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Impact of critical illness and withholding of early parenteral nutrition in the pediatric intensive care unit on long-term physical performance of children: a 4-year follow-up of the PEPaNIC randomized controlled trial

Abstract

Background

Many critically ill children face long-term developmental impairments. The PEPaNIC trial attributed part of the problems at the level of neurocognitive and emotional/behavioral development to early use of parenteral nutrition (early-PN) in the PICU, as compared with withholding it for 1 week (late-PN). Insight in long-term daily life physical functional capacity after critical illness is limited. Also, whether timing of initiating PN affects long-term physical function of these children remained unknown.

Methods

This preplanned follow-up study of the multicenter PEPaNIC randomized controlled trial subjected 521 former critically ill children (253 early-PN, 268 late-PN) to quantitative physical function tests 4 years after PICU admission in Leuven or Rotterdam, in comparison with 346 age- and sex-matched healthy children. Tests included handgrip strength measurement, timed up-and-go test, 6-min walk test, and evaluation of everyday overall physical activity with an accelerometer. We compared these functional measures for the former critically ill and healthy children and for former critically ill children randomized to late-PN versus early-PN, with multivariable linear or logistic regression analyses adjusting for risk factors.

Results

As compared with healthy children, former critically ill children showed less handgrip strength (p < 0.0001), completed the timed up-and-go test more slowly (p < 0.0001), walked a shorter distance in 6 min (p < 0.0001) during which they experienced a larger drop in peripheral oxygen saturation (p ≤ 0.026), showed a lower energy expenditure (p ≤ 0.024), performed more light and less moderate physical activity (p ≤ 0.047), and walked fewer steps per day (p = 0.0074). Late-PN as compared with early-PN did not significantly affect these outcomes.

Conclusions

Four years after PICU admission, former critically ill children showed worse physical performance as compared with healthy children, without impact of timing of supplemental PN in the PICU. This study provides further support for de-implementing the early use of PN in the PICU.

Trial registration ClinicalTrials.gov, NCT01536275; registered on February 22, 2012.

Background

Many critically ill children face long-term health problems and impaired physical, neurocognitive, emotional, and behavioral development [1,2,3,4,5,6]. These sequelae are observed up to years after hospital discharge and can negatively affect health-related quality of life and academic performance [7, 8]. Qualitative scales and questionnaires are valuable tools for documenting developmental impairments in the daily life functioning of the children after critical illness [6,7,8]. Certain domains have also been extensively documented with the use of objective, quantitative measurements such as anthropometrics to assess growth and a wide range of neurocognitive function tests to evaluate neurocognitive development [4, 5, 9,10,11]. General assessment of long-term physical functional capacity in daily life after critical illness, however, still remains limited to the use of scales and questionnaires [12,13,14].

Several pre-admission and disease-related factors may play a role in bringing about the developmental impairments, but also the medical care provided during the pediatric intensive care unit (PICU) stay may contribute, providing leverage points for identifying interventions able to alleviate these poor outcomes [4, 9,10,11, 15, 16]. One such intervention is avoiding the early use of supplemental parenteral nutrition (PN) in the PICU, as shown in the long-term follow-up of the multicenter randomized controlled PEPaNIC trial. This study had first shown that, as compared with initiating parenteral nutrition (PN) within 24 h after admission to supplement insufficient enteral nutrition (early-PN), withholding of supplemental PN in the first week in the PICU (late-PN) improved short-term PICU outcomes [17]. However, as underfeeding has been related to worse cognitive performance, behavioral problems, and impaired physical development of otherwise healthy children [18,19,20,21,22,23], there were concerns about potential adverse long-term consequences of the low caloric and macronutrient intake with late-PN for health and physical and neurocognitive development. Therefore, patients were invited for an extensive investigation of these outcomes 2 and 4 years after PICU admission, in comparison with healthy children. As compared with healthy children, former PICU patients showed worse health status, signs of impaired growth, worse neurocognitive functioning, more emotional and behavioral problems, and worse quality of life [8, 10, 11]. Importantly, as compared with early-PN, late-PN did not worsen any of these outcomes and even attenuated the impairments in executive functioning and visual-motor integration and reduced emotional/behavioral problems 2 and/or 4 years later [10, 11], with differential DNA methylation identified as plausible molecular basis of these effects [24, 25]. It remained unclear, however, whether the timing of initiating PN may also affect the patients’ long-term physical function.

In this study, we compared several quantitative measures of physical performance of former PEPaNIC patients 4 years after PICU admission with those of healthy children with a similar age and sex distribution and investigated whether late-PN versus early-PN differentially affected these outcomes.

Methods

Study design and participants

The PEPaNIC randomized controlled trial (RCT) enrolled 1440 critically ill children between June 2012 and July 2015 in the participating PICUs (University Hospitals Leuven, Belgium; Erasmus MC Sophia Children’s Hospital, Rotterdam, Netherlands; Stollery Children’s Hospital, Edmonton, Alberta, Canada; ClinicalTrials.gov, NCT01536275) [17]. The PEPaNIC RCT randomly assigned patients 1:1 to early (early-PN) or delayed (late-PN) initiation of supplemental PN when 80% of targeted calories per age and weight categories was not reached with enteral nutrition. In the early-PN group, supplemental PN was initiated within 24 h of PICU admission. In the late-PN group, supplemental PN was withheld in the first week in the PICU (meaning no PN in most children in view of PICU discharge before day 8). When enteral nutrition covered > 80% of calculated targets, supplemental PN was discontinued. After 1 week in the PICU, PN could be administered when necessary to both groups. In both groups, enteral nutrition was equally initiated as soon as possible and intravenous micronutrients were administered until fully enterally fed.

All surviving patients were eligible for a preplanned long-term follow-up 4 years after PICU admission, assessing health status and physical and neurocognitive development via interview, clinical assessments, and questionnaires. During PICU admission of the child, parents or legal guardians had provided consent to contact them for this long-term follow-up testing. A control group of healthy children, comparable to the patients for age and sex distribution, was recruited in parallel with the patients within the same time window and underwent identical assessments for comparison. Apart from unrelated children, healthy siblings and patients’ relatives were included to control as much as possible for genetic, socioeconomic, and environmental background. Healthy children could only participate if they had not been previously admitted to a neonatal ICU or PICU and had not been admitted to hospital with need for an intravenous line for 7 days or more. Additional exclusion criteria included a history of inborn chronic metabolic diseases requiring a specific diet, such as diabetes, and conditions that require home PN, such as short-bowel syndrome. If the burden of coming to the hospital was considered too high, examinations were performed during consented home visits. Assessors of the 4-year outcomes were physicians, physiotherapists, and experienced pediatric psychologists who had not been involved in the management of the patients during PICU stay and who were strictly masked to treatment allocation [11]. Parents and caregivers were not masked while the child was treated in the PICU, and they were not actively informed about the initial PEPaNIC trial results.

Parents, legal guardians, or the child if 18 years or older gave written informed consent according to local regulations. Each center’s institutional review boards approved the study (ML8052, NL49708.078, Pro00038098), which was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its amendments. The full study protocol has been published [11, 26]. Health status, anthropometrics, and neurocognitive outcomes have been reported [11]. Clinical assessment of physical functions reported in the present study was only performed for patients enrolled in Leuven or Rotterdam.

Outcomes

This study quantitatively assessed several measures of physical functional capacity of the participants, including handgrip strength, functional dynamic balance, functional exercise capacity, and overall daily physical activity.

Handgrip strength was measured with a Jamar Plus + digital hand dynamometer (Patterson Medical Ltd., Nottinghamshire, UK). Assessments were performed according to standardized testing position and conditions (including allowance of verbal encouragement) as advised by the American Society of Hand Therapists [27]. Average scores (kilograms) of three measurements were recorded and converted to percentage of force predicted for age and sex [28].

In the “timed up-and-go” test, assessing functional dynamic balance, the time was measured needed to stand up from an in height adjustable chair (in sitting position, both feet flat on the ground with a 90-degree angle at the knees), walk a 3 m distance, turn around a cone, walk back to the chair, and sit down again. A handheld stopwatch was used to register time in hundredths of a second. The fastest time of three trials was recorded.

The 6-min walk test was performed according to the American Thoracic Society guidelines [29] as a measure of functional exercise capacity and conducted along a straight, flat, corridor. Participants were instructed to walk, not run, as fast as possible for 6 minutes. The researcher offered support and gave time indications. The distance walked in 6 min was recorded to the nearest meter. Heart rate and peripheral oxygen saturation were measured before and after the test, and the corresponding differences were calculated. Changes in oxygen saturation were also noted as categorical variable indicating whether or not saturation dropped with 3% or more, as a measure of exertional oxygen desaturation [30].

Everyday overall physical activity was derived from an ActiGraph device (model wGT3X-BT, ActiGraph Corporation, Pensacola, FL), which records acceleration with a triaxial accelerometer and showed the greatest measurement properties for assessing common movement-related outcomes [31]. Participants were asked to wear the ActiGraph at the right hip for 7 consecutive days during waking hours and remove it only for sleeping and water-based activities (e.g., showering, bathing, or swimming). Parents/participants were asked to complete a daily log to record the time the monitor was worn or taken off. ActiGraph devices and logbooks were returned by post. Based on accelerometry output and log sheets, the data were first reduced manually to delete occasional periods of non-wear time. Participants’ ActiGraph data were only considered for evaluation if activity had been registered for at least 5 out of 7 days (of which at least one weekend day) for at least 8 h per day. Raw data extraction based on 60-s epochs was then performed with ActiLife Software 6.13.4 (ActiGraph Corporation). Several outcome parameters were derived, including total energy expenditure (kcal/kg/day and kcal/kg/hour monitored), degree of physical activity energy expenditure (expressed as metabolic equivalent of task (MET), which is the ratio of working metabolic rate relative to resting metabolic rate), activity intensity-based measures (daily time spent sedentary, or in light (< 3.0 METs), moderate (3.0–5.9 METs), vigorous (6.0–8.9 METs), or very vigorous (≥ 9.0 METs) activity (expressed as percentage of worn/monitored time, Additional file 1: Table S1)), number of Freedson bouts (period of at least 10 min in moderate to vigorous activity), number of sedentary bouts (period of at least 10 min in sedentary state), and number of steps (number/day and number/day/hour monitored). All data were averaged over the registered days.

Statistical analyses

The number of patients enrolled in this follow-up study was determined by the number of patients included in the primary RCT (n = 1440) and the fraction of missing data due to any type of loss to follow-up. Therefore, we could not perform an a priori sample size calculation. However, we calculated that a number of 198 participants would be needed per group to demonstrate a 5% difference [32] among healthy and former critically ill children or among early-PN and late-PN groups in handgrip strength predicted for age and sex with 95% certainty and 80% power.

Data are presented as numbers (proportions), medians (interquartile ranges), or beta-estimates (95% confidence intervals (CI)). Univariable comparisons were made with chi-square (Fisher’s exact) or Wilcoxon rank-sum tests, as appropriate. Multivariable linear or logistic regression analyses to investigate outcome differences between groups simultaneously adjusted for risk factors that may affect the studied outcomes, based on clinical practice and literature. To study outcome differences between patients and healthy control children, the risk factors were age, treatment center, sex, race, geographic origin, language, hand preference, history of malignancy, predefined syndrome (Additional file 1: Methods S1), and educational and occupational status of the parents/caregivers (Additional file 1: Methods S2). Multivariable analyses investigating outcome differences between early-PN and late-PN patients additionally adjusted for admission diagnosis, illness severity upon PICU admission (pediatric index of mortality 3 (PIM3) and pediatric logistic organ dysfunction (PeLOD) scores), malnutrition risk (Screening Tool for Risk on Nutritional Status and Growth), and parental smoking behavior before PICU admission. To assess whether patients who were infants (younger than 1 year) at randomization behaved differently from older children, p values for interaction between age-group and randomization were calculated. Finally, we further adjusted the analyses for BMI Z-score to investigate whether nutritional status could affect any association found with the physical outcomes. If necessary, data were square root transformed to obtain a near-normal distribution of the residuals to meet the linear regression model assumptions. Multicollinearity of the covariates was assessed with the use of the variance inflation factor and was generally not a problem [33].

Statistical analyses were performed with JMP©Pro16.1.0 (SAS Institute, Inc., Cary, NC). Two-sided p values of 0.05 or less were considered to indicate statistical significance. No corrections for multiple comparisons were done, as the studied outcomes are not independent [24, 34].

Results

Between March 8, 2016, and November 8, 2019, 521 PEPaNIC patients (253 early-PN, 268 late-PN) and 346 healthy children underwent physical function testing (Fig. 1). Demographics and medical characteristics of the participating children are shown in Table 1. Enteral, parenteral, and total macronutrient doses administered on each of the first 7 days of PICU admission for the participating early-PN and late-PN patients are shown in Additional file 1: Fig. S1. Former PICU patients who were tested for physical function (n = 521) were comparable for allocation to early-PN or late-PN, for most demographics upon PICU admission, and for PICU primary and secondary study endpoints with those patients who survived, but could not be reached, declined participation in functional testing, or could not be tested due to a practical problem (n = 624; Additional file 1: Table S2).

Fig. 1
figure 1

CONSORT diagram of study participants. aThese children survived but were physically or neurocognitively disabled (hampering assessment of physical function) or did not understand the instructions. bPractical reasons included, among others, insufficient time (as the physical function testing came last in the follow-up assessments, after a structured interview, anthropometric measurements, a clinical neurological examination, and extensive testing of neurocognitive functions), technical problems, age younger than 4 years, or partial follow-up performed in another center not participating in the PEPaNIC trial. ICU intensive care unit, PN parenteral nutrition, STRONGkids Screening Tool for Risk on Nutritional Status and Growth

Table 1 Participants’ characteristics

Physical function in former critically ill patients as compared with healthy children

We first compared the performance of former PICU patients with that of healthy children with univariable analyses (Table 2). Former PICU patients had less strength for both hands, needed more time to complete the timed up-and-go test, and were able to walk a shorter distance in 6 min. They showed a more pronounced decrease in peripheral oxygen saturation between the start and end of the walk test, with a higher proportion of children showing a decrease of 3% or more, whereas the corresponding rise in heart rate was comparable to that in healthy children. Registered ActiGraph wear time was slightly shorter in the former PICU patients than in the healthy children. Registered monitoring time revealed a lower total, but not physical activity energy expenditure in former PICU patients. The patients also spent a larger percentage of monitored time performing light activity and a smaller percentage in moderate activity, further underscored by a lower number of Freedson bouts, and walked fewer steps than healthy children. In subsequent multivariable analyses adjusting for risk factors, the differences remained, with no major impact of further adjusting for nutritional status at follow-up (Table 2, Additional file 1: Table S3).

Table 2 Physical outcomes at 4-year follow-up of former PEPaNIC patients in comparison with healthy control children

Physical function in former early-PN and late-PN patients

Patients who had been allocated to late-PN and patients who had been allocated to early-PN during PICU stay performed similarly for handgrip strength, timed up-and-go test, and all aspects of the 6-min walk test, both in univariable and in multivariable analyses (Table 3, Additional file 1: Table S4). Accelerometry output showed a few differences between the groups in univariable analyses, with late-PN patients spending a lower percentage of registered time in moderate or vigorous activity, in accordance with a lower number of Freedson bouts, as compared with early-PN patients. However, no significant differences were found in any of the accelerometry outcomes when adjusting for risk factors in multivariable analyses (Table 3, Additional file 1: Table S4). No interaction was found between age-group (infants versus older children) at the time of PICU admission and randomization to early-PN or late-PN (Additional file 1: Table S5). Further adjustment for nutritional status at follow-up did not change the conclusions (Additional file 1: Tables S4 and S5).

Table 3 Physical outcomes at 4-year follow-up of former PEPaNIC patients who had been randomized to early-PN or late-PN

Discussion

Children who have been critically ill performed worse for several quantitative measures of physical function 4 years after PICU admission, as compared with matched healthy children. They were weaker in handgrip strength and were slower in completing the timed up-and-go test. They also were able to walk a shorter distance in 6 min and showed a larger drop in peripheral oxygen saturation from before to after this test. Daily life overall physical activity was also affected, as illustrated by a lower energy expenditure, less intense physical activity, and fewer steps walked per day. Timing of initiating supplemental PN in the PICU when enteral nutrition was insufficient did not affect physical performance of the former PICU patients.

Four years after PICU admission, we documented a worse quantitatively measured physical performance and activity of children who have been critically ill as compared with healthy children. This may have wide health implications in view of the importance of adequate physical activity for healthy growth, body composition, cardiorespiratory and musculoskeletal fitness, cardiovascular and metabolic health, motor development, cognitive development, academic achievement, emotional regulation, pro-social behaviors and overall quality of life, during childhood, but also later in life [35, 36], many domains that are known to be affected in former PICU patients. Hence, these data should draw attention to the need of safely stimulating physical activity of these children, considering potential medical limitations and environmental factors [37].

The finding of a decreased physical functional capacity in the long term after PICU discharge is consistent with other studies, with a highly variable post-PICU follow-up time window [12]. However, virtually all these studies used qualitative assessments of general functional status based on a wide variety of questionnaires or scales [12,13,14, 38]. Only few objective quantitative data are available and this only from small studies (fewer than 50 patients), mostly performed in specific subgroups of former PICU patients. One study did measure handgrip strength of former PICU patients and healthy children, revealing numerically lower strength in the patients, but unfortunately both groups were not comparable for age, and strength was not statistically compared among the groups [38]. Children with severe burn injuries showed lower peak torque and average power output in strength measurements with isokinetic dynamometry 3–4 years later, as compared with healthy children [39]. Also their aerobic capacity, as measured by peak VO2 during a standardized treadmill exercise test, and peak heart rate remained lower. Among pediatric patients with acute respiratory distress syndrome, one-third exhibited mild-to-moderate impairments in pulmonary function testing approximately 10 months later, coinciding with a decreased physical functioning quality of life [40]. A significant number of pediatric survivors of acute hypoxemic respiratory failure showed long-term abnormalities in pulmonary function testing, but did not perceive limitations themselves in lifestyle, physical activity, or chronic pulmonary morbidity, although 6-min walk distance appeared lower than predicted [41, 42]. Interestingly, for a shorter distance walked, we observed a more pronounced decrease in peripheral oxygen saturation of former PICU patients in the 6-min walk test as compared with healthy children. The larger decrease translated into a higher odds of exertional oxygen desaturation and was not compensated for by a more pronounced rise in heart rate. Long-term exercise-induced deoxygenation has previously been shown to be highly prevalent in children who survived meningococcal septic shock [43].

Importantly, physical outcome measures were never worse for patients who had been exposed to an early macronutrient deficit in the PICU under the late-PN strategy, as compared with early full feeding of patients under the early-PN strategy. This is reassuring in view of the documented association between malnutrition in children and poorer physical function, such as lower handgrip strength [21,22,23], and further endorses de-implementation of the use of early-PN in the PICU. The present study also showed that, unfortunately, late-PN also did not improve any measure of physical function, unlike previously demonstrated beneficial effects on several measures of neurocognitive functioning and emotional and behavioral problems [10, 11]. In adult ICU patients, late-PN has been shown to reduce the risk of ICU-acquired muscle weakness and accelerated recovery from such weakness in ICU as compared with early-PN, but long-term impact on physical functional capacity remained unclear [44].

The major strengths of this study include the objective quantitative assessment of physical function measures as opposed to the use of (subjective) qualitative scales and questionnaires, as well as the large sample size of our cohort of critically ill children and own parallel control group of healthy children, as opposed to mostly small studies referring patient data to population norms. This study also has some limitations. First, in the comparison of former critically ill patients with healthy children, we cannot deduce to what extent the impaired physical function in PICU survivors may be explained by preexisting impairments or was evoked by the acute illness or associated treatments in the PICU. However, both previously healthy children with a normal baseline function and those with pre-PICU morbidity and baseline functional impairments have shown a functional decline after PICU discharge, although the capacity for functional recovery may be better in those children with a normal baseline function [45,46,47]. Second, information on in-hospital physiotherapy or on follow-up consultations and therapies beyond the study protocol were not systematically recorded. Also, no information was available on nutritional status of the participants at 4-year follow-up.

Conclusions

As compared with matched healthy children, former critically ill children performed worse for several quantitative measures of physical functional capacity 4 years after PICU admission, thus objectifying the adverse physical developmental legacy after pediatric critical illness. Delaying supplemental PN to beyond the first week in the PICU, previously shown to improve short-term outcome and certain long-term neurocognitive and behavioral problems as compared with the early use of PN, did not worsen any of the physical developmental impairments. This study thus provides further support for de-implementing the early use of PN in the PICU.

Availability of data and materials

Data sharing is offered under the format of collaborative projects. Proposals can be directed to the corresponding author.

Abbreviations

CI:

Confidence interval

ICU:

Intensive care unit

MET:

Metabolic equivalent of task

PeLOD:

Pediatric logistic organ dysfunction

PEPaNIC:

Early versus late parenteral nutrition in the pediatric intensive care unit

PICU:

Pediatric intensive care unit

PIM3:

Pediatric index of mortality 3

PN:

Parenteral nutrition

RCT:

Randomized controlled trial

STRONGkids:

Screening Tool for Risk on Nutritional Status and Growth

References

  1. Watson RS, Choong K, Colville G, Crow S, Dervan LA, Hopkins RO, Knoester H, Pollack MM, Rennick J, Curley MAQ. Life after critical illness in children-toward an understanding of pediatric post-intensive care syndrome. J Pediatr. 2009;198:16–24.

    Article  Google Scholar 

  2. Banwell BL, Mildner RJ, Hassall AC, Becker LE, Vajsar J, Shemie SD. Muscle weakness in critically ill children. Neurology. 2003;61:1779–82.

    CAS  PubMed  Article  Google Scholar 

  3. Mammen C, Al Abbas A, Skippen P, Nadel H, Levine D, Collet JP, Matsell DG. Long-term risk of CKD in children surviving episodes of acute kidney injury in the intensive care unit: a prospective cohort study. Am J Kidney Dis. 2012;59:523–30.

    PubMed  Article  Google Scholar 

  4. Mesotten D, Gielen M, Sterken C, Claessens K, Hermans G, Vlasselaers D, Lemiere J, Lagae L, Gewillig M, Eyskens B, Vanhorebeek I, Wouters PJ, Van den Berghe G. Neurocognitive development of children 4 years after critical illness and treatment with tight glucose control: a randomized controlled trial. JAMA. 2012;308:1641–50.

    CAS  PubMed  Article  Google Scholar 

  5. Madderom MJ, Reuser JJ, Utens EM, van Rosmalen J, Raets M, Govaert P, Steiner K, Gischler SJ, Tibboel D, van Heijst AFJ, Ijsselstijn H. Neurodevelopmental, educational and behavioral outcome at 8 years after neonatal ECMO: a nationwide multicenter study. Intensive Care Med. 2013;39:1584–93.

    PubMed  Article  Google Scholar 

  6. Ko MSM, Poh P-F, Heng KYC, Sultana R, Murphy B, Ng RWL, Lee JH. Assessment of long-term psychological outcomes after pediatric intensive care unit admission: a systematic review and meta-analysis. JAMA Pediatr. 2022;176:e215767.

    PubMed  Article  Google Scholar 

  7. Aspesberro F, Mangione-Smith R, Zimmerman JJ. Health-related quality of life following pediatric critical illness. Intensive Care Med. 2015;41:1235–46.

    PubMed  Article  Google Scholar 

  8. Hordijk J, Verbruggen S, Vanhorebeek I, Güiza F, Wouters P, Van den Berghe G, Joosten K, Dulfer K. Health-related quality of life of children and their parents 2 years after critical illness: pre-planned follow-up of the PEPaNIC international, randomized, controlled trial. Crit Care. 2020;24:347.

    PubMed  PubMed Central  Article  Google Scholar 

  9. Kachmar AG, Irving SY, Connolly CA, Curley MAQ. A systematic review of risk factors associated with cognitive impairment after pediatric critical illness. Pediatr Crit Care Med. 2018;19:e164–71.

    PubMed  Article  Google Scholar 

  10. Verstraete S, Verbruggen SC, Hordijk JA, Vanhorebeek I, Dulfer K, Güiza F, van Puffelen E, Jacobs A, Leys S, Durt A, Van Cleemput H, Eveleens RD, Garcia Guerra G, Wouters PJ, Joosten KF, Van den Berghe G. Long-term developmental effects of withholding parenteral nutrition for 1 week in the paediatric intensive care unit: a 2-year follow-up of the PEPaNIC international, randomised, controlled trial. Lancet Respir Med. 2019;7:141–53.

    PubMed  Article  Google Scholar 

  11. Jacobs A, Dulfer K, Eveleens RD, Hordijk J, Van Cleemput H, Verlinden I, Wouters PJ, Mebis L, Garcia Guerra G, Joosten K, Verbruggen SC, Güiza F, Vanhorebeek I, Van den Berghe G. Long-term developmental impact of withholding parenteral nutrition in paediatric-ICU: a 4-year follow-up of the PEPaNIC randomised controlled trial. Lancet Child Adolesc Health. 2020;4:503–14.

    PubMed  Article  Google Scholar 

  12. Procter C, Morrow B, Pienaar G, Shelton M, Argent A. Outcomes following admission to paediatric intensive care: a systematic review. J Paediatr Child Health. 2021;57:328–58.

    PubMed  Article  Google Scholar 

  13. Ong C, Hau Lee J, Leow MKS, Puthucheary ZA. Functional outcomes and physical impairments in pediatric critical care survivors: a scoping review. Pediatr Crit Care Med. 2016;17:e247–59.

    PubMed  Article  Google Scholar 

  14. Bossen D, de Boer RM, Knoester H, Maaskant JM, van der Schaaf M, Alsem MW, Gemke RJBJ, van Woensel JBM, Oosterlaan J, Engelbert RHH. Physical functioning after admission to the PICU: a scoping review. Crit Care Explor. 2021;3:e0462.

    PubMed  PubMed Central  Article  Google Scholar 

  15. Verstraete S, Van den Berghe G, Vanhorebeek I. What’s new in the long-term neurodevelopmental outcome of critically ill children. Intensive Care Med. 2018;44:649–51.

    CAS  PubMed  Article  Google Scholar 

  16. Verstraete S, Vanhorebeek I, Covaci A, Güiza F, Malarvannan G, Jorens PG, Van den Berghe G. Circulating phthalates during critical illness in children are associated with long-term attention deficit: a study of a development and a validation cohort. Intensive Care Med. 2016;42:379–92.

    CAS  PubMed  Article  Google Scholar 

  17. Fivez T, Kerklaan D, Mesotten D, Verbruggen S, Wouters PJ, Vanhorebeek I, Debaveye Y, Vlasselaers D, Desmet L, Casaer MP, Garcia Guerra G, Hanot J, Joffe A, Tibboel D, Joosten K, Van den Berghe G. Early versus late parenteral nutrition in critically ill children. N Engl J Med. 2016;374:1111–22.

    CAS  PubMed  Article  Google Scholar 

  18. Nyaradi A, Li J, Hickling S, Foster J, Oddy WH. The role of nutrition in children’s neurocognitive development, from pregnancy through childhood. Front Hum Neurosci. 2013;7:97.

    PubMed  PubMed Central  Article  Google Scholar 

  19. Gat-Yablonski G, De Luca F. Effect of nutrition on statural growth. Horm Res Paediatr. 2017;88:46–62.

    CAS  PubMed  Article  Google Scholar 

  20. Owino VO, Murphy-Alford AJ, Kerac M, Bahwere P, Friis H, Berkley JA, Jackson AA. Measuring growth and medium- and longer-term outcomes in malnourished children. Matern Child Nutr. 2019;15:e12790.

    PubMed  PubMed Central  Article  Google Scholar 

  21. Secker DJ, Jeejeebhoy KN. Subjective global nutritional assessment for children. Am J Clin Nutr. 2007;85:1083–9.

    CAS  PubMed  Article  Google Scholar 

  22. Orsso CE, Tibaes JRB, Oliveira CLP, Rubin DA, Field CJ, Heymsfield SB, Prado CM, Haqq AM. Low muscle mass and strength in pediatrics patients: why should we care? Clin Nutr. 2019;38:2002–15.

    PubMed  Article  Google Scholar 

  23. Mckirdy S, Nichols B, Williamson S, Gerasimidis K. Handgrip strength as a surrogate marker of lean mass and risk of malnutrition in paediatric patients. Clin Nutr. 2021;40:5189–95.

    PubMed  PubMed Central  Article  Google Scholar 

  24. Güiza F, Vanhorebeek I, Verstraete S, Verlinden I, Derese I, Ingels C, Dulfer K, Verbruggens SC, Garcia Guerra G, Joosten KF, Wouters PJ, Van den Berghe G. Effect of early parenteral nutrition during paediatric critical illness on DNA methylation as a potential mediator of impaired neurocognitive development: a pre-planned secondary analysis of the PEPaNIC international, randomised, controlled trial. Lancet Respir Med. 2020;8:288–303.

    PubMed  Article  Google Scholar 

  25. Jacobs A, Güiza F, Verlinden I, Dulfer K, Garcia Guerra G, Joosten K, Verbruggen SC, Vanhorebeek I, Van den Berghe G. Differential DNA methylation by early versus late parenteral nutrition in the PICU: a biological basis for its impact on emotional and behavioral problems documented 4 years later. Clin Epigenetics. 2021;13:146.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  26. Fivez T, Kerklaan D, Verbruggen S, Vanhorebeek I, Verstraete S, Tibboel D, Garcia Guerra G, Wouters PJ, Joffe A, Joosten K, Mesotten D, Van den Berghe G. Impact of withholding early parenteral nutrition completing enteral nutrition in pediatric critically ill patients (PEPaNIC trial): study protocol for a randomized controlled trial. Trials. 2015;16:202.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  27. Balogun JA, Akomolafe CT, Amusa LO. Grip strength: effects of testing posture and elbow position. Arch Phys Med Rehabil. 1991;72:280–3.

    CAS  PubMed  Google Scholar 

  28. Bohannon RW, Wang Y-C, Bubela D, Gershon RC. Handgrip strength: a population-based study of norms and age trajectories for 3- to 17-year-olds. Pediatr Phys Ther. 2017;29:118–23.

    PubMed  Article  Google Scholar 

  29. Laboratories ATSCoPSfCPF. ATS statement: guidelines for the 6-min walk test. Am J Respir Crit Care Med. 2002;166:111–7.

    Article  Google Scholar 

  30. Gupta R, Ruppel GL, Espiritu JRD. Exercise-induced oxygen desaturation during the 6-min walk test. Med Sci (Basel). 2020;8:8.

    CAS  Google Scholar 

  31. Phillips SM, Summerbell C, Hobbs M, Hesketh KR, Saxena S, Muir C, Hillier-Brown FC. A systematic review of the validity, reliability, and feasibility of measurement tools used to assess the physical activity and sedentary behaviour of pre-school aged children. Int J Behav Nutr Phys Act. 2021;18:141.

    PubMed  PubMed Central  Article  Google Scholar 

  32. Peterson MD, Zhang P, Saltarelli WA, Visich PS, Gordon PM. Low muscle strength thresholds for the detection of cardiometabolic risk in adolescents. Am J Prev Med. 2016;50:593–9.

    PubMed  Article  Google Scholar 

  33. Midi H, Sarkar SK, Rana S. Collinearity diagnostics of binary logistic regression model. J Interdiscip Math. 2010;13:253–67.

    Article  Google Scholar 

  34. Reiner A, Yekutieli D, Benjamini Y. Identifying differentially expressed genes using false discovery rate controlling procedures. Bioinformatics. 2003;19:368–75.

    CAS  PubMed  Article  Google Scholar 

  35. Rhodes RE, Guerrero MD, Vanderloo LM, Barbeau K, Birken CS, Chaput JP, Faulkner G, Janssen I, Madigan S, Mâsse LC, McHugh TL, Perdew M, Stone K, Shelley J, Spinks N, Tamminen KA, Tomasone JR, Ward H, Welsh F, Tremblay MS. Development of a consensus statement on the role of the family in the physical activity, sedentary, and sleep behaviours of children and youth. Int J Behav Nutr Phys Act. 2020;17:74.

    PubMed  PubMed Central  Article  Google Scholar 

  36. Lane-Cordova AD, Jerome GJ, Paluch AE, Bustamante EE, LaMonte MJ, Pate RR, Weaver RG, Webber-Ritchey KJ, Gibbs BB, Committee on Physical Activity of the American Heart Association Council on Lifestyle and Cardiometabolic Health. Supporting physical activity in patients and populations during life events and transitions: a scientific statement from the American Heart Association. Circulation. 2022;145:e117–28.

    PubMed  Article  Google Scholar 

  37. Hansen K, Tierney S. Every child with congenital heart disease should be exercising. Curr Opin Cardiol. 2022;37:91–8.

    PubMed  Article  Google Scholar 

  38. Ong C, Lee JH, Yang L, Wong JJM, Leow MKS, Puthucheary ZA. A cross-sectional study of the clinical metrics of functional status tools in pediatric critical illness. Pediatr Crit Care Med. 2021;22:879–88.

    PubMed  Article  Google Scholar 

  39. Cambiaso-Daniel J, Rivas E, Carson JS, Hundeshagen G, Lopez ON, Glover SQ, Herndon DN, Suman OE. Cardiorespiratory capacity and strength remain attenuated in children with severe burn injuries at over 3 years postburn. J Pediatr. 2018;192:152–8.

    PubMed  PubMed Central  Article  Google Scholar 

  40. Ward SL, Turpin A, Spicer AC, Treadwell MJ, Church GD, Flori HR. Long-term pulmonary function and quality of life in children after acute respiratory distress syndrome: a feasibility investigation. Pediatr Crit Care Med. 2017;18:e48-55.

    PubMed  PubMed Central  Article  Google Scholar 

  41. Weiss I, Ushay HM, DeBruin W, O’Loughlin J, Rosner I, Notterman D. Respiratory and cardiac function in children after acute hypoxemic respiratory failure. Crit Care Med. 1996;24:148–54.

    CAS  PubMed  Article  Google Scholar 

  42. Chakdour S, Vaidya PC, Angurana SK, Muralidharan J, Singh M, Singhi SC. Pulmonary functions in children ventilated for acute hypoxemic respiratory failure. Pediatr Crit Care Med. 2018;19:e464–71.

    PubMed  Article  Google Scholar 

  43. Plötz FB, van Vught H, Uiterwaal CSPM, Riedijk M, van der Ent CK. Exercise-induced oxygen desaturation as a late complication of meningococcal septic shock syndrome. JAMA. 2001;285:293–4.

    PubMed  Article  Google Scholar 

  44. Hermans G, Casaer MP, Clerckx B, Güiza F, Vanhullebusch T, Derde S, Meersseman P, Derese I, Mesotten D, Wouters PJ, Van Cromphaut S, Debaveye Y, Gosselink R, Gunst J, Wilmer A, Van den Berghe G, Vanhorebeek I. Effect of tolerating macronutrient deficit on the development of intensive-care unit acquired weakness: a subanalysis of the EPaNIC trial. Lancet Respir Med. 2013;1:621–9.

    PubMed  Article  Google Scholar 

  45. Knoester H, Bronner MB, Bos AP. Surviving pediatric intensive care: physical outcome after 3 months. Intensive Care Med. 2008;34:1076–82.

    PubMed  PubMed Central  Article  Google Scholar 

  46. Buysse CMP, Raat H, Hazelzet JA, Hop WCJ, Maliepaard M, Joosten KFM. Surviving meningococcal septic shock: health consequences and quality of life in children and their parents up to 2 years after pediatric intensive care unit discharge. Crit Care Med. 2008;36:596–602.

    PubMed  Article  Google Scholar 

  47. Choong K, Al-Harbi S, Siu K, Wong K, Cheng J, Baird B, Pogorzelski D, Timmons B, Gorter J-W, Thabane L, Khetani M, Canadian Critical Care Trials Group. Functional recovery following critical illness in children: the “wee-cover” pilot study. Pediatr Crit Care Med. 2015;16:310–8.

    PubMed  PubMed Central  Article  Google Scholar 

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Acknowledgements

The authors acknowledge the physiotherapists, psychologists, and other research team members involved in the study for their help with the physical functional testing and for the technical and administrative support. Furthermore, they thank the children and their parents for their willingness to participate in the study.

Funding

This work was supported by European Research Council Advanced Grants (AdvG-2012-321670 from the Ideas Program of the European Union 7th framework program and AdvG-2017-785809 from the Horizon 2020 Program to GVdB); by the Methusalem Program of the Flemish government (through the University of Leuven to GVdB, METH/08/07, and to GVdB and IV, METH14/06); by the Institute for Science and Technology, Flanders, Belgium (through the University of Leuven to GVdB, IWT-TBM150181 and IWT-TBM110685); by the Sophia Research Foundation (SSWO to SV); by the Stichting Agis Zorginnovatie (to SV); Nutricia Research B.V (to SV); by the Erasmus Trustfonds (to SV); and by an European Society for Clinical Nutrition and Metabolism (ESPEN) research grant (to SV). The funders of the study had no role in the design of the study, the collection, analysis, and interpretation of data, or in the writing of the manuscript.

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Authors and Affiliations

Authors

Contributions

IVa, AJ, KD, KJ, SV, and GVdB designed the study. AJ, LM, KD, RE, HVC, PJW, and IVe gathered the data. IVa statistically analyzed the data. IVa and GVdB wrote the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Greet Van den Berghe.

Ethics declarations

Ethics approval and consent to participate

Institutional Review Board approval was obtained at each participating site (Ethische Commissie Onderzoek UZ Leuven/KU Leuven: ML8052; Medisch Ethische Toetsings Commissie Erasmus MC: NL49708.078). The study was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its amendments. Written informed consent was acquired from parents, legal guardians, or the child if 18 years or older.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Supplementary Information

Additional file 1.

Compiled file with all Additional information: Additional methods describing the definition of “Syndrome” and the educational and occupational level of the participants’ parents. Additional tables describing cut-off points for intensity of activity measured by ActiGraph; characteristics of PEPaNIC patients who participated in physical function testing in comparison with those who survived but could not be reached, declined participation in functional testing or could not be tested due to a practical problem; multivariable analyses of physical outcomes at 4-year follow-up of former PEPaNIC patients in comparison with healthy control children and of former PEPaNIC patients who had been randomized to early-PN or late-PN, as well as interaction with age-group at randomization. Additional figure describing caloric intake of former critically ill patients during the first 7 days in PICU.

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Vanhorebeek, I., Jacobs, A., Mebis, L. et al. Impact of critical illness and withholding of early parenteral nutrition in the pediatric intensive care unit on long-term physical performance of children: a 4-year follow-up of the PEPaNIC randomized controlled trial. Crit Care 26, 133 (2022). https://doi.org/10.1186/s13054-022-04010-3

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Keywords

  • Critical illness
  • Children
  • PICU
  • Physical function
  • Strength
  • Long term