What s New in ICU Nutrition Research? Danielle Bear Principal Critical Care Dietitian St Thomas Hospital, London

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Transcription:

What s New in ICU Nutrition Research? Danielle Bear Principal Critical Care Dietitian St Thomas Hospital, London

Outline Individualised nutrition support Defining energy targets Feeding route Current research Energy expenditure Feeding route Nutrient losses on CRRT

Energy Targets

Energy Balance Larger energy deficit associated with worse outcomes Increased ICU LOS Increased days on MV Increased complications Increased mortality Rubinson et al, 2004; Villet et al, 2005, Dvir et al, 2006; Petros et al, 2006

Energy Balance

Energy Balance Study Outcome Permissive Underfeeding (Arabi et al, 2011) Decreased hospital mortality Decreased 180 day mortality Underfeeding Group The EDEN Study (Rice et al, 2012) No difference Increased trend toward d/c home over rehabilitation facility Full feeding Group

Conflicting Evidence ESPEN GUIDELINES ESPEN Guidelines on Ent eral Nut rit ion: Intensive care $ http:// intl.elsevierhealth.com/ j ournals/ clnu K.G. Kreymann a,, M.M. Berger b, N.E.P. Deutz c, M. Hiesmayr d, P. Jolliet e, G. Kazandj iev f, G. Nitenberg g, G. van den Berghe h, J. Wernerman i, DGEM: $$ C. Ebner, W. Hartl, C. Heymann, C. Spies a Depart ment of Int ensive Care Medicine, Universit y Hospit al Eppendorf, Hamburg, Germany b Soins Int ensifs Chirurgicaux et Cent re des Brûles, Cent re Hospit alier Universit aire Vaudois (CHUV)-BH 08.660, Lausanne, Swit zerland c Depart ment of Surgery, Maast richt Universit y, Maast richt, The Net herlands d Depart ment of Anaest hesiology and Int ensive Care, Medical Universit y of Vienna, Vienna, Aust ria e Depart ment of Int ensive Care, Universit y Hospit al Geneva, Geneva, Swit zerland f Depart ment of Anaest hesiology and Int ensive Care, Milit ary Medical Universit y, Sofi a, Bulgaria g Depart ment of Anaest hesia, Int ensive Care and Infect ious Diseases, Inst it ut Gust ave-roussy, Villej uif, France h Depart ment of Int ensive Care Medicine, Universit y Hospit al Gast huisberg, Leuven, Belgium i Depart ment of Anaest hesiology and Int ensive Care Medicine, Karolinska Universit y Hospit al, Huddinge, St ockholm, Sweden Received 20 January 2006; accept ed 20 January 2006 KEYWORDS Guideline; Clinical pract ice; Evidence-based; Enteral nutrition; Tube feeding; Oral nutritional sup- Summary Enteral nutrition (EN) via tube feeding is, today, the preferred way of feeding the critically ill patient and an important means of counteracting for the cat abolic st at e induced by severe diseases. These guidelines are int ended to give evidence-based recommendat ions for t he use of EN in pat ient s who have a complicat ed course during t heir ICU st ay, focusing part icularly on t hose who develop a severe inflammatory response, i.e. patients who have failure of at least one organ during their ICU stay.

Energy Targets

Energy Targets Study Outcome TICACOS (Singer et al, 2011) Lower hospital mortality Positive energy and protein balance Longer ICU LOS More days on mechanical ventilation Increased infection rates Intervention EPaNIC (Caesar et al, 2012) Fewer infections Shorter duration on mechanical ventilation Shorter ICU and Hospital LOS Late Group SPN (Heideggar et al, 2012) Reduced number of infections Reduced number of antibiotic days Shorter duration on mechanical ventilation SPN Group

Energy Targets Aims Patients groups, nutritional status LOS Sample sizes Outcomes Methodology Indirect calorimetry (once vs repeated) Predictive equations Protein targets rarely met

Energy Targets Intervention Control 3000 2500 Energy Targets (kcal/day) 2000 1500 1000 500 0 Singer Heideggar Caesar Rice Arabi Study Adapted from Singer & Cohen, 2012

Energy Targets More individualised approach Indirect Calorimetry SPN adjustments Repeated calculations/measurements of energy needs Calculate balances?meet protein intakes

Current Research A study comparing two methods of measuring energy expenditure in critically ill patients: Indirect Calorimetry (Deltatrac II) versus Sensewear Armband.

Aim: To determine level of agreement (bias and reliability in energy expenditure measurements between indirect calorimetry (deltatrac II) and the sensewear armband in mechanically ventilated, critically ill patients.

Adult ( 18 years) Inclusion Criteria Anticipated MV and artificial nutrition support >72hours Exclusion Criteria FiO 2 60% PEEP > 8mmHg Ventilated with nitric oxide ECMO HFOV CRRT Air leak in ventilation circuit Ventilated with AVEA ventilator Bolus feeding Nickel allergy Therapeutic cooling Study burden Liverpool Care pathway

Exclusion Percentage Excluded (%) Air leak in the ventilation circuit 39 Continuous renal replacement therapy 22 Expected mechanical ventilation <72 hours 9 PEEP > 8mmHg 9 Chest drains insitu 6 Decision made to limit/withdraw care 6 ECMO 4 Ventilated with AVEA ventilator 4 Fi0 2 > 60% 3 Trial burden 2 Non-English speaking 1 Therapeutic cooling 1

Interim Results Sex Diagnosis Age BMI SOFA FiO 2 (kg/m 2 ) (%) 1 Male OOHCA 60 30 1 21 2 Female Severe Respiratory Failure 30 16.7 4 35 3 Male OOHCA 50 27.8 3 30 4 Male Cardiogenic shock 44 24 6 30 Median - - 47 25.9 3.5 30 IQR - - 33.5-57.5 18.5-29.4 1.5-5.5 23.3-33.8

Interim Results Deltatrac II (kcal) Sensewear Armband (kcal) Percent difference (%) P value 1 2570 2034 21 2 1610 1402 13 3 3322 2259 32 4 2166 1887 13 Mean 2417 1895 19.8 0.07 (SD) (720.3) (181.4) (8.9)

Interim Results Bland Altman Plot

Conclusion - Bland Altman analysis shows wide limits of agreement. - Sensewear Armband appears more practical and user friendly than indirect calorimetry. - Completion of the study with adequate recruitment required.

Feeding Route Post-Pyloric Feeding Limited studies showing benefit May reduce incidence of pneumonia May improve nutrient provision in certain groups of patients High risk for GI intolerance Access may be an issue Cortrak Tiger 2 Davies et al, 2012; Acosta-Escribano et al, 2010; White et al, 2009; Hsu et al, 2009.

ECMO Gastric feeding leads to inadequate energy intake (mean 55% on ECMO) High percentage with large GRVs More than 70% requiring prokinetics within 24 hours 95% by 48 hours Feed interruptions Makikado et al, 2012; Lukas et al, 2010; Scott et al, 2004.

Results Energy Intake (as % of target) No. days energy intake adequate* (%) Protein Intake (as % of target) No. days protein intake adequate* (%) Nutrient delivery and adequacy of feeding Gastric Jejunal p value 79.2 (62.8-89.5) 92.3 (76.0-99.8) <0.016 135 (60.5) 133 (82.1) <0.001 71.1 (55.0-91.2) 91.9 (71.8-102.8) <0.027 131 (58.7) 127 (78.4) <0.001

Conclusions Jejunal feeding was associated with greater proportion of adequate feeding days. Daily estimated nutritional requirements were met using jejunal feeding though not with gastric feeding.

Observational study measuring essential nutrients in critically ill patients with severe acute kidney injury treated with and without continuous haemofiltration.

Aim: To serially measure plasma levels of vitamins, trace elements and amino acids in critically ill patients with severe AKI and to evaluate whether there are any additional losses into the filtrate during continuous veno-venous haemofiltration (CVVH).

Primary Outcome Difference in plasma concentrations of essential micronutrients between patients with and without CVVH. Secondary Outcomes a) Concentrations of trace elements, vitamins and amino acids in filtrate in patients on CVVH b) Differences in filtrate losses between patients on CVVH 30ml/kg/hr vs >30ml/kg/hr c) Differences in serum levels of micronutrients and amino acids between patients on CVVH 30ml/kg/hr vs > 30ml/kg/hr.

Inclusion Criteria Patients in the Critical Care Unit with severe AKI (Stage II or II) 18 years Exclusion Criteria Pre-existing dialysis dependent renal failure Life expectancy <48 hours Need for TPN Need for IV multivitamin or trace elements Jehovah s Witness Hb <7g/dl (unless being transfused for clinical reasons)

KDIGO Guidelines Stage Serum Creatinine Urine Output 1 1.5-1.9 times baseline or 0.3mg/dl (.26.4umol/L) increase in 48 hours <0.5ml/kg.hr for 6-12 hours 2 3 2.0-2.9 times baseline 3.0 times baseline OR increase in creatinine 4mg/dl (352umol/L) OR treatment with RRT <0.5ml/kg.hr for 12 hours <0.3ml/kg.hr 24 hours OR anuria 12 hours

A phase III, open, multi-centre, randomised controlled trial comparing the clinical and cost-effectiveness of early nutritional support in critically ill patients via the parenteral versus the enteral route

Primary objectives To estimate the effect of early nutritional support via the parenteral route (PN) compared with the enteral route (EN) on mortality at 30 days To estimate the incremental cost-effectiveness of early PN compared with early EN at one year.

Secondary objectives To compare PN with EN for: Duration of specific and overall organ support Infectious and non-infectious complications Duration of critical care unit and acute hospital length of stay Mortality at: discharge from the critical care unit and from hospital, 90 days and at one year Nutritional and health-related quality of life at 90 days and at one year Resource use and costs at 90 days and at one year Estimated lifetime incremental cost-effectiveness

Inclusion Criteria Exclusion Criteria Adult (defined as age 18 years or over) An unplanned admission (including planned admissions becoming unplanned e.g. unexpected post-operative complications) Expected to receive nutritional support for two or more days in your unit Not planned to be discharged within three days (defined by clinical judgment) from your unit. Who have been in a critical care unit for more than 36 hours (i.e. from the date/time of original admission to a critical care unit) Previously randomised into CALORIES Pre-existing contraindications to PN or EN Received PN or EN within the last seven days Admitted with a percutaneous endoscopic gastrostomy, percutaneous endoscopic jejunostomy, needle/surgical jejunostomy or nasojejunal tube in situ Admitted to the critical care unit for treatment of thermal injury (burns) Palliative care Patients whose expected stay in the UK is less than six months Pregnant

Where are we now? 25 active sites More joining > 1800 patients recruited so far Aiming 2400 Plan to finish recruitment November 2013

Questions