El presente estudio de caso tuvo como objetivo describir, analizar y comprender las experiencias de las enfermeras en la canalización de vías endovenosas en pacientes pediátricos en un hospital 2019, con un enfoque cualitativo. La muestra estuvo conformada por doce enfermeras que laboran en el servicio de pediatría del Hospital Regional, se determinó por saturación y redundancia incluyendo los criterios de inclusión y exclusión, se utilizó la técnica de recolección de datos, entrevista semiestructurada a profundidad, para el procesamiento de la información se empleó el método del análisis temático. En todo momento se cumplió con los criterios éticos y el rigor científico de la investigación. Entre los resultados se obtuvo que las enfermeras reconocen la expresión de sentimientos positivos a través de gratas experiencias vividas en su quehacer diario durante la canalización endovenosa, lo cual les genera no solo satisfacción profesional y personal sino el bienestar que logra en el paciente haciendo menos daño con menos venopunciones. Se encontró que las enfermeras viven experiencias difíciles y complicadas, les permite generar habilidades como el autocontrol, el entusiasmo, la automotivación, la empatía y dotarlas de defensas para la reacción positiva a la tensión y al estrés; y entre sus experiencias difíciles recurren a la ayuda espiritual como es Dios buscando fe y fortaleza; en la familia del paciente pediátrico buscan el soporte para generar un ambiente de confianza al momento de realizar la canalización y que sea más rápida y menos dolorosa para el paciente. / The objective of this case study was to describe, analyze and understand the experiences of nurses in the cannulation of intravenous lines in pediatric patients in a hospital in 2019, with a qualitative approach. The sample was made up of twelve nurses who work in the pediatric service of the Regional Hospital, it was determined by saturation and redundancy including theinclusion and exclusion criteria, the data collection technique, semi-structured in-depth interview, was used for the processing of The thematic analysis method was used to collect the information. The ethical criteria and scientific rigor of the research were met at all times. Amongthe results, it was obtained that nurses recognize the expression of positive feelings through pleasant experiences in their daily work during intravenous cannulation, which generates not only professional and personal satisfaction but also the well-being that it achieves in the patient,doing less harm. with fewer venipunctures. It was found that nurses live difficult and complicated experiences, allowing them to generate skills such as self-control, enthusiasm, self-motivation, empathy and providing them with defenses for a positive reaction to tension and stress; and among their difficult experiences they turn to spiritual help such as God seeking faithand strength; The family of the pediatric patient seeks support to generate an environment of trust when performing the canalization and to make it faster and less painful for the patient.

Background: The impact of COVID-19 on clinical outcomes in acute ischemic stroke patients receiving reperfusion therapy remains unclear. We therefore aimed to synthesize the available evidence to investigate the safety and short-term efficacy of reperfusion therapy in this patient population. Methods: We searched the electronic databases MEDLINE, Embase and Cochrane Library Reviews for randomized controlled trials and observational studies that investigated the use of intravenous thrombolysis, endovascular therapy, or a combination of both in acute ischemic stroke patients with laboratory-confirmed COVID-19, compared to controls. Our primary safety outcomes included any intracerebral hemorrhage (ICH), symptomatic ICH and all-cause in-hospital mortality. Short-term favorable functional outcomes were assessed at discharge and at 3 months. We calculated pooled risk ratios (RR) and 95% confidence intervals (CI) using DerSimonian and Laird random-effects model. Heterogeneity was evaluated using Cochran’s Q test and I2 statistics. Results: We included 11 studies with a total of 477 COVID-19 positive and 8,092 COVID-19 negative ischemic stroke patients who underwent reperfusion therapy. COVID-19 positive patients exhibited a significantly higher risk of experiencing any ICH (RR 1.54, 95% CI 1.16–2.05, p < 0.001), while the nominally increased risk of symptomatic ICH in these patients did not reach statistical significance (RR 2.04, 95% CI 0.97–4.31; p = 0.06). COVID-19 positive stroke patients also had a significantly higher in-hospital mortality compared to COVID-19 negative stroke patients (RR 2.78, 95% CI 2.15–3.59, p < 0.001). Moreover, COVID-19 positive stroke patients were less likely to achieve a favorable functional outcome at discharge (RR 0.66, 95% CI 0.51–0.86, p < 0.001) compared to COVID-19 negative patients, but this difference was not observed at 3-month follow-up (RR 0.64, 95% CI 0.14–2.91, p = 0.56). Conclusion: COVID-19 appears to have an adverse impact on acute ischemic stroke patients who undergo reperfusion therapy, leading to an elevated risk of any ICH, higher mortality and lower likelihood of favorable functional outcome.

Introduktion: Hepatit C är en global folkhälsoutmaning, med 58 miljoner som lever med kronisk infektion. Sverige har cirka 45 000 diagnostiserade fall, med hög odiagnostiserade förekomst. Hepatit C är ofta asymtomatisk, kan leda till allvarliga leverkomplikationer och död. Hepatit C är en blodsmitta och den vanligaste smittvägen är delade injektionsnålar/utrustning därav är intravenösa missbrukare en grupp som ofta drabbas. Behandlingen mot hepatit C har utvecklats med effektiva antivirala läkemedel sedan 2014, och nya riktlinjer innebär behandling för alla, även de med pågående missbruk. Eliminering av hepatit C är ett globalt hälsomål och kopplas till FN:s Agenda 2030 för hållbar utveckling. Syfte: Syftet med denna litteraturstudie var 1) beskriva olika interventioner som syftar till att eliminera hepatit C bland personer som missbrukar intravenösa droger genom att öka deltagande och 2) utvärdera interventionernas effekter avseende behandlingsdeltagande och behandlingsresultat. Metod: En strukturerad litteraturstudie genomfördes med tematisk analys och deduktiv ansats som analysmetod. Resultatet baseras på tio artiklar som kvalitetsgranskades. Resultat: Två teman identifierades; “Interventioner med fokus att öka delaktighet och deltagande av personer som injicerar droger i hepatit C-interventioner” och “Effekter på behandlingsdeltagande och behandlingsutfall”. Till dessa teman fanns även sex subteman. Resultaten visar att interventioner som inkluderar uppsökande verksamhet och integrerad vård har varit framgångsrika med att engagera personer som injicerar droger i hepatit C-vård. Slutsats: Eliminering av hepatit C är ett globalt mål som kan uppnås genom effektiva interventioner. Framgångsrik implementering av interventioner kräver ökad tillgänglighet, minskade hinder och förtroendeskapande interaktion. Det krävs fortsatt utveckling och breddning av interventioner. / Introduction: Hepatitis C is a global public health challenge, with 58 million people living with a chronic infection. Sweden has approximately 45 000 diagnosed cases, with a high prevalence of undiagnosed cases. Hepatitis C is often asymptomatic, can lead to severe liver complications and death. Hepatitis C is a bloodborne infection, and the most common route of transmissions is through shared injection needles/equipment hence intravenous drugs users are at a higher risk. Treatment for hepatitis C has evolved with effective antiviral drugs since 2014, and new guidelines advocate treatment for everyone, including those with ongoing substance abuse. Eliminating hepatitis C is a global health goal linked to the UN’s Agenda 2030 for sustainable development. Aim: The aim of this literature review was 1) to describe various interventions used to attempt the eradicate of hepatitis C among people who inject drugs, and 2) to evaluate the effects of the interventions in terms of treatment participation and treatment outcomes. Method: A structured literature review was conducted using thematic analysis with a deductive approach as the analysis method. The results are based on ten quality-reviewed articles. Results: Two themes were identified: "Interventions with a focus on increasing involvement and participation of people who inject drugs in hepatitis C interventions" and "Effects on treatmeant participation and treatment outcomes." Six subthemes also emerged within these themes. The results indicate that interventions involving outreach and integrated care have been successful in engaging people who inject drugs in hepatitis C care. Conclusion: Elimination of hepatitis C is a global goal achievable through effective interventions. Successful implementation requires increased accessibility, reduced barriers, and trust-building interaction. Continued development and expansion of interventions are necessary.

Η παρουσία σοβαρού ισχαιμικού πόνου πριν από τον ακρωτηριασμό κάτω άκρου πολύ συχνά συνοδεύεται από την ανάπτυξη πόνου φάντασμα. Ερευνήσαμε αν η εντατική περιεγχειρητική αναλγησία μειώνει την ανάπτυξη πόνου φάντασμα 6 μήνες μετά τον ακρωτηριασμό. Μεθοδολογία: Σε συνολικά 65 ασθενείς πραγματοποιήθηκε προγραμματισμένος ακρωτηριασμός κάτω άκρου. Οι ασθενείς τυχαιοποιήθηκαν σε 5 ομάδες αναλγησίας: (1) Οι ασθενείς της ομάδας Επι/Επι/Επι έλαβαν περιεγχειρητικά επισκληρίδια αναλγησία και επισκληρίδιο αναισθησία; (2) Οι ασθενείς της ομάδας PCA/Επι/Επι έλαβαν προεγχειρητικά ενδοφλέβια αναλγησία ελεγχόμενη από τον ασθενή (Patient Controlled Analgesia-PCA), μετεγχειρητικά επισκληρίδιο αναλγησία και επισκηρίδιο αναισθησία; (3) Οι ασθενείς της ομάδας PCA/Επι/PCA έλαβαν περιεγχειρητικά ενδοφλέβια PCA και επισκληρίδιο αναισθησία; (4) Οι ασθενείς της ομάδας PCA/ΓΑ/PCA έλαβαν περιεγχειρητικά ενδοφλέβια PCA και γενική αναισθησία (ΓΑ); (5) Οι ασθενείς της ομάδας ελέγχου έλαβαν συμβατική αναλγησία και ΓΑ. Η επισκηρίδιος αναλγησία ή η ενδοφλέβια PCA ξεκινούσε 48 ώρες προεγχειρητικά και συνεχιζόταν για 48 ώρες μετεγχειρητικά. Τα αποτελέσματα της κλίμακας πόνου VAS (Visual Analogue Scale) και της κλίμακας πόνου McGill καταγραφόταν περιεγχειρητικά και στον 1 και 6 μήνες. Αποτελέσματα: Στους 6 μήνες, η ενδιάμεσες (median) τιμές (ελάχιστη-μέγιστη, minimum–maximum) του πόνου φάντασμα (Phantom Limb Pain – PLP) και οι τιμές P (ομάδες παρέμβασης έναντι ομάδας ελέγχου) για την κλίμακα πόνου VAS (Visual Analogue Scale) ήταν οι ακόλουθες: 0 (0–20) για την ομάδα Επι/Επι/Επι (P = 0.001), 0 (0–42) για την ομάδα PCA/Επι/Επι (P = 0.014), 20 (0–40) για την ομάδα PCA/Επι/PCA (P = 0.532), 0 (0–30) για την ομάδα PCA/ΓΑ/ PCA (P = 0.008), και 20 (0–58) για την ομάδα ελέγχου. Οι τιμές για την κλίμακα πόνου McGill (McGill Pain Questionnaire) ήταν οι ακόλουθες: 0 (0–7) για την ομάδα Επι/Επι/Επι (P = 0.001), 0 (0–9) για την ομάδα PCA/Επι/Επι (P = 0.003), 6 (0–11) για την ομάδα PCA/Επι/PCA (P = 0.208), 0 (0–9) για την ομάδα PCA/ΓΑ/PCA (P = 0.003), και 7 (0–15) για την ομάδα ελέγχου. Στους 6 μήνες πόνος φάντασμα παρουσιάστηκε σε 1 από τους 13 ασθενείς της ομάδας Επι/Επι/Επι, σε 4 από τους 13 ασθενείς της ομάδας PCA/Επι/Επι, και σε 3 από τους 13 ασθενείς της ομάδας PCA/ΓΑ/PCA έναντι 9 από τους 12 ασθενείς της ομάδας ελέγχου (P=0.001, P=0.027, και P=0.009, αντίστοιχα). Ο πόνος κολοβώματος στους 6 μήνες ήταν ασήμαντος. Συμπεράσματα: Η χρήση εντατικήςς αναλγησίας, με χρήση επισκληριδίου ή ενδοφλέβιας PCA, η οποία ξεκινάει 48 ώρες προεγχειρητικά και συνεχίζεται για 48 ώρες μετεγχειρητικά, μειώνει τον πόνο φάντασμα στους 6 μήνες. Trial registration: Clinical Trials.gov, number NCT00443404 / Severe preamputation pain is associated with phantom limb pain (PLP) development in limb amputees. We investigated whether optimized perioperative analgesia reduces PLP at 6-month follow-up. Methods: A total of 65 patients underwent lower-limb amputation and were assigned to five analgesic regimens: (1) Epi/Epi/Epi patients received perioperative epidural analgesia and epidural anesthesia; (2) PCA/Epi/Epi patients received preoperative intravenous patient-controlled analgesia (PCA), postoperative epidural analgesia, and epidural anesthesia; (3) PCA/Epi/PCA patients received perioperative intravenous PCA and epidural anesthesia; (4) PCA/GA/PCA patients received perioperative intravenous PCA and general anesthesia (GA); (5) controls received conventional analgesia and GA. Epidural analgesia or intravenous PCA started 48 h preoperatively and continued 48 h postoperatively. The results of the visual analog scale and the McGill Pain Questionnaire were recorded perioperatively and at 1 and 6 months. Results: At 6 months, median (minimum–maximum) PLP and P values (intervention groups vs. control group) for the visual analog scale were as follows: 0 (0–20) for Epi/Epi/Epi (P _ 0.001), 0 (0–42) for PCA/Epi/Epi (P = 0.014), 20 (0–40) for PCA/Epi/PCA (P = 0.532), 0 (0–30) for PCA/GA/ PCA (P = 0.008), and 20 (0–58) for controls. The values for the McGill Pain Questionnaire were as follows: 0 (0–7) for Epi/Epi/Epi (P = 0.001), 0 (0–9) for PCA/Epi/Epi (P = 0.003), 6 (0–11) for PCA/Epi/PCA (P = 0.208), 0 (0–9) for PCA/GA/PCA (P = 0.003), and 7 (0–15) for controls. At 6 months, PLP was present in 1 of 13 Epi/Epi/Epi, 4 of 13 PCA/Epi/Epi, and 3 of 13 PCA/GA/PCA patients versus 9 of 12 control patients (P=0.001, P=0.027, and P=0.009, respectively). Residual limb pain at 6 months was insignificant. Conclusions: Optimized epidural analgesia or intravenous PCA, starting 48 h preoperatively and continuing for 48 h postoperatively, decreases PLP at 6 months. Trial registration: Clinical Trials.gov, number NCT00443404

A quantitative research design for a descriptive and contextual study to determine the critical care nurses knowledge and data preferences regarding the central venous and pulmonary artery catheters management and decision making after coronary arte.y bypass graft operations and the utmzation period of the pulmonary artery catheter after coronary artery bypass graft operations. The data was collected through a questionnaire completed by critical care nurses and retrospective analysis of patient records through a structured checklist. Data analysis indicated the following: critical care nurses have a knowledge deficit in the management of the central venous and pulmonary artery catheters and felt more competent and confident in the central venous measurements. The utilization period of the pulmonary artery catheter was 48% compared to the 100% of the central venous catheter. / Advanced Nursing Science / M.A. (Advanced Nursing Science)

Introduction : Chez les nouveau-nés prématurés, l’hyper-alimentation intraveineuse (HAIV) contribue à leur survie, mais elle est aussi une source importante de molécules oxydantes. L’absence d’une protection adéquate contre la lumière ambiante génère in vitro, via la photo-excitation de la riboflavine, du H2O2, des peroxydes organiques et un dérivé peroxydé de la vitamine C, l’ascorbylperoxyde (AscOOH). Plusieurs données du laboratoire associent l’infusion d’HAIV à des désordres lipidiques dans notre modèle animal. L’hypothèse est donc que l’AscOOH a un pouvoir oxydant et est responsable de certains des effets biologiques observés. Mes objectifs sont les suivants : 1) développer une méthode de dosage de l’AscOOH; 2) démontrer, à l’aide du modèle animal bien établi au laboratoire, des relations entre la concentration tissulaire de cette molécule et des paramètres métaboliques et l’état redox au foie et dans la circulation; et 3) confirmer l’effet physiologique de l’AscOOH dans un modèle cellulaire. Méthode : Différents étalons internes potentiels ont été testés pour le dosage de l’AscOOH par spectrométrie de masse après séparation sur HPLC (LC-MS). Les phases mobiles et conditions chromatographiques ont été optimisées. Pour l’objectif 2, des cobayes de 3 jours de vie (n=11) ont reçu par voie intraveineuse une dose d’AscOOH (entre 0 et 3,3mM). Les animaux ont été sacrifiés au 4e jour de traitement pour le prélèvement de tissus. Les concentrations tissulaires d’AscOOH ont été déterminées au LC-MS. La triglycéridémie et la cholestérolémie ont été mesurées à l’aide d’un kit commercial par spectrophotométrie. Le glutathion oxydé et réduit ont été mesurés par électrophorèse capillaire. Les relations linéaires obtenues sont exprimées par le ratio des carrés (r2), et traitées par ANOVA. Résultats : La validation du dosage de l’AscOOH par LC-MS a été réalisée. Chez les animaux, la concentration urinaire d’AscOOH par créatinine corrèle positivement avec la dose reçue, négativement avec la lipidémie, et négativement avec le redox sanguin et érythrocytaire, indiquant un milieu moins oxydé. Conclusion : La concentration urinaire d’AscOOH peut donc être un reflet de l’oxydation de l’HAIV en clinique. Nos données chez l’animal suggèrent une interaction de l’AscOOH avec le métabolisme hépatique produisant une chute de la concentration plasmatique de cholestérol et de triglycérides. Le modèle cellulaire n’a pas permis d’élucider le mécanisme moléculaire de l’action de l’AscOOH sur le métabolisme. / Introduction: Intravenous hyperalimentation (IVHA) often contributes to the survival of preterm newborns, but it is also an important source of oxidizing molecules. The lack of adequate protection from ambient light generates, in vitro, through the photo-excitation of riboflavin, H2O2, organic peroxides and a peroxidated derivative of vitamin C: ascorbylperoxide (AscOOH). Certain data from our laboratory linked the infusion of IVHA to lipid disorders in our animal model. The hypothesis is that AscOOH is an oxidant that is responsible for some of the biological effects observed. My objectives are: 1) to develop a method for quantitation of AscOOH, 2) to demonstrate, using the guinea pig model used by our laboratory, relations between the tissue concentration of this molecule and metabolic and redox parameters in the liver and plasma, and 3) to confirm the physiological effect of AscOOH in a cell culture model. Method: Different promising internal standards were tested for AscOOH quantitation by mass spectrometry after HPLC separation (LC-MS). Mobile phases and chromatography conditions have been optimized. For objective #2, 3 days old guinea pig pups (n = 11) received an intravenous dose of AscOOH (between 0 and 3.3mM). Animals were sacrificed on the 4th day of treatment for tissue gathering. Tissues AscOOH concentrations were determined by LC-MS. The triglyceride and cholesterol levels were measured by spectrophotometry using a commercial kit. The oxidized and reduced glutathione were measured by capillary electrophoresis. The linear relations obtained are expressed by the square of the correlation coefficient (r2), and processed by ANOVA. Results: The validation of the LC-MS method for AscOOH quantification has been achieved. In animals, the concentration of urinary AscOOH by creatinine correlates positively with the dose received, negatively with blood lipids, and negatively with blood and erythrocyte redox, indicating a less oxidized environment. Conclusion: The urinary AscOOH concentration may be a good indicator of the oxidation state of clinical IVHA. Our data in animals suggest an interaction between AscOOH and liver metabolism producing a drop in plasma concentration of cholesterol and triglycerides. The cell model was not able to clarify the molecular mechanism of AscOOH action on metabolism.

This thesis deals with a part of the treatment process in patients with acute ischemic stroke. Specifically, it examines the time interval from patient entry to a healthcare facility to initiation of treatment with intravenous thrombolysis - so called Door-to- Needle Time. The theoretical part describes the stroke and its division according to etiology. Furthermore, there are summarized clinical studies that have taken place in the world since the 1960s to the present, the development of care for patients with stroke in Czech Republic, recommended procedures of professional organizations in Czech Republic and the identification and management of treatment of stroke patients. In conclusion, the theoretical part summarizes the studies focused on the reduction of the Door-to-Needle Time, which took place in the world and in the Czech Republic. The aim of the practical part is to evaluate work procedures and conditions of health teams of individual stroke centers and to identify causes of Door-to-Needle Time median differences. The chosen method of research is a quantitative questionnaire survey in the form of an online Google Forms questionnaire sent to the leading members of these teams. Based on the research results, factors affecting reduction of Door-to-Needle Time median consists in to deepen and...

Introdução: O Cateter Central de Inserção Periférica (CCIP) é um dispositivo vascular central inserido através de veias periféricas que permite a infusão de soluções hiperosmolares e medicações por tempo prolongado. Complicações mecânicas e infecciosas podem ocorrer com seu uso, resultando em remoção não eletiva do cateter. Um escore de risco para remoção não eletiva do CCIP que considere conjuntamente o valor prognóstico ponderado de diversos fatores de risco representa uma ferramenta valiosa para o planejamento do cuidado de enfermagem com enfoque na prevenção ou atenuação dos fatores identificados, e consequente melhoria da qualidade da assistência. Objetivo: Elaborar um escore de risco para remoção não eletiva do cateter central de inserção periférica em neonatos. Método: Estudo de coorte com coleta prospectiva de dados realizado no período de 31 de agosto de 2010 a 30 de agosto de 2012 com 436 recém-nascidos internados em uma unidade de terapia intensiva neonatal de um hospital terciário em São Paulo submetidos à instalação de 524 CCIPs. As variáveis relacionadas às características clínicas do neonato, à técnica de inserção do cateter e à terapia intravenosa que indicou a instalação do CCIP foram analisadas quanto ao seu potencial preditivo para remoção não eletiva do CCIP através de análise bivariada, e posterior regressão logística. O escore de risco ponderado foi construído baseado na razão de chances das variáveis preditoras e sua acurácia foi avaliada através da área sob a curva ROC (Receiver Operating Characteristic). Resultados: O escore de risco foi composto pelos seguintes fatores de risco: diagnóstico de transtorno transitório do metabolismo (hipoglicemia, hiperglicemia, distúrbios do cálcio, magnésio, sódio e potássio), inserção prévia do CCIP, uso do CCIP 2.0 French de poliuretano com dupla via, infusão de múltiplas soluções endovenosas através do CCIP 1.9 French de silicone com única via, e posição não central da ponta do CCIP. Sua acurácia foi de 0,76 [IC 95%: 0,73-0,78]. Sua aplicação permitiu classificar os recém-nascidos em três categorias de risco: baixo (0 a 3 pontos), moderado (4 a 8 pontos) e alto ( 9 pontos) risco para remoção não eletiva. Conclusão: Recomenda-se a adoção de estratégias preventivas da remoção não eletiva do CCIP baseadas em evidência de acordo com a classificação e fatores de risco do recém-nascido. Além disso, sugere-se evitar a inserção de múltiplos cateteres, a posição não central da ponta do CCIP, e a instalação de cateteres de silicone de única via para a administração de cinco ou mais classes de soluções endovenosas. / Background: Peripherally Inserted Central Catheter (PICC) is a central vascular access device inserted via cannulation of a peripheral vein that allows the infusion of hyperosmolar solutions and medications over a prolonged dwell time. Mechanical and infectious complications can result from its use leading to nonelective removal of the device. A risk score for nonelective removal of PICC-lines that considers jointly a weighted prognostic value of several risk factors can represent a valuable tool for planning the nursing care focused on preventing or modifying identified risk factors, and thereby improving the quality of care. Aim: To develop a risk score for nonelective removal of PICCs in infants. Methods: A cohort study with prospective data collection between August 31, 2010 and August 30, 2012 in 436 infants admitted to a tertiary-level neonatal intensive care unit in São Paulo and submitted to 524PICC insertions. Variables related to the clinical characteristics of the neonate, the technique of catheter insertion, and intravenous therapy that indicated PICC were analysed for their nonelective predictive potential through bivariate analysis, followed by a logistic regression. Predictors were weighted points proportional to their odds ratio in order to develop the risk score. The accuracy of the risk score model was examined by calculating the area under the receiver operating curve (AUC). Results: The risk score was composed of the following risk factors: diagnose of transitory metabolic disorders (hyperglycaemia, hypoglycaemia, disorders of calcium, magnesium, sodium or potassium), previous PICC line insertion, insertion of 2.0 French dual-lumen polyurethane PICC, noncentral tip position, and multiple intravenous solutions in a 1.9 French single-lumen silicone PICC. The accuracy of the risk score was of AUC=0.76 [IC 95%: 0.73-0.78]. Its application allowed classify newborns into three nonelective removal risk categories: a low-risk group (0-3 points), a moderate-risk group (4-8 points), and a high-risk group ( 9 points). Conclusion: It is recommended the adoption of evidence-based preventive measures according to the classification and risk factors of the newborn in order to avoid nonelective removal of PICC. The avoidance of repeated PICC insertions, noncentral tip position, and placement of single-lumen silicone PICCs for administration of five or more intravenous solutions is suggested.

Com a finalidade de estudar a soroprevalência do Vírus da Imunodeficiência Humana, HIV, e infecções com transmissão relacionadas, entrevistamos e colhemos sangue de 197 usuários de drogas injetáveis, UDIs, amostrados através da metodologia de \"bola de neve\" (snow-balling), da cidade de Santos, São Paulo, Brasil. Nesta cidade a estimativa de UDIs, 10.000 indivíduos, compreende cerca de 2% de sua população. Soroprevalências de HIV, hepatites B e C, sífilis e HTLV (1 ou 2) foram obtidas e comparadas com 197 doadores de sangue pareados por idade e sexo. As soroprevalências encontradas foram de 62% para HIV, 75% para HCV, 75% para HBV, 34% para sífilis, e 25% para o HTLV (1 e 2) entre os UDIs, comparado com 0%; 2%; 23%; 12% e 1% entre os doadores do banco de sangue, respectivamente. Os fatores de risco para transmissões parenterais nesta comunidade de UDIs são mais importantes que para transmissão sexual, embora a última deva ser considerada quando se planejar estratégias de controle. Além disso, estimamos a Razão de Reprodutibilidade Basal, R0, para o HIV entre os UDIs. Usando um modelo clássico para infecções transmitidas por vetores de Macdonald adaptado para \"agulhas\", o valor de R0 foi estimado em 28 e 98, considerando uma distribuição dos inóculos infectantes como homogênea ou heterogênea respectivamente . Esta estimativa foi baseada somente em parâmetros de transmissão parenteral nesta comunidade de UDIs. Usando este modelo a estimativa da soroprevalência do HIV no equilíbrio (0,67) é bem próxima à soroprevalência observada (0,62). / In order to study the seroprevalence of HIV and infections with related transmission patterns, as hepatitis B and C, syphilis and HTLV (1 and 2), we interviewed and bled 197 IDUs, sampled by snow-balling and compared with 197 blood donors matched for age and sex, both groups from the city of Santos, Sao Paulo, Brazil. Seroprevalences found were 62% for HIV, 75% for HCV, 75% for HBV, 34% for syphilis and 25% for HTLV (1 or 2) among IDUs, which compare with 0.0%, 2%, 23%, 12%, and 1% for blood donors, respectively. The risk for parenterally transmitted infections in this IDUs community is higher than that for sexually transmitted one. We also estimated the Basic Reproduction Ratio, R0, for HIV among IDUs. Using a model adapted from the classical Macdonald\'s model for vector-born infection, the R0 resulted in 28 and 98, assuming an homogeneous or heterogeneous distribution of infective inoculae, respectively. This estimation was based only on parenteral transmission. Using this model the expected equilibrium for HIV seroprevalence (0.67) is close to the observed seroprevalence (0.62)

Com a finalidade de estudar a soroprevalência do Vírus da Imunodeficiência Humana, HIV, e infecções com transmissão relacionadas, entrevistamos e colhemos sangue de 197 usuários de drogas injetáveis, UDIs, amostrados através da metodologia de \"bola de neve\" (snow-balling), da cidade de Santos, São Paulo, Brasil. Nesta cidade a estimativa de UDIs, 10.000 indivíduos, compreende cerca de 2% de sua população. Soroprevalências de HIV, hepatites B e C, sífilis e HTLV (1 ou 2) foram obtidas e comparadas com 197 doadores de sangue pareados por idade e sexo. As soroprevalências encontradas foram de 62% para HIV, 75% para HCV, 75% para HBV, 34% para sífilis, e 25% para o HTLV (1 e 2) entre os UDIs, comparado com 0%; 2%; 23%; 12% e 1% entre os doadores do banco de sangue, respectivamente. Os fatores de risco para transmissões parenterais nesta comunidade de UDIs são mais importantes que para transmissão sexual, embora a última deva ser considerada quando se planejar estratégias de controle. Além disso, estimamos a Razão de Reprodutibilidade Basal, R0, para o HIV entre os UDIs. Usando um modelo clássico para infecções transmitidas por vetores de Macdonald adaptado para \"agulhas\", o valor de R0 foi estimado em 28 e 98, considerando uma distribuição dos inóculos infectantes como homogênea ou heterogênea respectivamente . Esta estimativa foi baseada somente em parâmetros de transmissão parenteral nesta comunidade de UDIs. Usando este modelo a estimativa da soroprevalência do HIV no equilíbrio (0,67) é bem próxima à soroprevalência observada (0,62). / In order to study the seroprevalence of HIV and infections with related transmission patterns, as hepatitis B and C, syphilis and HTLV (1 and 2), we interviewed and bled 197 IDUs, sampled by snow-balling and compared with 197 blood donors matched for age and sex, both groups from the city of Santos, Sao Paulo, Brazil. Seroprevalences found were 62% for HIV, 75% for HCV, 75% for HBV, 34% for syphilis and 25% for HTLV (1 or 2) among IDUs, which compare with 0.0%, 2%, 23%, 12%, and 1% for blood donors, respectively. The risk for parenterally transmitted infections in this IDUs community is higher than that for sexually transmitted one. We also estimated the Basic Reproduction Ratio, R0, for HIV among IDUs. Using a model adapted from the classical Macdonald\'s model for vector-born infection, the R0 resulted in 28 and 98, assuming an homogeneous or heterogeneous distribution of infective inoculae, respectively. This estimation was based only on parenteral transmission. Using this model the expected equilibrium for HIV seroprevalence (0.67) is close to the observed seroprevalence (0.62)