ABSTRACT
Bacterial infections are the most frequent cause of hospitalization in elderly patients. In the early eighties, the advantages of Outpatient parenteral Antibiotic therapy (OPAT) were identified in the United States, and suitable therapeutic programs were established. In order to understand the different ways of managing OPAT, a National OPAT Registry was set up in 2003 in Italy. This study analyzes data concerning bacterial infections in 176 elderly patients including demographics, therapeutic management, clinical response, and side-effects. Bone and joint infections (48.9%) and skin and soft tissue infections (27.8%) were the most common infections treated with OPAT. Teicoplanin (28.9%) and ceftriaxone (22.1%) were the top two antibiotics chosen. OPAT was mainly performed at a hospital infusion center (52.8%). The clinical success rate was high and side-effects were low (12.6% of cases). Management of bacterial infections in the elderly with an outpatient program is effective and safe.
Subject(s)
Ambulatory Care/methods , Anti-Bacterial Agents/administration & dosage , Bacterial Infections/drug therapy , Aged , Aged, 80 and over , Ceftriaxone/administration & dosage , Female , Humans , Infusions, Parenteral , Italy , Male , Teicoplanin/administration & dosageABSTRACT
In the early eighties, the advantages of outpatient parenteral antibiotic therapy (OPAT) (reduced costs, no hospitalization trauma in children, no immobilization syndrome in elderly, reduction in nosocomial infections by multiresistant organisms) were identified in the United States, and suitable therapeutic programs were established. Currently, more than 250,000 patients per year are treated according to an OPAT program. In order to understand the different ways of managing OPAT and its results, a National OPAT Registry was set up in 2003 in Italy. Analysis of data concerning osteomyelitis, septic arthritis, prosthetic joint infection and spondylodiskitis, allowed information to be acquired about 239 cases of bone and joint infections, with particular concern to demographics, therapeutic management, clinical response, and possible side effects. Combination therapy was the first-line choice in 66.9% of cases and frequently intravenous antibiotics were combined with oral ones. Teicoplanin (38%) and ceftriaxone (14.7%), whose pharmacokinetic/pharmacodynamic properties permit once-a-day administration, were the two top antibiotics chosen; fluoroquinolones (ciprofloxacin and levofloxacin) were the most frequently utilized oral drugs. Clinical success, as well as patients' and doctors' satisfaction with the OPAT regimen was high. Side-effects were mild and occurred in 11% of cases. These data confirm that the management of bone and joint infections in an outpatient setting is suitable, effective and safe.
Subject(s)
Ambulatory Care/methods , Anti-Bacterial Agents/administration & dosage , Arthritis, Infectious/therapy , Bone Diseases, Infectious/therapy , Aged , Aged, 80 and over , Anti-Bacterial Agents/adverse effects , Arthritis, Infectious/drug therapy , Bone Diseases, Infectious/drug therapy , Drug Therapy, Combination , Female , Humans , Injections , Italy , Male , Middle Aged , Treatment OutcomeABSTRACT
Between October and December 2000, a region-wide prevalence study of hospital-acquired infections (HAI) was conducted in all public hospitals (59 facilities with ca. 16000 beds; 560000 admission yearly) in Piemonte Region, Italy, and in the one hospital of the neighbouring autonomous region of Valle d'Aosta. The study population comprised a total of 9467 patients hospitalized for at least 24 h. The prevalence of HAI was 7.84%, with marked differences in prevalence among the participating hospitals (range: 0-47.8%). The higher relative frequency of urinary tract infections (UTI; 52.7%) was due to the inclusion of urine cultures obtained on the day of the study from asymptomatic UTI in catheterized patients. A significant correlation was found with major risk factors related to medical procedures (urinary catheter, mechanical ventilation, surgical drainage, intravascular catheters). Patients with HAI were found to be older and to have a greater mean length of stay in hospital. Multiple logistic regression analyses showed that lack of independence, indwelling urinary catheter and mechanical ventilation were the risk factors more significantly associated with HAI. The use of antibiotics, in particular prophylactic agents used in surgery (cephalosporins, glycopeptides), provided an incentive for corrective intervention in antibiotic administration and in training of healthcare workers.
Subject(s)
Cross Infection/epidemiology , Hospitals, Public/statistics & numerical data , Anti-Bacterial Agents/therapeutic use , Cross Infection/diagnosis , Cross Infection/drug therapy , Cross Infection/microbiology , Drug Utilization Review , Female , Hospital Units , Humans , Infection Control Practitioners , Italy/epidemiology , Male , Prevalence , Risk Factors , Sentinel Surveillance , Urinary Tract Infections/diagnosis , Urinary Tract Infections/epidemiology , Urinary Tract Infections/microbiologyABSTRACT
OBJECTIVE: To compare the antiviral activity, safety and tolerability of didanosine dosed once and twice daily when administered in combination with stavudine dosed twice daily in human immunodeficiency virus type 1 (HIV-1)-infected individuals with little or no previous exposure to antiretroviral drugs. DESIGN: Comparative, multicentre, randomized, open-label, short-term study. PATIENTS AND METHODS: Eighty-four HIV-1-infected adults with qualifying baseline CD4 cell counts of 200 to 500 cells/mm3 were included in the study. Of these, 43 patients received once daily didanosine plus twice daily stavudine (group A) and 41 subjects received twice daily didanosine plus twice daily stavudine (group B). The primary efficacy analysis used was the time-averaged difference (TAD) between treatment regimens of variations in plasma HIV-1 RNA levels from baseline over the first 12 weeks of therapy. Plasma HIV-1 RNA levels, CD4 cell counts and adverse events were monitored. RESULTS: At week 12, median HIV-1 RNA variations were -1.18 log10 copies/ml in group A and -0.88 log10 copies/ml in group B. For patients who were followed up to week 24, median variations of HIV-1 RNA levels from baseline were -1.21 log10 copies/ml in group A and -0.78 log10 copies/ml in group B. The TAD between the two treatment groups for variations from baseline plasma HIV-1 RNA levels over the first 12 weeks was 0.10 log10 copies/ml (95% confidence interval, -0.19 to 0.40), indicating equivalence. CONCLUSION: Once daily didanosine plus twice daily stavudine and twice daily didanosine plus twice daily stavudine are equally effective in reducing plasma HIV-1 RNA levels and increasing CD4 cell counts. Both regimens are safe and well tolerated.
Subject(s)
Didanosine/administration & dosage , HIV Infections/drug therapy , HIV-1 , Stavudine/administration & dosage , Adult , Aged , Anti-HIV Agents/administration & dosage , CD4 Lymphocyte Count , Drug Therapy, Combination , Female , HIV Infections/complications , Humans , Male , Middle Aged , RNA, Viral/blood , Reverse Transcriptase Inhibitors/administration & dosage , Risk FactorsABSTRACT
A retrospective survey on the epidemiology of H. Influenzae type b (Hib) meningitis was carried out in seven Italian hospitals. During the period 1987-1991, 95 (16.3%) Hib meningitis cases out of 581 bacterial meningitis cases were observed. The proportion of Hib meningitis was lowest in 1987 (11.3%); elevated in 1988 (17.9%); thereafter it did not change. A male preponderance was observed (Sex ratio 1.6). The age distribution showed that 93.7% of cases occurred in subjects < 5 years, 53.7% of cases in those < 1 year. Although Hib meningitis accounts for a small proportion of all bacterial meningitis, it is also a major problem in Italy in early childhood, because nearly all cases occur in children < 5 years.
Subject(s)
Meningitis, Haemophilus/epidemiology , Child, Preschool , Female , Humans , Infant , Italy/epidemiology , Male , Meningitis, Bacterial/epidemiology , Retrospective StudiesABSTRACT
Seven carriers of the Hepatitis B surface antigen who had acquired a form of chronic hepatitis D in the recent past were treated with lymphoblastoid alpha interferon (IFN) (10 MU three times weekly for 4 months, 6 MU three times weekly for other 8 months, with a 12 month follow-up after treatment). At the beginning of the study, these patients had a chronic active hepatitis with intrahepatic hepatitis D antigen but without signs of cirrhosis. By the end of therapy, five had normal amino-transferases and no trace of HDV-RNA in the serum. In two patients the liver enzymes and viremia relapsed during follow up; biochemical and virologic remission persisted after discontinuation of therapy in the other three patients. In the early non-cirrhotic stage of chronic hepatitis D, IFN may play a more consistent therapeutic role than in the average advanced case of the disease. Cytokine should be used as soon as a diagnosis of progressive hepatitis D is reached.
Subject(s)
Hepatitis D/therapy , Interferon-alpha/therapeutic use , Adult , Female , Hepatitis B Surface Antigens/analysis , Hepatitis D/microbiology , Hepatitis D/pathology , Hepatitis Delta Virus/genetics , Hepatitis Delta Virus/immunology , Hepatitis, Chronic/microbiology , Hepatitis, Chronic/pathology , Hepatitis, Chronic/therapy , Humans , Liver/pathology , Male , Pilot Projects , RNA, Viral/analysis , Time FactorsABSTRACT
The results of infection surveillance in orthopaedics are reported: the high incidence of hospital infections in patients undergoing major surgery, the paucity of microbiological data and the failure to standardise prophylaxis protocols were the most significant findings as well as providing a point of departure for programming future fields of intervention and for redefining the operating framework for continuous infection surveillance.
Subject(s)
Cross Infection/prevention & control , Orthopedics , Adolescent , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/therapeutic use , Child , Cross Infection/etiology , Female , Humans , Male , Middle Aged , Risk Factors , Surgical Wound Infection/etiology , Surgical Wound Infection/prevention & controlABSTRACT
A study was conducted on hospital infections in an emergency surgery ward. The survey lasted one year and confirmed the higher incidence of infections after contaminated and dirty operations. Rates of infection were also high after clean operations due to the large number of subjects at risk among the group examined. The most commonly encountered micro-organisms in the infections of surgical wounds were, in order, E. coli, Str. faecalis and Staph. aureus, the latter being only minimally responsive to the standard antibiotics. Several proposals are advanced for prophylaxis in the attempt to halt the circulation of strains with a multiple resistance to antibiotics.
Subject(s)
Cross Infection/epidemiology , Emergencies , Hospital Departments , Surgery Department, Hospital , Age Factors , Cross Infection/drug therapy , Cross Infection/etiology , Escherichia coli Infections/drug therapy , Escherichia coli Infections/epidemiology , Gastrointestinal Diseases/epidemiology , Gastrointestinal Diseases/etiology , Humans , Length of Stay , Microbial Sensitivity Tests , Risk Factors , Staphylococcal Infections/drug therapy , Staphylococcal Infections/epidemiology , Streptococcal Infections/drug therapy , Streptococcal Infections/epidemiologyABSTRACT
After a brief review of the data on cefotiam in the literature the report presents the results of microbiological research, a preliminary study into the drug's possible actions on phagocytosis and a polycentric clinical study of 93 cases of broncho-pleuro-pulmonary pathology and one sinusitis of the jaw. In vitro cefotiam was found to have an excellent inhibitory effect on gram positive and gram negative bacteria with MICs50 and 90 respectively 0.2 and 0.8 mcg/ml V. Staph. aureus, Str. pyogenes. E. Coli, K. pneumoniae and Pr. mirabilis. A dose-dependent increase in phagocytosis was noted. The clinical response was excellent with 90.43% (88/94) of the cases achieving clinical and radiological cure or very much improved. Cefotiam was very well tolerated with the appearance of 2/94 skin rashes (2.12%). The liver and kidney parameters showed no change at the end of treatment. No increase in enzymuria was noted during treatment with cefotiam.
Subject(s)
Bacteria/drug effects , Cefotaxime/analogs & derivatives , Phagocytosis/drug effects , Absorption , Cefotaxime/metabolism , Cefotaxime/pharmacology , Cefotaxime/therapeutic use , Cefotiam , Drug Evaluation , Drug Stability , Humans , Kinetics , Microbial Sensitivity Tests , Protein Binding/drug effects , Research , Tissue DistributionABSTRACT
The reasons for the use of a fat-soluble drug with an in vitro activity against Brucella spp in the treatment of brucellosis are presented. After a review of the literature a series of 222 cases subjected to various treatments is presented and it is concluded that an RMV-minocycline association offers the best antibacterial and kinetic characteristics.
Subject(s)
Anti-Bacterial Agents/therapeutic use , Brucellosis/drug therapy , Anti-Bacterial Agents/metabolism , Brucellosis/immunology , Drug Evaluation , Drug Therapy, Combination , Female , Humans , Macrophages/metabolism , Male , Neutrophils/metabolismABSTRACT
The significance of blood ammonia levels was assessed in 100 cases of viral hepatitis (82 cases of AVH B end 18 cases of AVH A). No valid correlation was noted between the course of blood ammonia levels and that of clinical symptoms or the other blood chemical parameters considered (transaminase, prothrombin time, bilirubinemia and parameters strictly related to the clinical course).
Subject(s)
Ammonia/blood , Hepatitis A/blood , Hepatitis B/blood , Acute Disease , Alanine Transaminase/blood , Female , Follow-Up Studies , Humans , MaleABSTRACT
Three hundred and forty-four patients at risk for HTLV/LAV infection were examined and seventy-seven were positive at the HTLV III/LAV Ab test. The clinical and laboratory study permitted to diagnose one case of AIDS, 26 cases of ARC and 50 cases of simple positivity at the HTLV III/LAV Ab test.
Subject(s)
Antibodies, Viral/analysis , Deltaretrovirus/immunology , Acquired Immunodeficiency Syndrome/diagnosis , Acquired Immunodeficiency Syndrome/epidemiology , Adolescent , Adult , Cytomegalovirus/immunology , Female , Heroin Dependence/complications , Herpesvirus 4, Human/immunology , Homosexuality , Humans , Italy , Male , Retroviridae Infections/diagnosis , Retroviridae Infections/epidemiology , Risk , Simplexvirus/immunology , Substance-Related Disorders/complicationsABSTRACT
Clinical research was conducted to evaluate the comparative therapeutic efficacy in respiratory pathology of 800 mg X 2 per diem bacampicillin v. 1000 mg X 2 per diem amoxicillin, both orally administered. The results were more or less identical and are interpreted as indicating the better constant absorption of the precursor, hence its higher concentration gradient that produces a higher antibiotic concentration in the lungs.
Subject(s)
Amoxicillin/therapeutic use , Ampicillin/analogs & derivatives , Bacterial Infections/drug therapy , Respiratory Tract Infections/drug therapy , Administration, Oral , Adolescent , Adult , Aged , Amoxicillin/administration & dosage , Ampicillin/administration & dosage , Ampicillin/therapeutic use , Bacteria/isolation & purification , Bronchitis/drug therapy , Bronchopneumonia/drug therapy , Female , Humans , Male , Middle Aged , Respiratory Tract Infections/microbiologyABSTRACT
Urinary enzyme excretion was studied in 56 patients treated with cephalosporins in order to evaluate their potential nephrotoxicity. Only in 4 out of 56 patients (7%) was increased NAG, gamma-GT, AlP excretion seen. A rapid return to normal values was observed just after the end of the therapy.
Subject(s)
Cephalosporins/adverse effects , Enzymes/urine , Kidney/drug effects , Acetylglucosaminidase/urine , Adolescent , Adult , Aged , Alkaline Phosphatase/urine , Cefotaxime/adverse effects , Cefotaxime/analogs & derivatives , Cefotetan , Cefotiam , Cefoxitin/adverse effects , Ceftriaxone/adverse effects , Cephamycins/adverse effects , Cephradine/adverse effects , Cephradine/analogs & derivatives , Child , Female , Humans , Male , Middle Aged , gamma-Glutamyltransferase/urineABSTRACT
In vitro cefoperazone proved more active against the tested gram-negative bacteria than either piperacillin or mezlocillin. When administered in 1 g venous bolus the antibiotic achieved high plasmatic concentrations that were still adequate after 8 hours. 33.2% was excreted by the kidneys and a considerable amount by the biliary way. Cefoperazone produced a clinical cure in 35/36 patients (97.22%). A disulfiram-like effect was noted in 18.18%.
Subject(s)
Cefoperazone/therapeutic use , Bacterial Infections/drug therapy , Bronchitis/drug therapy , Cefoperazone/blood , Cefoperazone/urine , Erysipelas/drug therapy , Humans , Kinetics , Mezlocillin/therapeutic use , Piperacillin/therapeutic use , Tonsillitis/drug therapy , Urinary Tract Infections/drug therapyABSTRACT
The Authors expose the bases of a rational antibiotic therapy according to their experience. They underline the risk of using antibiotics in situations in which they are not strictly necessary. They point out the importance of the dosage, the route of administration, the frequency of doses, the length of treatment and the control of seric drug levels of aminoglycosides, in case of creatinine clearance under 50 ml/min. They shortly review the different antibiotic combination.
Subject(s)
Anti-Bacterial Agents/administration & dosage , Bacterial Infections/drug therapy , Anti-Bacterial Agents/adverse effects , Anti-Bacterial Agents/blood , Brucellosis/drug therapy , Brucellosis/immunology , Complement System Proteins/deficiency , Diagnosis, Differential , Dose-Response Relationship, Drug , Drug Therapy, Combination , Humans , Pneumococcal Infections/drug therapy , Pneumococcal Infections/immunology , Salmonella Infections/drug therapy , Salmonella Infections/immunology , Streptococcal Infections/drug therapy , Streptococcal Infections/immunology , Tuberculosis/drug therapy , Tuberculosis/immunology , Virus Diseases/diagnosisABSTRACT
Certain clinical and epidemiological findings among 2262 AVH patients are reported. The patients were all admitted to the A. di Savoia Hospital for Infectious Diseases in Turin over a two-year period.
Subject(s)
Hepatitis, Viral, Human/epidemiology , Adolescent , Adult , Child , Child, Preschool , Cholestasis/diagnosis , Female , Hepatitis A/pathology , Hepatitis B/pathology , Hepatitis C/pathology , Hepatitis, Viral, Human/pathology , Humans , Infant , Infant, Newborn , Italy , Male , Occupations , Rural Population , Urban PopulationSubject(s)
Bacteria/drug effects , Bacterial Infections/drug therapy , Cephamycins/therapeutic use , Adolescent , Adult , Aged , Cefotetan , Female , Humans , Kinetics , Male , Middle AgedABSTRACT
Ceftriaxone effectively inhibited 332 out of 452 (73.45%) bacterial strains in vitro tests. 291 out of 365 (79.69%) gram negative and 41 out of 87 (47.12%) gram positive strains were inhibited. The tests showed ceftriaxone to be more effective than cephalothin, cephotaxime, cephuroxime, cephamandol and cephoxitin. Kinetic tests showed that cephtriaxone has a plasmatic half life of 7.25 hrs. 24 hours after administration of a 1000 mg venous bolus the drug was still present in the blood. Urinary elimination over a 24 hr. period amounted to means 486.8 mg (48.68%). The drug has liquor transfer capacity. 37 of the 38 patients treated showed complete clinical or clinicobacteriological cure. Improvement was noted in the 38th.