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Metrology part 1: definition of quality criteria

Squara, Pierre; Scheeren, Thomas W L; Aya, Hollmann D; Bakker, Jan; Cecconi, Maurizio; Einav, Sharon; Malbrain, Manu L N G; Monnet, Xavier; Reuter, Daniel A; van der Horst, Iwan C C; Saugel, Bernd
Any measurement is always afflicted with some degree of uncertainty. A correct understanding of the different types of uncertainty, their naming, and their definition is of crucial importance for an appropriate use of measuring instruments. However, in perioperative and intensive care medicine, the metrological requirements for measuring instruments are poorly defined and often used spuriously. The correct use of metrological terms is also of crucial importance in validation studies. The European Union published a new directive on medical devices, mentioning that in the case of devices with a measuring function, the notified body is involved in all aspects relating to the conformity of the device with the metrological requirements. It is therefore the task of the scientific societies to establish the standards in their area of expertise. Adopting the same understandings and definitions among clinicians and scientists is obviously the first step. In this metrologic review (part 1), we list and explain the most important terms defined by the International Bureau of Weights and Measures regarding quantities and units, properties of measurements, devices for measurement, properties of measuring devices, and measurement standards, with specific examples from perioperative and intensive care medicine.
PMID: 32185615
ISSN: 1573-2614
CID: 4504932

Current use of inotropes in circulatory shock

Scheeren, Thomas W L; Bakker, Jan; Kaufmann, Thomas; Annane, Djillali; Asfar, Pierre; Boerma, E Christiaan; Cecconi, Maurizio; Chew, Michelle S; Cholley, Bernard; Cronhjort, Maria; De Backer, Daniel; Dubin, Arnaldo; Dünser, Martin W; Duranteau, Jacques; Gordon, Anthony C; Hajjar, Ludhmila A; Hamzaoui, Olfa; Hernandez, Glenn; Kanoore Edul, Vanina; Koster, Geert; Landoni, Giovanni; Leone, Marc; Levy, Bruno; Martin, Claude; Mebazaa, Alexandre; Monnet, Xavier; Morelli, Andrea; Payen, Didier; Pearse, Rupert M; Pinsky, Michael R; Radermacher, Peter; Reuter, Daniel A; Sakr, Yasser; Sander, Michael; Saugel, Bernd; Singer, Mervyn; Squara, Pierre; Vieillard-Baron, Antoine; Vignon, Philippe; Vincent, Jean-Louis; van der Horst, Iwan C C; Vistisen, Simon T; Teboul, Jean-Louis
BACKGROUND:Treatment decisions on critically ill patients with circulatory shock lack consensus. In an international survey, we aimed to evaluate the indications, current practice, and therapeutic goals of inotrope therapy in the treatment of patients with circulatory shock. METHODS:From November 2016 to April 2017, an anonymous web-based survey on the use of cardiovascular drugs was accessible to members of the European Society of Intensive Care Medicine (ESICM). A total of 14 questions focused on the profile of respondents, the triggering factors, first-line choice, dosing, timing, targets, additional treatment strategy, and suggested effect of inotropes. In addition, a group of 42 international ESICM experts was asked to formulate recommendations for the use of inotropes based on 11 questions. RESULTS:A total of 839 physicians from 82 countries responded. Dobutamine was the first-line inotrope in critically ill patients with acute heart failure for 84% of respondents. Two-thirds of respondents (66%) stated to use inotropes when there were persistent clinical signs of hypoperfusion or persistent hyperlactatemia despite a supposed adequate use of fluids and vasopressors, with (44%) or without (22%) the context of low left ventricular ejection fraction. Nearly half (44%) of respondents stated an adequate cardiac output as target for inotropic treatment. The experts agreed on 11 strong recommendations, all of which were based on excellent (> 90%) or good (81-90%) agreement. Recommendations include the indications for inotropes (septic and cardiogenic shock), the choice of drugs (dobutamine, not dopamine), the triggers (low cardiac output and clinical signs of hypoperfusion) and targets (adequate cardiac output) and stopping criteria (adverse effects and clinical improvement). CONCLUSION/CONCLUSIONS:Inotrope use in critically ill patients is quite heterogeneous as self-reported by individual caregivers. Eleven strong recommendations on the indications, choice, triggers and targets for the use of inotropes are given by international experts. Future studies should focus on consistent indications for inotrope use and implementation into a guideline for circulatory shock that encompasses individualized targets and outcomes.
PMCID:7846624
PMID: 33512597
ISSN: 2110-5820
CID: 4799582

Assessment of mortality and performance status in critically ill cancer patients: A retrospective cohort study

van der Zee, Esther N; Noordhuis, Lianne M; Epker, Jelle L; van Leeuwen, Nikki; Wijnhoven, Bas P L; Benoit, Dominique D; Bakker, Jan; Kompanje, Erwin J O
INTRODUCTION/BACKGROUND:Given clinicians' frequent concerns about unfavourable outcomes, Intensive Care Unit (ICU) triage decisions in acutely ill cancer patients can be difficult, as clinicians may have doubts about the appropriateness of an ICU admission. To aid to this decision making, we studied the survival and performance status of cancer patients 2 years following an unplanned ICU admission. MATERIALS AND METHODS/METHODS:This was a retrospective cohort study in a large tertiary referral university hospital in the Netherlands. We categorized all adult patients with an unplanned ICU admission in 2017 into two groups: patients with or without an active malignancy. Descriptive statistics, Pearson's Chi-square tests and the Mann-Whitney U tests were used to evaluate the primary objective 2-year mortality and performance status. A good performance status was defined as ECOG performance status 0 (fully active) or 1 (restricted in physically strenuous activity but ambulatory and able to carry out light work). A multivariable binary logistic regression analysis was used to identify factors associated with 2-year mortality within cancer patients. RESULTS:Of the 1046 unplanned ICU admissions, 125 (12%) patients had cancer. The 2-year mortality in patients with cancer was significantly higher than in patients without cancer (72% and 42.5%, P <0.001). The median performance status at 2 years in cancer patients was 1 (IQR 0-2). Only an ECOG performance status of 2 (OR 8.94; 95% CI 1.21-65.89) was independently associated with 2-year mortality. CONCLUSIONS:In our study, the majority of the survivors have a good performance status 2 years after ICU admission. However, at that point, three-quarter of these cancer patients had died, and mortality in cancer patients was significantly higher than in patients without cancer. ICU admission decisions in acutely ill cancer patients should be based on performance status, severity of illness and long-term prognosis, and this should be communicated in the shared decision making. An ICU admission decision should not solely be based on the presence of a malignancy.
PMCID:8195393
PMID: 34115771
ISSN: 1932-6203
CID: 4924592

Transfusion practice in the bleeding critically ill: An international online survey-The TRACE-2 survey

de, Bruin S; Eggermont, D; van, Bruggen R; de, Korte D; Scheeren, T W L; Bakker, J; Vlaar, A P J; Abbasciano, R G; Antonelli, M; Aubron, C; van, Baarle F E H P; Cecconi, M; Dionne, J C; Duranteau, J; Gyatt, G; Hunt, B J; Juffermans, N P; Lance, M; Meier, J; Muller, M C A; Murphy, G J; Nielsen, N; Oczkowski, S J; Perner, A; Raasveld, S J; Schochel, H; Wijnberge, M
Background: Transfusion is very common in the intensive care unit (ICU), but practice is highly variable, as has recently been shown in non-bleeding critically ill patients practices survey. Bleeding patients in ICU require different blood products across a range of specific patient categories. We hypothesize that a large variety in transfusion practice exists in bleeding patients. Study design and methods: An international online survey was performed among physicians working in the ICU. Transfusion practice in massively and non-massively bleeding patients was examined, including transfusion ratios, thresholds, and the presence of transfusion guidelines.
Result(s): Six hundred eleven respondents filled in the survey of which 401 could be analyzed, representing 64 countries. Among the respondents, 52% had a massive transfusion protocol (MTP) available at their ICU. In massively bleeding patients, 46% of the respondents used fixed transfusion component ratios. Of those who used fixed blood ratios, the 1:1:1 ratio (red blood cell [RBC] concentrates: plasma: platelet concentrates) was most commonly used (33%). The presence of an MTP was associated with a more frequent use of fixed ratios (p <.001). For RBC transfusion in the general non-massively bleeding ICU population, a hemoglobin (Hb) threshold of 7.0[7.0-7.3] g/dl was reported. In the general ICU population, a platelet count threshold of 50[26-50] x 109/L was applied.
Discussion(s): Half of the centers had no massive transfusion protocol available. Transfusion practice in massively bleeding critically ill patients is highly variable and driven by the presence of an MTP. In the general non-massively bleeding ICU population restrictive transfusion triggers were chosen.
Copyright
EMBASE:2014670365
ISSN: 0041-1132
CID: 5135752

Topoisomerase 1 inhibition therapy protects against SARS-CoV-2-induced inflammation and death in animal models [PrePrint]

Yuin Ho, Jessica Sook; Wing-Yee Mok, Bobo; Campisi, Laura; Jordan, Tristan; Yildiz, Soner; Parameswaran, Sreeja; Wayman, Joseph A; Gaudreault, Natasha N; Meekins, David A; Indran, Sabarish V; Morozov, Igor; Trujillo, Jessie D; Fstkchyan, Yesai S; Rathnasinghe, Raveen; Zhu, Zeyu; Zheng, Simin; Zhao, Nan; White, Kris; Ray-Jones, Helen; Malysheva, Valeriya; Thiecke, Michiel J; Lau, Siu-Ying; Liu, Honglian; Junxia Zhang, Anna; Chak-Yiu Lee, Andrew; Liu, Wen-Chun; Aydillo, Teresa; Salom Melo, Betsaida; Guccione, Ernesto; Sebra, Robert; Shum, Elaine; Bakker, Jan; Kaufman, David A; Moreira, Andre L; Carossino, Mariano; Balasuriya, Udeni B R; Byun, Minji; Miraldi, Emily R; Albrecht, Randy A; Schotsaert, Michael; Garcia-Sastre, Adolfo; Chanda, Sumit K; Jeyasekharan, Anand D; TenOever, Benjamin R; Spivakov, Mikhail; Weirauch, Matthew T; Heinz, Sven; Chen, Honglin; Benner, Christopher; Richt, Juergen A; Marazzi, Ivan
The ongoing pandemic caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is currently affecting millions of lives worldwide. Large retrospective studies indicate that an elevated level of inflammatory cytokines and pro-inflammatory factors are associated with both increased disease severity and mortality. Here, using multidimensional epigenetic, transcriptional, in vitro and in vivo analyses, we report that Topoisomerase 1 (Top1) inhibition suppresses lethal inflammation induced by SARS-CoV-2. Therapeutic treatment with two doses of Topotecan (TPT), a FDA-approved Top1 inhibitor, suppresses infection-induced inflammation in hamsters. TPT treatment as late as four days post-infection reduces morbidity and rescues mortality in a transgenic mouse model. These results support the potential of Top1 inhibition as an effective host-directed therapy against severe SARS-CoV-2 infection. TPT and its derivatives are inexpensive clinical-grade inhibitors available in most countries. Clinical trials are needed to evaluate the efficacy of repurposing Top1 inhibitors for COVID-19 in humans.
PMID: 33299999
ISSN: 2692-8205
CID: 4843582

Attenuating hyperinflammation in COVID-19: A change in paradigm? [Editorial]

Molnar, Zsolt; Bakker, Jan
PMCID:7375956
PMID: 32741525
ISSN: 1557-8615
CID: 4581242

Objektive Verlegungskriterien und proaktives Verlegungsmanagement zur Steuerung von intensivmedizinischen Kapazitaten

Hiller, M; Spohn, K; Schutte, J K; Bracht, H; Hering, R; Bakker, J; Schroder, S
Despite the high number of intensive care beds in German hospitals compared to other European countries, intensive care medical shortages are common in daily clinical practice. This is due to a hardly established cross-departmental discharge and transfer management with missing objective discharge criteria, lack of personnel and bed closures. Aboveaverage lengths of stays and increased readmission rates to the intensive care unit also indicate an inefficient use of resources in German hospitals. Against this background, a systematic literature search was carried out on the current state of research on discharge criteria from the intensive care unit and transfer processes to follow-up wards. Between 1983 and 2020, 1,917 sources were found, 286 were selected as full text, 104 of which were considered relevant and used as the basis for this work. Approaches, such as a root cause analy- sis of bottleneck situations including the entire hospital system with its interdependent admission, transfer and discharge processes, and the use of electronic decision support in conjunction with standardised discharge criteria can improve the use of existing intensive care capacities and lead to safer and better patient flow. For better use of resources, the therapeutic outcome must be viewed along the entire clinical pathway in order to care for the right patient at the right place and at the right time. A standardised care transition management using objective discharge criteria could help to include the various stakeholders in the discharge decision and patient-transfer process to reflect patient-, caregiver-, process, and institution-specific factors, and ultimately to manage, proactively and efficiently, the available intensive care resources. Decision support in the discharge process using self-learning systems based on available data from patient data management systems is forward-looking, but must be validated more widely in clinical practice.
Copyright
EMBASE:2010366930
ISSN: 0170-5334
CID: 4750982

Transfusion practice in the bleeding critically ill; an international online survey-the trace-2 survey [Meeting Abstract]

De, Bruin S; Eggermont, D; Scheeren, T; Bakker, J; De, Korte D; Van, Bruggen R; Vlaar, A
Background: Transfusion practice on the intensive care unit (ICU) shifted from a liberal towards a more restrictive transfusion strategy during the last decades. However, current practice is still highly variable, as recently has been shown in non-bleeding critically ill patients. Bleeding patients are more complex and receive more and different blood products. Currently, no transfusion guideline for bleeding critically ill patients is available. Therefore, we hypothesized to find a great variety in transfusion practice in this patient population.
Aim(s): The aim of this survey was to study current transfusion practice in different bleeding subpopulations in the ICU and assess the availability and influence of transfusion guidelines.
Method(s): An online survey was performed among physicians working in the ICU only. The survey questioned transfusion practice in massively and non-massively bleeding ICU patients, including transfusion ratios of blood components and transfusion thresholds. Different relevant subpopulations were included. Also, the presence of transfusion guidelines was asked.
Result(s): A total of 611 physicians responded, of which 401 completed the survey, representing 64 countries. The majority of respondents work in high-income countries (72%) and 45% reports having a hospital wide transfusion protocol, 40% an ICU specific transfusion protocol, and 52% have a massive transfusion protocol available in their centre. In massively bleeding patients 67% of the respondents used conventional lab-based testing to guide their transfusion practice, 46% used fixed transfusion ratios and 41% used point of care visco-elastic tests. Of those who use fixed blood component ratio's, the 1:1:1 (red blood cell concentrates: plasma: platelet concentrates) was most commonly used (33%) followed by a 3:3:1 ratio (24%). In non-massively bleeding patients, different threshold were applied for different patient populations. In the general ICU population, a haemoglobin threshold of 7.0 [7.0-7.3] g/dl was used to transfuse red blood cells (RBCs). The highest variance in haemoglobin threshold was observed in patients treated with extracorporeal membrane oxygenation (ECMO) and in patients with haemorrhagic stroke or traumatic brain injury, with a haemoglobin threshold of 8.0 [7.0-9.0] g/dl each. In the general ICU population a platelet count threshold of 50 [26-50] x109 cells/l was applied. The highest threshold was observed in patients with haemorrhagic stroke or traumatic brain injury: 75 [50-100] cells/l. The presence of a hospital wide or an ICU specific transfusion guideline did not influence the applied transfusion thresholds in the non-massively bleeding patients. Summary/Conclusions: The majority of the respondents do not have an ICU specific transfusion guideline available in their centre. There is a high variance in the approach of both non-massive and massively bleeding ICU patients. In the general ICU population restrictive transfusion triggers are used. However, in ECMO and brain injury patients, physicians tend to transfuse more liberally
EMBASE:633986294
ISSN: 1423-0410
CID: 4774322

Effects of capillary refill time-vs. lactate-targeted fluid resuscitation on regional, microcirculatory and hypoxia-related perfusion parameters in septic shock: a randomized controlled trial

Castro, Ricardo; Kattan, Eduardo; Ferri, Giorgio; Pairumani, Ronald; Valenzuela, Emilio Daniel; Alegría, Leyla; Oviedo, Vanessa; Pavez, Nicolás; Soto, Dagoberto; Vera, Magdalena; Santis, César; Astudillo, Brusela; Cid, María Alicia; Bravo, Sebastian; Ospina-Tascón, Gustavo; Bakker, Jan; Hernández, Glenn
BACKGROUND:Persistent hyperlactatemia has been considered as a signal of tissue hypoperfusion in septic shock patients, but multiple non-hypoperfusion-related pathogenic mechanisms could be involved. Therefore, pursuing lactate normalization may lead to the risk of fluid overload. Peripheral perfusion, assessed by the capillary refill time (CRT), could be an effective alternative resuscitation target as recently demonstrated by the ANDROMEDA-SHOCK trial. We designed the present randomized controlled trial to address the impact of a CRT-targeted (CRT-T) vs. a lactate-targeted (LAC-T) fluid resuscitation strategy on fluid balances within 24 h of septic shock diagnosis. In addition, we compared the effects of both strategies on organ dysfunction, regional and microcirculatory flow, and tissue hypoxia surrogates. RESULTS:content difference ratio; and lactate/pyruvate ratio. There was no difference between CRT-T vs. LAC-T in 6 h-fluid boluses (875 [375-2625] vs. 1500 [1000-2000], p = 0.3), or balances (982[249-2833] vs. 15,800 [740-6587, p = 0.2]). CRT-T was associated with a higher achievement of the predefined perfusion target (62 vs. 24, p = 0.03). No significant differences in perfusion-related variables or hypoxia surrogates were observed. CONCLUSIONS:CRT-targeted fluid resuscitation was not superior to a lactate-targeted one on fluid administration or balances. However, it was associated with comparable effects on regional and microcirculatory flow parameters and hypoxia surrogates, and a faster achievement of the predefined resuscitation target. Our data suggest that stopping fluids in patients with CRT ≤ 3 s appears as safe in terms of tissue perfusion. Clinical Trials: ClinicalTrials.gov Identifier: NCT03762005 (Retrospectively registered on December 3rd 2018).
PMCID:7606372
PMID: 33140173
ISSN: 2110-5820
CID: 4660432

Prospective multicentre multifaceted before-after implementation study of ICU delirium guidelines: a process evaluation

Trogrlic, Zoran; van der Jagt, Mathieu; van Achterberg, Theo; Ponssen, Huibert; Schoonderbeek, Jeannette; Schreiner, Frodo; Verbrugge, Serge; Dijkstra, Annemieke; Bakker, Jan; Ista, Erwin
OBJECTIVE:We aimed to explore: the exposure of healthcare workers to a delirium guidelines implementation programme; effects on guideline adherence at intensive care unit (ICU) level; impact on knowledge and barriers, and experiences with the implementation. DESIGN/METHODS:A mixed-methods process evaluation of a prospective multicentre implementation study. SETTING/METHODS:Six ICUs. PARTICIPANTS/METHODS:4449 adult ICU patients and 500 ICU professionals approximately. INTERVENTION/METHODS:A tailored implementation programme. MAIN OUTCOME MEASURE/METHODS:Adherence to delirium guidelines recommendations at ICU level before, during and after implementation; knowledge and perceived barriers; and experiences with the implementation. RESULTS:Five of six ICUs were exposed to all implementation strategies as planned. More than 85% followed the required e-learnings; 92% of the nurses attended the clinical classroom lessons; five ICUs used all available implementation strategies and perceived to have implemented all guideline recommendations (>90%). Adherence to predefined performance indicators (PIs) at ICU level was only above the preset target (>85%) for delirium screening. For all other PIs, the inter-ICU variability was between 34% and 72%. The implementation of delirium guidelines was feasible and successful in resolving the majority of barriers found before the implementation. The improvement was well sustained 6 months after full guideline implementation. Knowledge about delirium was improved (from 61% to 65%). The implementation programme was experienced as very successful. CONCLUSIONS:Multifaceted implementation can improve and sustain adherence to delirium guidelines, is feasible and can largely be performed as planned. However, variability in delirium guideline adherence at individual ICUs remains a challenge, indicating the need for more tailoring at centre level.
PMID: 32948600
ISSN: 2399-6641
CID: 4609622