- Research article
- Open Access
Actuarial survival of a large Canadian cohort of preterm infants
BMC Pediatrics volume 5, Article number: 40 (2005)
The increased survival of preterm and very low birth weight infants in recent years has been well documented but continued surveillance is required in order to monitor the effects of new therapeutic interventions. Gestation and birth weight specific survival rates most accurately reflect the outcome of perinatal care. Our aims were to determine survival to discharge for a large Canadian cohort of preterm infants admitted to the neonatal intensive care unit (NICU), and to examine the effect of gender on survival and the effect of increasing postnatal age on predicted survival.
Outcomes for all 19,507 infants admitted to 17 NICUs throughout Canada between January 1996 and October 1997 were collected prospectively. Babies with congenital anomalies were excluded from the study population. Gestation and birth weight specific survival for all infants with birth weight <1,500 g (n = 3419) or gestation ≤30 weeks (n = 3119) were recorded. Actuarial survival curves were constructed to show changes in expected survival with increasing postnatal age.
Survival to discharge at 24 weeks gestation was 54%, compared to 82% at 26 weeks and 95% at 30 weeks. In infants with birth weights 600–699, survival to discharge was 62%, compared to 79% at 700–799 g and 96% at 1,000–1,099 g. In infants born at 24 weeks gestational age, survival was higher in females but there were no significant gender differences above 24 weeks gestation. Actuarial analysis showed that risk of death was highest in the first 5 days. For infants born at 24 weeks gestation, estimated survival probability to 48 hours, 7 days and 4 weeks were 88 (CI 84,92)%, 70 (CI 64, 76)% and 60 (CI 53,66)% respectively. For smaller birth weights, female survival probabilities were higher than males for the first 40 days of life.
Actuarial analysis provides useful information when counseling parents and highlights the importance of frequently revising the prediction for long term survival particularly after the first few days of life.
The improvement in survival rates for preterm and very low birth weight infants has been well documented during the last 20 years [1–3]. More recently, a marked reduction in mortality rates has been reported following the introduction and widespread use of antenatal steroids and exogenous surfactant [4–6]. Despite initial concerns, studies of later neurodevelopmental outcome have not shown an increase in major disability rates as a result of improved survival [7–9]. As our understanding of disease processes increases and new therapies continue to be developed, continued surveillance of up to date outcome data is essential in order to monitor the effectiveness of current practice.
Early reports of survival rates for high risk infants were based on birth weight alone, as assessment of gestational age was relatively imprecise prior to the introduction of routine first trimester ultrasound scans. Subsequently, survival data based on gestational age has become more widely reported [10, 11]. This information is more useful for obstetric decision-making in the prenatal period and there is increasing evidence that mortality and later morbidity in high risk infants relates more closely to gestation than to birth weight [10, 12]. Indeed a combination of both variables may give an even more accurate prediction of outcome once the infant is born .
Of further concern is that survival data in many published studies is derived from single tertiary units or collaborations of such centres which are not geographically based [1, 14]. This increases the likelihood of sample bias and may not give a true reflection of survival expectations for the population as a whole. The effects of gender and multiple births on survival have also been of interest in previous studies, many showing higher survival rates for females and/or singletons [11, 15–19]. This additional information may enhance our prediction of survival based on gestation or birth weight alone. More recently, attention has focused on the timing of infant death, specifically utilising actuarial survival analysis to predict future life expectancy from a given age [20–23]. This provides useful additional information when making decisions regarding ongoing management in the neonatal intensive care unit (NICU).
Our aims were to determine survival to discharge for a large Canadian cohort of high-risk infants (<1500 g or ≤30 weeks) representing admissions to 17 NICUs with 75% of tertiary level NICU beds in Canada, and to examine the effects of gestation, birth weight, gender and multiple birth on survival. Utilizing actuarial survival analysis, the effect of increasing postnatal age on expected survival to discharge was investigated.
The Canadian Neonatal Network comprised 17 tertiary NICUs across Canada in 1996 . It was funded by the Medical Research Council of Canada and other institutions (see acknowledgements) in 1996 to facilitate neonatal research by creating a national neonatal-perinatal database. The Canadian population in 1996 was about 30 million with approximately 357,000 births annually . This study included all infants with a birth weight <1500 grams or gestational age ≤30 weeks who were admitted to the Canadian Neonatal Network during a 22-month period between January 1996 and October 1997. Infants with congenital anomalies were excluded because they have different mortality and morbidity risks .
Prospective data were collected locally by trained research assistants and transmitted electronically to the Canadian Neonatal Network Coordinating Centre for verification and analysis. Collected data included demographic variables, obstetric information, neonatal illness severity (Score for Neonatal Acute Physiology, Version II [SNAP-II]) , therapeutic intensity (Neonatal Therapeutic Intensity Scoring System [NTISS])  and selected outcomes and resource use.
Definition of study variables
Study variables were defined according to the Canadian Neonatal Network SNAP Project Abstractor Manual . An admission was defined as a stay in the NICU for at least 24 hours or death/transfer to another unit within 24 hours. Gestational age was defined as the best obstetric estimate based on early prenatal ultrasound, obstetric examination and obstetric history, unless the post-natal pediatric estimate of gestation differed from the obstetric estimate by more than two weeks. In that case, the pediatric estimate of gestational age was used instead. An infant was defined as small-for-gestational age (SGA) if the birth weight was less than the 10th percentile for gestational age according to the growth charts established by Arbuckle  in 1989 for the Canadian population. SNAP-II  is a neonatal illness severity score calculated from 6 empirically weighted physiologic measurements made during the first 12 hours of admission to the NICU. NTISS  is a score of neonatal therapeutic intensity calculated from a checklist of 63 NICU therapies used in a 24 hour period, weighted according to invasiveness and cost. Chronic lung disease was defined as oxygen dependency at 36 weeks corrected GA for an infant who was born at ≤32 weeks gestation . Intraventricular hemorrhage (IVH) was defined according to the criteria of Papile  from head ultrasound performed before 14 days of life. Necrotizing enterocolitis (NEC) was defined according to Bell's criteria (stage 2 or higher)  and was classified as medical (clinical symptoms and signs plus evidence of pneumatosis on abdominal X'ray) or surgical (histological evidence of NEC on surgical specimen of intestine). Retinopathy of prematurity (ROP) was defined according to the International Classification for Retinopathy of Prematurity  and the Reese Classification of cicatrical disease . Nosocomial infection was defined using blood and cerebrospinal fluid culture results according to Freeman's criteria . Patent ductus arteriosus was defined as clinical diagnosis plus treatment with indomethacin or surgical ligation or both. Seizures were defined as clinically significant episodes witnessed by a nurse or physician and for which anti-convulsant treatment was given. Congenital anomalies were classified according to the WHO International Classification of Diseases, 9 th Revision (ICD-9) .
Data analysis was carried out on two populations – preterm babies with gestation age ≤30 weeks and Very Low Birth Weight (VLBW) babies with birth weight <1,500 grams. A two sample t-test was used to separately test the effect of gender and multiple births on population demographics, adverse outcome and resource use. Similarly a two sample t-test was used to test the effect of gender on survival proportions for each week of gestational age and each 100 grams birth weight range. For the actuarial analysis, the event of interest was death and the time-to-event was the number of days survived. Babies that survived to discharge had their length of stay included as right censored observations. The actuarial survival estimator which estimates the probability of survival to and beyond a set number of days was calculated in daily intervals for the first 60 days of life. The effect of gender, gestation age and birth weight on survival were studied by obtaining actuarial survival estimators for each category. The probability of survival to discharge, for an infant who has survived to a given day in the NICU, was calculated and graphed by gestational age and birth weight category.
Between January 8, 1996 and October 31, 1997, 19,507 infants were admitted to participating NICUs. Excluding those with congenital anomalies, there were 3,119 infants ≤30 weeks gestational age and 3,409 infants with birth weight <1,500 grams. Characteristics of the two groups are shown in Table 1. Of note, for infants <1,500 grams birth weight, 52% were born by caesarean section, 21% were outborn and 68% received antenatal steroids.
Survival to NICU discharge
Survival to discharge increased from 45% for infants weighing <600 g at birth to over 95% for those with birth weight >1200 g (Fig 1). There was a similar increase for gestational age groups with survival increasing from about 14% at 22 weeks to over 93% at 28 weeks and above (Fig 2).
Effect of gender on survival and morbidity
When analysed by gestational age groups, survival for male and female infants was not significantly different except for those born at 24 weeks gestation in whom survival for females was 17 (3, 29)% higher (Fig 3). When analysed according to birth weight groups, survival for females in the 600–699 g group was 7 (6,28)% significantly higher than for males (Fig 4). However, within many birth weight groups, females were significantly more mature than males and would therefore be expected to have higher survival as a consequence of gestational age (Tables 2 and 3). In contrast to survival, female infants had significantly (p < 0.05) lower incidence of chronic lung disease and severe intraventricular hemorrhage than male infants (Table 4). The high incidence of SGA among infants born at <1,500 g reflects the inherent tendency to select SGA infants when birth weight criteria is used to categorise infants instead of gestational age.
Multiple births and antenatal steroids
Of the 3119 infants born ≤30 weeks, 2,277 (73%) were singleton deliveries and 841 (27%) were the products of multiple gestation pregnancies (Table 5). There was no significant difference in survival, illness severity or resource use between the two groups. Antenatal steroid use was 7(4,11)% higher in multiple gestation for VLBW babies, and delivery by cesarean section was 9(5,13)% more likely in multiple gestation pregnancies for VLBW. Antenatal steroid use was 7(3,11)% higher in multiple gestation for preterm babies, and delivery by cesarean section was 9(6,13)% more likely in multiple gestation pregnancies for preterm. A full or partial course of antenatal steroids was given to 70% of infants ≤30 weeks gestation and to 68% of infants between <1,500 g birth weight. The use of antenatal steroids was lower in the most preterm infants ≤24 weeks gestation.
Actuarial survival curves are given in Figures 5, 6, 7, 8, 9 for the first 60 days. Points on the curves give S(t); the estimated probability of a baby surviving to at least t days. Babies that were discharged from the NICU can not afford to be ignored as these were most likely to be the longer lived observations. Babies that were discharged from the NICU were therefore included as censored observations in the analysis. By comparing the slope of the curve (which gives the instantaneous risk of death), the highest risk of death is within the first 6 days. Risk of death is higher for smaller babies and babies with lower GA. Risk of death also decreases with time. Figure 9 shows that actuarial survival is higher among females than males during the first 40 days, and narrows after that. Figures 10 and 11 give the probability of survival to discharge for an infant who has survived to a given day in the NICU, stratified by gestational age and birth weight respectively.
Since our study is based on a large, geographically defined Canadian cohort, it has greater relevance than those from single units and provides a more realistic picture of neonatal outcomes. In addition, our study cohort was derived from large regional centres with comparable levels of care conforming to current North American standards for neonatal intensive care. Our results are similar to those from previous publications on NICU outcomes, such as that of the NICHD Neonatal Network [1–4], the Vermont-Oxford Trials Network [38, 39] and the Australia-New Zealand Neonatal Network  (although some networks examined all live born infants instead of NICU admissions). Although improvement in survival rates were previously reported among the most preterm groups [1–4, 24, 38–40], more recent publications report no further improvement in outcomes [41, 42], and demonstrate the importance of reporting trends over time.
An advantage in survival for female infants has been reported by previous studies with the greatest difference apparent when stratified by birth weight groups [41–44]. In contrast, when analysed by gestational age, we found a gender difference in survival only for infants born at 24 weeks GA or less. This may reflect the fact that at any given birth weight, female infants tend to be more mature. It has also been previously suggested that the advantage in survival for female infants is related to a more favourable hormonal milieu in the female fetus leading to accelerated lung maturation compared to the male [45–48]. In the present era, it is also possible that the increased use of antenatal steroids and exogenous surfactant has improved overall survival but more notably in male compared to female infants. However, not all gender differences were eliminated and female infants continued to have lower incidences of chronic lung disease and severe intraventricular hemorrhage than male infants. Actuarial survival analysis also showed that female infants had lower mortality rates than male infants during the first 40 days of life, indicating a difference in time of death.
Actuarial analysis adds a further dimension to standard survival data and highlights several points of interest. For all gestational age and birth weight groups the risk of death is greatest during the first few days of life with relatively few deaths occurring after day 7. This emphasises the importance of revising the chances of survival at regular intervals especially during the first few days of life (as in figures 10 and 11). Such updated survival information is useful when informing parents and is necessary for ongoing management decisions. Furthermore, actuarial survival curves are helpful when studying the economic aspects of neonatal intensive care. The majority of deaths occur during the first few days of life and therefore the proportion of health care expenditure on eventual non-survivors is relatively small. With reference to research and health promotion, actuarial data aid the development of treatment strategies. Our data highlights where interventions would have the greatest benefit e.g. early deaths within the first few days and late deaths after the first 28 days. The effects of new interventions on survival patterns could then be monitored. Finally, this report extends the available information on various aspects of low birth weight infants previously reported by the Canadian Neonatal Network [24, 26, 27, 49–58].
One limitation of our survival data is that they only include infants admitted for neonatal intensive care. They do not take into account stillbirths after the onset of preterm labour nor delivery room deaths of live born infants. Therefore, they provide an overestimate of survival chances if used to counsel parents during preterm labour or as a guide to obstetric management. However, as most high risk pregnancies are currently managed in large perinatal centres, with skilled personnel certified in neonatal resuscitation, the majority of infants born at 24 weeks and above are successfully resuscitated and admitted for intensive care, and our results would be highly applicable to them. Discharge policies may affect survival rates but since infants are usually discharged only when they are sufficiently well, it is unlikely that discharge policies will significantly affect our results. For the actuarial survival analysis, survival to 60 days of life was considered. However, deaths may occur even after this time during the post-discharge period and these were not considered in the study.
Up to date survival rates are essential when evaluating perinatal services. Previously reported effect of gender on overall survival are no longer apparent among infants >24 weeks gestation but there is a gender difference in the time of death. Actuarial survival analysis emphasises the importance of frequently revising predictions for survival in high-risk infants, particularly during the first week of life.
Neonatal intensive care unit
Neonatal therapeutic intensity scoring system
Score for Neonatal Acute Physiology Version II
Very low birth weight
Hack M, Wright LL, Shankaran S, Tyson JE, Horbar JD, Bauer CR, Younes N: Very low birth weight outcomes of the National Institute of Child Health and Human Development Neonatal Network, November 1989 to October 1990. Am J Obstet Gynecol. 1995, 172: 457-464. 10.1016/0002-9378(95)90557-X.
Fanaroff AA, Wright LL, Stevenson DK, Shankaran S, Donovan EP, Ehrenkranz RA, Younes N, Korones SB, Stoll BJ, Tyson JE, Bauer CR, Oh W, Lemons JA, Papile LA, Verter J: Very low birthweight outcomes of the National Institute of Child Health and Human Development Neonatal Research Network, May 1991 through December 1992. Am J Obstet Gynecol. 1995, 173: 1423-1431. 10.1016/0002-9378(95)90628-2.
Stevenson DK, Wright LL, Lemons JA, Oh W, Korones SB, Papile LA, Bauer CR, Stoll BJ, Tyson JE, Shankaran S, Fanaroff AA, Donovan EF, Ehrenkranz RA, Verter J: Very low birth weight outcomes of the National Institute of Child Health and Human Development Neonatal Research Network, January 1993 through December 1994. Am J Obstet Gynecol. 1998, 179: 1632-1639. 10.1016/S0002-9378(98)70037-7.
Ferrara TB, Hoekstra RE, Couser RJ, Gaziano EP, Calvin SE, Payne NR, Fangman JJ: Survival and follow-up of infants born at 23–26 weeks of gestational age: effects of surfactant therapy. J Pediatr. 1994, 124: 119-124.
Jobe AH, Mitchell BR, Gunkel JH: Beneficial effects of the combined use of prenatal corticosteroids and postnatal surfactant on preterm infants. Am J Obstet Gynecol. 1993, 168: 508-513.
Corbet A, Bucciarelli R, Goldman S, Mammel M, Wold D, Long W: Decreased mortality rate among small premature infants treated at birth with a single dose of synthetic surfactant: a multicenter controlled trial. American Exosurf Pediatric Study Group 1. J Pediatr. 1991, 118: 277-284.
O'Shea TM, Preisser JS, Klinepeter KL, Dillard RG: Trends in mortality and cerebral palsy in a geographically based cohort of very low birth weight neonates born between 1982 to 1994. Pediatrics. 1998, 101: 642-647. 10.1542/peds.101.4.642.
O'Shea TM, Klinepeter KL, Goldstein DJ, Jackson BW, Dillard RG: Survival and developmental disability in infants with birth weights of 501 to 800 grams, born between 1979 and 1994. Pediatrics. 1997, 100: 982-986. 10.1542/peds.100.6.982.
Cooke RWI: Trends in incidence of cranial ultrasound lesions and cerebral palsy in very low birth weight infants 1982–93. Arch Dis Child Fetal Neonatal Ed. 1999, 80: F115-F117.
Wariyar U, Richmond S, Hey E: Pregnancy outcome at 24–31 weeks' gestation: neonatal survivors. Arch Dis Child. 1989, 64: 678-686.
Synnes AR, Ling EW, Whitfield MF, Mackinnon M, Lopes L, Wong G, Effer SB: Perinatal outcomes of a large cohort of extremely low gestational age infants (twenty-three to twenty-eight completed weeks of gestation). J Pediatr. 1994, 125: 952-60.
Phelps DL, Brown DR, Tung B, Cassady G, McClead RE, Purohit DM, Palmer EA: 28-Day Survival Rates of 6676 Neonates with Birth Weights of 1250 Grams or Less. Pediatrics. 1991, 87: 7-17.
Draper ES, Manktelow B, Field DJ, James D: Prediction of survival for preterm births by weight and gestational age: retrospective population based study. BMJ. 1999, 319: 1093-1097.
Hack M, Horbar JD, Malloy MH, Tyson JE, Wright E, Wright L: Very low birth weight outcomes of the National Institute of Child Health and Human Development Neonatal Network. Pediatrics. 1991, 87: 587-597.
Tyson JE, Younes N, Verter J, Wright LL: Viability, morbidity, and resource use among newborns of 501 to 800 g birth weight. National Institute of Child Health and Human Development Neonatal Research Network. JAMA. 1996, 276: 1645-1651. 10.1001/jama.276.20.1645.
Brothwood M, Wolke D, Gamsu H, Benson J, Cooper D: Prognosis of the very low birth weight baby in relation to gender. Arch Dis Child. 1986, 61: 559-564.
Resnick MB, Carter RL, Ariet M, Bucciarelli RL, Evans JH, Furlough RR, Ausbon WW, Curran JS: Effect of birth weight, race, and sex on survival of low-birth-weight infants in neonatal intensive care. Am J Obstet Gynecol. 1989, 161: 184-7.
Hoffman EL, Bennett FC: Birth Weight Less than 800 Grams: Changing Outcomes and Influences of Gender and Gestation Number. Pediatrics. 1990, 86: 27-34.
Khoury MJ, Marks JS, McCarthy BJ, Zaro SM: Factors affecting the sex differential in neonatal mortality: The role of respiratory distress syndrome. Am J Obstet Gynecol. 1985, 151: 777-782.
Cartlidge PHT, Stewart JH: Survival of very low birth weight and very preterm infants in a geographically defined population. Acta Paediatrica. 1997, 86: 105-110.
Cooper TR, Berseth CL, Adams JM, Weisman LE: Actuarial survival in the Premature Infant Less than 30 Weeks' Gestation. Pediatrics. 1998, 101: 975-978. 10.1542/peds.101.6.975.
Meadow W, Reimshisel T, Lantos J: Birth weight specific mortality for extremely low birth weight infants vanishes by four days of life: epidemiology and ethics in the neonatal intensive care unit. Pediatrics. 1996, 97: 636-643.
Gould JB, Benitz WE, Liu H: Mortality and time to death in very low birth weight infants: California, 1987 and 1993. Pediatrics. 2000, 105: e37-10.1542/peds.105.3.e37.
Lee SK, McMillan DD, Ohlsson A, Pendray M, Synnes A, Whyte R, Chien LY, Sale J: Variations in practice and outcomes of the Canadian NICU Network 1996–7. Pediatrics. 2000, 106: 1070-9. 10.1542/peds.106.5.1070.
Synnes A, Berry M, Jones H, Pendray M, Stewart SD, Lee SK, for The Canadian Neonatal Network: Infants with congenital anomalies admitted to neonatal intensive care units. Am J Perinatology. 2004, 21: 199-208. 10.1055/s-2004-828604.
Richardson DK, Corcoran JD, Escobar GJ, Lee SK, for the Canadian NICU Network the Kaiser Permanente Neonatal Minimum Sata Set Wide Area Network and the SNAP-II Study Group: SNAP-II and SNAPPE-II: Simplified newborn illness severity and mortality risk scores. J Pediatr. 2001, 138: 92-100. 10.1067/mpd.2001.109608.
Gray JE, Richardson DK, McCormick MC, Workman-Daniels K, Goldman DA: Neonatal therapeutic intervention scoring system (NTISS): a therapy-based severity of illness assessment tool. Pediatrics. 1992, 90: 561-567.
Canadian Neonatal Network Abstractor Manual, Vancouver, BC. 1995
Arbuckle TE, Sherman GJ: An analysis of birth weight by gestational age in Canada. CMAJ. 1989, 140: 157-165.
Shennan AT, Dunn MS, Ohlsson A, Lennox K, Hoskins EM: Abnormal pulmonary outcomes in preterm infants: prediction from oxygen requirement in the neonatal period. Pediatrics. 1988, 82: 527-532.
Papile LA, Munsick-Bruno G, Schaefer A: Relationship of cerebral intra-ventricular hemorrhage and early childhood handicaps. J Pediatr. 1983, 103: 272-277.
Bell MJ, Ternberg JL, Feigin RD, Keating JP, Marshall R, Barton L, Brotherton T: Neonatal necrotizing enterocolitis. Therapeutic decisions based upon clinical staging. Ann Surg. 1978, 187: 1-7.
Committee members: An international classification of retinopathy of prematurity. Pediatrics. 1984, 74: 127-133.
Reese AB, King MJ, Owens WC: a classification of retrolental fibroplasia. Am J Opthalmol. 1953, 36: 1333-
Freeman J, Epstein MF, Smith NE, Platt R, Sidebottom DG, Goldman DA: Extra hospital stay and antibiotic usage with nocosomial coagulase negative staphylococcal bacteremia in two neonatal intensive care unit populations. Am J Dis Child. 1990, 144: 324-329.
WHO International Classification of Diseases, 9 th Revision. WHO, Geneva. 1975
Horbar JD, Badger J, Lewit EM, Rogowski J, Shiono PH: Hospital and patient characteristics associated with variation in 28-day mortality rates for very low birth weight infants. Pediatrics. 1997, 99: 149-156. 10.1542/peds.99.2.149.
The investigators of the Vermont-Oxford Trials Network: Very low birth weight outcomes for 1990. Pediatrics. 1993, 91: 540-545.
Donoghue D: Australia & New Zealand Neonatal Network Neonatal Network Series Number 2. AIHW National Perinatal Statistics Unit, Sydney. 1997, ISSN 1326-012X, AIHW Catalogue no. PER 5
Tucker J, McGuire W: Epidemiology of preterm birth. BMJ. 2004, 329: 675-678. 10.1136/bmj.329.7467.675.
Battin M, Ling EW, Whitfield MF, Mackinnon M, Effer SB: Has the outcome for extremely low gestational age (ELGA) infants improved following recent advances in neonatal intensive care?. Am J Perinatol. 1998, 15: 469-477.
Hack M, Fanaroff AA: Outcomes of children of extremely low birthweight and gestational age in the 1990's. Early Hum Devel. 1999, 53: 193-218. 10.1016/S0378-3782(98)00052-8.
Hack M, Friedman H, Fanaroff AA: Outcomes of extremely low birth weight infants. Pediatrics. 1996, 98: 931-937.
Cummings JJ, D'Eugenio DB, Gross SJ: A controlled trial of dexamethasone in preterm infants at high risk for bronchopulmonary dysplasia. N Engl J Med. 1989, 320: 1505-10.
Khosla SS, Brehier A, Eisenfeld AJ, Ingleson LD, Parks PA, Rooney SA: Effects of estrogen on fetal rabbit lung maturation: morphological and biochemical studies. Pediatr Res. 1981, 15: 1274-1281.
Zachman RD, Morison JC, Curet LB, Gustafson N, the Collaborative Group on Antenatal Steroid Therapy: Lecithin:sphingomyelin ratio in the amniotic fluid of male and female fetuses. J Reprod Med. 1989, 34: 203-206.
Nielson HC: Testosterone regulation of sex differences in fetal lung development. Proc Soc Exp Biol Med. 1992, 199: 446-452.
Chien LY, Ohlsson A, Seshia M, Boulton J, Sankaran K, Lee SK, The Canadian Neonatal Network: Variation in antenatal corticosteroid treatment – a persistent problem 30 years later. Obstetr & Gynecol. 2002, 99: 401-408. 10.1016/S0029-7844(01)01732-X.
Chan KJ, Ohlsson A, Synnes A, Lee DSC, Chien LY, Lee SK, The Canadian NICU Network: Survival, morbidity and resource use of <25 weeks gestation infants. Am J Obstet Gynecol. 2001, 185: 220-226. 10.1067/mob.2001.115280.
Synnes A, Chien LY, Peliowski A, Baboolal R, Lee SK, The Canadian Neonatal Network: Variations in Intraventricular Hemorrhage Incidence Rates among Canadian Neonatal Intensive Care Units. J Pediatr. 2001, 138: 525-531. 10.1067/mpd.2001.111822.
Chien LY, Whyte R, Thiessen P, Matthew D, Aziz K, Lee SK, The Canadian Neonatal Network: Improved outcome of preterm infants when delivered in tertiary care centers. Obstet & Gynecol. 2001, 98: 247-252. 10.1016/S0029-7844(01)01438-7.
Lee SK, McMillan DD, Ohlsson A, Boulton J, Lee DSC, Ting S, Liston R, The Canadian Neonatal Network: Benefit of preterm birth at tertiary care centers is related to gestational age. Am J Obstet Gynecol. 2003, 188: 617-622. 10.1067/mob.2003.139.
Lee SK, Lee DCS, Andrews WL, Baboolal R, Pendray M, Stewart SD, The Canadian Neonatal Network: Higher mortality among infants admitted to neonatal intensive care units at nights. J Pediatr. 2003, 143: 592-597. 10.1067/S0022-3476(03)00367-6.
Sankaran K, Puckett B, Lee DSC, Seshia M, Boulton J, Qiu ZG, Lee SK, Canadian Neonatal Network: Variations in incidence of necrotizing enterocolitis in Canadian neonatal intensive care units. J Pediatr Gastro Nutr. 2004, 39: 366-372. 10.1097/00005176-200410000-00012.
Hayter M, Anderson L, Claydon J, Magee LA, Little R, Liston RM, Lee SK, Dadelszen PV, Canadian Neonatal Network: Variations in early and intermediate neonatal outcomes for inborn babies admitted to a Canadian NICU and born of hypertensive pregnancies. JOGC. 2005, 27: 25-32.
Shah P, Shah V, Qiu ZG, Ohlsson A, Lee SK, Canadian Neonatal Network: Improved outcomes of outborn preterm infants if admitted to perinatal centers vs free-standing pediatric hospitals. J Pediatr. 2005, 146: 626-631. 10.1016/j.jpeds.2005.01.030.
Lau J, Magee F, Qiu ZG, Hoube J, von Dadelszen P, Lee SK: Maternal-fetal chorioamnionitis is associated with higher neonatal mortality, morbidity and resource use than maternal chorioamnionitis. Am J Obstet Gynecol. 2005, 193: 708-713. 10.1016/j.ajog.2005.01.017.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2431/5/40/prepub
This study was supported by Grant 40503 and Grant 00152 from the Medical Research Council of Canada. Additional funding was provided by the B.C.'s Children's Hospital Foundation; Calgary Regional Health Authority; Dalhousie University Neonatal-Perinatal Research Fund; Division of Neonatology, Children's Hospital of Eastern Ontario; Child Health Program, Health Care Corporation of St John's; The Neonatology Program, Hospital for Sick Children; Lawson Research Institute; Midland Walwyn Capital Inc; Division of Neonatology, Hamilton Health Sciences Corporation; Mount Sinai Hospital; North York General Hospital Foundation; Saint Joseph's Health Centre; University of Saskatchewan Neonatal Research Fund; University of Western Ontario; Women's College Hospital.
Members of the Canadian Neonatal Network: Shoo K. Lee (Coordinator, Canadian Neonatal Network); Wayne Andrews (Charles A. Janeway Child Health Centre, St John's, NF); Ranjit Baboolal (North York Hospital, N. York, ON); Jill Boulton (St Joseph's Health Centre, London, ON; previously at Mt Sinai Hospital, Toronto, ON); David Brabyn (Royal Columbian Hospital, New Westminster, BC); David S.C. Lee (St Joseph's Health Centre; London, ON); Derek Matthew (Victoria General Hospital (Victoria, BC); Douglas D. McMillan (Foothill's Hospital, Calgary, AB); Christine Newman (Hospital for Sick Children; Toronto, ON); Arne Ohlsson (Mt Sinai Hospital, Toronto, ON; formerly at Women's College Hospital, Toronto, ON); Abraham Peliowski (Royal Alexandra Hospital, Edmonton, AB); Margaret Pendray (Children's & Women's Health Centre of British Columbia (Vancouver, BC); Koravangattu Sankaran, (Royal University Hospital, Saskatoon, SK); Barbara Schmidt (Hamilton Health Sciences Corporation, Hamilton, ON); Mary Seshia (Health Sciences Centre, Winnipeg, MB); Anne Synnes (Children's and Women's Health Centre of British Columbia, Vancouver, BC; formerly at Montreal Children's Hospital, Montreal, PQ); Paul Thiessen (Children's & Women's Health Centre of British Columbia (Vancouver, BC); Robin Walker (Children's Hospital of Eastern Ontario and Ottawa General Hospital, Ottawa, ON); Robin Whyte (IWK-Grace Health Centre for Women, Children and Families, Halifax, NS); Catherine M. G. Cronin (Winnipeg Regional Health Authority).
Coordinating centre staff (Vancouver, BC): Aireen Wingert; Stella Karuri; Sarka Lisonkova.
The author(s) declare that they have no competing interests.
Huw Jones interpreted data and drafted the manuscript. Stella Karuri performed statistical analysis and interpretation. Shoo K Lee was the principal investigator and interpreted the data and drafted the manuscript. Catherine Cronin, Arne Ohlson and Abraham Peliowski and Anne Synnes were site investigators. All these individuals read and approved the final manuscript. The CNN represents all site investigators, and was responsible for organization and administration of the SNAP study, and subsequent data flow.
Huw P Jones and Shoo K Lee contributed equally to this work.
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Jones, H.P., Karuri, S., Cronin, C.M. et al. Actuarial survival of a large Canadian cohort of preterm infants. BMC Pediatr 5, 40 (2005). https://doi.org/10.1186/1471-2431-5-40
- Birth Weight
- Neonatal Intensive Care Unit
- Actuarial Survival
- Antenatal Steroid
- Birth Weight Group