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BRATISLAVSKE LEKARSKE LISTY
BRATISLAVA MEDICAL JOURNAL



Volume 97 / No. 11 / 1996


IMIPENEM-RESISTANT Ps. AERUGINOSA BACTERAEMIA IN CANCER PATIENTS: RISK FACTORS, CLINICAL FEATURES AND OUTCOME

IMIPENEM REZISTENTNA Ps. AERUGINOSA AKO ETIOLOGICKY POVODCA BAKTERIEMII U ONKOLOGICKYCH PACIENTOV: RIZIKOVE FAKTORY, KLINICKE PRIZNAKY A VYSLEDOK LIECBY

KRCMERY Jr. V., TRUPL J., KUNOVA A., SPANIK S., ILAVSKA I., HELPIANSKA L., BEZAKOVA I., DRGONA L., ORAVCOVA E., STUDENA M., LACKA J., SEVCIKOVA L., KOREN P., KUKUCKOVA E., STOPKOVA K., KRUPOVA I., GRAUSOVA S., SVEC J.

Ninety nine patients with 101 bacteraemic episodes due to Ps. aeruginosa (PA) within 6 years were divided into two groups according to their resistance to imipenem – 91 due to imipenem sensitive (ISPA) and 10 due to resistant (IRPA). Risk factors, the clinical course and the outcome were evaluated and compared. Acute leukaemia, prolonged neutropenia, previous therapy with amikacin, third generation of cephalosporins, imipenem and prophylaxis by quinolones were significantly more frequently associated with IRPA.
Imipenem resistant PA bacteraemia were associated with higher incidence of septic shock (40 % vs 19.8 %, p<0.02) and death (33.3 %) than ISPA bacteraemias. Since 1992, when first IRPA appeared, the incidence of imipenem resistance increased tenfold, and in 1994, up to 10 % of PA causing bloodstream infections in cancer patients in our center were imipenem resistant. (Tab. 3, Ref. 8.)
Key words: imipenem, Ps. aeruginosa, bacteraemia, cancer patient, infection.

Bratisl Lek Listy 1996; 96: 647–651


BREAKTHROUGH BACTERAEMIC AND FUNGAEMIC EPISODES DURING ANTIMICROBIAL PROPHYLAXIS AND THERAPY IN CANCER PATIENTS: ANALYSIS OF RISK FACTORS, ETIOLOGY, THERAPY AND OUTCOME IN 123 EPISODES

"BREAKTHROUGH" BAKTERIEMIE A FUNGEMIE POCAS ANTIMIKROBIALNEJ PROFYLAXIE A TERAPIE U ONKOLOGICKYCH PACIENTOV: ANALYZY RIZIKOVYCH FAKTOROV, ETIOLOGIA, TERAPIA A VYSLEDOK LIECBY V 123 PRIPADOCH

SPANIK S., KRCMERY JR. V., TRUPL J., ILAVSKA I., HELPIANSKA L., DRGONA L., SALEK T., MARDIAK J., KUKUCKOVA E., STUDENA M., PICHNA P., ORAVCOVA E., GREY E., KOREN P., MINARIK T., LACKA J., SUFLIARSKY J.

One hundred twenty three breakthrough bacteraemias (BB) during 5 years in a National Cancer Institute, among 9986 admissions and 979 bacteraemic episodes were analysed. 123 BB were caused by 323 microbes, only 116 were resistant (31.5 %) to currently administered antimicrobials. Sixty seven of 123 bacteraemic episodes were catheter associated confirmed by isolation of the same organisms from the blood and catheter tip. 77/123 BE were polymicrobial. The most frequently isolated strains were coagulase negative staphylococci (30.5 %), Corynebacteria (10 %), Ps. aeruginosa (10 %), Str. faecalis (9 %) and Viridans streptococci (8.5 %). Gram-positive aerobes accounted for two-thirds of all organisms isolated during breakthrough bacteraemic and fungaemic episodes. Mixed polymicrobial breakthrough bacteraemic and fungaemic episodes were more frequently associated with vascular catheter insertion and neutropenia, and had a less favourable outcome in comparison to monomicrobial infections. The relapse was associated more frequently with catheter related bacteraemic and fungaemic episodes, but the overall mortality rate was similar independently from catheter insertion. Breakthrough bacteraemic and fungaemic episodes were associated more frequently with acute leukaemia. Polymicrobial breakthrough bacteraemic and fungaemic episodes were associated more frequently in neutropenic episodes and in venous catheters.
Regarding the outcome, an extraction of the catheter with no dependence on variable and modification of antimicrobial therapy were essential for the improvement in the prognosis. (Tab. 5, Ref. 20.)
Key words: bacteraemia, fungaemia, antimicrobial prophylaxis, therapy in cancer patients, cancer.

Bratisl Lek Listy 1996; 97: 652–659


IMUNOPATOGENETICKE MECHANIZMY AUTOIMUNITNYCH PROCESOV: PORUCHA REGULACNYCH MECHANIZMOV IMUNUNITY, GENETICKA DETERMINACIA AUTOIMUNITY, EFEKTOROVE MECHANIZMY AUTOIMUNITNYCH PROCESOV A ICH TERAPEUTICKE OVPLYVNENIE

IMMUNOPATHOGENIC MECHANISMS OF AUTOIMMUNE PROCESSES: BREAKDOWN OF REGULATORY MECHANISMS OF IMMUNITY, GENETIC DETERMINATION OF AUTOIMMUNITY, EFFECTOR MECHANISMS OF AUTOIMMUNE PROCESSES AND THEIR THERAPY

BUC M.

Autoimmune diseases represent a great social and medical problem. 5 to 7 % of population suffer from these chronic debilitating disorders. Our knowledge about the immune system and the genetic determination of its components and processes has considerably increased in the fast few years. The purpose of the two articles on autoimunity published in the previous and this issue is to offer a reader a topical status of the development in this field. Autoantigens, their presentation to T lymphocytes and superantigens were discussed in the first article. The breakdown of regulatory mechanisms of immunity, the genetic basis of autoimmunity, the effector mechanisms responsible for tissue damages and their therapy are reviewed in the presented article. (Tab. 4, Fig. 1.)
Key words: apoptosis, autoimmunity, cytokines, HLA complex, hormones and immunity, immunocomplexes, subpopulations of T and B lymphocytes, T-cell vaccination.

Bratisl Lek Listy 1996; 97: 660–668


INTRAKAVITARNY TROMBUS – NEOBVYKLA KOMPLIKACIA PRI ULCEROZNEJ KOLITIDE

INTRACAVITARY THROMBOSIS – AN UNUSUAL COMPLICATION OF CROHN'S DISEASE

SASVARY F., MURIN J., DURIS I., PONTUCH P., SEDLAK T., LABAS P.

The statement of echocardiographic differential diagnosis of intracavitary masses is not simple even for an experienced echocardiographist. It is mainly caused by the resemblance in echo-densities of thrombi and myxoma. Atypical localization of masses makes the differential diagnosis even more difficult.
Authors report a case of a 30 year-old man with the history of ulcerative colitis, in whom sepsis occured as a complication of an inflammatory bowel disease. They report the diagnosis of thrombus in the right atrium, probably of infectious genesis, formed on the endocardium which had been damaged by a catheter tip and potenciated by activated coagulatory system.
In the documented period, histological examinations of colonoscopic and peroperative biopsies were performed repetitively. Neither these examinations answered the question of differential diagnosis between ulcerative colitis and Crohn's disease.
The authors report an echocardiographic diagnosis and they follow-up the genesis and subsequent disappearance of the pathological mass in the right atrium which was finally diagnosed as a thrombus. The final diagnosis was based on the clinical follow-up and disappearance of the mass. (Fig. 3, Ref. 7.)
Key words: inflammatory bowel disease, thrombosis, echocardiography, parenteral nutrition.

Bratisl Lek Listy 1996; 97: 669–672


MIESTO PENICILINOV V LIECBE INFEKCII RESPIRACNEHO SYSTEMU

THE ROLE OF PENICILLINS IN THE THERAPY OF RESPIRATORY TRACT INFECTIONS

LACKA J., STRAKOVA A., GREY E., KRALOVICOVA K., KRCMERY Jr. V.

The development of antimicrobial resistance in main pathogens of respiratory system infections (S. pneumoniae, H. Influenzae, B. catarrhalis) reduces the range of unprotected penicillins indications. The inhibitors of beta-lactamase rendered back the original spectrum of antimicrobial activity to aminopenicillins and ureidopenicillins, and withheld them within the most frequently used armamentarium of antimicrobial drugs for the therapy of more severe infections. The prescription of penicillins is ruled according to the localization of infection, most frequent pathogens and by the epidemiologic situation. A combined antibiotic therapy is indicated in severe infections. An important indication area is the prophylactic administration of penicillins in recurring tonsilopharynigitis, recurring otitis media and eradication of meningococcal carriership. (Tab. 1, Ref. 3.)
Key words: penicillins, beta-lactamase inhibitor, respiratory tract infections.

Bratisl Lek Listy 1996; 97: 673–674


ETIOLOGY OF BACTERAEMIA IN PATIENTS WITH VARIOUS MALIGNANCIES: IS THERE ASSOCIATION BETWEEN CERTAIN ANTINEOPLASTIC DRUGS AND MICROORGANISM?

ETIOLOGIA BAKTERIEMIE PRI ROZNYCH MALIGNYCH OCHORENIACH: EXISTUJE SPOJENIE MEDZI URCITYMI ANTINEOPLASTIKAMI A MIKROORGANIZMAMI?

BALAZ M., DEMITROVICOVA A., SPANIK S., DRGONA L., KRUPOVA I., GRAUSOVA S., KRALOVICOVA K., KRCHNAKOVA A., TRUPL J., KUNOVA A., KRCMERY Jr. V.

The authors studied a relationship between particular bacterial or fungal organisms isolated from blood cultures and type of malignancy and antineoplastic drugs in 237 cancer patients. Sixty four had acute myelogenous leukemia (AML), 43 non-Hodgkin's lymphoma (NHL) and 140 solid tumors (ST). All patients had at least one positive blood cultures for one or more microorganism drawn during 1–10 days after cytotoxic chemotherapy. viridans streptococcal bacteremia was more frequently observed in patients with AML (12.5 %) and NHL (27.9 %) than ST (4.3 %, p<0.01 and 0.03). The incidence of anaerobic bacteria was similar in patients with NHL and ST, and in both groups significantly higher (p<0.05) than in AML. Enterobacteriaceae caused bacteremia less frequently in patients with AML than in those with ST (12.5 vs 27.8 %, p<0.05) . However, the highest incidence of Stenotrophomonas maltophilia bacteremia was seen in patients with AML (6.3 % vs 2.3 %, p<0.04 and 0.03). Concerning fungemia, Candida albicans occurred significantly more frequently in blood cultures in patients with NHL, and molds in patients with AML. Cytarabine and metothrexate seems to be more frequently associated with viridans streptococci, cytarabine and mitoxanthrone with Stenotrophomonas maltophilia, B. fragilis with cisplatin and 5-fluorouracil, Fusarium spp., Mucorales and Aspergillus spp. with acute leukaemia (AL) treated with cytarabine and mitoxantrone. The association of other pathogens with an underlying disease or chemotherapeutic regimen could not be documented. (Tab. 1, Ref. 19.)
Key words: bacteramia, various malignancies, antineoplastic drugs, microorganism.

Bratisl Lek Listy 1996; 97: 675–679


DO LOW VANCOMYCINE SERUM LEVELS PREDICT FAILURES OF VANCOMYCINE THERAPY IN NEUTROPENIC CANCER PATIENTS?

MOZNO PREDPOVEDAT NEUSPESNOST TERAPIE VANKOMYCINOM U NEUTROPENICKYCH ONKOLOGICKYCH PACIENTOV NA ZAKLADE NIZKYCH HLADIN VANKOMYCINU V SERE?

NETRIOVA J., HALKO J., STUDENA-MRAZOVA M., KUKUCKOVA E., STOPKOVA K., KRALOVICOVA K., DEMITROVICOVA A., GRAUSOVA S., KRUPOVA I., TRUPL J., KRCMERY Jr. V.

Vancomycine serum levels were measured in 198 cancer patients with documented grampositive bacteremia and twenty two failed. Failures were analyzed for risk factors of therapy failure. Only 8 of 22 showed low serum peak or through vancomycin levels. One patient was treated less than 7 days, 9 had persisting and 4 catheter associated bacteremia. Bacteremias due to VAN resistant strains were excluded.
In 14 out of 22 patients, multiple or one risk factor could be determined, but in 8 patients, no risk factor was found. Hence the, case control study was conducted to compare the group of failures in 22 patients with a group of patients with underlying disease and neutropenia treated successfully within the same period and same antibiotic policy at the same cancer center, by VAN for gram-positive bacteremia. Persisting, catheter associated and enterococcal bacteremias were the only statistical significant risk factors predicting a therapy failure in cancer patients. Neither Vancomycine serum peak nor through levels predicted the outcome: failure or cure of gram-positive bacteremia in cancer patients. (Tab. 1, Ref. 5.)
Key words: Vancomycine, serum level, bacteraemia, cancer, neutropenic cancer patients.

Bratisl Lek Listy 1996; 97: 680–683


BACTEREMIA IN CANCER PATIENTS WITH SOLID TUMORS UNDERGOING CHEMOTHERAPY VERSUS SURGERY: RISK FACTORS, ETIOLOGY AND OUTCOME IN 276 PATIENTS

BAKTERIEMIA U ONKOLOGICKYCH PACIENTOV SO SOLIDNYMI NADORMI PODROBENYCH CHEMOTERAPII VERSUS CHIRURGICKEJ LIECBE: RIZIKOVE FAKTORY, ETIOLOGIA A VYSLEDKY LIECBY U 276 PACIENTOV

GRAUSOVA S., KRCMERY Jr. V., STOPKOVA K., KOREN P., SEPESI J.

Risk factors, etiology, symptomatology and outcome of bacteremia in 276 patients with solid tumors were evaluated. A group of 78 patients with solid tumors and surgical therapy was compared with 172 patients with solid tumors but treated solely by chemotherapy. The most frequently observed risk factors of bacteremia in patients after surgery were the vascular and urinary catheter insertions, wound as source of bacteremia, staphylococci, enterococci and Enterobacteriaceae as etiologic agents. Comparing the group of therapeutically treated patients with solid tumors, with the group of those treated only by chemotherapy, a statistically significant difference in risk factors between both groups was observed only in the incidence of catheter insertion (more frequently in surgically treated patients), neutropenia (more frequently in those treated by chemotherapy). Wound as source of bacteremia was more frequently observed in those after surgery. Enterobacteriaceae and enterococci were significantly more frequently observed in patients with solid tumors treated by surgery. Surprisingly, patients after surgery the mortality due to septic shock was lower in (6.4 % vs 16.9 %, p<0.03) than in the control group of patients with solid tumors treated solely by chemotherapy. (Tab. 1, Ref. 5.)
Key words: chemotherapy, bacteraemia, cancer patients, solid tumor, surgery.

Bratisl Lek Listy 1996; 97: 684–687


MELANOCYTOSIS NEUROCUTANEA

MELANOCYTOSIS NEUROCUTANEA

KOPECKY S., BOLDISOVA O.

An 11-month-old girl with a large "swimming-suit" neavus whose head began to enlarge at the age of 3 months was subdued to sonographic and computer tomographic examinations. The latter revealed a complete obstructive hydrocephalus of all brain ventricles. The section and histologic examinations indicated that the obstruction was caused by extensive melanocytosis of leptomeninges at the cerebellar base, pons and spinal cord thus blocking out the outlets of the IVth brain ventricle. (Fig. 8, Ref. 8.)
Key words: melanocytosis neurocutanea, hydrocephalus, brain, brain ventricle, central nervous system.

Bratisl Lek Listy, 1996: 97: 688–692


VYUZITIE TESTU DOMINANTNE LETALNYCH MUTACII PRE STUDIUM GENETICKEHO RIZIKA KONTINUALNE POSOBIACEHO IONIZUJUCEHO ZIARENIA S NIZKYM DAVKOVYM PRIKONOM

APPLICATION OF THE DOMINANT LETHAL MUTATION TEST IN THE STUDY OF GENETIC RISKS OF CONTINUOUS EXPOSITION TO LOW DOSE RATE IONIZING RADIATION

BREZANI P.

Background: Dissension in data on the effectivity of ionizing radiation at a low-dose rate do not enable to judge the extent of the genetic risk of such exposition. This estimation, however, is especially important in cases of irradiation of female germ cells in which the lesions can cumulate and persist for a long period.
Objectives: The aim of this study is to judge the mutagenic effectivity of continuous irradiation on the basis of a model experiment founded on the test of dominantly lethal mutations.
Methods: Sexually mature female ICR mice were continuously irradiated by gama rays at daily dose rates 0.01 and 0.05 Gy to a total accumulated dose of 1 Gy. The frequency of genetic lesions induced by irradiation in dictyotene oocytes was evaluated by means of the test of dominantly lethal mutations within the periods of 1–2 and 21–22 weeks after the ultimation of irradiation.
Results: Continuous irradiation significantly increased the frequency of dominantly lethal mutations in germ cells of female mice. Induced lesions manifest themselves mostly in form of increased values of preimplantation lethality. The level of dominantly lethal mutations persists on a significantly increased level also in the period of 21–22 weeks after the ultimation of irradiation.
Conclusion: Continuous irradiation of female mice represents a significant risk factor which induces a long-term increase in frequency of genetic lesions in germ cells. The negative selection of lesions in the preimplantation period can be subsequently the cause of decreased reproductive abilities of irradiated animals. (Tab. 1, Fig. 2, Ref. 13.)
Key words: dominant lethal mutations, continuous irradiation, low dose rate, female mice.

Bratisl Lek Listy 1996; 97: 693–696