Skip to Content
A home for paediatricians. A voice for children and youth.
CPS

Discharge planning of the preterm infant

Posted: Mar 4, 2022


The Canadian Paediatric Society gives permission to print single copies of this document from our website. For permission to reprint or reproduce multiple copies, please see our copyright policy.

Principal author(s)

Nicole Anderson, Michael Narvey, Canadian Paediatric Society, Fetus and Newborn Committee

Paediatr Child Health 2022 27(2):129 (Abstract)

Abstract

“When will my baby come home?” is one of the most common questions asked by parents of preterm infants admitted to the neonatal intensive care unit (NICU). While the hospital course varies based on the gestational age at birth and the attainment of “physiological maturity”, the aim of this statement is to provide guidance for the safe discharge of infants born before 37 weeks. The discharge process should start at the time of admission to NICU, and with a plan for assessing physiological markers including thermoregulation, control of breathing, respiratory stability, and adequate weight gain as an indication of feeding skills. Importantly, the infant’s family unit is a crucial part of the care team and their involvement in the NICU will promote confidence, decrease anxiety, increase resilience, and help ensure a safe discharge environment.

Keywords: Apnea; Discharge; Late preterm; NICU; Psychosocial; Thermoregulation

This statement amalgamates and updates two previous Canadian Paediatric Society documents: ‘Going home: Facilitating discharge of the preterm infant’ and ‘Safe discharge of the late preterm infant’ [1][2].

Search strategy

A combined MEDLINE and Embase search was performed for studies from January 2014 up to May 2020, using identified keywords. Reference lists of publications were reviewed. The timeline was chosen to identify new literature published since previous CPS statements on this topic. A total of 178 references were retrieved, of which full text articles were reviewed. Levels of evidence and grades of recommendation were assigned in accordance with the Oxford Centre for Evidence-Based Medicine guideline [3] (Levels of evidence and grades of recommendation).

Definitions and frequency

A preterm infant is defined as any infant born before the 37th week of gestation. The World Health Organization (WHO) defines an infant born between 33 to 37 weeks as moderate to late preterm [4]. Very preterm infants are those born between 28 to 32 6/7 weeks gestational age (GA). Extremely preterm infants are defined as any infant born less than 28 weeks GA. The preterm birth rate in Canada hovers around 8% of all live births, of which approximately 70% are born from 34 0/7 to 36 6/7 weeks, with the remaining 30% being born before 34 weeks GA [5][6].

Admission to the neonatal intensive care unit (NICU)

The preterm infant’s journey may begin well before admission to the NICU, with a prolonged hospital admission for the mother, frequent perinatal ultrasounds, and close surveillance of the pregnancy. In some cases, the delivery of a preterm infant comes without warning. Regardless of scenario, admission to the NICU is a stressful and anxiety-provoking experience. Every infant admitted to the NICU experiences a unique hospital course that is often commensurate with their GA, with length of NICU admission being inversely correlated [7][8]. Complications such as sepsis, necrotizing enterocolitis, retinopathy of prematurity [9], or bronchopulmonary dysplasia (BPD) can individually or in combination contribute to length of stay. After recovering from such conditions, the safe discharge of a preterm infant is, at a minimum, dependent on the attainment of physiological maturity.

Physiological maturity

Thermoregulation

The weight and GA whereby an infant can maintain normothermia in an open cot is both infant-dependent and centre-specific. Though there is evidence supporting earlier weaning from the incubator with earlier discharge [10], one Cochrane review concluded that transfer to a cot at less than 1700 grams (versus greater than 1700 grams) did not lead to earlier discharge [11]. Studies on kangaroo care or skin-to skin-contact between caregiver and infant have been shown to promote normothermia at discharge, among other benefits [12][13].

Control of breathing

In one observational study, all infants born 28 weeks GA had apnea of prematurity (AOP)[14]. The incidence of AOP followed an inverse relationship with GA, affecting 50% of those born at 30 weeks versus 7% born at 34 to 35 weeks. One systematic review in late preterm infants indicated an absolute risk of AOP of 0.87 % [15]. Caffeine (a methylxanthine) is one of the most commonly prescribed medications in the NICU and is the mainstay of pharmacological treatment for AOP [16]. Although there is variation as to when caffeine is discontinued, most centres will opt to do so between 32 and 37 weeks postmenstrual age (PMA). This timing is due to the fact that AOP is less common beyond 36 weeks GA [17][18]. The mean half-life of caffeine is approximately 100 hours but varies with GA at birth and chronological age [19]-[21]. Thus, a minimum 5- to 7-day period of monitoring in the NICU after caffeine discontinuation is suggested. A longer period of observation may be necessary for infants born at less than 29 weeks GA [17]. There is no current literature to support shorter durations of monitoring after discontinuation of caffeine. For infants with AOP who have not been treated with caffeine, an apneic-free period is more difficult to discern. The risk for recurrence of apneic events after a period of 3 versus 7 days from the last event shows minimal risk reduction. Therefore, practitioners may reasonably choose a minimum 3-day observation period and consider a longer period for infants with a more severe or prolonged course of AOP [22][23].

While it is preferable to discontinue caffeine in hospital, continuing caffeine at home may be considered as part of a shared decision between the family and health care team. Importantly, AOP is not an identified risk factor for sudden infant death syndrome (SIDS), and there is no evidence suggesting clear benefit of home monitoring in the context of AOP or SIDS prevention [24][25]. SIDS prevention strategies, including safe sleep, should be reviewed (and modelled) during the NICU stay [26][27]. A premature infant born at 32 weeks GA in the NICU should be placed supine during sleep to promote tolerance of this position before discharge [28].

Respiratory stability

Respiratory stability is achieved when an infant no longer requires ventilatory support and (preferably) is not receiving supplemental oxygenation. Preterm infants often require ventilatory support, with appropriate de-escalation during their NICU stay. A retrospective study of 224 infants <27 weeks GA found a correlation between earlier attempts at extubation and shorter lengths of stay [29]. Clinicians should also consider that reintubation (within 14 days of first extubation) may be associated with adverse outcomes [30].

BPD is clinically diagnosed when supplemental oxygen or mechanical ventilation is provided beyond 36 weeks GA, although this definition is constantly evolving [31][32]. Oxygen saturation targets in the NICU remain inconclusive, but most authors suggest a target of 90% to 95% [32]-[34]. Diuretics, steroids (inhaled or systemic), and home oxygen may be part of the discharge plan for infants with BPD [35]. For appropriate infants and families, home oxygen is preferable to a prolonged NICU admission. Arranging for home oxygen support may help to increase growth, decrease mean pulmonary artery pressure, and (when used at night) improve sleep duration [32].

BPD-associated pulmonary hypertension (PH) is an important diagnosis because it carries significant mortality [36]. The prevalence of PH is proportional to BPD severity, with up to 39% of infants with this condition being classified as having severe BPD [37]. Screening for PH in high-risk infants, along with evaluation of comorbidities including intermittent hypoxemia, aspiration, gastroesophageal reflux, structural airway abnormalities, pulmonary artery or vein stenosis, and left ventricular dysfunction, should be pursued in the NICU as well as followed up post-discharge [38].

To minimize further risk in infants with compromised pulmonary reserve, health care practitioners should promote a smoke-free home environment and infection prevention strategies, such as handwashing. Moreover, adherence to the routine immunization schedule, along with respiratory syncytial virus (RSV) prophylaxis when criteria are met, is essential [39].

Feeding and weight gain

The establishment of oral feeding is a significant milestone during an NICU admission. Establishing breastfeeding should be encouraged when that is the mother’s goal. In preterm infants, barriers to oral feeding may include an immature suck and swallow mechanism, invasive ventilatory support, cardiorespiratory instability, and ‘nil per os’ (NPO) status, all of which can make feeding skills difficult to attain. Organized non-nutritive sucking has been observed in infants around 28 to 29 weeks PMA, with subsequent attainment of exclusive breastfeeding at 32 to 38 weeks [40][41]. One recent study showed the median PMA for establishment of full oral feeds was 37.1 weeks and 34.7 weeks for extremely preterm and very preterm infants, respectively [42].

There has been a recent shift to infant-driven and standardized feeding algorithms for preterm babies [43][44]. Introduction of the ‘safe individualized nipple-feeding competence’ (or SINC) approach to feeding extremely preterm infants on non-invasive respiratory support has allowed earlier development of feeding skills than the traditional approach of waiting until respiratory support has been discontinued [45]. Importantly, however, SINC implementation requires a standardized and educated team. For infants born <32 weeks, SINC has been shown to achieve earlier attainment of first breast or nipple feeds [45]. One recent randomized controlled trial (RCT) comparing SINC with “regular care” showed an effect on weight gain but not on transition to full oral feeds or length of hospitalization [45]. Hence, there is a need for evidence-based tools that assess preterm infant readiness to initiate oral feeds [46].

When caring for preterm babies, practitioners should provide the tools necessary for mothers to provide as much human milk as possible. Initiation relies on lactogenesis, a transitional process that is altered by a premature birth [47]. Also, breast milk supply can be negatively affected by concerns about adequacy of amount, difficulties with expression, and physical separation from the infant [48]. Promotion of breastfeeding should begin with maternal obstetrical care and continue from point of admission throughout the NICU stay. Studies have shown a significant association between initiation of early pumping and first oral feeding at breast and breast milk feeding at discharge [49]-[51]. Skin-to-skin care has been shown to improve breastfeeding efficacy and duration post-discharge [52]. Galactogogues for breast milk production, such as metoclopramide and domperidone, increase serum prolactin by inhibition of dopamine [48]. Evidence in this area is limited by heterogeneity in trial design and outcome measures. However, domperidone appears to be more efficacious in increasing breast milk production [47][53].

Mothers who plan to breastfeed their infant post-discharge can begin to introduce solid foods at 4 to 6 months to meet iron requirements, while continuing to breastfeed. There should be appropriate supports in place (e.g., referral to a lactation consultant) to support breastfeeding past discharge [54]. Factors associated with shorter duration of breastfeeding post-NICU include lower maternal socioeconomic status (SES), lower maternal education, and maternal smoking. Mothers with these risk factors require additional support during the discharge planning process [52].

Reflux is reported in approximately one-in-ten preterm infants [55]. Routine pharmacological intervention treatment of reflux is not recommended [56]. However, as per the guidelines developed by the European Society for Pediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) with the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN), when a pharmacological is needed, proton pump inhibitors (PPIs) are the treatment of first line [57]. Given the likelihood of prolonged use in the outpatient setting and the side effect profile, practitioners should review the ongoing need for a PPI at the time of discharge [56][58].

Education on how to administer medications and supplements, including iron, vitamin D and, if appropriate, calcium and/or phosphate, should be provided to caregivers. Guidance on monitoring and length of treatment should be shared with the family’s health care provider (HCP). Iron supplementation should continue for 6 to 12 months chronological age (depending on birth weight) for infants who are breastfed exclusively to 6 months of age [59]. For infants requiring additives to human milk or formula feeding, caregivers should be taught and given opportunities to prepare feeds before NICU discharge [60]. Use of fortified human milk is usually limited to hospital settings, such that alternatives needed to meet the infant’s nutritional requirements must be anticipated and planned before discharge. Inaccurate mixing of feeds is a common mistake and can lead to electrolyte disturbance and poor growth. After discharge, consultation with an outpatient dietitian and the infant’s primary HCP should guide the duration of treatment with milk additives.

There is no standard minimum weight at which an infant can be discharged, but timing is guided by weight criteria for infant car seats. Families who anticipate going home before their infant weighs 2.2 kg (5 lbs) must make sure they have a car seat with a ~1.8 kg (4 lb) minimum weight.

Family readiness and home environment

As an infant nears the physiological maturity necessary for safe discharge, caregivers and the infant’s environment must be adequately prepared for life at home. While there is an abundance of literature on the negative psychosocial effects of having a preterm infant in the NICU, it is essential to consider each family’s sources of support, including cultural networks and care practices [58][61]-[68].

Family readiness should be assessed throughout the NICU admission. Family-centred or integrated care frameworks (or an equivalent centre-specific initiative) provide a basis for NICU assessment and support. Families should be both involved with and informed of their infant’s care, and collaborative care helps increase resilience and readiness for homecoming and decreases risk for hospital readmission [69]-[74]. Preparation also improves neonatal outcomes [75][76]. Data from locations with an early discharge program (often complemented by outreach and home support) have clearly demonstrated that collaboration between caregivers and medical teams means safer transitions home [77][78].

Typical newborn care, as outlined in ‘Facilitating discharge from hospital of the healthy term infant[79], is important for context. The following steps are always part of discharge education:

  • Highlight and involve family caregivers in early newborn care routines, such as bathing.
  • Ask that the infant’s car seat be brought to the NICU and review safety measures, including adequate fit and use.
  • Make sure parents know and can recognize early signs of illness, such as fever, dehydration, and respiratory distress.

Late preterm infants

Late preterm infants may appear to be mature but still lack key elements of physiological maturity that facilitate safe discharge home. Before discharge, late preterm newborns must demonstrate respiratory and temperature stability, adequate feeding skills, and euglycemia. Deficits in these areas can interact to put infants at risk [80]. For example, a late preterm infant may become hypothermic and feed poorly, which can lead to lethargy that prompts an unnecessary work-up for sepsis and hospitalization.

Late preterm infants are at risk for problems post-discharge and require timely follow-up by community care providers. Those with stable weight and bilirubin levels may be discharged in the first week post-birth, provided there is a follow-up appointment within 72 h of discharge. Bilirubin levels in this population peak later, remain elevated for longer, and achieve higher peak values compared with term infants [81][82]. A clinician should arrange for follow-up within 24 to 48 h from discharge with appropriate public health services.

Support following NICU discharge

The psychosocial effects of having a preterm baby often linger, with many families requiring ongoing support at home [83]-[85]. In some birthing centres, home-based support programs follow preterm infants post-discharge. This population is frequently re-hospitalized during infancy, requiring ongoing health care resources. Home-based discharge teams can help mitigate such needs [72][86]-[90]. The positive outcomes of these programs include improved breastfeeding, parent-infant interactions, and neurodevelopmental outcomes [72]. When an infant is being discharged into a remote community, liaising directly with the child’s primary care provider in-community is recommended. There may be a role for supportive web-based or telemedicine programs [91][92].

A checklist of recommendations

The following checklist is based on recommendations reached by consensus and drawn from several evidence-based resources, with a general evidence level of 2 [3]. For a printable version of this checklist, click here.

Within the first 72 h of admission and before delivery, if possible:

  • Describe what physiological maturity means to parents or caregivers, and explain—in general terms at first—the expected course of care in the NICU.
  • Encourage the family to become part of the infant’s health care team. Introduce and explain supportive resources, such as social work.
  • Encourage and support breastfeeding. Explain early feeding goals and why related behaviours and routine checks (e.g., glucose levels) are reassessed at regular intervals during the NICU admission.
  • Explore whether communication would be preferred in a different language and, if so, arrange for translation.

Before discharge:

  • Maintain the infant’s body temperature within normal range (36.5°C to 37.5°C) when appropriately dressed for the ambient temperature.
  • Consider discontinuing caffeine, but observe the infant for 5 to 7 days for possible apneic events. When caffeine has not been administered, an observed apnea-free period of 3 to 7 days is recommended. 
  • Arrange follow-up with appropriate paediatric subspecialists (e.g., ophthalmology for infants at risk for retinopathy of prematurity(ROP)).
  • Evaluate infants for broncho-pulmonary dysplasia (BPD)-associated hypertension and, if present, arrange appropriate follow-up.
  • Ensure appropriate weight gain and maintenance, and plan a post-discharge feeding regimen with parents.
  • Educate parents and caregivers regarding routine care:
    • Typical newborn feeding and sleep patterns and behaviours
    • Bathing routine and safety
    • Safe sleep and SIDS prevention
    • Car and home safety
    • Cardiopulmonary resuscitation (CPR) training, when appropriate and if parents are interested in learning
    • How to administer medication(s) and nutritional supplements, when needed. Review dosing and use as often as needed, prepare feeds with specified additives with parents, and explain and review nasogastric tube use feeding, when needed.
    • Car seat installation and safe use
    • Early signs of illness, including fever, dehydration, and respiratory distress
    • Promote hand hygiene, a safe home environment, and smoking cessation
    • Provide contact information for supportive community resources
  • As timing of discharge nears, re-evaluate caregiver readiness for different aspects of at-home care.
  • Ascertain need for government support programs and help to complete paperwork, when needed.

At discharge:

  • Confirm and document newborn metabolic screen. Arrange for repeat screen if necessary.
  • Confirm and document hearing screen.
  • Arrange outpatient ROP screening, as appropriate.
  • Encourage adherence to the routine immunization schedule (in accordance with infant age and condition) and arrange for respiratory syncytial virus (RSV) prophylaxis when local criteria are met.
  • Perform and document a comprehensive physical examination, including growth parameters.
  • Review medications and consider weaning before discharge, when appropriate.
  • Provide written prescriptions for medications and instructions for administration. Confirm that parents understand the correct dosage and suspensions, and that medications are readily accessible at home.
  • Consider nutritional follow-up for infants at risk for post-discharge growth failure.
  • Ensure timely, appropriate follow-up has been arranged with the infant’s community care team. This should include:
    • A written summary of infant’s NICU course
    • Confirming the most responsible physician or practitioner who will follow the infant as outpatient
    • Confirming that a parental care team is in place (with psychosocial supports, as needed).
  • Refer for neurodevelopmental follow-up as per clinic-specific criteria (e.g., infants weighing less than 1250 grams at birth).

Acknowledgements

This position statement was reviewed by the Community Paediatrics and Nutrition and Gastroenterology Committees of the Canadian Paediatric Society. It has also been reviewed by the College of Family Physicians of Canada.


CANADIAN PAEDIATRIC SOCIETY FETUS AND NEWBORN COMMITTEE (2020-2021)

Members: Gabriel Altit MD, Nicole Anderson MD (Resident Member), Heidi Budden MD (Board Representative), Leonora Hendson MD (past member), Souvik Mitra MD, Michael R. Narvey MD (Chair), Eugene Ng MD, Nicole Radziminski MD, Vibhuti Shah MD (past member)

Liaisons: Radha Chari MD (The Society of Obstetricians and Gynaecologists of Canada), James Cummings MD (Committee on Fetus and Newborn, American Academy of Pediatrics), William Ehman MD (College of Family Physicians of Canada), Danica Hamilton RN (Canadian Association of Neonatal Nurses), Chloë Joynt MD (CPS Neonatal-Perinatal Medicine Section Executive), Chantal Nelson PhD (Public Health Agency of Canada)

Principal authors: Nicole Anderson MD, Michael Narvey MD


References

  1. Jefferies AL; Canadian Paediatric Society, Fetus and Newborn Committee. Going home: Facilitating discharge of the preterm infant. Paediatr Child Health 2014;19(1):31-36.
  2. Whyte RK; Canadian Paediatric Society, Fetus and Newborn Committee. Safe discharge of the late preterm infant. Paediatr Child Health 2010;15(10):655-60.
  3. Oxford Centre for Evidence-Based Medicine: Levels of Evidence (March 2009) (Accessed June 14, 2021).
  4. World Health Organization: Preterm Birth (19 February 2018) (Accessed June 14, 2021).
  5. Farwell KD, Shahmirzadi L, El-Khechen D, et al. Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: Results from 500 unselected families with undiagnosed genetic conditions. Genet Med 2015;17(7):578-86.
  6. Statistics Canada. Table 13-10-0425-01. Live births, by weeks of gestation. Release date September 29, 2020 (Accessed July 5, 2021).
  7. Hintz SR, Bann CM, Ambalavanan N, Cotten CM, Das A, Higgins RD. Predicting time to hospital discharge for extremely preterm infants. Pediatrics 2010;125(1):e146-54.
  8. Rawlings JS, Scott JS. Postconceptional age of surviving preterm low-birth-weight infants at hospital discharge. Arch Pediatr Adolesc Med 1996;150(3):260-2.
  9. Jefferies AL; Canadian Paediatric Society, Fetus and Newborn Committee. Retinopathy of prematurity: An update on screening and management. Pediatr Child Health 2016;21(2)101-4.
  10. Barone G, Corsello M, Papacci P, et al. Feasibility of transferring intensive cared preterm infants from incubator to open crib at 1600 grams. Ital J Pediatr 2014;40:41.
  11. New K, Flenady V, Davies MW. Transfer of preterm infants from incubator to open cot at lower versus higher body weight. Cochrane Database Syst Rev 2011;(9):CD004214.
  12. Jefferies AL; Canadian Paediatric Society, Fetus and Newborn Committee. Kangaroo care for the preterm infant and family. Paediatr Child Health 2012;17(3):141-6.
  13. Conde-Agudelo A, Díaz-Rossello JL. Kangaroo mother care to reduce morbidity and mortality in low birthweight infants. Cochrane Database Syst Rev 2016;(8):CD002771.
  14. Henderson-Smart DJ. The effect of gestational age on the incidence and duration of recurrent apnoea in newborn babies. Aust Paediatr J 1981;17(4):273-6.
  15. Teune MJ, Bakhuizen S, Gyamfi Bannerman C, et al. A systematic review of severe morbidity in infants born late preterm. Am J Obstet Gynecol 2011;205(4):374.e1-9.
  16. Abdel-Hady H, Nasef N, Shabaan AE, Nour I. Caffeine therapy in preterm infants. World J Clin Pediatr 2015;4(4):81-93.
  17. Eichenwald EC, Aina A, Stark AR. Apnea frequently persists beyond term gestation in infants delivered at 24 to 28 weeks. Pediatrics 1997;100(3 Pt 1):354-9.
  18. Ji D, Smith PB, Clark RH, et al. Wide variation in caffeine discontinuation timing in premature infants. J Perinatol 2020;40(2):288-93.
  19. Charles BG, Townsend SR, Steer PA, Flenady VJ, Gray PH, Shearman A. Caffeine citrate treatment for extremely premature infants with apnea: Population pharmacokinetics, absolute bioavailability, and implications for therapeutic drug monitoring. Ther Drug Monit 2008;30(6):709-16.
  20. Koch G, Datta AN, Jost K, Schulzke SM, van den Anker J, Pfister M. Caffeine Citrate dosing adjustments to assure stable caffeine concentrations in preterm neonates. J Pediatr 2017;191:50-66.e1.
  21. Le Guennec JC, Billon B, Paré C. Maturational changes of caffeine concentrations and disposition in infancy during maintenance therapy for apnea of prematurity: Influence of gestational age, hepatic disease, and breast-feeding. Pediatrics 1985;76(5):834-40.
  22. Darnall RA, Kattwinkel J, Nattie C, Robinson M. Margin of safety for discharge after apnea in preterm infants. Pediatrics 1997;100(5):795-801.
  23. Lorch SA, Srinivasan L, Escobar GJ. Epidemiology of apnea and bradycardia resolution in premature infants. Pediatrics 2011;128(2):e366-73.
  24. Ramanathan R, Corwin MJ, Hunt CE, et al. Cardiorespiratory events recorded on home monitors: Comparison of healthy infants with those at increased risk for SIDS. JAMA 2001;285(17):2199-207.
  25. Strehle EM, Gray WK, Gopisetti S, Richardson J, McGuire J, Malone S. Can home monitoring reduce mortality in infants at increased risk of sudden infant death syndrome? A systematic review. Acta Paediatr 2012;101(1):8-13.
  26. Task Force on Sudden Infant Death Syndrome; Moon RY. SIDS and other sleep-related infant deaths: Expansion of recommendations for a safe infant sleeping environment. Pediatrics 2011;128(5):e1341-67.
  27. Public Health Agency of CanadaJoint Statement on Safe Sleep: Reducing Sudden Infant Deaths in Canada. October 2021 (Accessed December 6, 2021).
  28. American Academy of Pediatrics, Committee on Fetus and Newborn. Hospital discharge of the high-risk neonate. Pediatrics 2008;122(5):1119-26.
  29. Robbins M, Trittmann J, Martin E, Reber KM, Nelin L, Shepherd E. Early extubation attempts reduce length of stay in extremely preterm infants even if re-intubation is necessary. J Neonatal Perinatal Med 2015;8(2):91-7.
  30. Shalish W, Kanbar L, Kovacs L, et al. The impact of time interval between extubation and reintubation on death or bronchopulmonary dysplasia in extremely preterm infants. J Pediatr 2019;205:70-76.e2.
  31. Jobe AH, Bancalari E. Bronchopulmonary dysplasia. Am J Respir Crit Care Med 2001;163(7):1723-9.
  32. Hayes D, Wilson KC, Krivchenia K, et al. Home oxygen therapy for children. An official American Thoracic Society Clinical Practice Guideline. Am J Respir Crit Care Med 2019;199(3):e5-e23.
  33. Askie LM, Henderson-Smart DJ, Irwig L, Simpson JM. Oxygen-saturation targets and outcomes in extremely preterm infants. N Engl J Med 2003;349(10):959-67.
  34. Primhak R. Oxygen titration strategies in chronic neonatal lung disease. Paediatr Respir Rev 2010;11(3):154-7.
  35. Bhandari A, Panitch H. An update on the post-NICU discharge management of bronchopulmonary dysplasia. Semin Perinatol 2018;42(7):471-7.
  36. Berkelhamer SK, Mestan KK, Steinhorn R. An update on the diagnosis and management of bronchopulmonary dysplasia (BPD)-associated pulmonary hypertension. Semin Perinatol 2018;42(7):432-43.
  37. Arjaans S, Zwart EAH, Ploegstra MJ, et al. Identification of gaps in the current knowledge on pulmonary hypertension in extremely preterm infants: A systematic review and meta-analysis. Paediatr Perinat Epidemiol 2018;32(3):258-67.
  38. Krishnan U, Feinstein JA, Adatia I, et al. Evaluation and management of pulmonary hypertension in children with bronchopulmonary dysplasia. J Pediatr 2017;188:24-34.e1.
  39. Robinson JL, Le Saux N; Canadian Paediatric Society, Infectious Diseases and Immunization Committee. Preventing hospitalization for respiratory syncytial virus infection. Paediatr Child Health 2015;20(6): 321-6.
  40. Nyqvist KH. Early attainment of breastfeeding competence in very preterm infants. Acta Paediatr 2008;97(6):776-81.
  41. Nyqvist KH, Sjödén PO, Ewald U. The development of preterm infants' breastfeeding behavior. Early Hum Dev 1999l;55(3):247-64.
  42. Khan Z, Sitter C, Dunitz-Scheer M, et al. Full oral feeding is possible before discharge even in extremely preterm infants. Acta Paediatr 2019;108(2):239-44.
  43. Bozkurt O, Dizdar EA, Bidev D, Sari FN, Uras N, Oguz SS. Prolonged minimal enteral nutrition versus early feeding advancements in preterm infants with birth weight ≤1250 g: A prospective randomized trial. J Matern Fetal Neonatal Medicine 2020:1-7.
  44. Celen R, Tas Arslan F, Soylu H. Effect of SINC feeding protocol on weight gain, transition to oral feeding, and the length of hospitalization in premature infants: A randomized controlled trial. JPEN J Parenter Enteral Nutr 2021;45(3):567-77.
  45. Dalgleish SR, Kostecky LL, Blachly N. Eating in "SINC": Safe Individualized Nipple-Feeding Competence, a quality improvement project to explore infant-driven oral feeding for very premature infants requiring noninvasive respiratory support. Neonatal Netw 2016;35(4):217-27.
  46. Crowe L, Chang A, Wallace K. Instruments for assessing readiness to commence suck feeds in preterm infants: Effects on time to establish full oral feeding and duration of hospitalisation. Cochrane Database Syst Rev 2016;(8):CD005586.
  47. Asztalos EV. Supporting mothers of very preterm infants and breast milk production: A review of the role of galactogogues. Nutrients 2018;10(5):600.
  48. Alves E, Magano R, Amorim M, Nogueira C, Silva S. Factors influencing parent reports of facilitators and barriers to human milk supply in neonatal intensive care units. J Hum Lact 2016;32(4):695-703.
  49. Parker LA, Sullivan S, Krueger C, Mueller M. Association of timing of initiation of breastmilk expression on milk volume and timing of lactogenesis stage II among mothers of very low-birth-weight infants. Breastfeed Med 2015;10(2):84-91.
  50. Casavant SG, McGrath JM, Burke G, Briere C-E. Caregiving factors affecting breastfeeding duration within a neonatal intensive care unit. Adv Neonatal Care 2015;15(6):421-8.
  51. Casey L, Fucile S, Dow KE. Determinants of successful direct breastfeeding at hospital discharge in high-risk premature infants. Breastfeed Med 2018;13(5):346-51.
  52. Briere C-E, McGrath J, Cong X, Cusson R. An integrative review of factors that influence breastfeeding duration for premature infants after NICU hospitalization. J Obstet Gynecol Neonatal Nurs 2014;43(3):272-81.
  53. Asztalos EV, Campbell-Yeo M, da Silva OP, . Enhancing human milk production with domperidone in mothers of preterm infants. J Hum Lact 2017;33(1):181-7.
  54. UNICEF, WHO. Protecting, promoting and supporting breastfeeding: The baby-friendly hospital initiative for small, sick and preterm newborns. August 5, 2020 (Accessed June 14, 2021).
  55. Jadcherla SR, Khot T, Moore R, Malkar M, Gulati IK, Slaughter JL. Feeding methods at discharge predict long-term feeding and neurodevelopmental outcomes in preterm infants referred for gastrostomy evaluation. J Pediatr 2017;181:125-30.e1.
  56. Choosing Wisely Canada. Five Things Physicians and Patients Should Question. August 2020 (Accessed June 14, 2021).
  57. Rosen R, Vandenplas Y, Singendonk M, et al. Pediatric gastroesophageal reflux clinical practice guidelines: Joint recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition. J Pediatr Gastroenterol Nutr 2018;66(3):516-54.
  58. D'Agostino JA, Passarella M, Martin AE, Lorch SA. Use of gastroesophageal reflux medications in premature infants after NICU discharge. Pediatrics 2016;138(6):e20161977.
  59. Unger SL, Fenton TR, Jetty R, Critch JN, O'Connor DL. Iron requirements in the first 2 years of life. Paediatr Child Health 2019;24(8):555-6:
  60. Vollrath K, Rosenberg A, Gabrielski L, et al. NICU discharge feeding bundle improves accuracy of postdischarge feeding preparation and potentially prevents readmission. Adv Neonatal Care 2019;19(2):90-6.
  61. Bry A, Wigert H. Psychosocial support for parents of extremely preterm infants in neonatal intensive care: A qualitative interview study. BMC Psychol 2019;7(1):76.
  62. Calsina SP, Gutierrez NO, Del Fresno SC, Besa ME, Codina LC, Tricas JG. Anxiety and depression in mothers of preterm infants. Intervention strategies and literature review. Matronas Profesion 2018;19(1):21-7.
  63. Cano Giménez E, Sánchez-Luna M. Providing parents with individualised support in a neonatal intensive care unit reduced stress, anxiety and depression. Acta Paediatr 2015;104(7):e300-5.
  64. Cheng C, Franck LS, Ye XY, Hutchinson SA, Lee SK, O'Brien K. Evaluating the effect of family integrated care on maternal stress and anxiety in neonatal intensive care units. J Reprod Infant Psychol 2021;39(2):166-79.
  65. Hawes K, McGowan E, O'Donnell M, Tucker R, Vohr B. Social emotional factors increase risk of postpartum depression in mothers of preterm infants. J Pediatr 2016;179:61-7.
  66. Lee SY, Chau JPC, Choi KC, Lo SHS. Feasibility of a guided participation discharge program for very preterm infants in a neonatal intensive care unit: A randomized controlled trial. BMC Pediatr 2019;19(1):402.
  67. Trumello C, Candelori C, Cofini M, et al. Mothers' depression, anxiety, and mental representations after preterm birth: A study during the infant's hospitalization in a neonatal intensive care unit. Front Public Health 2018;6:359.
  68. Treyvaud K, Spittle A, Anderson PJ, O'Brien K. A multilayered approach is needed in the NICU to support parents after the preterm birth of their infant. Early Hum Deve 2019;139:104838.
  69. Aydon L, Hauck Y, Murdoch J, Siu D, Sharp M. Transition from hospital to home: Parents' perception of their preparation and readiness for discharge with their preterm infant. J Clin Nurs 2018;27(1-2):269-77.
  70. Chen Y, Zhang J, Bai J. Effect of an educational intervention on parental readiness for premature infant discharge from the neonatal intensive care unit. J Adv Nurs 2016;72(1):135-46.
  71. Griffin T. Family-centered care in the NICU. J Perinat Neonatal Nurs 2006;20(1):98-102.
  72. Hannan KE, Hwang SS, Bourque SL. Readmissions among NICU graduates: Who, when and why? Semin Perinatol 2020;44(4):151245.
  73. Lakshmanan A, Agni M, Lieu T, et al. The impact of preterm birth <37 weeks on parents and families: A cross-sectional study in the 2 years after discharge from the neonatal intensive care unit. Health Qual Life Outcomes 2017;15(1):38.
  74. Mikkelsen G, Frederiksen K. Family-centred care of children in hospital – A concept analysis. J Adv Nurs 2011 May;67(5):1152-62.
  75. Lv B, Gao X-R, Sun J, et al. Family-centered care improves clinical outcomes of very-low-birth-weight infants: A quasi-experimental study. Front Pediatr2019;7:138.
  76. Raiskila S, Axelin A, Rapeli S, Vasko I, Lehtonen L. Trends in care practices reflecting parental involvement in neonatal care. Early Hum Dev 2014;90(12):863-7.
  77. Brødsgaard A, Zimmermann R, Petersen M. A preterm lifeline: Early discharge programme based on family-centred care. J Spec Pediatr Nurs 2015;20(4):232-43.
  78. Koreska M, Petersen M, Andersen BL, Brødsgaard A. Supporting families on their journey towards a normal everyday life – Facilitating partnership in an early discharge program for families with premature infants. J Spec Pediatr Nurs 2020;25(1):e12274.
  79. Lemyre B, Jefferies AL, O'Flaherty P; Canadian Paediatric Society, Fetus and Newborn Committee. Facilitating discharge from hospital of the healthy term infant. Paediatr Child Health 2018;23(8):515-31:
  80. Barkemeyer BM. Discharge planning. Pediatr Clin North Am 2015;62(2):545-56.
  81. Sarici SU, Serdar MA, Korkmaz A, et al. Incidence, course, and prediction of hyperbilirubinemia in near-term and term newborns. Pediatrics 2004;113(4):775-80.
  82. Wang ML, Dorer DJ, Fleming MP, Catlin EA. Clinical outcomes of near-term infants. Pediatr 2004;114(2):372-6.
  83. Ireland S, Ray RA, Larkins S, Woodward L. Perspectives of time: A qualitative study of the experiences of parents of critically ill newborns in the neonatal nursery in North Queensland interviewed several years after the admission. BMJ Open 2019;9(5):e026344.
  84. Leahy-Warren P, Coleman C, Bradley R, Mulcahy H. The experiences of mothers with preterm infants within the first-year post discharge from NICU: Social support, attachment and level of depressive symptoms. BMC Pregnancy Childbirth 2020;20(1):260.
  85. McAndrew S, Acharya K, Westerdahl J, et al. A prospective study of parent health-related quality of life before and after discharge from the neonatal intensive care unit. J Pediatr 2019;213:38-45.e3.
  86. Kuint J, Lerner-Geva L, Chodick G, et al. Type of re-hospitalization and association with neonatal morbidities in infants of very low birth weight. Neonatology 2019;115(4):292-300.
  87. Liu Y, McGowan E, Tucker R, Glasgow L, Kluckman M, Vohr B. Transition Home Plus Program reduces Medicaid spending and health care use for high-risk infants admitted to the neonatal intensive care unit for 5 or more days. J Pediatr 2018;200:91-97.e3
  88. Luu TM, Lefebvre F, Riley P, Infante-Rivard C. Continuing utilisation of specialised health services in extremely preterm infants. Arch Dis Child Fetal Neonatal Ed 2010;95(5):F320-5.
  89. Patra K, Greene MM. Health care utilization after NICU discharge and neurodevelopmental outcome in the first 2 years of life in preterm infants. Am J Perinatol 2018;35(5):441-7.
  90. Vohr B, McGowan E, Keszler L, O'Donnell M, Hawes K, Tucker R. Effects of a transition home program on preterm infant emergency room visits within 90 days of discharge. J Perinatol 2018;38(2):185-90.
  91. Luu TM, Xie LF, Peckre P, et al. Web-Based intervention to teach developmentally supportive care to parents of preterm infants: Feasibility and acceptability study. JMIR Res Protoc 2017;6(11):e236.
  92. Robinson C, Gund A, Sjöqvist B-A, Bry K. Using telemedicine in the care of newborn infants after discharge from a neonatal intensive care unit reduced the need of hospital visits. Acta Paediatr 2016;105(8):902-9.

Disclaimer: The recommendations in this position statement do not indicate an exclusive course of treatment or procedure to be followed. Variations, taking into account individual circumstances, may be appropriate. Internet addresses are current at time of publication.

Last updated: Feb 8, 2024