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"en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Prevention, identification and management of pain.</p> <p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">vNRS, numeric rating scale; VAS, visual analogue scale; ESCID, Pain Indicating Behaviors Scale (Escala de Conductas Indicadores de Dolor); BPS, Behavioral Pain Scale; CPOT, Critical-Care Pain Observation Tool; ANI, Analgesia Nociception Index; NOL, nociception level index; IMV, invasive mechanical ventilation; Cx, surgeries.</p> <p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Reproduced from<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> (with permission).</p>"
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"textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Patients who survive critical illness can present physical, psychological or cognitive symptoms following discharge. If these symptoms persist for months, they may be regarded as sequelae or adverse events, many of which are avoidable, and which constitute what is known as post-intensive care syndrome (PICS).<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> These alterations are a consequence of both the critical disease itself and the medical interventions surrounding it. Preventive measures are therefore essential, are considered to be safe, and represent adherence to the good clinical practice guides based on scientific evidence. Failure to adopt such measures can lead to errors that may result in harm to the critically ill patient.</p><p id="par0010" class="elsevierStylePara elsevierViewall">Since the term was introduced in 2010, the interest and number of studies on PICS have grown exponentially.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,3</span></a> Patient quality of life and functional capacity are closely related to the above alterations – hence the importance of preventing the syndrome during admission to the Intensive Care Unit (ICU) and of monitoring those individuals at risk of suffering PICS.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Prevention</span><p id="par0015" class="elsevierStylePara elsevierViewall">The prevention of PICS is based on the comprehensive and multidisciplinary management of the critically ill patient through implementation of the ABCDEF (<span class="elsevierStyleBold">A</span>ssess/treat pain, <span class="elsevierStyleBold">B</span>reathing/awakening trials, <span class="elsevierStyleBold">C</span>hoice of sedatives, <span class="elsevierStyleBold">D</span>elirium reduction, <span class="elsevierStyleBold">E</span>arly mobility and exercise, <span class="elsevierStyleBold">F</span>amily) bundle,<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> along with recently added strategies grouped under the acronym GHIRN (<span class="elsevierStyleBold">G</span>ood communication, <span class="elsevierStyleBold">H</span>andout materials, <span class="elsevierStyleBold">R</span>edefined ICU architectural design, <span class="elsevierStyleBold">R</span>espirator, <span class="elsevierStyleBold">N</span>utrition) (Fig. 1),<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5–7</span></a> which are described below:</p><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Assess/treat pain: identification, prevention and management of pain</span><p id="par0020" class="elsevierStylePara elsevierViewall">Pain in the critically ill patient can be caused by tissue damage inherent to the primary disease condition, invasive procedures, immobilization and mobilization. Pain activates the autonomic nervous system and can cause hemodynamic dysfunction, respiratory alterations, coagulopathy or immune system alterations. Sustained pain stimuli can produce hyperalgesia and an amplified response to minimally harmful stimuli, resulting in chronic pain. If not adequately identified, prevented and treated, this situation can have a psychological impact on the patient, in addition to the physiological effects commented above. Pain recall is an independent predictor of the development of posttraumatic stress disorder (PTSD).<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Excessive analgesic use can also lead to undesired side effects such as gastrointestinal hypomotility, gastric bleeding, renal dysfunction, and tolerance or withdrawal symptoms.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Frequent (at least every 4 h) and protocolized pain assessments should be made using validated scales. In patients that are able to communicate, we can use the Verbal Numerical Rating Scale (vNRS) and the Visual Analogue Scale (VAS),<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> both scoring pain from 0 to 10 points, while behavioral scales are needed in case of patients unable to communicate, such as the Pain Indicating Behaviors Scale (<span class="elsevierStyleItalic">Escala de Conductas Indicadores de Dolor</span> [ESCID])<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">11</span></a> from 0 to 10 points, the Critical-Care Pain Observation Tool (CPOT)<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">12</span></a> scoring 0 to 8 points, or the Behavioral Pain Scale (BPS)<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a> that scores from 3 to 12 points. In patients subjected to deep sedation and neuromuscular relaxation, where changes in behavior or gestures are not seen, we can useobjective instrumental methods that analyze components of the sympathetic and parasympathetic autonomic nervous system and which identify pain based on a numerical score.<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">14,15</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The monitoring of pain in patients who are able or unable to communicate is one of the quality indicators of the Spanish Society of Intensive and Critical Care Medicine and Coronary Units (<span class="elsevierStyleItalic">Sociedad Española de Medicina Intensiva, Crítica y Unidades Coronarias</span> [SEMICYUC]) in critically ill patients.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The treatment of pain initially should be based on non-pharmacological measures such as music therapy, relaxation techniques (e.g., mindfulness), massages and local cold application (cold packs). If these measures fail, drug treatment should be introduced adapted to the intensity of the pain and the clinical condition of the patient. In this context, multimodal strategies are indicated, combining opioids (fentanyl, remifentanil or morphic chloride) with non-opioid analgesics (paracetamol, nonsteroidal anti-inflammatory drugs [NSAIDs]), coadjuvants (dexmedetomidine, corticosteroids or ketamine), neuropathic pain analgesics (gabapentin, carbamazepine or pregabalin) or regional analgesia (epidural, muscle blocks, etc), seeking to control the pain and reduce the opioid doses and side effects (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Breathing/awakening trials: reduction of sedation and spontaneous breathing trial</span><p id="par0045" class="elsevierStylePara elsevierViewall">For decades, sedatives have helped to reduce pain, stress and discomfort in critically ill mechanically ventilated patients . However, many studies have also demonstrated their potential short- and long-term negative effects, such as respiratory depression, hemodynamic instability and metabolic acidosis, in addition to a prolongation of mechanical ventilation (MV), ICU stay and an increased risk of delirium.<a class="elsevierStyleCrossRefs" href="#bib0085"><span class="elsevierStyleSup">17,18</span></a> For this reason, mild sedation strategies are currently recommended (Richmond Agitation Sedation Scale [RASS] −2 to +1), except in the presence of absolute indications of deep sedation: severe acute respiratory distress syndrome (ARDS), intracranial hypertension (ICH), status epilepticus, hypothermia or the use of neuromuscular blockers (NMBs).<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">19</span></a> Thus, the new sedation strategies should seek the minimum necessary dose, favoring patient cooperation and communication, the withdrawal of respiratory support and early mobility.</p><p id="par0050" class="elsevierStylePara elsevierViewall">Some studies have shown that daily sedative interruption strategies are safe and improve the outcomes in terms of days without MV as well as shortening ICU stay,<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">20</span></a> though mild sedation protocols are also effective and pose fewer risks.<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">19</span></a> In fact, daily assessment of the interruption of sedation, spontaneous breathing trials, the monitoring of sedation, adequate indication and the monitoring of neuromuscular block as well as of sedation during neuromuscular block, are regarded as quality indicators by the SEMICYUC.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">In order to achieve the aims of sedation, it is essential to make use of validated scales that measure the level of sedation, such as the RASS,<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">21</span></a> which yields a score of −5 to +4 points, or the Riker Sedation Agitation Scale (SAS),<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">22</span></a> with a score of 1–7 points. In patients undergoing deep sedation or neuromuscular relaxation, objective tools such as the bispectral index (BIS)<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">23</span></a> and the train-of-four (TOF),<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a> should be used. Conscious or superficial sedation is considered when the patient presents RASS 0, −1 or −2, while deep sedation is defined as RASS −3, −4 or −5 and BIS between 40−60. Bispectral levels under 40 are associated with oversedation. Such levels have been observed in up to 35% of all critically ill patients<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> – a fact that must be considered given its deleterious impact and safety concerns for the patient (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>).</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0060" class="elsevierStylePara elsevierViewall">In the context of patient quality care and safety projects, the SEMICYUC and the working group in sedation, analgesia and delirium (GTSAD) propose the inclusion of the “Zero Overdose” project as a practical teaching tool to enhance global awareness of convenience, safety and management in order to maximize the clinical outcomes and minimize the harmful effects of excessive sedation.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Choice of sedatives</span><p id="par0065" class="elsevierStylePara elsevierViewall">In order to reduce stress and discomfort in mechanically ventilated patients, it is advisable to guarantee adequate analgesia, discard and treat delirium, and favor the previously mentioned non-pharmacological strategies, such as environmental enhancement, postural measures, relaxation and music therapy, among others. If this proves to be ineffective, pharmacological approach should be considered according to the objective of sedation, which should be established on an individualized basis and adapted dynamically to the clinical condition of the patient.</p><p id="par0070" class="elsevierStylePara elsevierViewall">Preferably, and except in the presence of an absolute indication of deep sedation,<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">19</span></a> superficial and conscious sedation should be provided with drugs such as dexmedetomidine, propofol or remifentanil.</p><p id="par0075" class="elsevierStylePara elsevierViewall">In those cases where deep sedation is justified, short half-life drugs such as propofol or ketamine should be chosen or inhaled sedatives such as isoflurane should be used,<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> avoiding benzodiazepines due to their association with delirium, increased ICU stay and estimated costs.<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> The latter drugs are only indicated in alcohol deprivation, refractory status epilepticus or in cases of difficult sedation as the second or third step where isoflurane is not available or contraindicated<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>). Adequate sedation is a relevant quality indicator in the critically ill patient.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a></p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Delirium reduction: evaluate, prevent and treat delirium</span><p id="par0080" class="elsevierStylePara elsevierViewall">Delirium, defined as acute brain dysfunction characterized by attention, consciousness and cognition alterations with an acute and fluctuating course is a frequent condition in the ICU. It is associated with modifiable risk factors such as benzodiazepine use, deep sedation or blood transfusions, as well as with non-modifiable factors such as patient age, dementia, prior condition, urgent surgery or trauma, and high severity scores. Thus, the appearance of delirium is potentially modifiable.<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">19</span></a></p><p id="par0085" class="elsevierStylePara elsevierViewall">A relationship has been demonstrated between the appearance of delirium and poorer global cognitive and executive function , three and 12 months after discharge,<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a> as well as an independent association between duration of delirium and long-term cognitive alterations.<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> Hence the prediction, detection and management of delirium constitute a guarantee of quality and safety. The identification of delirium and its non-pharmacological prevention are quality indicators in the critically ill patient, with the former being a relevant indicator.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a></p><p id="par0090" class="elsevierStylePara elsevierViewall">There are validated predictive models that can help in identifying those patients at an increased risk of suffering delirium during ICU stay, such as the Early Prediction Model for Delirium (E- PRE-DELIRIC) at the time of admission to the ICU, and the Prediction Model of Delirium (PRE-DELIRIC)<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a> in the first 24 h of stay, facilitating the early application of preventive strategies.</p><p id="par0095" class="elsevierStylePara elsevierViewall">Following the good practice recommendations of the working groups of the SEMICYUC,<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a> regular assessment of the appearance of delirium should be carried out during admission, using validated tools in all patients, particularly in those with a high risk of developing the disorder. In this way, early identification proves possible, with the adoption of the measures required to shorten its duration and avoid the development of alterations in the long term. The available validated tools include the Confusion Assessment Method for the ICU (CAM-ICU)<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a> and the Intensive Care Delirium Screening Checklist (ICDSC).<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">The strategies for the prevention and treatment of delirium may include non-pharmacological interventions<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> based on preservation of the sleep-wake cycle, early mobility, prolonged family visits, technological tools to help in communication and neurocognitive development, orientatition measures such as natural light or the use of clocks and televisions, the avoidance of mechanical restraints, etc. Moreover, if these measures prove insufficient, preventive drug treatments can be prescribed, such as nocturnal low-dose dexmedetomidine or melatonin to favor the sleep-wake cycle, with the avoidance of benzodiazepines – particularly at high doses and in continuous infusion. In relation to pharmacological treatment, the drugs of choice are α-2-agonists (dexmedetomidine or clonidine), with typical (haloperidol) or atypical antipsychotics (quetiapine, risperidone, olanzapine) being held in reserve in case of refractory agitation or psychotic symptoms, administered at the lowest dose possible and adjusted to the duration of the agitation symptoms of the patient. Valproic acid may be used in cases of delirium that fail to respond to these agents<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7,36</span></a> (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>).</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Early mobility and exercise</span><p id="par0105" class="elsevierStylePara elsevierViewall">The survivors of critical illness suffer long-term physical sequelae, including ICU acquired weakness (ICUAW) which can be seen in 25%–50% of all patients and limits their physical function and quality of life.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a> The main risk factor in this regard is confinement to bed and prolonged immobilization.</p><p id="par0110" class="elsevierStylePara elsevierViewall">The beneficial effects of mobilization strategies include the prevention of polyneuropathy and myopathy in the critically ill patient, improvement of quality of life, a shortening of ICU and hospital stay and a decrease of in-hospital mortality. The main techniques used for early mobility include kinesitherapy, transference and locomotion training, neuromuscular electrical stimulation and cycle ergometry.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a></p><p id="par0115" class="elsevierStylePara elsevierViewall">In order to implement these measures, it is essential to incorporate a physiotherapist within the ICU team to gradually introduce exercises (classified as in-bed and out-bed) according to the clinical condition of the patient. In-bed exercises include passive mobilization (when the patient is unable to collaborate), postural changes (active and passive), sitting in bed andactive mobilization (the patient collaborates with resistance and/or active exercises). Out-bed exercises, on the other hand, are based on control of the trunk (sitting at the edge of the bed), standing, transfers to the chair (active or passively) and walking (with different levels of aid).</p><p id="par0120" class="elsevierStylePara elsevierViewall">In recent years, projects have been introduced that go beyond rehabilitation and exercise in the ICU, moving patients safely to outdoor spaces such as hospital gardens, which offers both, physical and psychological benefits.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a></p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Family: family inclusion and empowerment</span><p id="par0125" class="elsevierStylePara elsevierViewall">The families of critically ill patients become the interlocutors of their wishes and needs. In addition, the presence of relatives can help reduce anxiety, thereby lessening the risk of delirium, minimizing the use of restraints and self-removal of medical devices (thereby reducing self-inflicted injury),avoiding, therefore, delays in clinical recovery and long-term sequelae. Accordingly, protocols have been adopted for some time seeking to integrate families with unrestricted visits and encouraging their participation and preparation in the critically ill patient care plan.</p><p id="par0130" class="elsevierStylePara elsevierViewall">The clinical practice guides based on scientific evidence offer strong recommendations on the need for patient and family education in the interventions that are going to be carried out, their indications, scope, advantages, limitations and risks.<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a></p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Good communication</span><p id="par0135" class="elsevierStylePara elsevierViewall">The inability of critically ill patients to communicate, especially in those subjected to mechanical ventilation, can cause distress, feelings of isolation and fears of not having their needs met. This in turn can result in anxiety, depression or PTSD.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a></p><p id="par0140" class="elsevierStylePara elsevierViewall">Methods should be adopted to guarantee correct communication, allowing patients at all times to express their physical, emotional and spiritual needs. This can be done through simple techniques such as gestures, writing or letters, words, phrases or image cards. Other more sophisticated tools include augmented and alternative communication systems.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Handout materials and holistic and personalized care</span><p id="par0145" class="elsevierStylePara elsevierViewall">Patient isolation, with disconnection from usual life and separation from the home and familiar environment, can give rise to psychological disorders. In order to prevent such problems, it is important to incorporate non-pharmacological interventions such as music therapy adapted to the preferences of the patient, allowing the use of personal electronic devices, access to news in the ICU, the strategic placement of photographs and the creation of an environment as close to that of home as possible.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Redefined ICU architectural design</span><p id="par0150" class="elsevierStylePara elsevierViewall">In recent years, several studies have proposed redesigning the areas within the ICU, seeking to prevent delirium and reduce anxiety and stress in patients. The proposals include large spaces with natural light and separation from noise and technical devices, with spaces for families, television screens or means allowing direct communication with relatives and orientation elements (clocks, calendars, etc.). In addition, augmented sensory devices are proposed, such as virtual reality headsets, loudspeakers, sound-lowering earphones, etc., along with early mobilization protocols.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Respirator: adaptation to the respirator</span><p id="par0155" class="elsevierStylePara elsevierViewall">MV poses the main challenge in the prevention of sequelae, since the technique is often stressful and painful. This makes it necessary to use analgosedation and – in some cases – neuromuscular blockers. On the other hand, the prolongation of MV implies longer bed confinement, ICUAW, and problems in establishing effective communication with the patient. Lastly, patient-respirator asynchrony can prolong MV, with an increased risk of lung and muscle injuries that lead to physical sequelae such as dyspnea or limited lung capacity. It is important to correct such asynchrony, adapting the respiratory to the patient and not the other way around, to avoid oversedation.<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a></p><p id="par0160" class="elsevierStylePara elsevierViewall">Several studies have analyzed the sequelae in survivors of ARDS, documenting persistent alteration of diffusion capacity of carbon monoxide(DLCO test) and functional limitations referred to exercise as evidenced by the SF-36 or SF-12 tools and the 6-minute walking test (6MWT).<a class="elsevierStyleCrossRefs" href="#bib0215"><span class="elsevierStyleSup">43–46</span></a> Over the short term, the pulmonary sequelae appear to be related to lung injury and the duration of MV, though, over the long term, the extrapulmonary causes (loss of muscle mass, ICUAW, etc.) determine the functional prognosis.</p><p id="par0165" class="elsevierStylePara elsevierViewall">In order to avoid these sequelae, and in addition to an adequate ventilatory strategy, other measures should be adopted to avoid prolonged MV, identify and correct asynchronies, ensure adequate management of analgosedation, and guarantee adequate nutrition and early rehabilitation.<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">47</span></a></p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Nutrition</span><p id="par0170" class="elsevierStylePara elsevierViewall">Malnutrition in critically ill patients is closely related to ICUAW. Thus, a key strategy for avoiding physical sequelae is to guarantee adequate patient nutrition based on the catabolic/anabolic processes.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">48</span></a> The latest clinical guides on nutrition in the ICU<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">49</span></a> consider all critically ill patients admitted for over 48 h to be at risk of malnutrition. Apart from the body mass index (BMI) and basal metabolic rate (BMR), it may be useful to use the GLIM (Global Leadership Initiative on Malnutrition) criteria.<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">50</span></a> The GLIM is a useful and validated tool for application in the hospital setting at the time of patient admission, and can be used to establish an early nutritional diagnosis with subsequent intervention.</p><p id="par0175" class="elsevierStylePara elsevierViewall">It is advisable to start with oral feeding rather than using the enteral or parenteral route, in the first 48 h of admission, on a continuous basis and ensuring tolerance with the use of prokinetic agents, if needed. In the early phase it is advisable to administer a hypocaloric diet, affording a gradual increase in calorie supply after the third day, with protein 1.3 g/kg/day, without exceeding 5 mg/kg/min of glucose or carbohydrates, or 1.5 g/kg/day of lipids.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">49</span></a> It should be remembered that physical activity may improve the effects of nutritional therapy.</p></span></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Therapeutic approach to PICS</span><p id="par0180" class="elsevierStylePara elsevierViewall">The conceptual changes in Intensive Care Medicine have done away with the old model of the intensivist enclosed within the ICU walls. The new model of critical illness focuses not only on the period in which the patient is admitted to the ICU but also on the previous period (early detection of serious illness in the ward) and the period after discharge from hospital<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">51</span></a> (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a>), seeking not only to ensure survival but also survival with quality of life (patient return to work, social, family and other activities as before admission). Accordingly, despite the preventive measures adopted during admission to the ICU, we need to identify patients at risk for posterior assessment in the intensive care outpatient clinic to detect and treat the sequelae.</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><p id="par0185" class="elsevierStylePara elsevierViewall">The risk factors warranting patient enrollment in follow-up programs differ among the existing protocols and consensuses.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,52,53</span></a> The points below may be seen as a summary of what has been published to date. The risk factors include concrete conditions (e.g., sepsis, ARDS, cardiac arrest, etc.) that have been described in some documents<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a>:<ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">1</span><p id="par0190" class="elsevierStylePara elsevierViewall">Patients receiving ventilatory support for more than 48 h (invasive or noninvasive, or high-flow mechanical ventilation).</p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">2</span><p id="par0195" class="elsevierStylePara elsevierViewall">Patients with an ICU stay of over 5 days.</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">3</span><p id="par0200" class="elsevierStylePara elsevierViewall">Patients who have suffered multiorgan dysfunction (two or more organs).</p></li><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel">4</span><p id="par0205" class="elsevierStylePara elsevierViewall">Patients who have suffered delirium during ICU admission.</p></li><li class="elsevierStyleListItem" id="lsti0025"><span class="elsevierStyleLabel">5</span><p id="par0210" class="elsevierStylePara elsevierViewall">Patients who in the opinion of the supervising physician should be evaluated in the intensive care outpatient clinic.</p></li></ul></p><p id="par0215" class="elsevierStylePara elsevierViewall">Such follow-up is focused on patients with recovery potential, excluding those with unrecoverable sequelae or with severe cognitive or psychiatric disorders or severe neurological or neuromuscular diseases or disabilites prior to admission. While such differentiation is complex, it is crucial for adequate patient selection.</p><p id="par0220" class="elsevierStylePara elsevierViewall">The patient history prior to admission to the ICU must be considered and documented. Based on the recommendation that “the prediction of post-ICU problems and anticipatory guidance is a task ICU clinicians should try to take on”,<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> an evaluation is needed of the patient functional capacities prior to admission to the ICU and which in turn should be documented in the case history and physical examination, to serve as a reference in the post-ICU assessment, reporting it during the transfer of competences once the patient leaves the ICU.</p><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Timing of first evaluation</span><p id="par0225" class="elsevierStylePara elsevierViewall">The first Spanish working protocol<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">52</span></a> on patient follow-up in the intensive care outpatient clinic established a timing of three months from hospital discharge. Recent recommendations from other societies suggest earlier evaluation (4 weeks after hospital discharge). Likewise, rather than establishing a prior timing of evaluations, they advocate continued assessments over the course of recovery, adapted to each individual patient and the needs of the affected spheres.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> In other words, serial evaluations are recommended, based on sub-spheres, using the recommended tools, and which will be presented in the course of the document, establishing an order of priorities proportional to the level of severity, with a view to the care that will be provided by the post-ICU team.</p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">PICS follow-up team</span><p id="par0230" class="elsevierStylePara elsevierViewall">The team in charge of follow-up is to be coordinated by the specialist in Intensive Care Medicine, and although the characteristics of each team may vary depending on the possibilities of each center, a number of services are essential for guaranteeing the quality of patient care after hospital discharge (these moreover also being essential for the application of preventive measures during admission). Integration of the services of mental health (psychiatry and clinical psychology) and rehabilitation is crucial, and it is advisable to incorporate specialists in endocrinology and nutrition, due to the nutritional problems which some patients may continue to have after hospital discharge.</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Assessment in the clinic</span><p id="par0235" class="elsevierStylePara elsevierViewall">The activities to be carried out in the clinic can be summarized as: anamnesis (from hospital discharge), physical exploration, and evaluation of the domains that conform PICS (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Psychological sphere assessment</span><p id="par0240" class="elsevierStylePara elsevierViewall">Since the psychological disorders associated with PICS are anxiety, depression and PTSD, validated screening tools should be used to identify them, with referral to the corresponding specialist on the team, where applicable. The most widely used scales are described below. <ul class="elsevierStyleList" id="lis0010"><li class="elsevierStyleListItem" id="lsti0030"><span class="elsevierStyleLabel">1</span><p id="par0245" class="elsevierStylePara elsevierViewall">Anxiety and depression. Hospital Anxiety and Depression Scale (HADS).<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a> The HADS combines two subscales of 7 items that evaluate the symptoms of depression (HADS-D subscale) and anxiety (HADS-A subscale).</p></li><li class="elsevierStyleListItem" id="lsti0035"><span class="elsevierStyleLabel">2</span><p id="par0250" class="elsevierStylePara elsevierViewall">PTSD. Any of the following scales can be used to assess the symptoms of PTSD:<ul class="elsevierStyleList" id="lis0015"><li class="elsevierStyleListItem" id="lsti0040"><span class="elsevierStyleLabel">•</span><p id="par0255" class="elsevierStylePara elsevierViewall">Impact of Event Scale (IES)-Revised.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a> This is a 22-item detection instrument based on the DSM-IV criteria. It has been adapted and validated in Spanish. In turn, the short IES-6<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">56</span></a> has slightly lower sensitivity and specificity than the original IES-R.</p></li><li class="elsevierStyleListItem" id="lsti0045"><span class="elsevierStyleLabel">•</span><p id="par0260" class="elsevierStylePara elsevierViewall">Posttraumatic Stress Disorder Symptom Severity Scale - Revised (<span class="elsevierStyleItalic">Escala de Gravedad de Síntomas Revisada [EGS-R] del Trastorno de Estrés Postraumático</span>).<a class="elsevierStyleCrossRef" href="#bib0285"><span class="elsevierStyleSup">57</span></a> This is a 21-item tool in correspondence with the diagnostic criteria of the DSM-V. The scale has been validated in the Spanish population and constitutes a modified and updated version of the EGS of 1997, which showed good psychometric properties.</p></li></ul></p></li></ul></p></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Cognitive sphere assessment</span><p id="par0265" class="elsevierStylePara elsevierViewall">The evaluation of cognitive function is a complex task that requires the participation of specialists trained in this area. However, screening for cognitive problems using simple tools proves useful for prompt and adequate patient referral to these specialized teams. The Montreal Cognitive Assessment (MoCA) test<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">58</span></a> is a simple questionnaire and is recommended for use by non-specialized personnel.</p></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Physical sphere assessment</span><p id="par0270" class="elsevierStylePara elsevierViewall">Physical function is one of the most affected spheres following discharge from the ICU. Its classical assessment comprises muscle strength and respiratory function. The former can be evaluated using a number of tests (6-minute walking test<a class="elsevierStyleCrossRefs" href="#bib0295"><span class="elsevierStyleSup">59,60</span></a> or the get up and go test<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">61</span></a>) and objective measurement devices such as the dynamometer. In this regard, the measurements obtained must be compared against those obtained in the healthy population (in our setting we have the assessments published by Luna et al.<a class="elsevierStyleCrossRef" href="#bib0310"><span class="elsevierStyleSup">62</span></a>). Respiratory function in turn should be evaluated by spirometry and also the DLCO test. The protocol and interpretation of spirometry and DLCO are to be based on the standardization and guidelines of the American Thoracic Society (ATS) and the European Respiratory Society (ERS).<a class="elsevierStyleCrossRefs" href="#bib0315"><span class="elsevierStyleSup">63–66</span></a> On the other hand, in recent years nutritional assessment has also been incorporated, since nutritional-metabolic optimization may have a positive impact upon functional recovery of the patient. There are no validated scales for the type of patients we are dealing with, however. The introduction of the GLIM criteria<a class="elsevierStyleCrossRef" href="#bib0335"><span class="elsevierStyleSup">67</span></a> for malnutrition, which are based on three phenotypical parameters (weight loss, low body mass index and reduced muscle mass) and two etiological factors (reduced food intake and inflammation), with the help of ultrasound, could be of use - though the screening and diagnosis of malnutrition in these cases remains to be clarified.</p></span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Quality of life</span><p id="par0275" class="elsevierStylePara elsevierViewall">Health-related quality of life (HRQoL) questionnaires are used to measure patient physical, social and mental status. Different questionnaires are available, though perhaps the most widely used are the 12-item Short Form healthy survey (SF-12),<a class="elsevierStyleCrossRef" href="#bib0340"><span class="elsevierStyleSup">68</span></a> a short version of the SF-36 that explores physical and mental health through different items in 8 domains, and the EuroQol-5D-5L,<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a> which is a generic and simple multiple-choice response instrument.</p></span></span></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Conclusions</span><p id="par0280" class="elsevierStylePara elsevierViewall">The sequelae frequently seen among survivors of critical illness are currently encompassed within what is known as post-intensive care syndrome (PICS), which comprises a series of symptoms in the physical, cognitive and psychological spheres. The first measure in the approach to PICS is prevention, and in this regard, bundles have been proposed for comprehensive and multidisciplinary symptoms management during the critical illness process. In addition to the prevention measures, it is important to identify patients at risk in order to ensure their post-hospital discharge assessment by the post-ICU follow-up team, which will detect, evaluate and treat the possible sequelae.</p></span><span id="sec0115" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Conflict of interest</span><p id="par0285" class="elsevierStylePara elsevierViewall">None.</p></span></span>"
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"titulo" => "Prevention"
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"titulo" => "Breathing/awakening trials: reduction of sedation and spontaneous breathing trial"
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"titulo" => "Therapeutic approach to PICS"
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1 => "Analgesia"
2 => "Sedation"
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1 => "Analgesia"
2 => "Sedación"
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4 => "Paquete medidas ABCDEF"
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"titulo" => "Abstract"
"resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">Survivors of critical illness may present physical, psychological, or cognitive symptoms after hospital discharge, encompassed within what is known as post-intensive care syndrome. These alterations result from both the critical illness itself and the medical interventions surrounding it. For its prevention, the implementation of the ABCDEF bundle (<span class="elsevierStyleBold">A</span>ssess/treat pain, <span class="elsevierStyleBold">B</span>reathing/awakening trials, <span class="elsevierStyleBold">C</span>hoice of sedatives, <span class="elsevierStyleBold">D</span>elirium reduction, <span class="elsevierStyleBold">E</span>arly mobility and exercise, <span class="elsevierStyleBold">F</span>amily) has been proposed, along with additional strategies grouped under the acronym GHIRN (<span class="elsevierStyleBold">G</span>ood communication, <span class="elsevierStyleBold">H</span>andout materials, <span class="elsevierStyleBold">R</span>edefined ICU architectural design, <span class="elsevierStyleBold">R</span>espirator, <span class="elsevierStyleBold">N</span>utrition). In addition to these preventive measures during the ICU stay, high-risk patients should be identified for subsequent follow-up through multidisciplinary teams coordinated by Intensive Care Medicine Departments.</p></span>"
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"resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0095" class="elsevierStyleSimplePara elsevierViewall">Los supervivientes de la enfermedad crítica pueden presentar síntomas físicos, psicológicos o cognitivos tras el alta hospitalaria, que se engloban en lo que se conoce como síndrome post-cuidados intensivos. Estas alteraciones son consecuencia tanto del propio proceso crítico como de las actuaciones sanitarias que ocurren en torno al mismo. Para su prevención se ha propuesto la aplicación del paquete de medidas ABCDEF (<span class="elsevierStyleBold">A</span>sses/treat pain, <span class="elsevierStyleBold">B</span>reathing/awakening trials, <span class="elsevierStyleBold">C</span>hoice of sedatives, <span class="elsevierStyleBold">D</span>elirium reduction, <span class="elsevierStyleBold">E</span>arly mobility and exercise, <span class="elsevierStyleBold">F</span>amily) al que recientemente se han sumado otras, agrupadas en las siglas GHIRN (<span class="elsevierStyleBold">G</span>ood comunication, <span class="elsevierStyleBold">H</span>andout materials, Redefined <span class="elsevierStyleBold">I</span>CU architectural design, <span class="elsevierStyleBold">R</span>espirator, <span class="elsevierStyleBold">N</span>utrition). Además de estas medidas de prevención durante el ingreso en la UCI, los pacientes de riesgo deben ser identificados para un posterior seguimiento mediante equipos multidisciplinares coordinados por los Servicios de Medicina Intensiva.</p></span>"
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"nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Giménez-Esparza C, Relucio MÁ, Nanwani-Nanwani KL, Añón JM. Impacto de la seguridad del paciente en los resultados. Desde la prevención al tratamiento del síndrome post-cuidados intensivos. Med Intensiva. 2024. <span class="elsevierStyleInterRef" id="intr0005" href="https://doi.org/10.1016/j.medin.2024.03.004">https://doi.org/10.1016/j.medin.2024.03.004</span></p>"
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"en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Prevention, identification and management of pain.</p> <p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">vNRS, numeric rating scale; VAS, visual analogue scale; ESCID, Pain Indicating Behaviors Scale (Escala de Conductas Indicadores de Dolor); BPS, Behavioral Pain Scale; CPOT, Critical-Care Pain Observation Tool; ANI, Analgesia Nociception Index; NOL, nociception level index; IMV, invasive mechanical ventilation; Cx, surgeries.</p> <p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Reproduced from<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> (with permission).</p>"
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"en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Sedation-Agitation.</p> <p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">MV, mechanical ventilation; RASS, Richmond Agitation Sedation Scale; SAS, Riker Sedation-Agitation Scale; BIS, bispectral index; ARDS, acute respiratory distress syndrome; ICH, intracranial hypertension; NMB, neuromuscular block.</p> <p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Reproduced from<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> (with permission).</p>"
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"en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Analgosedation algorithm in the critically ill patient.</p> <p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">NRS, numeric rating scale; VAS, visual analogue scale; ESCID, Pain Indicating Behaviors Scale (Escala de Conductas Indicadores de Dolor); BPS, Behavioral Pain Scale; COPT, Critical-Care Pain Observation Tool; ANI, Analgesia Nociception Index; NOL, nociception level index; RASS, Richmond Agitation Sedation Scale; SAS, Riker Sedation-Agitation Scale; BIS, bispectral index; ARDS, acute respiratory distress syndrome; ICH, intracranial hypertension; NMB, neuromuscular block; BZD, benzodiazepines; CAM-ICU, Confusion Assessment Method for the ICU; ICDSC, Intensive Care Delirium Screening Checklist.</p> <p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Reproduced from<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> (with permission).</p>"
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"en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Prevention, identification and management of delirium.</p> <p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">BZD, benzodiazepines; CAM-ICU, Confusion Assessment Method for the ICU; ICDSC, Intensive Care Delirium Screening Checklist.</p> <p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Reproduced from<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> (with permission).</p>"
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"en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Critical illness model.</p> <p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">PICS, post-intensive care syndrome; ABCDEF, bundle: <span class="elsevierStyleBold">A</span>ssess/treat pain, <span class="elsevierStyleBold">B</span>reathing/awakening trials, <span class="elsevierStyleBold">C</span>hoice of sedatives, <span class="elsevierStyleBold">D</span>elirium reduction, <span class="elsevierStyleBold">E</span>arly mobility and exercise, <span class="elsevierStyleBold">F</span>amily; GHIRN, bundle of measures: <span class="elsevierStyleBold">G</span>ood communication, <span class="elsevierStyleBold">H</span>andout materials, Redefined <span class="elsevierStyleBold">I</span>CU architectural design, <span class="elsevierStyleBold">R</span>espirator, <span class="elsevierStyleBold">N</span>utrition.</p> <p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Reproduced from.<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">51</span></a></p>"
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"leyenda" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">DLCO: Carbon monoxide lung diffusion test. ATS: American Thoracic Society. ERS: European Respiratory Society. HADS: Hospital anxiety (HADS-A) and depression scale (HADS-D). PTSD: Posttraumatic Stress Disorder; IES-R: Impact of Event Scale-Revised. MoCA: Montreal Cognitive Assessment test. SF-12: 12-item Short Form health survey.</p>"
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0 => """
<table border="0" frame="\n
\t\t\t\t\tvoid\n
\t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Questionnaires/tools \t\t\t\t\t\t\n
\t\t\t\t\t\t</th><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Domain \t\t\t\t\t\t\n
\t\t\t\t\t\t</th><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Comments/Cut-off points \t\t\t\t\t\t\n
\t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Spirometry (in addition DLCO test) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Physical/Pulmonary \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Alterations of the spirometric pattern according to ATS/ERS.<a class="elsevierStyleCrossRefs" href="#bib0315"><span class="elsevierStyleSup">63–66</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Dynamometry \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Physical/Neuromuscular \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><85% of the healthy population.<a class="elsevierStyleCrossRef" href="#bib0310"><span class="elsevierStyleSup">62</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Walking test \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Physical \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Comprehensive assessment of the respiratory, cardiovascular, metabolic, musculoskeletal and neurosensory system response of the individual during the exercise. There are some contraindications to the walking test, such as recent or uncontrolled cardiac or coronary disorders, or incapacity to understand the test. The result should be interpreted with respect to the healthy population reference values.<a class="elsevierStyleCrossRef" href="#bib0295"><span class="elsevierStyleSup">59</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Get up and go test \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Physical \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Functional assessment is used to measure the patient’s mobility and capacity to stand up from a chair, walk a short distance, and sit down again. \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The standard test procedure is as follows: \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The patient is seated in a standard chair with armrests. \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The patient is instructed to stand up from the chair without help and walk a short distance (about 3 m or 10 feet). \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The patient walks to the indicated point at a normal or safe maximum pace, without running. \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">On reaching the indicated point, the patient turns around and returns to the chair. \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The patient sits down in the chair again. \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The test evaluates <span class="elsevierStyleBold"><span class="elsevierStyleItalic">mobility, stability, coordination and balance</span></span>, as well as the risk of falls.<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">61</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">HADS-A \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Psychiatric \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">A score of ≥ 8 points identifies symptoms of <span class="elsevierStyleBold"><span class="elsevierStyleItalic">anxiety</span></span><a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a>. \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">HADS-D \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Psychiatric \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">A score of ≥8 points identifies symptoms of <span class="elsevierStyleBold"><span class="elsevierStyleItalic">depression</span></span>.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">PTSD Symptomseverity scale-Revised \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Psychiatric \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Global cut-off point of 20, and partial cut-off points above 3, 3, 5 and 5 corresponding to the re-experimentation, avoidance, cognitive alterations/negative mood state, and activation increase subscales, respectively.<a class="elsevierStyleCrossRef" href="#bib0285"><span class="elsevierStyleSup">57</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">IES-R \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Psychiatric \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The patients are required to identify the traumatic event and respond to the 22 items exploring its perception. Each item is scored from 0 (nothing) to 4 (extreme), yielding a total score of 0 (minimum) to 88 (maximum). In addition, there are subscales for the items that evaluate intrusion, avoidance and hyper-alertness. A score of ≥ 33 has been used as a cut-off point for indicating the significant presence of <span class="elsevierStyleBold"><span class="elsevierStyleItalic">post-traumatic stress symptoms</span></span>.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">MoCA test \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Cognitive \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Evaluation of <span class="elsevierStyleBold"><span class="elsevierStyleItalic">global cognitive function,</span></span> including executive function, working memory/attention, episodic memory and language.<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">58</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Score: 18−25: mild cognitive impairment \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Score 10−17: moderate cognitive impairment \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Score < 10: severe cognitive impairment.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">SF-12 \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Quality of life \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Domains related to <span class="elsevierStyleBold"><span class="elsevierStyleItalic">physical health</span></span>: general health, physical activities, common role activities and body pain. Domains related to <span class="elsevierStyleBold"><span class="elsevierStyleItalic">mental health</span></span>: vitality, social activities, emotion influenced by limitations in role activities, and general mental health. Two “summary” scores are calculated – physical health and mental health – based on the weighted means of the 8 domains. A score of <50 indicates poor health-related quality of life compared with the reference population, while a score of >50 indicates good health-related quality of life.<a class="elsevierStyleCrossRef" href="#bib0340"><span class="elsevierStyleSup">68</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">EuroQoL-5D-5L \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Quality of life \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Composed of two parts: the first part includes evaluations of <span class="elsevierStyleBold"><span class="elsevierStyleItalic">mobility, self-care, common activities, pain and anxiety/depression</span></span>. The responses generate a 5-digit number expressing the selected level in each domain (e.g., “11111” or “21123”), where each digit represents the selected level in each dimension (1, 2, 3, 4 or 5, corresponding to “no problem”, “slight problem”, “moderate problem”, “severe problem” and “extreme problem”, respectively). \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The health status corresponding to those 5 digits (the index) can be consulted and compared with the general population. \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">The second part includes a visual analogue scale consisting of a vertical line on which the patients trace a horizontal line at the level which they feel represents their current health status.<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td></tr></tbody></table>
"""
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"en" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Tools for assessing post-intensive care syndrome.</p>"
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"titulo" => "References"
"seccion" => array:1 [
0 => array:2 [
"identificador" => "bibs0005"
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0 => array:2 [
"titulo" => "Improving long-term outcomes after discharge from intensive care unit: report from a stakeholders’ conference"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "D.M. Needham"
1 => "J. Davidson"
2 => "H. Cohen"
3 => "R.O. Hopkins"
4 => "C. Weinert"
5 => "H. Wunsch"
]
]
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"host" => array:1 [
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"doi" => "10.1097/CCM.0b013e318232da75"
"Revista" => array:6 [
"tituloSerie" => "Crit Care Med."
"fecha" => "2012"
"volumen" => "40"
"paginaInicial" => "502"
"paginaFinal" => "509"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/21946660"
"web" => "Medline"
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0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Follow-up program after intensive care unit discharge"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "M. Busico"
1 => "A. das Neves"
2 => "F. Carini"
3 => "M. Pedace"
4 => "D. Villalba"
5 => "C. Foster"
]
]
]
]
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"host" => array:1 [
0 => array:2 [
"doi" => "10.1016/j.medin.2018.12.005"
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"tituloSerie" => "Med Intensiva."
"fecha" => "2019"
"volumen" => "43"
"paginaInicial" => "243"
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"link" => array:1 [
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"url" => "https://www.ncbi.nlm.nih.gov/pubmed/30833016"
"web" => "Medline"
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"identificador" => "bib0015"
"etiqueta" => "3"
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"titulo" => "The impact of the patient post-intensive care syndrome components upon caregiver burden"
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"etal" => true
"autores" => array:6 [
0 => "J. Torres"
1 => "D. Carvalho"
2 => "E. Molinos"
3 => "C. Vales"
4 => "A. Ferreira"
5 => "C.C. Dias"
]
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