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1.
Arch Dis Child Fetal Neonatal Ed ; 106(5): 561-567, 2021 Sep.
Article in English | MEDLINE | ID: covidwho-1455687

ABSTRACT

IMPORTANCE: The current neonatal resuscitation guidelines recommend positive pressure ventilation via face mask or nasal prongs at birth. Using a nasal interface may have the potential to improve outcomes for newborn infants. OBJECTIVE: To determine whether nasal prong/nasopharyngeal tube versus face mask during positive pressure ventilation of infants born <37 weeks' gestation in the delivery room reduces in-hospital mortality and morbidity. DATA SOURCES: MEDLINE (through PubMed), Google Scholar and EMBASE, Clinical Trials.gov and the Cochrane Central Register of Controlled Trials through August 2019. STUDY SELECTION: Randomised controlled trials comparing nasal prong/nasopharyngeal tube versus face mask during positive pressure ventilation of infants born <37 weeks' gestation in the delivery room. DATA ANALYSIS: Risk of bias was assessed using the Covidence Collaboration Tool, results were pooled into a meta-analysis using a random effects model. MAIN OUTCOME: In-hospital mortality. RESULTS: Five RCTs enrolling 873 infants were combined into a meta-analysis. There was no statistical difference in in-hospital mortality (risk ratio (RR 0.98, 95% CI 0.63 to 1.52, p=0.92, I2=11%), rate of chest compressions in the delivery room (RR 0.37, 95% CI 0.10 to 1.33, p=0.13, I2=28%), rate of intraventricular haemorrhage (RR 1.54, 95% CI 0.88 to 2.70, p=0.13, I2=0%) or delivery room intubations in infants ventilated with a nasal prong/tube (RR 0.63, 95% CI 0.39,1.02, p=0.06, I2=52%). CONCLUSION: In infants born <37 weeks' gestation, in-hospital mortality and morbidity were similar following positive pressure ventilation during initial stabilisation with a nasal prong/tube or a face mask.


Subject(s)
Intubation/methods , Masks , Nasopharynx , Positive-Pressure Respiration/methods , Respiratory Distress Syndrome, Newborn/therapy , Bronchopulmonary Dysplasia/complications , Cerebral Intraventricular Hemorrhage/complications , Delivery Rooms , Enterocolitis, Necrotizing/complications , Equipment Failure , Hospital Mortality , Humans , Intensive Care, Neonatal , Intubation/instrumentation , Positive-Pressure Respiration/instrumentation , Respiratory Distress Syndrome, Newborn/complications , Respiratory Distress Syndrome, Newborn/mortality , Treatment Outcome
2.
J Vasc Surg ; 73(6): 1881-1888.e3, 2021 06.
Article in English | MEDLINE | ID: covidwho-1096146

ABSTRACT

OBJECTIVE: The hypercoagulability seen in patients with novel coronavirus disease 2019 (COVID-19) likely contributes to the high temporary hemodialysis catheter (THDC) malfunction rate. We aim to evaluate prophylactic measures and their association with THDC patency. METHODS: A retrospective chart review of our institutions COVID-19 positive patients who required placement of a THDC between February 1 to April 30, 2020, was performed. The association between heparin locking, increased dosing of venous thromboembolism (VTE) prophylaxis and systemic anticoagulation on THDC patency was assessed. Proportional hazards modeling was used to perform a survival analysis to estimate the likelihood and timing of THDC malfunction with the three different prophylactic measures. We also determined the mortality, rate of THDC malfunction and its association with d-dimer levels. RESULTS: A total of 48 patients with a mortality rate of 71% were identified. THDC malfunction occurred in 31.3% of patients. Thirty-seven patients (77.1%) received heparin locking, 22 (45.8%) received systemic anticoagulation, and 38 (79.1%) received VTE prophylaxis. Overall, the rate of THDC malfunction was lower at a trend level of significance, with heparin vs saline locking (24.3% vs 54.6%; P = .058). The likelihood of THDC malfunction in the heparin locked group is lower than all other groups (hazard ratio [HR], 0.07; 95% confidence interval [CI], 0.01-0.45]; P = .005). The rate of malfunction in patients with subcutaneous heparin (SQH) 7500 U three times daily is significantly lower than of the rate for patients receiving none (HR, 0.03; 95% CI, 0.001-0.74; P = .032). A trend level significant association was found for SQH 5000 U vs none (P = .417) and SQH 7500 vs 5000 U (P = .059). Systemic anticoagulation did not affect the THDC malfunction rate (P = .240). Higher d-dimer levels were related to greater mortality (HR, 3.28; 95% CI, 1.16-9.28; P = .025), but were not significantly associated with THDC malfunction (HR, 1.79; 95% CI, 0.42, 7.71; P = .434). CONCLUSIONS: Locking THDCs with heparin is associated with a lower malfunction rate. Prospective randomized studies will be needed to confirm these findings to recommend locking THDC with heparin in patients with COVID-19. Increased VTE prophylaxis suggested a possible association with improved THDC patency, although the comparison lacked sufficient statistical power.


Subject(s)
Anticoagulants/therapeutic use , COVID-19/complications , Central Venous Catheters , Equipment Failure , Heparin/therapeutic use , Renal Dialysis/instrumentation , Venous Thromboembolism/etiology , Venous Thromboembolism/prevention & control , Aged , Cohort Studies , Female , Humans , Male , Retrospective Studies , Time Factors
4.
J Intensive Care Med ; 36(5): 604-611, 2021 May.
Article in English | MEDLINE | ID: covidwho-999444

ABSTRACT

BACKGROUND: Patients with COVID-19 and ARDS on prolonged mechanical ventilation are at risk for developing endotracheal tube (ETT) obstruction that has not been previously described in patients with ARDS due to other causes. The purpose of this report is to describe a case series of patients with COVID-19 and ARDS in which ETT occlusion resulted in significant clinical consequences and to define the pathology of the obstructing material. METHODS: Incidents of ETT occlusion during mechanical ventilation of COVID-19 patients were reported by clinicians and retrospective chart review was conducted. Statistical analysis was performed comparing event rates between COVID-19 and non-COVID 19 patients on mechanical ventilation over the predefined period. Specimens were collected and submitted for pathological examination. FINDINGS: Eleven COVID-19 patients experienced endotracheal tube occlusion over a period of 2 months. Average age was 69 (14.3, range 33-85) years. Mean APACHE III score was 73.6 (17.3). All patients had AKI and cytokine storm. Nine exhibited biomarkers for hypercoagulability. Average days on mechanical ventilation before intervention for ETT occlusion was 14 (5.18) days (range of 9 to 23 days). Five patients were discharged from the ICU, and 4 expired. Average documented airway resistance on admission was 14.2 (3.0) cm H2O/L/sec. Airway resistance before tube exchange was 28.1 (8.0) cm H2O /L/sec. No similar events of endotracheal tube occlusion were identified in non-COVID patients on mechanical ventilation during the same time period. Microscopically, the material consisted of mucin admixed with necrotic cell debris, variable numbers of degenerated inflammatory cells, oral contaminants and red blood cells. INTERPRETATION: Patients with COVID-19 and ARDS on prolonged mechanical ventilation are at risk for developing ETT obstruction due to deposition of a thick, tenacious material within the tube that consists primarily of mucin and cellular debris. Clinicians should be aware of this dangerous but treatable complication.


Subject(s)
Airway Obstruction , COVID-19/complications , Intubation, Intratracheal , Respiration, Artificial , Respiratory Distress Syndrome , APACHE , Aged , Airway Obstruction/etiology , Airway Obstruction/pathology , Airway Obstruction/therapy , COVID-19/epidemiology , COVID-19/therapy , Duration of Therapy , Equipment Failure/statistics & numerical data , Female , Humans , Intubation, Intratracheal/adverse effects , Intubation, Intratracheal/instrumentation , Male , Mortality , Respiration, Artificial/instrumentation , Respiration, Artificial/methods , Respiration, Artificial/statistics & numerical data , Respiratory Distress Syndrome/etiology , Respiratory Distress Syndrome/mortality , Respiratory Distress Syndrome/therapy , Retreatment/methods , Retreatment/statistics & numerical data , Retrospective Studies , SARS-CoV-2 , Treatment Outcome , United States/epidemiology
5.
BMC Nephrol ; 21(1): 486, 2020 11 16.
Article in English | MEDLINE | ID: covidwho-926325

ABSTRACT

BACKGROUND: Critically ill coronavirus disease 2019 (COVID-19) patients have a high risk of acute kidney injury (AKI) that requires renal replacement therapy (RRT). A state of hypercoagulability reduces circuit life spans. To maintain circuit patency and therapeutic efficiency, an optimized anticoagulation strategy is needed. This study investigates whether alternative anticoagulation strategies for RRT during COVID-19 are superior to administration of unfractionated heparin (UFH). METHODS: Retrospective cohort study on 71 critically ill COVID-19 patients (≥18 years), admitted to intensive care units at a tertiary health care facility in the southwestern part of Germany between February 26 and May 21, 2020. We collected data on the disease course, AKI, RRT, and thromboembolic events. Four different anticoagulatory regimens were administered. Anticoagulation during continuous veno-venous hemodialysis (CVVHD) was performed with UFH or citrate. Anticoagulation during sustained low-efficiency daily dialysis (SLEDD) was performed with UFH, argatroban, or low molecular weight heparin (LMWH). Primary outcome is the effect of the anticoagulation regimen on mean treatment times of RRT. RESULTS: In patients receiving CVVHD, mean treatment time in the UFH group was 21.3 h (SEM: ±5.6 h), in the citrate group 45.6 h (SEM: ±2.7 h). Citrate anticoagulation significantly prolonged treatment times by 24.4 h (P = .001). In patients receiving SLEDD, mean treatment time with UFH was 8.1 h (SEM: ±1.3 h), with argatroban 8.0 h (SEM: ±0.9 h), and with LMWH 11.8 h (SEM: ±0.5 h). LMWH significantly prolonged treatment times by 3.7 h (P = .008) and 3.8 h (P = .002), respectively. CONCLUSIONS: UFH fails to prevent early clotting events in the dialysis circuit during COVID-19. For patients, who do not require effective systemic anticoagulation, regional citrate dialysis is the most effective strategy. For patients, who require effective systemic anticoagulation, the usage of LMWH results in the longest circuit life spans. The proposed anticoagulatory strategies are safe, can easily be monitored, and allow an individualized treatment.


Subject(s)
Acute Kidney Injury/therapy , Anticoagulants/administration & dosage , Betacoronavirus , Coronavirus Infections/epidemiology , Pneumonia, Viral/epidemiology , Renal Replacement Therapy/methods , Acute Kidney Injury/blood , Acute Kidney Injury/epidemiology , Adult , Aged , Arginine/analogs & derivatives , Blood Coagulation , COVID-19 , Citric Acid/administration & dosage , Comorbidity , Coronavirus Infections/blood , Critical Care , Critical Illness , Equipment Failure , Female , Germany/epidemiology , Heparin/administration & dosage , Heparin, Low-Molecular-Weight/administration & dosage , Humans , Male , Middle Aged , Pandemics , Pipecolic Acids/administration & dosage , Pneumonia, Viral/blood , Renal Replacement Therapy/instrumentation , Retrospective Studies , SARS-CoV-2 , Sulfonamides , Tertiary Care Centers
6.
Blood Purif ; 50(3): 390-398, 2021.
Article in English | MEDLINE | ID: covidwho-917824

ABSTRACT

INTRODUCTION: The coronavirus disease 2019 (COVID-19) pandemic led to increased demand nationwide for dialysis equipment, including supplies and machines. To meet the demand in our institution, our surge plan included rapid mobilization of a novel continuous renal replacement treatment (CRRT) machine named SAMI. The SAMI is a push-pull filtration enhanced dialysis machine that can conjugate extremely high single-pass solute removal efficiency with very precise fluid balance control. MATERIAL AND METHODS: Machine assembly was conducted on-site by local biomedical engineers with remote assistance by the vendor. One 3-h virtual training session of 3 dialysis nurses was conducted before SAMI deployment. The SAMI was deployed in prolonged intermittent replacement therapy (PIRRT) mode to maximize patients covered per machine per day. Live on-demand vendor support was provided to troubleshoot any issues for the first few cases. After 4 weeks of the SAMI implementation, data on treatments with the SAMI were collected, and a questionnaire was provided to the nurse trainees to assess device usability. RESULTS: On-site installation of the SAMI was accomplished with remote assistance. Delivery of remote training was successfully achieved. 23 PIRRT treatments were conducted in 10 patients. 7/10 of patients had CO-VID-19. The median PIRRT dose was 50 mL/kg/h (IQR [interquartile range] 44 - 62 mL/kg/h), and duration of the treatment was 8 h (IQR 6.3 - 8 h). Solute control was adequate. The user response was favorable to the set of usability questions involving user interface, on-screen instructions, machine setup, troubleshooting, and the ease of moving the machine. CONCLUSION: Assembly of the SAMI and training of nurses remotely are possible when access to vendor employees is restricted during states of emergency. The successful deployment of the SAMI in our institution during the pandemic with only 3-h virtual training supports that operating the SAMI is simple and safe.


Subject(s)
Acute Kidney Injury/therapy , COVID-19/complications , Continuous Renal Replacement Therapy/instrumentation , Hemodialysis Units, Hospital/organization & administration , Intermittent Renal Replacement Therapy/instrumentation , Pandemics , SARS-CoV-2 , Acute Kidney Injury/blood , Acute Kidney Injury/etiology , Anticoagulants/administration & dosage , Attitude of Health Personnel , Continuous Renal Replacement Therapy/methods , Continuous Renal Replacement Therapy/nursing , Data Collection , Dialysis Solutions/administration & dosage , Disposable Equipment , Education, Nursing, Continuing , Equipment Design , Equipment Failure , Heparin/administration & dosage , Humans , Intermittent Renal Replacement Therapy/methods , Intermittent Renal Replacement Therapy/nursing , Maintenance and Engineering, Hospital/organization & administration , Medical Waste Disposal , Prescriptions , Robotics , Surveys and Questionnaires , Virtual Reality
7.
Int J Environ Res Public Health ; 17(18)2020 Sep 06.
Article in English | MEDLINE | ID: covidwho-750677

ABSTRACT

Since the emergence of the COVID-19 pandemic, the use of face masks by healthy individuals for prevention has been attracting public attention. However, efficacy depends on proper usage. We set out to determine the prevalence of wearing masks to prevent COVID-19 and compliance with appropriate measures for the correct use of face masks among the general public in Japan where wearing medical masks is a "cultural" normality. This cross-sectional study was based on an internet-based survey completed by 2141 people (50.8% men, aged 20-79 years) who were selected among registrants of an Internet research company between 1 April and 6 April 2020. Participants were asked to indicate how often they wore masks for prevention and to what extent they practiced appropriate measures suggested by the World Health Organization. The prevalence of wearing masks was 80.9% and compliance rates with appropriate measures ranged from 38.3% to 83.5%. Only 23.1% complied with all recommendations. Compliance rates were overall low in men and persons with low household incomes. Our results, hence show that many citizens implement inaccurate measures when using face masks. Therefore, providing guidance on correct usage is essential when encouraging the use of face masks to prevent COVID-19.


Subject(s)
Coronavirus Infections/prevention & control , Equipment Failure , Masks , Pandemics/prevention & control , Pneumonia, Viral/prevention & control , Adult , Aged , Betacoronavirus , COVID-19 , Cross-Sectional Studies , Female , Humans , Japan , Male , Middle Aged , SARS-CoV-2 , Young Adult
8.
Skeletal Radiol ; 49(11): 1873-1877, 2020 Nov.
Article in English | MEDLINE | ID: covidwho-723995

ABSTRACT

The ongoing coronavirus disease 2019 (COVID-19) pandemic has increased the need for safe and efficient testing as a key containment strategy. Drive-through testing with nasopharyngeal swab has been implemented in many places in the USA as it allows for expeditious testing of large numbers of patients, limits healthcare workers' risk of exposure, and minimizes the use of personal protective equipment. We present a case where the aluminum shaft of the nasopharyngeal swab fractured during specimen collection at a drive-through testing facility and was suspected to have remained in the asymptomatic patient. Initial evaluation with a series of radiographs covering the skull base, neck, chest, and abdomen did not reveal the swab. On further clinical evaluation, the swab was found endoscopically, lodged between the left inferior turbinate and nasal floor, and was removed by an otorhinolaryngologist. Using a phantom model, we aimed to delineate an imaging technique to better visualize the aluminum shaft of the nasopharyngeal swab on radiographs to help in identification. A technique using lower tube voltage (kVp) with tight collimation centered at the nasal bones area produced the best visualization of the aluminum shaft of the swab. Recognition that aluminum foreign bodies may be difficult to visualize radiographically and  optimization of radiograph acquisition technique may help guide clinical management in unusual cases. Further evaluation with computed tomography or endoscopy should be considered in suspected cases where radiographs are negative.


Subject(s)
Betacoronavirus , Clinical Laboratory Techniques/instrumentation , Coronavirus Infections/diagnosis , Equipment Failure , Foreign Bodies/diagnostic imaging , Pneumonia, Viral/diagnosis , Specimen Handling/instrumentation , Aged, 80 and over , Aluminum , COVID-19 , COVID-19 Testing , Humans , Male , Pandemics , Radiography/methods , SARS-CoV-2 , Surgical Instruments
9.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi ; 34(8): 1036-1040, 2020 Aug 15.
Article in Chinese | MEDLINE | ID: covidwho-719850

ABSTRACT

At present, the 2019-nCoV epidemic situation is in severe and complex period. In order to prevent the virus from invading and infecting, it is very important and urgent for medical personnel to protect themselves. However, in the process of using protective equipment by medical personnel, the performance of device related pressure injuries (DRPI) caused by pain, numbness, redness, and even breakage caused by the equipment has seriously endangered the health of medical personnel. This article, based on Prevention and Treatment of Pressure Ulcers/Injuries: Quick Reference Guide 2019, references, and clinical experiences of wound specialists in West China Hospital of Sichuan University, summarize the preventive and protective measures of West China Hospital for medical personnel to prevent DRPI, so as to provide clinical preventive measurements for medical personnel.


Subject(s)
Coronavirus Infections/epidemiology , Equipment Failure , Personal Protective Equipment/adverse effects , Pneumonia, Viral/epidemiology , Wounds and Injuries/prevention & control , Betacoronavirus , COVID-19 , China , Health Personnel , Humans , Pandemics , Pressure , SARS-CoV-2
11.
Rev Invest Clin ; 72(3): 144-150, 2020.
Article in English | MEDLINE | ID: covidwho-617020

ABSTRACT

The emergence of coronavirus disease 19 pandemic and novel research on the high transmissibility of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has raised controversies over the use of face masks to prevent community transmission. Specific regulations need to be fulfilled to use a face mask as part of the personal protective equipment and high quality of evidence supporting its use to prevent respiratory viral infections, including SARS-CoV-2, is lacking. However, its widespread use is becoming a standard practice in some countries and discrepancies between health authorities on their policy have led to controversy. The aim of this review is to provide an outlook on recent research in this matter and areas of opportunity.


Subject(s)
Betacoronavirus , Communicable Disease Control/instrumentation , Coronavirus Infections/prevention & control , Masks , Pandemics/prevention & control , Pneumonia, Viral/prevention & control , Aerosols , Air Microbiology , Betacoronavirus/isolation & purification , COVID-19 , Communicable Disease Control/legislation & jurisprudence , Communicable Disease Control/methods , Coronavirus Infections/epidemiology , Coronavirus Infections/transmission , Disease Outbreaks , Disease Transmission, Infectious/prevention & control , Equipment Design , Equipment Failure , Humans , Influenza A Virus, H1N1 Subtype , Influenza, Human/epidemiology , Influenza, Human/virology , Particle Size , Pneumonia, Viral/epidemiology , Pneumonia, Viral/transmission , Procedures and Techniques Utilization , Program Evaluation , Respiratory Protective Devices , SARS-CoV-2 , Severe Acute Respiratory Syndrome/epidemiology , Survival Rate
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