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1.
J Vasc Access ; 23(4): 532-537, 2022 Jul.
Article in English | MEDLINE | ID: mdl-33618564

ABSTRACT

BACKGROUND: Venous Access Devices (VADs) are the most used devices in COVID-19 patients. OBJECTIVE: Identify VADs implanted, catheter related thrombosis (CRT), catheter-related bloodstream infection (CRBSI), and accidental remove of VADs in both COVID-19 positive and COVID-19 free patients. Successive analysis was conducted comparing COVID-19 positive patients with COVID-19 free with inverse probability propensity score weights using simple regression to account for these two confounders (peripheral tip as central/peripheral and hospitalization as no/yes). METHODS: This multicenter, retrospective cohort study collected data from seven hospitals in Lombardy during the pandemic period from February 21st to May 31st 2020. RESULTS: A total of 2206 VADs were evaluated, 1107 (50.2%) of which were inserted in COVID-19 patients. In COVID-19 cohort the first choice was Long Peripheral Cannula in 388 patients (35.1%) followed by Midline Catheter in 385 (34.8%). The number of "central tip" VADs inserted in COVID-free inpatients and COVID-19 positive were similar (307 vs 334). We recorded 42 (1.9%) CRT; 32 (79.2%) were observed in COVID-19 patients. A total of 19 CRBSI were diagnosed; 15 (78.95%) were observed in COVID-19. Accidental removals were the more represented complication with 123 cases, 85 (69.1%) of them were in COVID-19. COVID-19 significantly predicted occurrence of CRT (OR = 2.00(1.85-5.03); p < 0.001), CRSB (OR = 3.82(1.82-8.97); p < 0.001), and Accidental Removal (OR = 2.39(1.80-3.20); p < 0.001) in our propensity score weighted models. CONCLUSIONS: CRT, CRBSI, and accidental removal are significantly more frequent in COVID-19 patients. Accidental removals are the principal complication, for this reason, the use of subcutaneously anchored securement is recommended for a shorter period than usual.


Subject(s)
COVID-19 , Catheter-Related Infections , Catheterization, Central Venous , Central Venous Catheters , COVID-19/epidemiology , Catheter-Related Infections/epidemiology , Catheterization, Central Venous/adverse effects , Catheters , Humans , Retrospective Studies
2.
J Vasc Access ; 22(6): 997-999, 2021 Nov.
Article in English | MEDLINE | ID: mdl-32669027

ABSTRACT

We describe the case of a coronavirus disease patient with midline who, during ventilation with continuous positive airway pressure helmet with underarm fastening straps, presented thrombosis of the axillary vein in the armpit. The tip of the midline ended in the armpit. The thrombosis has been resolved with anticoagulant therapy with low molecular weight heparin of 100 IU/kg bid without giving pulmonary embolism. In an emergency context like this, the need to resort to ventilation strategies even in departments generally not accustomed to the use of these devices and to the management of this type of patients, the need to use and adapt the available material (e.g. being unable to renounce to use underarm fastening straps) obliges us to consider the use of alternative strategies also in the field of vascular access. After this case, we began to consider techniques that allow us to prevent the catheter from ending in the armpit, with benefit. It is essential to continue to observe this patient.


Subject(s)
COVID-19 , Thrombosis , Axillary Vein/diagnostic imaging , Continuous Positive Airway Pressure , Head Protective Devices , Humans , SARS-CoV-2
3.
J Vasc Access ; 18(3): 238-242, 2017 May 15.
Article in English | MEDLINE | ID: mdl-28218360

ABSTRACT

PURPOSE: In recent years, a large variety of medical devices has become available. Every device must be efficient, safe and cost effective, but it is not enough to use it properly without considering the environment in which it will be employed. We applied this kind of analysis to subcutaneously anchored sutureless devices (SAS). METHODS: This is a one-center prospective observational study on safety, effectiveness and cost effectiveness of an SAS device (SecurAcath, Interrad) for securement of peripherally inserted central catheter (PICC) in 30 adult cancer patients with treatment expected to be >60 days. RESULTS: During 4963 catheter days and after 709 dressing changes (documented by 373 pictures), the use of SAS was associated with no episode of PICC dislodgement and a lower incidence of complications if compared to traditional securement devices. Insertion, management and removal of SAS were not associated with an increased pain perception by the patients. Cost effectiveness was particularly evident for long dwelling PICCs. CONCLUSIONS: Our study suggests that SAS is a highly effective and cost-effective method for securement of medium- to long-term PICCs with expected duration longer than 30 days. The introduction of SAS had a positive impact on our healthcare organization.


Subject(s)
Antineoplastic Agents/administration & dosage , Catheterization, Peripheral/instrumentation , Catheters, Indwelling , Administration, Intravenous , Catheter-Related Infections/economics , Catheter-Related Infections/etiology , Catheter-Related Infections/therapy , Catheterization, Peripheral/adverse effects , Catheterization, Peripheral/economics , Catheters, Indwelling/adverse effects , Catheters, Indwelling/economics , Cost-Benefit Analysis , Device Removal , Equipment Design , Equipment Failure , Health Care Costs , Humans , Italy , Prospective Studies , Technology Assessment, Biomedical , Time Factors
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