ABSTRACT
OBJECTIVE: To describe and quantify resource use and direct health costs associated with skin and skin structure infections (SSSIs) caused by Gram-positive bacteria in adults receiving outpatient parenteral antimicrobial therapy (OPAT), administered by Hospital at Home units (HaH) in Spain. METHODS: Observational, multicenter, retrospective study. We included patients of both sexes included in the HaH-based OPAT Registry during 2011 to 2017 who were hospitalized due to SSSIs caused by Gram-positive bacteria. Resource use included home visits (nurses and physician), emergency room visits, conventional hospitalization stay, HaH stay and antibiotic treatment. Costs were quantified by multiplying the natural units of the resources by the corresponding unit cost. All costs were updated to 2019 euros. RESULTS: We included 194 episodes in 189 patients from 24 Spanish hospitals. The most frequent main diagnoses were cellulitis (26.8%) and surgical wound infection (24.2%), and 94% of episodes resulted in clinical improvement or cure after treatment. The median HaH stay was 13 days (interquartile range [IR]:8-22.7), and the conventional hospitalization stay was 5 days (IR: 1-10.7). The mean total cost attributable to the complete infectious process was 7,326 (95% confidence interval: 6,316-8,416). CONCLUSIONS: Our results suggest that OPAT administered by HaH is a safe and efficient alternative for the management of these infections and could lead to lower costs compared with hospital admission.
Subject(s)
Anti-Bacterial Agents , Outpatients , Adult , Male , Female , Humans , Retrospective Studies , Financial Stress , Hospitals , Gram-Positive Bacteria , Ambulatory Care/methodsABSTRACT
OBJECTIVE: Clostridioides difficile infection (CDI) is associated with increased hospital stays and mortality and a high likelihood of rehospitalization, leading to increased health resource use and costs. The objective was to estimate the economic burden of recurrent CDI (rCDI). METHODS: Observational, retrospective study carried out in six hospitals. Adults aged ≥18 years with ≥1 confirmed diagnosis (primary or secondary) of rCDI between January 2010 and May 2018 were included. rCDI-related resource use included days of hospital stay (emergency room, ward, isolation and ICU), tests and treatments. For patients with primary diagnosis of rCDI, the complete hospital stay was attributed to rCDI. When diagnosis of rCDI was secondary, hospital stay attributed to rCDI was estimated using 1:1 propensity score matching as the difference in hospital stay compared to controls. Controls were hospitalizations without CDI recorded in the Spanish National Hospital Discharge Database. The cost was calculated by multiplying the natural resource units by the unit cost. Costs (euros) were updated to 2019. RESULTS: We included 282 rCDI episodes (188 as primary diagnosis): 66.31% of patients were aged ≥65 years and 57.80% were female. The mean hospital stay (SD) was 17.18 (23.27) days: 86.17% of rCDI episodes were isolated for a mean (SD) of 10.30 (9.97) days. The total mean cost (95%-CI) per episode was 10,877 (9,499-12,777), of which the hospital stay accounted for 92.56. CONCLUSIONS: There is high cost and resource use associated with rCDI, highlighting the importance of preventing rCDI to the Spanish National Health System.
Subject(s)
Clostridioides difficile , Clostridium Infections , Adolescent , Adult , Clostridioides , Clostridium Infections/epidemiology , Cost of Illness , Female , Hospitalization , Hospitals , Humans , Neoplasm Recurrence, Local , Recurrence , Retrospective StudiesABSTRACT
La exposición a productos químicos con contaminación cutánea y/o ocular es un motivo de consulta a urgencias. Se describen las características (epidemiológicas, toxicológicas, clínicas, terapéuticas y evolutivas) de los pacientes atendidos en un área hospitalaria de descontaminación química, durante un periodo de 18 meses. Fueron 36pacientes, con una media de edad de 42,8 (16,7) años, y de los cuales 24 (66,7%)eran mujeres. Los productos implicados con mayor frecuencia fueron los cáusticos (52,8%), disolventes o desengrasantes (19,4%), pegamentos (13,9%) y sprays de defensa personal (8,3%). Los accidentes domésticos (41,7%) y laborales (36,1%) fueron las causas más frecuentes, pero también hubo agresiones (8,3%) y una tentativa suicida. La afectación fue ocular (75%), cutánea (19,4%) o mixta (2 casos). Un paciente se contaminó la cara al ingerir ácido sulfúrico en un intento de suicidio, y falleció pocas horas más tarde. El tratamiento aplicado inicialmente fue agua, agua y jabón o diphotérine. El seguimiento oftalmológico se realizó en el 100% de los casos con afectación ocular, y tres de ellos presentaron secuelas. También refirió secuelas una de las exposiciones cutáneas (AU)
Exposure to chemicals harmful to the skin and/or eyes is a common reason for seeking emergency care. Our aim was to describe the characteristics of patients treated in the chemical decontamination unit of an area referral hospital. This 18-month descriptive observational study evaluated the epidemiologic, toxicologic, clinical, and therapeutic characteristics of cases treated by a chemical decontamination unit within an emergency department. Thirty-six patients with a mean(SD) age of 42.8 (16.7) years were identified; 24 (66.7%) were women. The chemical products involved were usually caustic substances (52.8%), solvents or degreasers (19.4%), glues (13.9%), or self-defense sprays (8.3%). Accidents in the home (41.7%) or workplace (36.1%) were the most common reasons for chemical contamination; violent attacks accounted for 8.3% of the cases and there was 1 suicide attempt. The eye (75%), skin (19.4%) or both (2 cases) were affected. The patient who committed suicide injured his face when ingesting sulfuric acid and died a few hours later. First aid consisted of rinsing with water, water and soap, or diphoterine. Follow-up eye care was given to all patients whose eyes were contaminated; 3 patients reported persistent eye symptoms. One patient reported a residual skin lesion (AU)
Subject(s)
Humans , Chemical Compound Exposure , Poisoning/therapy , Emergency Treatment/methods , Decontamination , Emergency Medical Services/statistics & numerical dataABSTRACT
Oxidative stress contributes to the pathogenesis of diabetes mellitus and its sequelae nephropathy. The kidneys are especially prone to damage by free radicals. We therefore tested the effect of the flavonoid mixture silymarin, a free radical scavenger, on the activity and gene expression of superoxide dismutase, glutathione peroxidase and catalase, as well as on renal tissue morphology in rats with alloxan-induced diabetes mellitus. Alloxan-intoxicated rats were treated with silymarin 20 days after alloxan administration for 9 weeks. Alloxan-induced tissue damage and decreased the activity of the three enzymes, SOD (U/mg prot.): 14.4±1.75 vs 112±6.45 control, p<0.05, n=6; GSHPx (µM NADPH/min/mg prot.): 0.02±0.002 vs 0.121±0.01 control, p<0.05, n=6; CAT (k/seg/mg prot.): 0.022±0.003 vs 0.044±0.002 control, p<0.05, n=6. Silymarin treatment prevented tissue damage and restored the activity (SOD: 110.7±12.9U/mg prot.; GSHPx: 0.329±0.031 µM NADPH/min/mg prot.; CAT: 0.054±0.002 k/seg/mg prot., n=6) and gene expression of the three antioxidant enzymes after 20 days of alloxan administration (SOD: 12.00±0.57 control, 9.00±0.1 diabetic p<0.05, 11.00±0.20 silymarin treated; GSHPx: 6.01±0.78 control, 9.03±0.3 diabetic p<0.05, 7.02±0.07 silymarin treated; CAT: 9.03±1.07 control, 12.02±0.60 diabetic p<0.05, 8.06±0.31 silymarin treated, n=6). It is suggested in this study that recuperative effect of silymarin on the renal tissue damage induced by alloxan may be related to an increase in the activity and recovery of gene expression of antioxidant enzymes which in addition to the glutathione system constitute some of the most important defense mechanisms against free radicals damage. As these results show, silymarin may be considered potentially in the treatment of diabetic nephropathy.
Subject(s)
Antioxidants/pharmacology , Diabetes Mellitus, Experimental/drug therapy , Diabetic Nephropathies/prevention & control , Kidney/drug effects , Plant Extracts/therapeutic use , Silybum marianum/chemistry , Silymarin/pharmacology , Alloxan , Animals , Antioxidants/metabolism , Antioxidants/therapeutic use , Diabetes Mellitus, Experimental/metabolism , Diabetes Mellitus, Experimental/pathology , Diabetic Nephropathies/chemically induced , Kidney/metabolism , Kidney/pathology , Male , Oxidative Stress/drug effects , Phytotherapy , Plant Extracts/pharmacology , Rats , Rats, Wistar , Silymarin/therapeutic useABSTRACT
No disponible
Subject(s)
Humans , Decontamination/methods , 35514 , Eye , Skin , Chemical Hazard Release , Toxicity Tests , Protective Devices , Environmental ExposureABSTRACT
Alloxan has been widely used to produce experimental diabetes mellitus syndrome. This compound causes necrosis of pancreatic beta-cells and, as is well known, induces oxidant free radicals which play a relevant role in the etiology and pathogenesis of both experimental and human diabetes mellitus. Previously we have reported hypoglycemic and antilipoperoxidative actions of silymarin in serum and pancreatic tissue respectively. The aim of this study was to test whether silymarin could reduce the hyperglycemia and revert the pancreatic damage in alloxan treated rats, tested with silymarin in two protocols: using both compounds simultaneously for four or eight doses, or using the compound 20 days after alloxan administration for 9 weeks. Serum glucose and insulin were determined, and pancreatic fragments were used for histology and insulin immunohistochemistry. Pancreatic islets were isolated to assess insulin and Pdx1 mRNA expression by RT-PCR. Our results showed that 72 hours after alloxan administration, serum glucose increased and serum insulin decreased significantly, whereas pancreatic tissue presented morphological abnormalities such as islet shrinkage, necrotic areas, loss of cell organization, widespread lipoid deposits throughout the exocrine tissue, and loss of beta cells, but insulin and glucagon immunoreactivity was scattered if any. In contrast the pancreatic tissue and both insulin and glucose serum levels of rats treated with silymarin were similar to those of control animals. In addition, insulin and glucagon immunoreactive cells patterns in Langerhans islets were also normal, and normal insulin and Pdx1 mRNA expression patterns were detected during pancreatic recovery in Langerhans islets. The overall results suggest that silymarin induces pancreatic function recovery demonstrated by insulin and glucagon expression protein and normoglycemia after alloxan pancreatic damage in rats.