The first consensus standardised neonatal parenteral nutrition formulations were implemented in many neonatal units in Australia in 2012. The current update involving 49 units from Australia, New Zealand, Singapore, Malaysia and India was conducted between September 2015 and December 2017 with the aim to review and update the 2012 formulations and guidelines.
A systematic review of available evidence for each parenteral nutrient was undertaken and new standardised formulations and guidelines were developed.
Five existing preterm Amino acid-Dextrose formulations have been modified and two new concentrated Amino acid-Dextrose formulations added to optimise amino acid and nutrient intake according to gestation. Organic phosphate has replaced inorganic phosphate allowing for an increase in calcium and phosphate content, and acetate reduced. Lipid emulsions are unchanged, with both SMOFlipid (Fresenius Kabi, Australia) and ClinOleic (Baxter Healthcare, Australia) preparations included. The physicochemical compatibility and stability of all formulations have been tested and confirmed. Guidelines to standardise the parenteral nutrition clinical practice across facilities have also been developed.
The 2017 PN formulations and guidelines developed by the 2017 Neonatal Parenteral Nutrition Consensus Group offer concise and practical instructions to clinicians on how to implement current and up-to-date evidence based PN to the NICU population.
Parenteral nutrition (PN) is an essential component in the management of many newborn infants, admitted to Newborn Intensive Care Units (NICUs). All New South Wales (NSW) NICUs and subsequently other Australian NICUs formed a PN Consensus Group in 2010. Formulations were standardised in July 2011 with further amendments in 2012 and 2013. The Consensus Group recommendations and the improved nutritional outcomes following the implementation of consensus formulations were published in 2014 [1, 2]. Although nutritional intakes improved significantly, amino acid targets were not achieved in extremely preterm infants.
In February 2015, the group reconvened in Sydney, now comprising 49 tertiary and non-tertiary NICUs from Australia, New Zealand, Malaysia, Singapore and India who participated in the consensus meeting in-person or via video link. A survey was conducted to explore the clinical PN practice in each NICU . Outcomes of 2010 consensus formulations were presented, gaps in knowledge identified, topics for updating the formulations prioritised with tasks distributed to participants.
In September 2017, delegates reconvened, evidence was reviewed and guidelines and formulations were updated. A systematic literature search was undertaken and detailed reports were developed for each component of PN. Levels of evidence (LOE) and grades of recommendation (GOR) were allocated according to National Health and Medical Research Council (NHMRC) criteria . Physicochemical compatibility and stability of updated formulations were checked and confirmed compliant by a compounding pharmaceutical facility (Baxter Pharmaceuticals Pty Ltd). The new formulations were commissioned and released in March 2018. The updated PN guidelines are based on the majority consensus of the PN Consensus Group. Where good published evidence was unavailable, recommendations were discussed and, if necessary, voted upon. Time was allowed for thorough literature review, free and open discussion and an exchange of good practice tips among units. Each member of the group was given the opportunity to provide comments and suggestions to the consensus group for their consideration. They are written balancing the potential benefits of PN against associated risks. These practice guidelines do not account for every clinical situation, particularly for infants that are acutely unwell or unstable. The professional judgement of the health professional in these individual cases must take precedence.
Outcomes of the consensus
The survey of Australian and New Zealand NICUs in 2015 demonstrated that 97% of extremely preterm infants weighing < 1000 g and 88% of very preterm infants 1000–1500 g are commenced on PN from day 1 of life, and 77% of NICUs administer PN to any infant > 1500 g who fails to establish enteral feeds by day 3–5 of life . The current recommendation remains the same as the 2012 recommendation (Table 1).
Parenteral calorie recommendations remain similar, including consideration of the updated 2014 American Academy of Pediatrics (AAP) Committee on Nutrition recommendation of a parenteral caloric intake of 90–115 kcal/kg/day in preterm infants  and the ESPGHAN 2005 recommendation of 90–110 kcal/kg/day for extremely low birth weight (ELBW) infants .
The 2017 updated starter PN solution infused at 60 ml/kg/day (33 kcal/kg/day) and new starter concentrated PN solution at 40 ml/kg/day and lipid emulsion at 1 g/kg/day (10 kcal/kg/day) provides approximately 43 kcal/kg/day. The standardised preterm PN solution infused at 135 ml/kg/day (70.2 kcal/kg/day) and new concentrated preterm PN at 100 ml/kg/day and lipid emulsion at 3 g/kg/day (30 kcal/kg/day) provides approximately 100 kcal/kg/day (Level of Evidence [LOE] II, Grade of Recommendation [GOR] B).
The 2017 consensus agreement is similar to the 2012 recommendation: Standardised PN should be formulated to provide recommended nutrient intakes (RNI) in a total fluid intake of 150 ml/kg/day. This includes 135 ml/kg/day of AA/dextrose formulation and 15 ml/kg/day water in the 20% lipid emulsion. The 2012 agreement on starting fluid intake at 60 ml/kg/day with daily increase by 20–30 ml/kg/day to an average maximum of 150 ml/kg/day remains. Alternatively, for those units who opt for a total water intake below 150 ml/kg/day, or unwell babies with multiple non-protein intravenous infusions such as inotropes, opioid analgesics contributing to a significant proportion of fluid volume, the new concentrated PN solutions provide an adequate nutrient and mineral intake on a lower volume.
There is no definitive evidence about what dose of parenteral amino acid is appropriate and when to initiate parenteral AA supplementation in neonates. Delay in administering amino acids could result in a protein catabolic state and could impact on growth and development in preterm neonates. However, potential benefits of improved nitrogen balance, growth and infant health may be outweighed by the infant’s ability to utilise high intakes of parenteral amino acid, especially in the days after birth, resulting in high concentrations of amino acids, ammonia and urea, and an exacerbation of metabolic acidosis. The 2017 consensus agreement incorporates the findings of three new systematic reviews that evaluated the efficacy and safety of parenteral AA in preterm neonates [7,8,9].
The Consensus Group recommendations remained unchanged: (1) commence parenteral AA within the first 24 h of birth (LOE I, GOR C); (2) commence parenteral AA at 2 g/kg/day (LOE I, GOR C) and; (3) incrementally increase amino acid infusions to a maximum 4 g/kg/day by day 3–5 of life in preterm neonates (LOE I, GOR C). The Consensus Group considered the safety of (1) commencement parenteral AA in excess of 3 to 3.5 g/kg/day and (2) maintenance AA intake in excess of 4.5 g/kg/day has not been proven in clinical trials.
Consensus recommendations regarding carbohydrates remain unchanged. Proposed standard preterm and term PN formulations contain 10 and 12% dextrose respectively, providing 13.5 g/kg/day (9.4 mg/kg/min) and 17 g/kg/day (11.8 mg/kg/min) at 135 ml/kg/day respectively (LOE I, GOR C).
The Consensus Group reconsidered the findings of two systematic reviews, which reported no benefit of introducing lipids before two to five days [10, 11]. As the composition of growth was not assessed in these studies, it is uncertain if increased energy intake derived from early lipid infusion is protective against induced protein catabolism in the preterm neonate. Further, it is possible to prevent essential fatty acid deficiency with introduction of as little as 0.5 to 1 g/kg/day of lipid (linoleic acid) infusion . The Consensus Group agreed to commencement of parenteral lipid on day 1 of PN administration, particularly for extremely preterm neonates (LOE I, GOR C).
Several types of intravenous lipid emulsions (IVLE) are available for neonatal use. Recent systematic reviews have shown no statistically significant differences between IVLEs with respect to clinically important outcomes including mortality, growth, chronic lung disease, sepsis, severe ROP ≥ stage 3, and cholestasis by using any specific preparation in newborns [12,13,14] (LOE I, GOR C). The 2015 Survey revealed 67% of units in ANZ use both mixed 30% soybean oil/25% olive oil/30% medium-chain triglyceride oil/15% fish oil IVLE (SMOFlipid [Fresenius Kabi, Australia]) and mixed 80% olive oil/20% soybean oil IVLE (ClinOleic [Baxter Healthcare, Australia]) . All units use water and fat soluble vitamins added to lipid emulsion. The consensus 2017 proposed both SMOFlipid and ClinOleic as suitable lipid preparations and anticipate individual units will take cost and waste minimisation into consideration when choosing the specific type of lipid preparation most suited to their needs.
All lipid emulsions with added fat and water soluble vitamins discussed above are formulated to provide 1 g of lipid (SMOFlipid or ClicOleic) in 6 mL of lipid emulsion with vitamins (Soluvit N and Vitalipid N Infant). Thus, 1 g lipid/kg/day equates to 6 mL lipid emulsion with vitamins/kg/d, which equates to an energy intake of 10 kcal/kg/day. Similarly, 2 g lipid/kg/day equates to 12 ml/kg/day lipid emulsion with vitamins and 3 g lipid/kg/day equates to 18 ml/kg/day lipid emulsion with vitamins. There are variations in terms of starting dose of lipid emulsions. However, a starting dose 1 g/kg/day was safely tolerated in most clinical trials. The consensus agreed to commence lipids at 1 g/kg/day. There is no evidence that gradual increments in the infusion rate of lipids improve fat tolerance. The majority consensus was to increase by 1 g/kg (6 mL/kg) each day to 3 g/kg/day (18 mL/kg/day). If lipid infusion is increased in increments of 0.5 to 1.0 g/kg/day, it may be possible to monitor for hypertriglyceridemia . The lipid emulsions contain 80% water (6 mL lipid emulsion with vitamins contains 5 mL water; 12 mL lipid emulsion with vitamins contains 10 mL water; 18 mL lipid emulsion with vitamins contains 15 mL water). In view of benefits associated with restricted fluid intake , the group proposed to include the water content of lipid infusions in the total fluid intake, which equates to 15 ml/kg/day of water when the lipid intake reaches 3 g/kg/day (LOE I, GOR B).
Sodium, potassium and chloride
The 2017 consensus reaffirmed the consensus reached in 2012, agreeing to minimal sodium intake of approximately 1 mmol/kg/d on day 1 using a starter PN formulation. Sodium in starter formulation is a component of organic phosphate (sodium glycerophosphate which contains 2 mmol Na per mmol of phosphate) and can only be altered by replacing with other sodium free nutrients. The currently designed starter and standard formulations will increase sodium from 1 mmol/kg/day on day 1 (starter formulation) to a maximum 4.6 mmol/kg/day in preterm infants and 3.4 mmol/kg/day in term infants at 135 ml/kg/day (standard formulations) (LOE II, GOR C). The new starter concentrated PN solutions will gradually increase sodium from 1.2 mmol/kg/day on day 1 in the starter concentrated PN to a maximum 5.0 mmol/kg/day in the concentrated preterm PN in extremely preterm infants. A Cochrane review assessing the benefits and harms of higher versus lower sodium intakes in preterm infants is currently underway .
The Consensus Group agreed on minimal potassium intake using starter PN formulation, with an increase in standard formulations to a maximum 3.0 mmol/kg/d in preterm and 2.7 mmol/kg/day in term infants (LOE III-2, GOR C). This is unchanged from the previous consensus and complies with AAP and ESPGHAN 2005 recommendations [5, 6].
With respect to chloride, the 2013 consensus was to adopt a trial recommendation that the first 3 mmol/kg/day of anion is provided as chloride, next 6 mmol/kg/day of anion is provided as acetate and thereafter as chloride again . However, there have been concerns about hypercarbia in some infants using 2013 formulations. Moreover, 2017 consensus formulations contain organic phosphate (sodium glycerophosphate) resulting in an increase of pH of the formulations. Therefore, the 2017 consensus is to reduce the acetate content to a maximum of 3.5 mmol/kg/day in the updated standard formulations (LOE II, GOR C).
Calcium, phosphorus and magnesium
There is a wide range in the recommended doses of calcium (Ca) and phosphorus (P) delivered by PN in preterm infants. American Academy of Pediatrics 2014 recommends 1.5–2.0 mmol/kg/day of Ca and 1.5–1.9 mmol/kg/day of phosphorus whereas ESPGHAN 2005 recommends 1.3–3 mmol/kg/day of Ca and 1.0–2.3 mmol/kg/day of P, with optimal Ca:P ratio between 1.3–1.7 [5, 6]. However, these recommendations are based on in-utero accretion rates. While a number of clinical studies evaluated the efficacy and safety of various parenteral intakes of Ca and P in preterm infants, none of them tested the ESPGHAN recommended maximum intake levels of 3 mmol/kg/day of Ca and 2.3 mmol/kg/day of P in preterm neonates, so the safety of this level of intake is unreported [18,19,20,21]. One RCT used inorganic phosphate for an estimated maximum P intake 2.6 mmol/kg/day with a maximal Ca intake 2 mmol/kg/day .
Until recently, only inorganic phosphate has been registered by Therapeutics Goods Administration Australia and higher intakes of calcium and phosphate intravenously were not possible while maintaining compatibility to prevent calcium-phosphate precipitation [20, 21]. Recently, organic phosphate in the form of sodium glycerophosphate has been registered. Substitution of inorganic phosphate by organic phosphate improves physicochemical compatibility with trial evidence reported increased mineral intake and mineral retention .
Due to a paucity of studies on the safety of maximum parenteral RDIs for Ca and P and the availability of organic phosphate with improved physicochemical stability, the 2017 consensus increased the parenteral Ca and P intakes to a maximum of 2.3 mmol/kg/day and 1.8 mmol/kg/day respectively. Furthermore, there is additional 0.19 mmol/kg/day P from ClinOleic or SMOFLipid at 3 g/kg/day.
The 2017 consensus regarding magnesium (Mg) is unchanged. A minimum Mg intake of 0.2 mmol/kg/day and maximum 0.3 mmol/kg/day is considered appropriate for LBW infants. (LOE III-3, GOR C).
The lipid emulsion contains water and fat soluble vitamins (Soluvit N and Vitalipid N Infant [Fresenius Kabi, Australia]). There was no change with respect to vitamins in the 2017 consensus.
In the absence of a formulation with the optimal mixture of trace elements, the 2012 consensus was to add zinc, selenium and iodine as individual trace elements to all AA/dextrose formulations. Trace elements were not added to the starter formulation due to physicochemical compatibility concerns. The 2018 formulations contain organic phosphate allowing addition of trace elements in all formulations including the starter formulation without any physicochemical instability. Other trace elements, including copper, manganese and molybdenum, can be added to the formulations in infants who are on exclusive PN for more than 2–4 weeks with minimal enteral intake.
Our previous and current consensus is to add heparin 0.5 IU/ml to AA/dextrose formulations (LOE I, GOR C) and remains the same.
Physicochemical stability of the latest formulations have been tested and confirmed to be stable for up to 61 days at 2–8 °C and 5 days at below 25 °C (Baxter Healthcare, Australia).
The majority consensus 2017 recommended a hanging time of 48 h for PN solution. Due to concerns of microbial contamination with longer hanging times [22,23,24], a range of 24–48 h hanging time was agreed for lipid infusions (LOE II, GOR C).
Route of administration
In neonates, umbilical vessels can be used for PN . Umbilical venous catheters compared to peripheral venous catheter reduces insertion attempts with no increase in risk of infection or necrotising enterocolitis . The risk of complication may increase if umbilical venous catheters are left in place for more than 14 days [26, 27].
Peripherally inserted central catheters (PICCs) should be used preferentially to provide central venous access in neonates receiving prolonged PN as PICC use results in improved nutrient intake and fewer insertion attempts [6, 28].
As phlebitis of peripheral veins were reported when the osmolality of the intravenous solution exceeded 600 mOsm , peripheral veins have been recommended for short term venous access [6, 29]. The group has developed a peripheral preterm PN solution (see below) with reduced mineral content that can be used to run through the peripheral cannula for short periods of time, although there is limited evidence for the role of minerals in the development of tissue injury. Although extravasation injury occurs in up to 10% of infants managed only with peripheral infusion of PN , it is unclear if the risk of peripheral PN is greater than the risk of peripheral crystalloid infusion.
The formulations that have been developed as a result of the 2017 consensus are predominantly intended for administration via a central vein. American Society of Parenteral and Enteral Nutrition (ASPEN) recommends the osmolarity of peripheral parenteral nutrition solutions be limited to 900 mOsm/L to lower the risk of phlebitis due to infiltration based on a study that evaluated the feasibility of infusing a 900 mOsm/L solution through peripheral veins in 15 adult participants . A prospective study reported that administration of PN with an osmolarity ≤1000 mOsm/L resulted in an 8% (15 of 181) incidence of extravasation/phlebitis, whereas peripheral administration of PN with osmolarity > 1000 mOsm/L resulted in a 30% (40 of 134) incidence of extravasation/phlebitis, suggesting that peripheral administration of PN in neonates should be limited to 1000 mOsm/L.  Another retrospective, matched-cohort study that included 151 neonates found that administration of PN with osmolarity > 1000 mOsm/L vs ≤1000 mOsm/L significantly increased infiltration (17% vs 7%; odds ratio [OR], 2.47; 95% confidence interval [CI], 1.24–4.94; P = .01) and the combined composite end point of phlebitis or infiltration (45% vs 34%; OR, 1.65; 95% CI, 1.07–2.54; P = .02). In multivariate analysis, osmolarity > 1000 mOsm/L vs ≤1000 mOsm/L was an independent risk factor for developing complications (OR, 1.67; 95% CI, 1.08–2.52; P = .02) .
The 2017 Consensus Group concluded that PN solutions with osmolality below 1000 mosm/L can be administered peripherally for short term use provided that close monitoring of the IV site for any extravasation/phlebitis is followed. In view of the dearth of evidence, the group agreed to continue the peripheral PN formulation in case of concerns regarding the amount of calcium infused through peripheral veins.
PN in late preterm (34+0to 36+ 6 weeks) and term neonates
There is paucity of data on the efficacy and safety of PN in this age group. Two small studies enrolled late preterm and term neonates, but neither reported on major clinical outcomes [33, 34]. PN is widely used in Australian facilities in late preterm and term neonates who are not enterally fed. The 2017 Consensus Group followed the human milk approach to develop the PN formulations for this group and nutrient intake estimates are based on the average composition and intake of human milk .
Updated consensus formulations
Table 1 provides the summary of recommendations and strength of evidence for recommendations. Based on these recommendations, the 2017 group developed 8 AA/dextrose formulations and 2 lipid formulations in different volumes. Six of these AA/dextrose formulations are the improved versions of 2012 formulations. These are summarised in Table 2. Two new AA/dextrose formulations have been proposed and the contents and indications of these formulations are shown in Tables 3-4. Suggested lipid formulations are shown in Table 5. Additional file 1: Tables S1 and S2 show the nutrient intakes provided by the standard formulations in comparison to the recommended nutrient intakes (RNI).
Cessation of PN
There is no clear evidence to guide practice. The risk of late onset sepsis with intravenous access and the cost of PN are to be considered. The 2015 consensus survey found the majority of the NICUs in ANZ cease AA/dextrose formulation once the infant tolerates 120–140 ml/kg/day of enteral feeds .
Mature human milk contains 3.4 g of fat per 100 mL. The 2015 consensus survey reported that the majority of NICUs cease IV lipids once the infant tolerates 100–120 mL/kg/day of enteral feeds .
Biochemical monitoring on PN
PN administration requires careful clinical and laboratory monitoring. High blood urea nitrogen, hyperglycaemia, metabolic acidosis, hypertriglyceridemia and conjugated hyperbilirubinemia are frequently encountered biochemical abnormalities on PN. In addition to routine observations, periodic measurements of the following biochemical parameters are suggested during PN therapy. Suggested monitoring by the group is shown in Additional file 1: Table S3.
No data are available to determine the effect of higher versus lower amino acid and lipid intake in PN in ‘sick’ infants (e.g., infants with moderate-severe respiratory distress, receiving cardiovascular support, possible sepsis, acidosis); and ‘surgical’ or postoperative infants or infants post-cardiopulmonary bypass.
Blood Urea Nitrogen [Conversion blood urea nitrogen = blood urea divided by 2.14]: In the Cochrane review comparing higher versus lower amino acid intake in parenteral nutrition, six studies reported BUN levels . The criteria for abnormal blood urea nitrogen differed between the studies and varied from > 10 mmol/L to 21.4 mmol/L. There was a significant increase in abnormal blood urea nitrogen level from higher amino acid intake in all these studies although a threshold level was not clear. Given the data supporting the importance of early amino-acid administration in premature infants, limiting amino acid intake based on serum BUN alone is not warranted. BUN levels up to 14.3 mmol/L may be considered acceptable in VLBW infants on PN provided there are no other parameters to suggest protein intolerance (eg hyperammonaemia > 122 μmol/L) .
Hyperglycaemia (> 8.3 mmol/L) is not uncommon in ELBW infants . If blood glucose > 10 mmol/L (moderate hyperglycaemia) [37, 38], further management to control hyperglycaemia should be considered including reducing the glucose infusion rate (e.g. changing over to 7.5% Dextrose PN).
Defined as serum level of direct bilirubin > 20% of total serum bilirubin or serum level of direct bilirubin > 34 mmol/L [mg/dL × 17.10] .
Hypertriglyceridemia (HT) (plasma triglyceride > 2.8 mmol/L)
ESPGHAN 2005 Guidelines recommend monitoring of triglycerides in preterm and term infants and suggest a triglyceride level of 2.8 mmol/L as the upper limit . The 2015 Consensus survey revealed 62% of respondents monitor plasma triglyceride levels either routinely or in specific circumstances . A retrospective review from an Australian NICU in which routine triglyceride monitoring is in place showed HT incidence of 32.5% in 23–25 weeks and 16.1% in 26–28 weeks. Severe HT (> 4.5 mmol/L) was noted in 10% in 23–25 weeks and 4.5% in 26–28 weeks. HT was associated with a significant increase in mortality (unadjusted OR 3.5; 95% CI 1.13–10.76; 0.033) and severe retinopathy of prematurity (unadjusted OR 4.06; 95% CI 1.73–9.59; 0.002) on univariate analysis. Further multivariate analysis with adjustment for gestation and birthweight showed no significant association with HT .
Prolonged PN usage
The current formulations do not contain copper, manganese and molybdenum. Infants (e.g. post-surgical infants) who are exclusively on PN for long periods (> 4 weeks) may be at risk of trace element deficiency such as copper deficiency, which is associated with pancytopenia and osteoporosis . These can be added to the current formulations for those infants on exclusive PN for more than 4 weeks .
PN in non-tertiary neonatal facilities
Many non-tertiary nurseries manage preterm and growth restricted term neonates, who may receive partial PN while establishing enteral feeds. As there is no clear evidence for this practice, the benefits of PN in this setting needs to be balanced against the potential risks of therapy, staff skill mix and the resource availability. Short term PN using peripheral preterm PN via peripheral cannula is appropriate for these infants if enteral feeding cannot be established by day 3–5 of life.
This updated consensus proposed a total of 8 AA/dextrose formulations, 3 ClinOleic lipid/vitamin admixtures and 2 SMOFlipid lipid/vitamin admixtures to cater for the need of the majority of the NICU population in the network. Recommendations are based on the majority consensus and mostly meet the recommended nutrient intakes when administered at recommended volumes. It is important to note that the 2017 Consensus Group considered recommendations from ESPGHAN guidelines published in 2005 . Future meetings are planned to review and optimise these formulations, which will consider the more recent ESPGHAN guidelines published in 2018 . While the number of formulations seems large, it is expected that individual units may choose to limit their formulations based on their current practice, size, the spectrum of their NICU population and preference. In view of the large number of formulations and significant improvement in the formulations from 2012, colour coded posters, handouts and worksheets have been developed to assist the frontline staff in the safe prescription of PN. Coloured labels have been developed for clear identification of each formulation. Most facilities in the Australian and New Zealand region procure PN formulations from the same commercial pharmaceutical companies. Formulations and guidelines to standardise parenteral nutrition practice across the Australasian region have the potential to improve nutrition and clinical outcomes of neonates. Standardisation of the formulations across Australia resulted in reduced practice variation and reduced labour costs in compounding the formulations with the pharmaceutical companies passing on the cost savings to the NICUs. Other potential benefits of standardisation, such as error minimisation in PN prescribing and ordering, will be investigated prospectively.
The 2017 PN formulations and guidelines developed by the 2017 Neonatal Parenteral Nutrition Consensus Group offer concise and practical instructions to clinicians on how to implement current and up-to-date evidence based PN to the NICU population. In comparison to the previous formulations, the updated formulations have higher amino acid and other nutrients, particularly calcium and phosphate with the change from inorganic to organic phosphate. These PN solutions and guidelines have the potential to standardise the nutritional practice and improve both the quality and process of nutritional care and patient outcomes in the region.
Availability of data and materials
American Academy of Pediatrics
Extremely Low Birth Weight
European Society of Paediatric Gastroenterology, Hepatology and Nutrition
Grade of recommendation
Low Birth Weight
Level of evidence
Neonatal intensive care unit
New South Wales
Recommended Nutrient Intakes
Bolisetty S, Osborn D, Sinn J, Lui K. Australasian Neonatal Parenteral Nutrition Consensus Group. Standardised neonatal parenteral nutrition formulations-an Australasian group consensus 2012. BMC Pediatr. 2014;14:48.
Bolisetty S, Pharande P, Nirthanakumaran L, Do TQ, Osborn D, Smyth J, et al. Improved nutrient intake following implementation of the consensus standardised parenteral nutrition formulations in preterm neonates – a before-after intervention study. BMC Pediatr. 2014;14:309.
Tan A, Osborn D, Sinn J, Schindler T, Lui K, Bolisetty S. Neonatal Parenteral Nutrition Consensus Group Survey: Proceedings of the Neonatal Parenteral Nutrition Consensus Group 2015 Meeting. Sydney; 2015.
NHMRC Levels of evidence and grades for recommendations for developers of guidelines. 2009. www.nhmrc.gov.au/about-us/publications/guide-development-evaluation-and-implementation-clinical-practice-guidelines.
American Academy of the Pediatric (AAP). Committee on Nutrition: Nutritional needs of the preterm infant. In: Kleinman RE, editor. Pediatric Nutrition. 7th ed. IL, USA: AAP; 2014. p. 83–121.
Koletzko B, Goulet O, Hunt J, Krohn K, Shamir R. 1. Guidelines on Paediatric Parenteral Nutrition of the European Society of Paediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) and the European Society for Clinical Nutrition and Metabolism (ESPEN), Supported by the European Society of Paediatric Research (ESPR). J Pediatr Gastr Nutr. 2005;41(Suppl 2):S1–87.
Trivedi A, Sinn JKH. Early versus late administration of amino acids in preterm infants receiving parenteral nutrition. Cochrane Database Syst Rev 2013, Issue 7. Art. No.:CD008771. DOI: https://doi.org/10.1002/14651858. CD008771.pub2.
Leenders EKSM, de Waard M, van Goudoever JB. Low- versus high-dose and early versus late parenteral amino-acid administration in very-low-birth-weight infants: a systematic review and meta-analysis. Neonatol. 2018;113:187–205.
Osborn DA, Schindler T, Jones LJ, Sinn JKH, Bolisetty S. Higher versus lower amino acid intake in parenteral nutrition for newborn infants. Cochrane Database Syst Rev 2018, Issue 3. Art. No.:CD005949. DOI: https://doi.org/10.1002/14651858. CD005949.pub2.
Simmer K, Rao SC. Early introduction of lipids to parenterally-fed preterm infants. Cochrane Database Syst Rev 2005, Issue 2. Art. No.:CD005256. DOI: https://doi.org/10.1002/14651858. CD005256.
Vlaardingerbroek H, Veldhorst MA, Spronk S, van den Akker CH, van Goudoever JB. Parenteral lipid administration to very-low-birth-weight infants--early introduction of lipids and use of new lipid emulsions: a systematic review and meta-analysis. Am J Clin Nutr. 2012;96:255–68.
Hojsak I, Colomb V, Braegger C, Bronsky J, Campoy C, Domellöf M, et al. ESPGHAN committee on nutrition position paper. Intravenous lipid emulsions and risk of hepatotoxicity in infants and children: a systematic review and meta-analysis. J Pediatr Gastr Nutr. 2016;62:776–92.
Kapoor V, Glover R, Malviya MN. Alternative lipid emulsions versus pure soy oil based lipid emulsions for parenterally fed preterm infants. Cochrane Database Syst Rev 2015, Issue 12. Art. No.:CD009172. DOI: https://doi.org/10.1002/14651858. CD009172.pub2.
Edward RR, Innes JK, Marino LV, Calder PC. Influence of different intravenous lipid emulsions on growth, development and laboratory and clinical outcomes in hospitalised paediatric patients: a systematic review. Clin Nutr. 2018;37:765–83.
Bell EF, Acarregui MJ. Restricted versus liberal water intake for preventing morbidity and mortality in preterm infants. Cochrane Database Syst Rev 2008, Issue 3. Art. No.:CD000503. DOI: https://doi.org/10.1002/14651858. CD000503.
Chan W, Chua MYK, Teo E, Osborn DA, Birch P. Higher versus lower sodium intake for preterm infants. Cochrane Database Syst Rev 2017, Issue 4. Art. No.:CD012642. DOI: https://doi.org/10.1002/14651858. CD012642.
Peters O, Ryan S, Matthew L, Cheng K, Lunn J. Randomised controlled trial of acetate in preterm neonates receiving parenteral nutrition. Arch Dis Childhood-Fetal. 1997;77:F12–5.
Koo WW, Tsang RC, Succop P, Krug-Wispe SK, Babcock D, Oestreich AE. Minimal vitamin D and high calcium and phosphorus needs of preterm infants receiving parenteral nutrition. J Pediatr Gastr Nutr. 1989;8:225–33.
Devlieger H, Meyers Y, Willems L, de Zegher F, Van Lierde S, Proesmans W, et al. Calcium and phosphorus retention in the preterm infant during total parenteral nutrition. A comparative randomized study between organic and inorganic phosphate as a source of phosphorus. Clin Nutr. 1993;12:277–81.
Prestridge LL, Schanler RJ, Shulman RJ, Burns PA, Laine LL. Effect of parenteral calcium and phosphorus therapy on mineral retention and bone mineral content in very low birth weight infants. J Pediatr. 1993;122:761–8.
Pereira-da-Silva L, Costa AB, Pereira L, Filipe AF, Virella D, Leal E, et al. Early high calcium and phosphorus intake by parenteral nutrition prevents short-term bone strength decline in preterm infants. J Pediatr Gastr Nutr. 2011;52:203–9.
Fox M, Molesky M, Van Aerde JE, Muttitt S. Changing parenteral nutrition administration sets every 24 h versus every 48 h in newborn infants. Can J Gastroenterol. 1999;13:147–51.
Balegar VK, Azeem MI, Spence K, Badawi N. Extending total parenteral nutrition hang time in the neonatal intensive care unit: is it safe and cost effective? J Paediatr Child H. 2013;49:E57–61.
Matlow AG, Kitai I, Kirpalani H, Chapman NH, Corey M, Perlman M, et al. A randomized trial of 72- versus 24-hour intravenous tubing set changes in newborns receiving lipid therapy. Infec Cont Hosp Ep. 1999;20:487–93.
Loisel DB, Smith MM, MacDonald MG, Martin GR. Intravenous access in newborn infants: impact of extended umbilical venous catheter use on requirement for peripheral venous lines. J Perinatol. 1996;16:461–6.
Butler-O'Hara M, Buzzard CJ, Reubens L, McDermott MP, DiGrazio W, D'Angio CT. A randomized trial comparing long-term and short-term use of umbilical venous catheters in premature infants with birth weights of less than 1251 grams. Pediatr. 2006;118:e25–35.
Seguin J, Fletcher MA, Landers S, Brown D, Macpherson T. Umbilical venous catheterizations: audit by the study Group for Complications of perinatal care. Am J Perinat. 1994;11:67–70.
Ainsworth SB, McGuire W. Percutaneous central venous catheters versus peripheral cannulae for delivery of parenteral nutrition in neonates. Cochrane Database Syst Rev 2015, Issue 10. Art. No.:CD004219. DOI: https://doi.org/10.1002/14651858. CD004219.pub4.
Gazitua R, Wilson K, Bistrian BR, Blackburn GL. Factors determining peripheral vein tolerance to amino acid infusions. Arch Surg-Chicago. 1979;114:897–900.
August D, Teitelbaum D, Albina J, Bothe A, Guenter P, Heitkemper M, et al. Guidelines for the use of parenteral and enteral nutrition in adult and pediatric patients. JPEN Parenter Enter. 2002;26:1SA–138SA.
Metjian TA, Seri I, Jew RK. Osmolarity of peripherally administered hyperalimentation and the incidence of phlebitis in the neonatal intensive care unit. Presented at 35th Annual ASHP Clinical Meeting; NV, USA; 2000 Dec 3–7.
Dugan S, Le J, Jew RK. Maximum tolerated osmolarity for peripheral administration of parenteral nutrition in pediatric patients. JPEN-Parenter Enter. 2014;38:847–51.
Hata S, Kubota A, Okada A. A pediatric amino acid solution for total parenteral nutrition does not affect liver function test results in neonates. Surg Today. 2002;32:800–3.
Makay B, Duman N, Ozer E, Kumral A, Yesilirmak D, Ozkan H. Randomized, controlled trial of early intravenous nutrition for prevention of neonatal jaundice in term and near-term neonates. JPEN-Parenter Enter. 2007;44:354–8.
Amino acids and proteins. In Koletzko B, Poindexter B, Uauy R, editors. Nutritional care of preterm infants. Basel: Karger; 2014, p. 55.
Hays SP, Smith EO, Sunehag AL. Hyperglycemia is a risk factor for early death and morbidity in extremely low birth-weight infants. Pediatr. 2006;118:1811–8.
Bottino M, Cowett RM, Sinclair JC. Interventions for treatment of neonatal hyperglycemia in very low birth weight infants. Cochrane Database Syst Rev 2011, Issue 10. Art. No.:CD007453. DOI: https://doi.org/10.1002/14651858. CD007453.pub3.
Sinclair JC, Bottino M, Cowett RM. Interventions for prevention of neonatal hyperglycemia in very low birth weight infants. Cochrane Database Syst Rev 2009, Issue 3. Art. No:CD007615. DOI: https://doi.org/10.1002/14651858. CD007615.pub2.
Duvanel CB, Fawer CL, Cotting J, Hohlfeld P, Matthieu JM. Long-term effects of neonatal hypoglycemia on brain growth and psychomotor development in small-for-gestational-age preterm infants. J Pediatr. 1999;134:492–8.
Lucas A, Morley R, Cole TJ. Adverse neurodevelopmental outcome of moderate neonatal hypoglycaemia. BMJ. 1988;297:1304–8.
American Academy of Pediatrics Subcommittee on Hyperbilirubinemia. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatr. 2004;114:297–316.
Reading RF, Ellis R, Fleetwood A. Plasma albumin and total protein in preterm babies from birth to eight weeks. Early Hum Dev. 1990;22:81–7.
Zlotkin SH, Casselman CW. Percentile estimates of reference values for total protein and albumin in sera of premature infants (<37 weeks of gestation). Clin Chem. 1987;33:411–3.
Sinclair R, Lui K, Bolisetty S. Hypertriglyceridaemia in extremely preterm infants receiving parenteral lipid emulsions. Presented at 21st Annual Congress of Perinatal Society of Australia and New Zealand; Canberra; 2017 April 2–5.
Mihatsch W, Shamir R, van Goudoever JB, Fewtrell M, Lapillonne A, Lohner S, et al. ESPGHAN/ESPEN/ESPR/CSPEN guidelines on pediatric parenteral nutrition: Guideline development process for the updated guidelines. Clin Nutr. 2018;37(6 Pt B):2306–8.
We thank all the frontline medical and nursing staff for providing feedback during the development of these guidelines.
No external or internal funding was provided for the development of these guidelines.
Ethics approval and consent to participate
Consent for publication
Authors have no competing (financial or non-financial) interests to declare.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1 Table S1. 2017 consensus formulations and comparison to recommended parenteral nutrient intakes in preterm neonates. Values are per kg per day, unless otherwise indicated. Table S2. 2017 consensus formulations and comparison to recommended parenteral nutrient intakes in term neonates. Values are per kg per day, unless otherwise indicated. Table S3. Suggested routine PN biochemistry orders.
About this article
Cite this article
Bolisetty, S., Osborn, D., Schindler, T. et al. Standardised neonatal parenteral nutrition formulations – Australasian neonatal parenteral nutrition consensus update 2017. BMC Pediatr 20, 59 (2020). https://doi.org/10.1186/s12887-020-1958-9
- Parenteral nutrition