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Risk factors in critical illness myopathy during the early course of critical illness: a prospective observational study

Critical Care volume 14, Article number: R119 (2010) Cite this article

Abstract

Introduction

Non-excitable muscle membrane indicates critical illness myopathy (CIM) during early critical illness. We investigated predisposing risk factors for non-excitable muscle membrane at onset of critical illness.

Methods

We performed sequential measurements of muscle membrane excitability after direct muscle stimulation (dmCMAP) in 40 intensive care unit (ICU) patients selected upon a simplified acute physiology (SAPS-II) score ≥ 20 on 3 successive days within 1 week after ICU admission. We then investigated predisposing risk factors, including the insulin-like growth factor (IGF)-system, inflammatory, metabolic and hemodynamic parameters, as well as suspected medical treatment prior to first occurrence of abnormal dmCMAP. Nonparametric analysis of two-factorial longitudinal data and multivariate analysis were used for statistical analysis.

Results

22 patients showed abnormal muscle membrane excitability during direct muscle stimulation within 7 (5 to 9.25) days after ICU admission. Significant risk factors for the development of impaired muscle membrane excitability in univariate analysis included inflammation, disease severity, catecholamine and sedation requirements, as well as IGF binding protein-1 (IGFBP-I), but did not include either adjunctive hydrocortisone treatment in septic shock, nor administration of neuromuscular blocking agents or aminoglycosides. In multivariate Cox regression analysis, interleukin-6 remained the significant risk factor for the development of impaired muscle membrane excitability (HR 1.006, 95%-CI (1.002 to 1.011), P = 0.002).

Conclusions

Systemic inflammation during early critical illness was found to be the main risk factor for development of CIM during early critical illness. Inflammation-induced impairment of growth-factor mediated insulin sensitivity may be involved in the development of CIM.

Introduction

ICU-acquired muscle weakness is a serious complication of critical illness. It has been recognized as the clinical manifestation of an ICU-acquired peripheral neuromuscular pathology [1] that, with regard to muscle pathology, is characterized by atrophy of type II muscle fibres and thick filament myopathy [2].

Diagnosis of critical illness myopathy (CIM) is either based on clinical proof of muscle weakness after awakening from analgesia and sedation, measurement of short duration low amplitude muscle unit potentials, depending on voluntary muscle contraction, or histological confirmation of muscle pathology [2]. As muscle biopsies are not routinely taken at the onset of critical illness neither approach is suitable to diagnose CIM at early critical illness.

Recent studies described measurements of muscle membrane excitability after direct muscle stimulation as a valid electrophysiological marker indicating CIM in critically ill patients [2–5]. As the investigation of muscle membrane excitability is independent of voluntary muscle contraction, it enables the detection of CIM during early critical illness when clinical evaluation is generally not applicable. Attempts to determine predisposing risk factors for CIM have yielded mixed results [6–8]. Illness severity [9], duration of immobility [10], systemic inflammation, hyperglycemia [8, 11, 12], and the use of corticosteroids or neuromuscular blocking agents [6] are disputed risk factors. Recent data suggest a relation between growth factor-mediated dysregulation of glucose and protein metabolism due to systemic inflammation and the development of myopathy [13, 14].

Measurement of muscle membrane excitability during early critical illness offers a unique opportunity to better understand and investigate early markers and potential risk factors for non-excitable muscle membrane.

The objective of this study is to investigate predisposing risk factors for the development of non-excitable muscle membrane during early critical illness, particularly considering concentration patterns of the insulin-like growth factor (IGF)-system prior to first proof of pathologically reduced muscle membrane excitability.

Materials and methods

This study presents a subanalysis of 40 patients of a recent prospective observational study [5] that investigated the predictive value of certain electrophysiological measurements on the development of ICU-acquired weakness. Validating muscle membrane excitability at the onset of critical illness turned out to be most valuable for an early prediction of ICU-acquired weakness in immobile, sedated patients adding important information to clinical estimation of the patients' motor function upon emergence from sedation. Mechanically ventilated ICU patients on an operative ICU who featured simplified acute physiology (SAPS-II) scores of 20 or higher on three successive days within one week after ICU admission were included in the study. Sequential electrophysiological measurements including measurement of muscle membrane excitability had been performed at study enrollment and every three days until pathological findings were detected or clinical evaluation of muscle strength by Medical Research Council (MRC) score was possible.

Details of electrophysiological measurements are reported elsewhere [5], in brief we assessed the compound muscle amplitude with concentric needle electrodes after direct stimulation of the muscle. Comparable with measurement of compound muscle amplitude after nerve stimulation, this is a quantitative method and the normal data in critically ill patients are 3 mV or more [3]. Patients with non-excitable muscle membrane after direct muscle stimulation show reduced amplitudes of less than 3 mV, whereas patients with an acute neuropathy show normal amplitudes within the muscle after direct muscle stimulation. Measurement of muscle membrane excitability diagnoses myopathy but cannot exclude an additional axonal motor neuropathy. Here we focused on a risk factor analysis of non-excitable muscle membrane from the beginning of critical illness until first proof of non-excitable muscle membrane. Hence, we excluded patients being pretreated on other ICUs for more than 24 hours and only included values of risk factors of the first eight days of critical illness in the analysis. The study was approved by our local review board. Written informed consent was obtained from legal proxies.

Patients were treated following standard operating procedures of intensive care incorporating severe sepsis bundles [15]. Systemic inflammation, sepsis or severe sepsis [see Table E1 in Additional file 1] accompanied by organ dysfunction [see Table E2 in Additional file 1] was classified according to consensus conference criteria [16, 17].

Inflammatory cytokines (IL-6 and IL-10), IGF-I and its binding proteins (IGFBP-I, IGFBP-III) were analysed from blood samples, drawn between days 3 and 7 as well as between days 8 and 10 after ICU admission.

Hemodynamic parameters and blood glucose levels were recorded four times daily considering least favorable values within six-hour intervals. Illness severity, SAPS-II [18], sepsis-related organ failure assessment (SOFA) [19] and other clinical data were recorded on a daily basis. Methods are further described in Additional file 1.

Statistical analysis

Results are expressed as median and 25th/75th percentiles for continuous variables and proportions for qualitative parameters, respectively. We used nonparametric tests for statistical testing.

Changes in interesting clinical outcomes with respect to time were analyzed using nonparametric analysis of longitudinal data in a two-factorial design (1st factor: compound muscle action potential after direct muscle stimulation (dmCMAP) normal versus dmCMAP abnormal patients, 2nd factor: repetitions in time), focusing on values during the first eight days after ICU admission or within a first interval between days 3 and 7, and a second interval between days 8 and 10 after ICU admission. Therefore, we compared all time points simultaneously on the corresponding response curves [20].

In univariate and subsequently in multivariate Cox' proportional hazard regressions (stepwise backward procedure), we tested risk factors impairing muscle membrane excitability (as a dependent variable). For all parameters we included values from days of first IL-6 measurements in the analysis. Hazard ratios (HR) with their 95% confidence intervals (CI) and the corresponding P values were calculated for each risk factor. P values less than 0.05 (two-sided) were considered as statistically significant.

We evaluated the diagnostic test performance of IL-6 and SOFA to indicate the development of myopathy by receiver operating characteristics (ROC) analysis using abnormal dmCMAP amplitude less than 3 mV as electrophysiological parameter for diagnosis of myopathy and IL-6 as well as SOFA as test variables. We combined the diagnostic tests regarding sensitivity and specificity of SOFA and IL-6 to indicate myopathy with the help of the known 'believe-the-positive' rule.

All tests should be understood as constituting exploratory data analysis, such that no adjustments for multiple testing have been made. We used SPSS, Version 14 (SPSS, Inc., Chicago, IL, USA), and SAS, Version 9.1 (SAS Institute, Inc., Cary, NC, USA).

Results

Patient characteristics

Forty patients at the onset of critical illness were enrolled in the study. Twenty-two patients developed abnormal muscle membrane excitability in terms of reduced compound muscle action potential after direct muscle stimulation (dmCMAP abnormal) within 7 (5 to 9.25) days after admission to ICU as reported earlier [5]. Eighteen patients showed normal muscle membrane excitability (dmCMAP normal). Patients with abnormal dmCMAP revealed significant paresis (MRC 2.6 (1.84 to 3.27)) after emergence from sedation compared with patients with normal dmCMAP (MRC 4.1 (4 to 4.84); (P < 0.0001). ICU length of stay was significantly prolonged in dmCMAP abnormal patients (26 (18 to 38) days) compared with dmCMAP normal patients (13 (8 to 18) days; P < 0.0001). Patients' characteristics upon admission and within the first eight days after ICU admission are shown in Table 1.

Table 1 Patients' characteristics within the first week after ICU admission in patients without and with critical illness myopathy
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Risk factors of critical illness myopathy in dmCMAP normal and dmCMAP abnormal patients within the first week after ICU admission.

Within the first eight days after ICU admission, patients with abnormal dmCMAP had significantly more days with systemic inflammatory response syndrome, severe sepsis, and dysfunction of two or more organs compared with patients with normal dmCMAP (Table 1 and Figure 1).

Figure 1
figure 1

Critical illness myopathy and disease severity scores. Normal (≥3 mV) and abnormal (< 3 mV) direct muscle stimulation compound muscle action potentials (dmCMAP), (a) simplified acute physiology score-II (SAPS-II) and (B) sequential organ failure assessment (SOFA) score on the first eight days after ICU admission. Patients with impaired muscle membrane excitability had significantly higher SAPS-II and SOFA scores during the first eight days after ICU admission. Nonparametric analysis of longitudinal data in a two-factorial design (1st factor: dmCMAP normal versus dmCMAP abnormal, 2nd factor: repetitions in time. The statistical analysis was the same for Figures 1 to 6, either focusing on values from the first eight days after ICU admission (Figures 1, 2, 4 and 5) or referring to a first and second interval between days 3 and 7 after ICU admission and between days 8 and 10 after ICU admission, respectively (Figures 3 and 6).

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Moreover, patients with abnormal dmCMAP received significantly higher doses of norepinephrine within the first week after ICU admission (Figure 2). Hemodynamic stability in terms of circulatory shock was significantly impaired within the first eight days compared with dmCMAP normal patients (Figure 2). There was no difference regarding frequency and cumulative dosage of adjunctive hydrocortisone therapy within the first week after ICU admission between the two groups (Table 1).

Figure 2
figure 2

Critical illness myopathy and hemodynamic variables. Normal (≥3 mV) and abnormal (< 3 mV) direct muscle stimulation compound muscle action potentials (dmCMAP), (a) mean shock index and (b) daily norepinephrine dosage on the first eight days after ICU admission. Patients with impaired muscle membrane excitability had significantly higher shock indices and required significantly higher daily norepinephrine dosages during the first eight days after ICU admission.

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DmCMAP abnormal patients received significantly higher doses of analgesics and sedation and more neuromuscular blocking agents; however, the cumulative dosage of neuromuscular blocking agents was low within both groups (Table 1).

IL-6 plasma levels were significantly higher within the first week (day 5 (3 to 7)) in patients with abnormal dmCMAP. In the second week (day 8 (6 to 10.25)), IL-6 decreased in both groups but remained significantly higher in dmCMAP abnormal patients. There was no difference between the two groups regarding IL-10 plasma levels (Figure 3).

Figure 3
figure 3

Critical illness myopathy and systemic inflammation. Normal (≥3 mV) and abnormal (< 3 mV) direct muscle stimulation compound muscle action potentials (dmCMAP), (a) IL-6 plasma levels, (b) IL-10 plasma levels at median day (25th/75th percentile) 5 (3 to 7) and median day 8 (6 to 10,25). Patients with impaired muscle membrane excitability had significantly higher IL-6 plasma levels but no significant differences of IL-10 plasma levels at both measurement intervals.

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Daily blood glucose levels (Figure 4), total carbohydrate intake, insulin requirement (Table 1), and the insulin per kcal carbohydrate intake (Figure 4) were not significantly different between the two groups within the first week. Patients with abnormal dmCMAP had a significantly higher plasma osmolarity and sodium plasma levels during the first eight days after ICU admission than dmCMAP normal patients (Figure 5).

Figure 4
figure 4

Critical illness myopathy and glycemic control. Normal (≥3 mV) and abnormal (< 3 mV) direct muscle stimulation compound muscle action potentials (dmCMAP), (a) mean blood glucose levels and (b) insulin in relation to daily carbohydrate intake on the first eight days after ICU admission. Mean blood glucose levels and insulin in relation to daily carbohydrate intake did not differ significantly in patients with impaired muscle membrane excitability compared with patients with normal membrane excitability.

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Figure 5
figure 5

Critical illness myopathy and plasma homeostasis. Normal (≥3 mV) and abnormal (< 3 mV) direct muscle stimulation compound muscle action potentials (dmCMAP), (a) plasma sodium, (b) plasma osmolarity, (c) plasma pH and (d) plasma urea (multiply by factor 0.46 for blood urea nitrogen (BUN) conversion) over the first eight days after ICU admission. Patients with impaired muscle membrane excitability had significantly higher plasma sodium, plasma osmolarity, plasma pH and plasma urea during the first eight days after ICU admission.

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IGF-I was reduced in dmCMAP abnormal patients at both test intervals (87.2 ng/ml (65.9 to 119.5) versus 104.5 ng/ml (74.4 to 136.9) and 76.1 ng/ml (55.1 to 119.5) versus 87.2 ng/ml (65.8 to 122)), but differences did not reach statistical significance. Plasma levels of IGFBP-III were not different between both groups whereas IGFBP-I as a marker reflecting impaired insulin sensitivity was significantly higher in dmCMAP abnormal patients at both test intervals (Figure 6).

Figure 6
figure 6

Critical illness myopathy and insulin sensitivity. Normal (≥3 mV) and abnormal (< 3 mV) direct muscle stimulation compound muscle action potentials (dmCMAP), (a) insulin-like growth factor binding protein (IGFBP)-1 plasma levels, (b) IGFBP-3 plasma levels at median day (25th/75th percentile) 5 (3 to 7) and median day 8 (6 to 10,25). Patients with impaired muscle membrane excitability had significantly higher IGFBP-1 plasma levels but no significant differences of IGFBP-3 plasma levels at both measurement intervals.

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Cox' regressions analysis

Separate (univariate) Cox regression analyses for risk factors impairing muscle membrane excitability are shown in Table 2. Analyses included values from day of first IL-6 measurements.

Table 2 Risk factors leading to impaired muscle membrane excitability
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In univariate analysis severity of illness, sepsis-related organ dysfunction, inflammation, catecholamine requirements, sedation requirements and an impaired insulin sensitivity turned out as significant risk factors for the development of impaired muscle membrane excitability within the early course of critical illness. An increased osmolarity, adjunctive hydrocortisone treatment in septic shock, administration of neuromuscular blocking agents and aminoglycosides were not significantly correlated with the development of impaired muscle membrane excitability.

In the backward selection of multivariate Cox regression analysis (Figure 7) the extent of inflammation as reflected by IL-6 plasma levels and the fentanyl dosage remained as independent risk factors for the development of impaired muscle membrane excitability.

Figure 7
figure 7

Multivariate Cox' proportional hazard regression after backward selection for variables, that were considered as risk factors impairing muscle membrane excitability (as dependent variable). For the particular parameter values from the day of first blood sampling for IL-6 were included in the analysis. Hazard ratios (HR) with (95% confidence intervals (CI) and P values for each variable. HC, adjunctive hydrocortisone treatment in septic shock; IGFBP, insulin-like growth factor-binding protein; IL-6, interleukin-6; SOFA, sequential organ failure assessment score.

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Sensitivity and specificity

Sensitivity and specificity of SOFA score to predict abnormal membrane excitability was highest on day 4 at a cut-off value of 10 (sensitivity = 65% and specificity = 93.8%). The cut-off value for IL-6 predicting abnormal membrane excitability was observed at 230 pg/ml, featuring sensitivity of 71.4% and specificity of 93.3%. According to the 'believe the positive' rule applied in a combined cross tabulation of patients with SOFA scores of 10 or more at day 4 after ICU admission and/or IL-6 plasma levels of 230 pg/ml or more, we observed a sensitivity of 85.7% and a specificity of 86.7% of this combination for predicting development of abnormal dmCMAP.

Discussion

In this observational study we investigated predisposing risk factors leading to non-excitable muscle membrane indicating CIM during early critical illness. The main finding was a significant relation between muscle membrane inexcitability, disease severity and IL-6 plasma levels.

In the absence of a reliable clinical parameter identifying patients at risk of developing CIM during early critical illness, when motor function is not assessable due to analgesia and sedation, current data on risk factors leading to CIM are derived mostly from prospective cohort studies relating data from ICU admission with patients' motor function once assessable [6]. One excellent study investigating risk factors for combined critical illness neuromyopathy [9] during early critical illness showed that illness severity, determined through acute physiology and chronic health evaluation (APACHE) III scores, predicted the later development of critical illness neuromyopathy. In our study, sequential measurements of muscle membrane excitability offers the opportunity to focus on CIM and to determine the time frame in which CIM originates during early critical illness, thereby improving stratification of predisposing risk factors for CIM.

Univariate analysis indicated illness severity, IL-6, hemodynamic impairment, decreased insulin sensitivity as well as analgesia and sedation as predisposing risk factors. However, only IL-6 and dosage of analgesia emerged as independent risk factors from multivariate analysis. Interestingly, we did not observe any significant relation between development of non-excitable muscle membrane and application of low-dose hydrocortisone, aminoglycosides or neuromuscular blocking agents, which have frequently been incriminated as being involved in the development of CIM.

Large prospective randomized studies have shown that glycemic control is associated with the development of neuromuscular dysfunction [11, 12]. In our study, we did not observe a difference in blood glucose levels between dmCMAP normal and abnormal patients because we aimed for glycemic control below 150 mg/dl in all of our patients. However, despite comparable blood glucose levels between the groups, IGFBP-1 was significantly higher in abnormal dmCMAP patients. In agreement with other reports [21, 22] we consider increased IGFBP-1 as a parameter indicative of impaired insulin sensitivity. Hence, our data suggest that significantly impaired insulin sensitivity during early critical illness was related to development of abnormal muscle membrane excitability.

In parallel, dmCMAP abnormal patients revealed a significant hyperosmotic state within the first days of critical illness. Hyperosmolality is related to illness severity [23] and has been described as a risk factor for critical illness neuropathy [24]. It is worth noting that the study by Garnacho-Montero and colleagues [24] did not differentiate between myopathy and neuropathy. In our study, hyperosmolality during the first days after ICU admission was significantly related to electrophysiological-proven muscle pathology. It can be speculated that this hyperosmotic state may have led to osmotic stress-induced reduction of cellular insulin sensitivity in our patients, which has been shown in adipocytes under experimental conditions [25].

However, alteration of insulin sensitivity and plasma osmolality are most likely related to systemic inflammation in our study. Our data are in agreement with the general perception that systemic inflammation and sepsis-related organ dysfunction are major triggers for the development of CIM [6, 8, 9, 26]. Earlier experimental data inducing inflammation in rats by intravenous inoculation of endotoxin showed that IL-6 increased muscle fatigue [27] and decreased muscle contractility of the diaphragm [28]. Interestingly, recent clinical data indicate a relation between IL-6 and reduced muscle strength in elderly people [29]. Our data reveal a possible role of IL-6 in the development of non-excitable muscle membrane during early critical illness finally leading to muscle weakness.

IL-6 seems to be an important mediator leading to muscle protein breakdown [30]. One mechanism may lie in the inhibition of growth factor-mediated (e.g. IGF-I) intracellular signaling by IL-6 [13, 31]. IGF-I plays a central role in glucose uptake and protein synthesis, and was shown to be downregulated in inflammation and sepsis [13]. Impairment of IGF-I may be due to inflammation-induced upregulation of high-affinity IGFBP-1 which prevents IGF-I receptor binding [32]. In vitro [33] and later in vivo [14], it has been shown that an increase of IGFBP-1 reduced the IGF-I-mediated glucose uptake and reduced protein synthesis in skeletal muscle within an experimental setting. In line with this, our data suggest that impaired growth factor-mediated intracellular signaling due to systemic inflammation may be involved in the development of CIM.

Corticosteroids are controversially discussed as aggravating factors of CIM [6, 7, 9, 34]. It is well established that high-dose application of corticosteroids, for example in patients with chronic obstructive pulmonary disease, results in selective loss of thick myosin filaments in skeletal muscle fibers [35], a so-called steroid-induced myopathy [36].

Nevertheless, these reports refer to steroid myopathy as a result of high-dose steroid application. A link between 'low-dose hydrocortisone' treatment as adjunctive therapy during septic shock and development of CIM has been postulated [15], but never proven. Several data indicate that moderate doses of steroids do not prolong mechanical ventilation due to muscle weakness but are related to significantly more ventilator-free days and earlier spontaneous breathing capacity [37]. In an earlier study we did not observe an association between low-dose hydrocortisone application and development of paresis [5, 34]. In this study we were able to show that low-dose hydrocortisone application does not provoke impaired muscle membrane excitability, suggesting that steroid involvement in CIM development is dose dependent [8].

Furthermore, dosage of analgesics and sedatives was significantly associated with the development of non-excitable muscle membrane. Interpreting higher doses of analgesics and sedatives as higher degrees of immobilization, this finding is in line with recent studies describing that immobilization aggravated neuromuscular weakness in an experimental setting [38] and that early physical mobilization resulted in a better clinical outcome of motor function [10].

For clinicians it is difficult to estimate patients at risk for the development of CIM. The APACHE-III score has been cited as being able to identify patients at risk for critical illness neuromyopathy [9]. In our study we used the SOFA score because it is widely accepted in the ICU setting, and has been validated to monitor organ dysfunction-related to sepsis [19]. Our results indicate that a SOFA score of 10 or above and/or IL-6 plasma levels of 230 pg/ml or more at the onset of critical illness disclose high-risk patients for the development of non-excitable muscle membrane.

The following limitations of this study need to be addressed. Although we observed a statistically significant effect for IL-6 as a main risk factor for non-excitable muscle membrane, it has to be stressed that the overall effect was small, which may be due to small sample size. It also needs to be mentioned that blood samples were collected at two different time points only and that the course of inflammatory parameters was not followed daily. However, this was designed as a pilot study for hypothesis generation. The clinical significance has to be addressed in further studies.

Conclusions

Systemic inflammation during early critical illness turned out to be the main risk factor for the development of non-excitable muscle membrane indicating CIM. It may be hypothesized that inflammation-induced impairment of growth factor-mediated intracellular signaling is involved in the pathophysiology of CIM. Furthermore, adjunctive treatment with low-dose hydrocortisone during septic shock was not associated with development of CIM.

Key messages

  • Non-excitable muscle membrane indicates CIM during early critical illness.

  • Inflammation, disease severity, decreased insulin sensitivity, catecholamine and sedation requirement turned out to be significantly related to the development of impaired muscle membrane excitability.

  • IL-6 and dosage of analgesia emerged as independent risk factors from multivariate analysis.

  • Inflammation-induced impairment of growth-factor-mediated insulin sensitivity may be involved in the development of CIM.

  • In contrast to prior assumptions we could not observe any significant relation between development of CIM and application of low-dose hydrocortisone in septic shock.

Abbreviations

APACHE:

acute physiology and chronic health evaluation

CI:

confidence interval

CIM:

critical illness myopathy

dmCMAP:

compound muscle action potential after direct muscle stimulation

HR:

hazard ratio

IGF:

insulin-like growth factor

IGFBP:

insulin-like growth factor binding protein

IL:

interleukin

MRC:

Medical Research Council

ROC:

receiver operating characteristic

SAPS:

simplified acute physiology score

SOFA:

sepsis-related organ failure assessment.

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Acknowledgements

We thank Mrs Anne Goessinger for her outstanding support in performing laboratory investigations. This study was granted by the Deutsche Forschungsgemeinschaft (KFO 192, WE 4386/1-1).

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    Authors and Affiliations

    1. Clinic of Anesthesiology and Intensive Care Medicine, Charité University Medicine, Campus Virchow-Klinikum, Augustenburger Platz 1, Berlin, 13353, Germany

      Steffen Weber-Carstens, Maria Deja, Susanne Koch, Florian Bubser, Claudia D Spies & Didier Keh

    2. Clinic of Anesthesiology and Intensive Care Medicine, Charité University Medicine, Campus Charité Mitte, Charitéplatz 1, Berlin, 10117, Germany

      Steffen Weber-Carstens, Maria Deja, Susanne Koch, Florian Bubser, Claudia D Spies & Didier Keh

    3. Clinic of Endocrinology, Diabetes and Nutritional Medicine, Charité University Medicine, Campus Benjamin Franklin, Hindenburgdamm 30, Berlin, 12203, Germany

      Joachim Spranger

    4. Institute of Medical Biometry, Charité University Medicine, Campus Charité Mitte, Charitéplatz 1, Berlin, 10117, Germany

      Klaus D Wernecke

    5. Muscle Research Unit, Experimental and Clinical Research Center, Charité University Medicine, Campus Berlin Buch, Lindenberger Weg 80, Berlin, 13125, Germany

      Simone Spuler

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    1. Steffen Weber-Carstens
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    Correspondence to Steffen Weber-Carstens.

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    The authors declare that they have no competing interests.

    Authors' contributions

    SW-C conceived of the study, performed data and statistical analysis, wrote the final manuscript and is head of the project, which is funded by the Deutsche Forschungsgemeinschaft. MD and DK participated in the design of the study, in data analysis and in writing the final manuscript. SK performed the electrophysiological measurements and analysis. JS and DK performed laboratory data measurements and analysis. FB programmed the data base and participated in data collection and analysis. KW prepared the statistical part of the manuscript and performed the statistical analysis. CS critically revised the manuscript and gave final approval. SS critically revised the electrophysiological data analysis and participated in writing the paper. All authors read and approved the final manuscript.

    Steffen Weber-Carstens, Maria Deja contributed equally to this work.

    Electronic supplementary material

    13054_2010_8503_MOESM1_ESM.DOCX

    Additional file 1: Further description of methods and definitions. The additional file contains additional information on exclusion criteria, electrophysiologic measurements, general ICU care, and laboratory testing [39]. Two tables within this file explain the conditions required for defining systemic inflammatory response syndrome, sepsis, severe sepsis, or septic shock (E1) and organ dysfunction (E2). (DOCX 17 KB)

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    Weber-Carstens, S., Deja, M., Koch, S. et al. Risk factors in critical illness myopathy during the early course of critical illness: a prospective observational study. Crit Care 14, R119 (2010). https://doi.org/10.1186/cc9074

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    • DOI: https://doi.org/10.1186/cc9074

    Keywords

    Critical Care

    ISSN: 1364-8535