, General Hospital Leskovac, Leskovac, Serbia
  • Tomislav Tasić Department of Gastroenterology and Hepatology, General Hospital Leskovac, Leskovac, Serbia
  • Biljana Radovanović Dinić Clinic for Gastroenterology and Hepatology, Clinical Center Niš, Niš, Serbia
  • Daniela Benedeto Stojanov Clinic for Gastroenterology and Hepatology, Clinical Center Niš, Niš, Serbia
Ključne reči: helicobacter pylori||, ||helicobacter pylori, helicobacter infection||, ||infekcija, helicobacter, disease eradication||, ||bolest, eradikacija, clinical protocols||, ||protokoli, klinički, probiotics||, ||probiotici, treatment outcome||, ||lečenje, ishod,

Sažetak


Uvod/Cilj. Pojedine studije ukazuju na dobrobit primene različitih probiotskih sojeva u kombinaciji sa antibioticima u eradikaciji infekcije prouzrokovane bakterijom Helicobacter pylori (H. pylori). Cilj ove studije bio je da se proceni efekat koadministracije multiplih probiotskih sojeva i trostruke eradikacione terapije za H. pylori. Metode. U ovu prospektivnu studiju bilo je uključeno 167 bolesnika sa dispeptičkim simptomima i hroničnim gastritisom kod kojih je dijagnostikovana H. pylori infekcija i koji su randomizirani u dve grupe. Grupa I, od 77 bolesnika, podvrgnuta je trostrukoj eradikacionoj terapiji u trajanju od 7 dana, sa lansoprazolom 2 × 30 mg pola sata pre obroka, amoksicilinom 2 × 1 000 mg na 12 sati i klaritromicinom 2 × 500 mg na 12 sati. Posle 7. dana nastavljena je terapija lansoprazolom u dozi od 30 mg pola sata pre doručka još 4 nedelje. Grupa II, sastavljena od 90 bolesnika, podvrgnuta je istoj terapiji kao i bolesnici grupe I, uz dodatak kulture probiotika u vidu jedne kapsule, koja je sadržala Lactobacillus Rosell-52, Lactobacillus Rosell-11, Bifidobacterium Rosell-1755 i Saccharomyces boulardii, od početka eradikacione terapije, u trajanju od 4 nedelje. Kontrola eradikacije H. pylori infekcije izvršena je 8 nedelja nakon terapije brzim ureaza testom i patohistološkom procenom endoskopskih biopsija ili testom antigena u stolici na H. pylori. Rezultati. Eradikacija H. pylori infekcije postignuta je kod 93,3% bolesnika koji su dobijali probiotik uz eradikacionu terapiju i kod 81,8% bolesnika koji su bili samo na eradikacionoj terapiji bez probiotika. Razlika u uspehu eradikacije H. pylori bila je statistički značajna, (p < 0,05). Učestalost ispoljavanja neželjenih efekata eradikacione terapije bila je veća u grupi I bolesnika koji nisu bili na probiotiku (28,6%), nego u grupi II koja je dobijala probiotik (17,7%), ali razlika nije bila statistički značajna. Zaključak. Dodatkom multiplih probiotiskih kultura trostrukoj eradikacionoj terapiji H. pylori infekcije postiže se značajno bolji stepen eracikacije sa manje neželjenih efekata primene antibiotika.

Biografije autora

Saša Petar Grgov, Department of Gastroenterology and Hepatology, General Hospital Leskovac, Leskovac, Serbia
Sef odeljenja za gastroenterologiju i hepatologiju
Tomislav Tasić, Department of Gastroenterology and Hepatology, General Hospital Leskovac, Leskovac, Serbia

clinical doctor

Biljana Radovanović Dinić, Clinic for Gastroenterology and Hepatology, Clinical Center Niš, Niš, Serbia
profesor of faculty
Daniela Benedeto Stojanov, Clinic for Gastroenterology and Hepatology, Clinical Center Niš, Niš, Serbia
docent of faculty

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2017/03/13
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