Video Abstract

Video Abstract

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OBJECTIVES

To examine the prevalence, characteristics, clinical course, and length of stay (LOS) among 4 groups of infants who were transferred for convalescence and subsequently discharged from the hospital; failed transfer for convalescence and were (a) either readmitted, or (b) transferred again; and were not transferred for convalescence.

METHODS

Among very low birth weight infants hospitalized at US Vermont Oxford Network centers between 2006 and 2020, we examined the distribution of characteristics, delivery room and NICU usage measures, outcomes, and LOS among the 4 groups of infants.

RESULTS

Among 641 712 infants, a total of 28 985 (4.5%) infants were transferred for convalescent care; of 28 186 infants, 182 (0.65%) died before hospital discharge and 2551 (9.1%) failed the transfer (1771 [6.3%] were readmitted and 780 [2.8%] were transferred again). There were major regional and NICU variations in the practice of the transfer for convalescence; New England (18.8%) had the highest whereas East South Central (2.2%) had the lowest percentage of transfer for convalescence. Infants who transferred for convalescence and were discharged from the hospital had a similar LOS and similar distribution of NICU usage measures and outcomes to infants who were not transferred for convalescence. Infants who failed the transfer for convalescence had a longer LOS than infants who were transferred for convalescence and then discharged from the hospital.

CONCLUSIONS

The rates of transfer for convalescence and transfer for convalescence failure were low. Future studies should weigh the risks and benefits of transfer for convalescence, which might differ on the basis of geography.

What’s Known on the Subject:

Studies examining the transfer of very low birth weight infants for convalescent care are limited, with contradictory findings on the safety of the practice.

What This Study Adds:

Transfer for convalescence and failed transfer for convalescence rates were 4.5% and 9.1%, respectively. Morbidities and hospital stay were similar between infants discharged from the hospital and infants transferred for convalescence who were subsequently discharged from the hospital.

Regionalization of neonatal care has played an important role in improving outcomes of high-risk infants. To avoid overcrowding of specialty hospitals, regionalized systems depend on the transfer of infants to a lower level of care once their acuity improves.1  Transfer for convalescence (TFC), although poorly studied, has been shown to have several benefits in small, single-center studies conducted in the 1980s, including more efficient utilization of intensive care beds,2  improved parental visitation and familial bonding,2  easier transitioning to local providers and services before discharge home,2  and cost-effectiveness,3,4  especially when the stay of the transferred infants to community hospitals exceeds 1 week.4  However, a study of 148 very low birth weight (VLBW) infants cared for during 2004 and 2006 reported that 19% of infants transferred for convalescent care were readmitted to a higher level of care before hospital discharge, raising concerns about the capabilities of the community hospitals and the medical needs of these infants.5 

To address the limited number of studies on TFC, we used data from Vermont Oxford Network (VON), a nonprofit voluntary worldwide collaboration of health care professionals dedicated to improving the quality, safety, and value of care for newborns.6  We compared, on a national level, the prevalence, characteristics, clinical course, and length of stay (LOS) of infants who were transferred for convalescence, infants who failed TFC, and infants who were not transferred for convalescence but were discharged from the hospital. We also examined risk factors associated with failed TFC.

We used data submitted by VON members in the United States from January 1, 2006, to December 31, 2020, for infants with a birth weight of 401 to 1500 g or 22 to 29 weeks’ gestation who were born in the member hospital or admitted within 28 days of birth without first having gone home. Member NICUs contribute data from medical records using uniform definitions.7  All data undergo automated checks for quality and completeness at the time of submission. The University of Vermont’s committee for human research determined that use of VON’s de-identified research repository for this analysis was not human subjects research.

VON collects data on initial disposition (home, transferred, died, still hospitalized as of first birthday), posttransfer disposition for transferred infants (home, transferred again, died, readmitted, still hospitalized as of first birthday), disposition after readmission for readmitted infants (home, transferred, died, still hospitalized as of first birthday), and ultimate disposition (home, died, still hospitalized as of first birthday). Reason for transfer is collected for only the initial disposition (extracorporeal membrane oxygenation, growth/discharge planning, medical/diagnostic services, surgery, chronic care, or other). Initial and subsequent LOS for transferred infants are also collected. For outborn infants, day of life at admission to the VON center is recorded. Infants who transfer between VON member NICUs are counted at the earlier NICU.

NICU types for VON members are collected through the VON annual membership survey: Type A—restriction on assisted ventilation or no surgery, Type B—major surgery, and Type C—cardiac surgery requiring bypass. For outborn infants, birth hospital name was collected in 2015, and American Academy of Pediatrics NICU level of birthplace was determined from publicly available hospital data. American Hospital Association data were used to examine hospital ownership (government-owned, nonprofit, investor-owned). NICU census regions and divisions were classified according to the U.S. Census Bureau classifications as: West (Mountain and Pacific), Midwest (East North Central and West North Central), South (South Atlantic, East South Central, and West South Central), and Northeast (New England and Mid-Atlantic).8 

We examined delivery room (DR) (tracheal intubation) and NICU (conventional ventilation, high-frequency ventilation, postnatal steroids, nasal continuous positive airway pressure, inhaled nitic oxide) usage measures and measures at discharge or transfer (oxygen, monitor, enteral feeding). These measures were only recorded while the infants were at VON centers. For infants transferred for convalescence, updated measures at discharge were only recorded for readmitted infants.

Examined outcome variables have been previously defined9  and included respiratory distress syndrome, focal intestinal perforation/necrotizing enterocolitis (NEC), early-onset sepsis (≤day 3 of life), late-onset sepsis (>day 3 of life), severe intraventricular hemorrhage, severe retinopathy of prematurity (ROP), chronic lung disease, and pneumothorax. We also examined survival to discharge without a major morbidity (defined as ≥1 of: NEC/focal intestinal perforation, early-onset sepsis, late-onset sepsis, severe intraventricular hemorrhage, severe retinopathy of prematurity, chronic lung disease, pneumothorax, or cystic periventricular leukomalacia) and anthropometric variables (weight, head circumference, growth velocity) at disposition. Reporting hospitals tracked mortality and total LOS before hospital discharge and after transfer until ultimate disposition. Morbidities and anthropometric variables were only tracked until discharge from the VON hospital. For infants transferred for convalescence, updated morbidities and weight were only recorded for readmitted infants.

We identified 4 groups of infants among NICU survivors:

  1. infants who were discharged from the hospital as their initial disposition;

  2. infants who were transferred for their initial disposition with the reason for transfer being growth/discharge planning, labeled as TFC, and were then discharged from the hospital; and

  3. infants who failed TFC; that is, they were transferred for growth/discharge planning but then were either (a) readmitted to the original center they transferred from for the growth/discharge planning, or (b) transferred again to a different center.

We conducted descriptive analyses, examining among the 4 groups of infants the distribution of: (1) hospital, newborn, and maternal characteristics, and (2) DR and NICU usage measures and outcomes. We also examined the percentage of infants who transferred for convalescence from type C NICUs by region. We used logistic regression models with birth year modeled as a linear effect to examine whether changes over time in rates of TFC and failed TFC were significant. To examine the risk factors associated with failed TFC, we used modified Poisson regression models with robust variance estimation. The examined variables in the model included gestational age, birth weight z-score, outborn status, race/ethnicity, sex, presence of major congenital anomalies,7  DR intubation, respiratory distress syndrome, initial LOS, and weight z-score at transfer.

A total of 591 559 neonates were inborn at 836 VON centers and 77 204 neonates were outborn and transferred to 768 VON centers. Among the inborn infants, 27 051 (4.6%) died in the DR, resulting in 641 712 infants who were either born at or transferred to a VON NICU. A total of 28 985 (4.5%) infants transferred for growth/discharge planning. Data on the second disposition for infants transferred for growth/discharge planning were available for 28 186 infants, among whom 2551 (9.1%) failed the TFC, 1771 (6.3%) were readmitted, and 780 (2.8%) were transferred again (Fig 1). Moreover, 182 (0.65%) infants transferred for convalescence died before hospital discharge.

FIGURE 1

Disposition status of inborn and outborn infants. aInfants born in 2015 or later. VON did not identify the birth hospitals of outborn infants before 2015. bData missing for 1536 infants. cData missing for 5 infants. dData missing for 173 infants. eExcludes 280 infants born before 29 weeks gestational age and transferred within 4 days of birth. fData missing for 799 infants. gData missing for 41 infants. hData missing for 2 infants. iData missing for 8 infants.

FIGURE 1

Disposition status of inborn and outborn infants. aInfants born in 2015 or later. VON did not identify the birth hospitals of outborn infants before 2015. bData missing for 1536 infants. cData missing for 5 infants. dData missing for 173 infants. eExcludes 280 infants born before 29 weeks gestational age and transferred within 4 days of birth. fData missing for 799 infants. gData missing for 41 infants. hData missing for 2 infants. iData missing for 8 infants.

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Infant Characteristics by Initial Disposition Status (Discharged from the hospital Versus Transferred for Convalescence)

Table 1 shows hospital, newborn, and maternal characteristics by disposition status. Across regions, New England (18.8%) had the highest whereas East South Central (2.2%) had the lowest percentage of TFC. Compared with infants discharged from the hospital, infants transferred for convalescence were more than twice as likely to be outborn (26.9% vs 10.9%) and to be born at level C NICUs (48.2% vs 25.8%). More than 50% of infants transferred for convalescence were transferred to type A NICUs, but 15.5% were also transferred to hospitals without NICUs. Compared with infants discharged from the hospital, infants transferred for convalescence were less likely to be born at investor-owned hospitals (4.3% vs 9.1%) and more likely to be born at nonprofit hospitals (83.2% vs 76.2%).

TABLE 1

Hospital, Newborn, and Maternal Characteristics By Disposition Status

Discharged From the HospitalTransferred for ConvalescenceTransferred for Convalescence and Discharged From the HospitalTransferred for Convalescence and ReadmittedTransferred for Convalescence and Transferred Again
N = 485 931N = 28 985N = 25 458N = 1771N = 780
Regiona      
 New England 15 842 (3.3) 3672 (12.7) 3224 (12.7) 212 (12.0) 74 (9.5) 
 Middle Atlantic 55 078 (11.3) 3404 (11.7) 3000 (11.8) 172 (9.7) 115 (14.7) 
 East North Central 77 250 (15.9) 2544 (8.8) 2259 (8.9) 164 (9.3) 64 (8.2) 
 West North Central 36312 (7.5) 2022 (7.0) 1833 (7.2) 135 (7.6) 15 (1.9) 
 South Atlantic 100 586 (20.7) 8630 (29.8) 7501 (29.5) 565 (31.9) 241 (30.9) 
 East South Central 34 332 (7.1) 766 (2.6) 704 (2.8) 36 (2.0) 7 (0.9) 
 West South Central 66 558 (13.7) 1574 (5.4) 1372 (5.4) 95 (5.4) 34 (4.4) 
 Mountain 28 583 (5.9) 1310 (4.5) 1191 (4.7) 51 (2.9) 44 (5.6) 
 Pacific 71 390 (14.7) 5063 (17.5) 4374 (17.2) 341 (19.3) 186 (23.8) 
Outborn 53 032 (10.9) 7811 (26.9) 6642 (26.1) 642 (36.3) 232 (29.7) 
Birth hospital NICU levelb      
 No NICU or AAP level I 7073 (1.6) 395 (1.7) 342 (1.7) 26 (2.1) 5 (0.9) 
 Type A or AAP level II 94 270 (20.9) 3584 (15.7) 3152 (15.6) 120 (9.6) 149 (25.5) 
 Type B or AAP level III 232 413 (51.4) 7778 (34.0) 7037 (34.8) 277 (22.2) 257 (43.9) 
 Type C or AAP level IV 116 432 (25.8) 11 005 (48.2) 9645 (47.6) 822 (65.8) 171 (29.2) 
Transfer hospital NICU levelc      
 No NICU or AAP level I — 1945 (15.5) 1584 (14.3) 205 (27.4) 83 (23.6) 
 Type A or AAP level II — 7114 (56.7) 6457 (58.4) 380 (50.7) 162 (46.0) 
 Type B or AAP level III — 2231 (17.8) 1961 (17.7) 107 (14.3) 62 (17.6) 
 Type C or AAP level IV — 1247 (9.9) 1056 (9.5) 57 (7.6) 45 (12.8) 
Gestational age, wk, mean (SD) 28.7 (2.7) 28.5 (2.6) 28.6 (2.5) 27.5 (2.6) 27.4 (2.6) 
Gestational age      
 ≤26 wk 65 325 (13.4) 3891 (13.4) 3050 (12.0) 437 (24.7) 200 (25.6) 
 27–29 wk 196 598 (40.5) 12 424 (42.9) 11 074 (43.5) 698 (39.4) 295 (37.8) 
 ≥30 wk 227 635 (46.8) 14 014 (48.4) 11 834 (46.5) 1133 (64.0) 521 (66.8) 
Birth weight, g, mean (SD) 1119 (285) 1112 (282) 1127 (275) 986 (294) 981 (306) 
Male 239 851 (49.4) 14 441 (49.8) 12 541 (49.3) 980 (55.3) 406 (52.1) 
Major congenital anomalies 13 508 (2.8) 924 (3.2) 670 (2.6) 139 (7.8) 48 (6.2) 
Multiple gestation 130 196 (26.8) 8313 (28.7) 7373 (29.0) 454 (25.6) 210 (26.9) 
Antenatal corticosteroidsd 404 962 (83.6) 24 051 (83.8) 21 190 (83.8) 1449 (83.4) 648 (83.6) 
Cesarean delivery 359 789 (74.0) 20 837 (71.9) 18 326 (72.0) 1268 (71.7) 528 (67.7) 
Maternal hypertensione 149 368 (35.3) 7526 (33.1) 6722 (33.5) 430 (31.7) 181 (30.3) 
Chorioamnionitisf 49 002 (11.6) 2915 (12.9) 2587 (13.0) 176 (13.1) 98 (16.6) 
Maternal race or ethnicityg      
 Black 143 148 (29.6) 7733 (26.9) 6653 (26.4) 538 (30.6) 241 (31.1) 
 Hispanic 88 550 (18.3) 5038 (17.5) 4434 (17.6) 330 (18.8) 145 (18.7) 
 White 217 193 (44.9) 13 907 (48.4) 12 366 (49.0) 767 (43.7) 332 (42.8) 
 Asian American 22 096 (4.6) 1280 (4.5) 1124 (4.5) 85 (4.8) 38 (4.9) 
 Native American 3778 (0.8) 222 (0.8) 202 (0.8) 7 (0.4) 7 (0.9) 
 Other race 8725 (1.8) 528 (1.8) 464 (1.8) 29 (1.7) 12 (1.5) 
Hospital ownership      
 Government-owned 71 293 (14.7) 3616 (12.5) 3127 (12.3) 131 (7.4) 77 (9.9) 
 Nonprofit 370 342 (76.2) 24 126 (83.2) 21 269 (83.5) 1577 (89.0) 669 (85.8) 
 Investor-owned 44 293 (9.1) 1243 (4.3) 1062 (4.2) 63 (3.6) 34 (4.4) 
Discharged From the HospitalTransferred for ConvalescenceTransferred for Convalescence and Discharged From the HospitalTransferred for Convalescence and ReadmittedTransferred for Convalescence and Transferred Again
N = 485 931N = 28 985N = 25 458N = 1771N = 780
Regiona      
 New England 15 842 (3.3) 3672 (12.7) 3224 (12.7) 212 (12.0) 74 (9.5) 
 Middle Atlantic 55 078 (11.3) 3404 (11.7) 3000 (11.8) 172 (9.7) 115 (14.7) 
 East North Central 77 250 (15.9) 2544 (8.8) 2259 (8.9) 164 (9.3) 64 (8.2) 
 West North Central 36312 (7.5) 2022 (7.0) 1833 (7.2) 135 (7.6) 15 (1.9) 
 South Atlantic 100 586 (20.7) 8630 (29.8) 7501 (29.5) 565 (31.9) 241 (30.9) 
 East South Central 34 332 (7.1) 766 (2.6) 704 (2.8) 36 (2.0) 7 (0.9) 
 West South Central 66 558 (13.7) 1574 (5.4) 1372 (5.4) 95 (5.4) 34 (4.4) 
 Mountain 28 583 (5.9) 1310 (4.5) 1191 (4.7) 51 (2.9) 44 (5.6) 
 Pacific 71 390 (14.7) 5063 (17.5) 4374 (17.2) 341 (19.3) 186 (23.8) 
Outborn 53 032 (10.9) 7811 (26.9) 6642 (26.1) 642 (36.3) 232 (29.7) 
Birth hospital NICU levelb      
 No NICU or AAP level I 7073 (1.6) 395 (1.7) 342 (1.7) 26 (2.1) 5 (0.9) 
 Type A or AAP level II 94 270 (20.9) 3584 (15.7) 3152 (15.6) 120 (9.6) 149 (25.5) 
 Type B or AAP level III 232 413 (51.4) 7778 (34.0) 7037 (34.8) 277 (22.2) 257 (43.9) 
 Type C or AAP level IV 116 432 (25.8) 11 005 (48.2) 9645 (47.6) 822 (65.8) 171 (29.2) 
Transfer hospital NICU levelc      
 No NICU or AAP level I — 1945 (15.5) 1584 (14.3) 205 (27.4) 83 (23.6) 
 Type A or AAP level II — 7114 (56.7) 6457 (58.4) 380 (50.7) 162 (46.0) 
 Type B or AAP level III — 2231 (17.8) 1961 (17.7) 107 (14.3) 62 (17.6) 
 Type C or AAP level IV — 1247 (9.9) 1056 (9.5) 57 (7.6) 45 (12.8) 
Gestational age, wk, mean (SD) 28.7 (2.7) 28.5 (2.6) 28.6 (2.5) 27.5 (2.6) 27.4 (2.6) 
Gestational age      
 ≤26 wk 65 325 (13.4) 3891 (13.4) 3050 (12.0) 437 (24.7) 200 (25.6) 
 27–29 wk 196 598 (40.5) 12 424 (42.9) 11 074 (43.5) 698 (39.4) 295 (37.8) 
 ≥30 wk 227 635 (46.8) 14 014 (48.4) 11 834 (46.5) 1133 (64.0) 521 (66.8) 
Birth weight, g, mean (SD) 1119 (285) 1112 (282) 1127 (275) 986 (294) 981 (306) 
Male 239 851 (49.4) 14 441 (49.8) 12 541 (49.3) 980 (55.3) 406 (52.1) 
Major congenital anomalies 13 508 (2.8) 924 (3.2) 670 (2.6) 139 (7.8) 48 (6.2) 
Multiple gestation 130 196 (26.8) 8313 (28.7) 7373 (29.0) 454 (25.6) 210 (26.9) 
Antenatal corticosteroidsd 404 962 (83.6) 24 051 (83.8) 21 190 (83.8) 1449 (83.4) 648 (83.6) 
Cesarean delivery 359 789 (74.0) 20 837 (71.9) 18 326 (72.0) 1268 (71.7) 528 (67.7) 
Maternal hypertensione 149 368 (35.3) 7526 (33.1) 6722 (33.5) 430 (31.7) 181 (30.3) 
Chorioamnionitisf 49 002 (11.6) 2915 (12.9) 2587 (13.0) 176 (13.1) 98 (16.6) 
Maternal race or ethnicityg      
 Black 143 148 (29.6) 7733 (26.9) 6653 (26.4) 538 (30.6) 241 (31.1) 
 Hispanic 88 550 (18.3) 5038 (17.5) 4434 (17.6) 330 (18.8) 145 (18.7) 
 White 217 193 (44.9) 13 907 (48.4) 12 366 (49.0) 767 (43.7) 332 (42.8) 
 Asian American 22 096 (4.6) 1280 (4.5) 1124 (4.5) 85 (4.8) 38 (4.9) 
 Native American 3778 (0.8) 222 (0.8) 202 (0.8) 7 (0.4) 7 (0.9) 
 Other race 8725 (1.8) 528 (1.8) 464 (1.8) 29 (1.7) 12 (1.5) 
Hospital ownership      
 Government-owned 71 293 (14.7) 3616 (12.5) 3127 (12.3) 131 (7.4) 77 (9.9) 
 Nonprofit 370 342 (76.2) 24 126 (83.2) 21 269 (83.5) 1577 (89.0) 669 (85.8) 
 Investor-owned 44 293 (9.1) 1243 (4.3) 1062 (4.2) 63 (3.6) 34 (4.4) 

No. (%) unless otherwise noted. AAP, American Academy of Pediatrics. —, not applicable.

a

Total infants by region: New England, 19 514; Middle Atlantic, 58 482; East North Central, 79 794; West North Central, 38 334; South Atlantic, 109 216; East South Central, 35 098; West South Central, 68 132; Mountain, 29 893; Pacific, 76 453.

b

Birth hospital data missing for 7.8% of infants.

c

Transfer hospital data missing for 56.6% of transferred infants.

d

Exposure to antenatal corticosteroids defined as steroids administered intramuscular or intravenous to the mother during pregnancy at any time before delivery.

e

Hypertension variable added in 2008 and, thus, data missing for 13.3% of infants. Maternal hypertension defined as chronic or pregnancy-induced, with or without edema and proteinuria, or as maternal blood pressure >140 systolic or 90 diastolic before or during the present pregnancy.

f

Chorioamnionitis variable added in 2008 and, thus, data missing for 13.5% of infants.

g

Data missing for 0.5% of infants. For all other variables, <0.5% missing values.

Infant Characteristics by Transfer for Convalescence Status (Discharged From the Hospital Versus Failed TFC) and Risk Factors for Failed TFC

Compared with infants transferred for convalescence and discharged from the hospital, infants who failed TFC were more likely to be outborn, transfer to a hospital without a NICU, have a lower gestational age, and have a major congenital anomaly (Table 1). In a regression model, major congenital anomalies increased the risk of failed TFC by 2.51-fold (95% confidence interval 2.08–3.03) (Fig 2). Other factors associated with failed TFC included gestational age, birth weight z-score, outborn status, race, sex, DR intubation, respiratory distress syndrome, and weight z-score at transfer time.

FIGURE 2

Risk factors for failed transfer for convalescence based on modified Poisson multiple regression model.

FIGURE 2

Risk factors for failed transfer for convalescence based on modified Poisson multiple regression model.

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Infants who were discharged from the hospital had a similar clinical course to infants who were transferred for convalescence and then discharged from the hospital. For infants transferred for convalescence who were subsequently discharged from the hospital, oxygen (29.7%), monitor (84.2%), and any human milk (64.4%) were measured at the initial disposition; that is, at transfer but were measured at discharge to home for infants who were not transferred for convalescence (oxygen: 13.7%, monitor: 21.9%, any human milk: 49.1%) (Table 2). Infants who failed TFC had higher rates of DR intubation, conventional and high-frequency ventilation, postnatal steroids, and inhaled nitric oxide compared with infants who were transferred for convalescence and discharged from the hospital. For infants transferred for convalescence who were readmitted, oxygen (42.8%), monitor (71.0%), and any human milk (52.5%) were measured at the subsequent disposition after readmission.

TABLE 2

Clinical Course By Disposition Status

Discharged From the HospitalTransferred for Convalescence and Discharged From the HospitalTransferred for Convalescence and ReadmittedTransferred for Convalescence and Transferred Again
N = 485 931N = 25 458N = 1771N = 780
DR intubation 205 522 (42.3) 11 195 (44.1) 1059 (59.9) 487 (62.6) 
Conventional ventilation 263 563 (54.3) 14 910 (58.6) 1424 (80.4) 595 (76.3) 
High-frequency ventilation 74 428 (15.3) 3688 (14.5) 542 (30.7) 220 (28.2) 
Postnatal steroids 40 917 (8.4) 1524 (6.0) 290 (16.4) 127 (16.3) 
Nasal CPAP after initial resuscitation 380 378 (78.3) 19 851 (78.0) 1446 (81.7) 600 (76.9) 
Inhaled nitric oxidea 12 207 (2.9) 600 (3.0) 118 (8.6) 35 (5.8) 
Oxygen at discharge or transferb 66 660 (13.7) 7553 (29.7) 758 (42.8) 422 (54.1) 
Monitor at discharge or transferb 106 446 (21.9) 21 373 (84.2) 1258 (71.0) 701 (89.9) 
Enteral feeding at discharge or transferb     
 None 2226 (0.5) 959 (3.8) 102 (5.8) 67 (8.7) 
 Any human milk 238 259 (49.1) 16 258 (64.4) 930 (52.5) 436 (56.3) 
 Formula only 245 258 (50.5) 8017 (31.8) 738 (41.7) 271 (35.0) 
Discharged From the HospitalTransferred for Convalescence and Discharged From the HospitalTransferred for Convalescence and ReadmittedTransferred for Convalescence and Transferred Again
N = 485 931N = 25 458N = 1771N = 780
DR intubation 205 522 (42.3) 11 195 (44.1) 1059 (59.9) 487 (62.6) 
Conventional ventilation 263 563 (54.3) 14 910 (58.6) 1424 (80.4) 595 (76.3) 
High-frequency ventilation 74 428 (15.3) 3688 (14.5) 542 (30.7) 220 (28.2) 
Postnatal steroids 40 917 (8.4) 1524 (6.0) 290 (16.4) 127 (16.3) 
Nasal CPAP after initial resuscitation 380 378 (78.3) 19 851 (78.0) 1446 (81.7) 600 (76.9) 
Inhaled nitric oxidea 12 207 (2.9) 600 (3.0) 118 (8.6) 35 (5.8) 
Oxygen at discharge or transferb 66 660 (13.7) 7553 (29.7) 758 (42.8) 422 (54.1) 
Monitor at discharge or transferb 106 446 (21.9) 21 373 (84.2) 1258 (71.0) 701 (89.9) 
Enteral feeding at discharge or transferb     
 None 2226 (0.5) 959 (3.8) 102 (5.8) 67 (8.7) 
 Any human milk 238 259 (49.1) 16 258 (64.4) 930 (52.5) 436 (56.3) 
 Formula only 245 258 (50.5) 8017 (31.8) 738 (41.7) 271 (35.0) 

Data are n (%) unless otherwise noted. CPAP, continuous positive airway pressure.

a

Variable added in 2001 and, thus, data are missing for 13.0% of infants. For all other variables, <0.5% missing values.

b

Oxygen, monitor, and enteral feeding were measured at hospital discharge for infants who were discharged from the hospital but were measured at initial transfer for transferred infants who were subsequently discharged from the hospital and for transferred infants who were transferred again. For transferred infants who were subsequently readmitted, these variables were measured at discharge (1158 were discharged from the hospital) or transfer after the readmission.

Infants who transferred for convalescence and were then discharged from the hospital had similar outcomes to infants who were discharged from the hospital without being transferred (Table 3). However, infants who transferred for convalescence and were in the VON hospital at the recommended age for a retinal exam were less likely to receive a retinopathy of prematurity exam (82.0% vs 94.5%) than infants who were not transferred for convalescence. The median postmenstrual age and the mean weight at initial disposition were 3.7 weeks and 793 g, respectively, lower for infants who transferred for convalescence and were subsequently discharged from the hospital than those who were discharged from the hospital at their initial disposition. At discharge home, the median postmenstrual age (37.6 weeks) was similar for both groups.

TABLE 3

Outcomes By Disposition Status

OutcomesDischarged From the Hospital N = 485 931Transferred for Convalescence and Discharged From the Hospital N = 25 458Transferred for Convalescence and Readmitted N = 1771Transferred for Convalescence and Transferred Again N = 780
Respiratory distress syndrome 342 503 of 485 798 (70.5) 17 748 of 25 443 (69.8) 1422 of 1770 (80.3) 649 of 778 (83.4) 
Necrotizing enterocolitis/focal intestinal perforation 22 324 of 485 841 (4.6) 921 of 25 452 (3.6) 265 of 1771 (15.0) 47 of 780 (6.0) 
 Necrotizing enterocolitis surgery 9083 of 485 830 (1.9) 330 of 25 453 (1.3) 117 of 1771 (6.6) 21 of 780 (2.7) 
Early onset sepsis 6504 of 485 749 (1.3) 355 of 25 443 (1.4) 42 of 1769 (2.4) 15 of 779 (1.9) 
Late-onset sepsis 48 746 of 485 475 (10.0) 2071 of 25 217 (8.2) 337 of 1771 (19.0) 107 of 773 (13.8) 
Infants with cranial sonogram within 28 d, among infants in hospital at 28 d 425 642 of 446 552 (95.3) 13 392 of 13 765 (97.3) 1693 of 1749 (96.8) 464 of 470 (98.7) 
 Severe intraventricular hemorrhage 21 527 of 451 753 (4.8) 1056 of 22 577 (4.7) 191 of 1710 (11.2) 71 of 726 (9.8) 
Retinal exam, among infants in hospital at recommended age 344 874 of 365 097 (94.5) 10 886 of 13 282 (82.0) 1206 of 1378 (87.5) 374 of 429 (87.2) 
 Severe retinopathy of prematurity 22 593 of 410 913 (5.5) 530 of 12 602 (4.2) 239 of 1453 (16.4) 34 of 421 (8.1) 
 Retinopathy of prematurity surgery 12 963 of 485 733 (2.7) 369 of 25 441 (1.5) 186 of 1771 (10.5) 24 of 779 (3.1) 
Chronic lung diseasea 115 570 of 447 189 (25.8) 3989 of 19 866 (20.1) 696 of 1581 (44.0) 211 of 522 (40.4) 
Pneumothorax 14 512 of 485 839 (3.0) 780 of 25 453 (3.1) 96 of 1770 (5.4) 37 of 780 (4.7) 
Survived to discharge 485 931 of 485 931 (100) 25 458 of 25 458 (100) 1708 of 1761 (97.0) 715 of 739 (96.8) 
 Survival without morbidities 314 759 of 485 906 (64.8) 18 569 of 25 458 (72.9) 645 of 1761 (36.6) 401 of 739 (54.3) 
Any major surgery 58 552 of 485 654 (12.1) 2943 of 25 445 (11.6) 867 of 1771 (49.0) 204 of 779 (26.2) 
Infant characteristics at discharge or transfer     
 Postmenstrual age at initial disposition, wk, median (IQR) 37.6 (36.1–39.6) 33.9 (32.3–35.6) 33.9 (31.9–36.6) 33.4 (31.3–37.1) 
 Postmenstrual age at discharge home, wk, median (IQR) 37.6 (36.1–39.6) 37.6 (36.3–39.6) 41.1 (38.4–46.1) 41.0 (38.0–47.9) 
 Weight, g, mean (SD) at initial disposition 2594 (778) 1801 (731) 1885 (1021) 1903 (1125) 
 Weight, g, mean (SD) at disposition after readmissionb   3191 (1357)  
 Head circumference, cm, mean (SD) at initial dispositionc 32.6 (2.3) 29.2 (2.9) 29.2 (3.8) 29.2 (4.2) 
 Weight gain velocity, g/kg/d, mean (SD) at initial dispositiond 12.9 (2.4) 11.2 (4.2) 11.5 (4.9) 11.2 (4.5) 
OutcomesDischarged From the Hospital N = 485 931Transferred for Convalescence and Discharged From the Hospital N = 25 458Transferred for Convalescence and Readmitted N = 1771Transferred for Convalescence and Transferred Again N = 780
Respiratory distress syndrome 342 503 of 485 798 (70.5) 17 748 of 25 443 (69.8) 1422 of 1770 (80.3) 649 of 778 (83.4) 
Necrotizing enterocolitis/focal intestinal perforation 22 324 of 485 841 (4.6) 921 of 25 452 (3.6) 265 of 1771 (15.0) 47 of 780 (6.0) 
 Necrotizing enterocolitis surgery 9083 of 485 830 (1.9) 330 of 25 453 (1.3) 117 of 1771 (6.6) 21 of 780 (2.7) 
Early onset sepsis 6504 of 485 749 (1.3) 355 of 25 443 (1.4) 42 of 1769 (2.4) 15 of 779 (1.9) 
Late-onset sepsis 48 746 of 485 475 (10.0) 2071 of 25 217 (8.2) 337 of 1771 (19.0) 107 of 773 (13.8) 
Infants with cranial sonogram within 28 d, among infants in hospital at 28 d 425 642 of 446 552 (95.3) 13 392 of 13 765 (97.3) 1693 of 1749 (96.8) 464 of 470 (98.7) 
 Severe intraventricular hemorrhage 21 527 of 451 753 (4.8) 1056 of 22 577 (4.7) 191 of 1710 (11.2) 71 of 726 (9.8) 
Retinal exam, among infants in hospital at recommended age 344 874 of 365 097 (94.5) 10 886 of 13 282 (82.0) 1206 of 1378 (87.5) 374 of 429 (87.2) 
 Severe retinopathy of prematurity 22 593 of 410 913 (5.5) 530 of 12 602 (4.2) 239 of 1453 (16.4) 34 of 421 (8.1) 
 Retinopathy of prematurity surgery 12 963 of 485 733 (2.7) 369 of 25 441 (1.5) 186 of 1771 (10.5) 24 of 779 (3.1) 
Chronic lung diseasea 115 570 of 447 189 (25.8) 3989 of 19 866 (20.1) 696 of 1581 (44.0) 211 of 522 (40.4) 
Pneumothorax 14 512 of 485 839 (3.0) 780 of 25 453 (3.1) 96 of 1770 (5.4) 37 of 780 (4.7) 
Survived to discharge 485 931 of 485 931 (100) 25 458 of 25 458 (100) 1708 of 1761 (97.0) 715 of 739 (96.8) 
 Survival without morbidities 314 759 of 485 906 (64.8) 18 569 of 25 458 (72.9) 645 of 1761 (36.6) 401 of 739 (54.3) 
Any major surgery 58 552 of 485 654 (12.1) 2943 of 25 445 (11.6) 867 of 1771 (49.0) 204 of 779 (26.2) 
Infant characteristics at discharge or transfer     
 Postmenstrual age at initial disposition, wk, median (IQR) 37.6 (36.1–39.6) 33.9 (32.3–35.6) 33.9 (31.9–36.6) 33.4 (31.3–37.1) 
 Postmenstrual age at discharge home, wk, median (IQR) 37.6 (36.1–39.6) 37.6 (36.3–39.6) 41.1 (38.4–46.1) 41.0 (38.0–47.9) 
 Weight, g, mean (SD) at initial disposition 2594 (778) 1801 (731) 1885 (1021) 1903 (1125) 
 Weight, g, mean (SD) at disposition after readmissionb   3191 (1357)  
 Head circumference, cm, mean (SD) at initial dispositionc 32.6 (2.3) 29.2 (2.9) 29.2 (3.8) 29.2 (4.2) 
 Weight gain velocity, g/kg/d, mean (SD) at initial dispositiond 12.9 (2.4) 11.2 (4.2) 11.5 (4.9) 11.2 (4.5) 
a

Among infants born before 33 weeks. Data missing for 1.1% of eligible infants.

b

Data missing for 2.2% of readmitted infants.

c

Data missing for 3.6% of infants.

d

Data missing for 4.7% of infants.

For all other variables, <0.5% missing values.

Infants who failed TFC and were transferred again had a higher rate of all the examined morbidities than infants who transferred for convalescence and were then discharged from the hospital (Table 3). Among infants who transferred for convalescence and were then discharged from the hospital, rates of any major surgery and survival to discharge without morbidities were 11.6% and 72.9%, whereas they were 26.2% and 54.3%, respectively, among infants who transferred for convalescence and transferred again. Among infants who transferred for convalescence and were readmitted, rates of any major surgery and survival to discharge without morbidities were 49.0% and 36.6%, respectively; the higher-outcome rates reported in this group might be partially because of the longer reporting period given their readmission.

The median total LOS (59 days) was the same if infants were discharged from the hospital or if they transferred for convalescence and were then discharged from the hospital (Fig 3). However, the LOS was much higher if infants failed the TFC.

FIGURE 3

LOS (days) by disposition status. LOS data missing for 1,155 infants. The line represents the median (50th percentile). The borders of the box plot represent the 25th and 75th percentiles. The whiskers represent the minimum and maximum LOS. IQR, interquartile range.

FIGURE 3

LOS (days) by disposition status. LOS data missing for 1,155 infants. The line represents the median (50th percentile). The borders of the box plot represent the 25th and 75th percentiles. The whiskers represent the minimum and maximum LOS. IQR, interquartile range.

Close modal

We observed major regional variation in TFC from type C NICUs (Table 4). In the South Atlantic region among 26 type C NICUs, the percentage of TFC ranged between 0% and 84%. West South Central had the lowest variation; the percentage of TFC ranged between 0% and 13%. In 7 regions, there were type C NICUs that did not TFC any infants.

TABLE 4

Transfers for Convalescence From Type C NICUs By Region

RegionNumber of Type C NICUs% Transferred for Convalescence
MinimumQ1MedianQ3Maximum
New England 12.4 14.5 21.4 25.2 65.2 
Middle Atlantic 15 0.8 4.8 8.0 12.2 31.2 
East North Central 20 3.2 6.8 10.3 32.8 
West North Central 11 0.95 6.8 13.4 23.0 
South Atlantic 26 2.0 5.8 13.0 83.8 
East South Central 0.4 3.2 5.8 53.2 
West South Central 21 1.1 3.0 4.9 13.0 
Mountain 12 2.1 4.4 11.6 56.4 
Pacific 24 3.4 15.1 23.1 68.1 
RegionNumber of Type C NICUs% Transferred for Convalescence
MinimumQ1MedianQ3Maximum
New England 12.4 14.5 21.4 25.2 65.2 
Middle Atlantic 15 0.8 4.8 8.0 12.2 31.2 
East North Central 20 3.2 6.8 10.3 32.8 
West North Central 11 0.95 6.8 13.4 23.0 
South Atlantic 26 2.0 5.8 13.0 83.8 
East South Central 0.4 3.2 5.8 53.2 
West South Central 21 1.1 3.0 4.9 13.0 
Mountain 12 2.1 4.4 11.6 56.4 
Pacific 24 3.4 15.1 23.1 68.1 

Q1, quarter 1; Q3, quarter 2.

The rate of TFC decreased significantly from 9.8% in 2006% to 3.9% in 2020 (P <.001) (Table 5). However, there was no significant trend over time in the overall rate of failed TFC (P = .28). The rate of TFC decreased over time across all regions (Supplemental Fig 4).

TABLE 5

Percentage of Transfers for Convalescence and Failed Transfers in 2006 and 2020

Region% Transferred for Convalescence% Transfers That Failed
2006202020062020
New England 26.3 13.5 10.3 10.7 
Middle Atlantic 9.6 4.4 8.7 7.7 
East North Central 5.7 1.9 11.3 7.2 
West North Central 7.8 2.7 5.3 5.0 
South Atlantic 9.4 6.3 6.6 12.1 
East South Central 4.7 1.1 8.3 0.0 
West South Central 3.3 1.6 15.4 1.3 
Mountain 14.6 2.6 9.2 2.1 
Pacific 14.7 4.4 10.8 6.3 
Overall 9.8 3.9 9.4 8.5 
Region% Transferred for Convalescence% Transfers That Failed
2006202020062020
New England 26.3 13.5 10.3 10.7 
Middle Atlantic 9.6 4.4 8.7 7.7 
East North Central 5.7 1.9 11.3 7.2 
West North Central 7.8 2.7 5.3 5.0 
South Atlantic 9.4 6.3 6.6 12.1 
East South Central 4.7 1.1 8.3 0.0 
West South Central 3.3 1.6 15.4 1.3 
Mountain 14.6 2.6 9.2 2.1 
Pacific 14.7 4.4 10.8 6.3 
Overall 9.8 3.9 9.4 8.5 

In a study of >665 000 VLBW infants, we show that the overall rate of TFC was low at 4.5% and decreased by 60% over time. New England (18.8%) had the highest whereas East South Central (2.2%) had the lowest percentage of TFC from type C NICUs. We also show that the rate of failed TFC was 9.1%; 6.3% of infants were readmitted and 2.8% were transferred again. Having a major congenital anomaly was the strongest risk factor for a failed TFC. Among the infants transferred for convalescence, <1% died before hospital discharge.

From a regionalized systems perspective, the practice of TFC is necessary because it promotes the intent of achieving risk-appropriate care in a resource-efficient manner when intensive care is no longer required.1  However, the major regional differences and the decrease over time in TFC bring into question the potential contributors driving this variation. Potential contributors include state and financial policies. A review of state policies supporting neonatal transfer showed that only 16 of the 34 states (47%) with a transfer policy noted a TFC component, whereas 25 of the 31 states (81%) with a transfer reimbursement policy did not specifically address TFC reimbursement.10  However, even within regions, we observed enormous variation in TFC among tertiary NICUs. Potential contributors to NICU variation in the TFC practice include high NICU census and competition between hospitals. High NICU census has been previously associated with increased likelihood of discharging moderately preterm infants11  and might also contribute to the TFC of VLBW infants as suggested by parents’ perception of the reason for TFC of their VLBW infants.12  On the opposite end, a hospital receiving reimbursement for care of an infant, has no incentive to TFC the infant because another institution would receive the convalescing care reimbursement.13,14  We are not sure how hospital ownership might affect the TFC practice, but we found that infants who transferred for convalescence were less likely to be born at investor-owned hospitals and more likely to be born at nonprofit hospitals than infants who were discharged from the hospital.

Beyond state- and NICU-level contributors to TFC, sociodemographic factors, parental preferences, and geography might also play a role. Two previous studies have shown that TFC was associated with having private insurance coverage,15,16  which might indicate that this elective nature of transfer might be more likely covered by private insurers.15  However, this has not been replicated in another study.5  We are unsure if parental preferences might impact TFC or if that is a decision solely made by the NICU personnel or the insurance provider. A study based on 236 families showed that <50% of families wanted the TFC, citing their trust with the medical team at the high-level NICU.12  Geographic proximity of the patient’s home to community hospitals with sufficient facilities15  and nursing staff appropriately trained to care for these high-risk infants is another important contributor to TFC.

The overall rate of failed TFC was 9.1%. However, the rate of failed transfer was 15.4% if infants were transferred to hospitals without a NICU and 7.7% if infants were transferred to hospitals with level II NICUs. In a study of 148 VLBW infants who transferred to community hospitals with mostly level II nurseries, 19% were readmitted to an intensive care setting before discharge from the hospital with feeding intolerance, severe apnea, respiratory distress, infection, or ROP surgery being the main causes for readmission.5  In another study of 2178 infants born <37 weeks’ gestation, 13% of infants failed TFC, with the most common reason for transfer to a level IV NICU being admission for specialized radiology services, followed by apnea.17  We did not have data on the reasons for failed TFC. Additionally, we do not know why some infants transferred for convalescence were readmitted (6.3%) whereas others were transferred to different centers (2.8%) and whether these transferred infants also received high-acuity care. Thus, the overall TFC failure rate might be somewhere between 6.3% and 9.1%.

Although failure in TFC might be expected in certain cases given this high-risk group, failure might also signal the nonreadiness of these infants to transfer or the poor communication between the transferring and the receiving hospital about the medical needs of the infant and the capabilities of the receiving hospital.5,18  Some risk factors for infants who failed TFC included having a major congenital anomaly, being outborn, having a lower gestational age, and having respiratory distress syndrome.

Infants who transferred for convalescence and were discharged from the hospital were less likely to receive retinal exams at the recommended age (82.0%) compared with infants who were discharged from the hospital (94.5%). We did not have data on whether these infants who transferred for convalescence and were subsequently discharged from the hospital received retinal examination at the center they transferred to. In a previous study, infants transferred for convalescence were twice (risk ratio = 2.16; 95% confidence interval: 1.05–4.44) as likely to not receive ROP follow-up care compared with infants who were not transferred for convalescence.19  Similarly, another study of 401 to 1000-g infants showed that infants transferred for convalescence were less compliant with a neurodevelopmental assessment at 18 to 22 months’ corrected age.16  This emphasizes the importance of communication between the transferring and the receiving hospital to ensure adequate follow-up care needs are delivered to these high-risk infants.

Studies examining duration of hospitalization among VLBW or extremely low birth weight infants transferred to the community hospital compared with infants discharged from the hospital from the regional center have either reported a similar,18  a trend toward a longer,5  or a shorter LOS.16,20  In our study, the median total LOS (59 days) was the same for infants who were discharged from the hospital and infants who were transferred for convalescence and then discharged from the hospital. However, the median total LOS was longer by >1 month for infants who failed the TFC.

Strengths of our study include a large sample size of VLBW infants, allowing us to examine on a national level regional TFC practices. We also had data on initial and subsequent LOS among transferred infants until they were discharged from the hospital. Limitations include lack of data on the reasons for the regional variation in the TFC rates. Additionally, most of our measures were from the initial LOS at the VON center; we only had updated measures for infants who were transferred for convalescence and readmitted. We also did not have data on the cost-effectiveness of TFC, the longer-term outcomes such as readmission rates and emergency department utilization, and the reasons for the failed TFC. We used the term “convalescent care” for the care received by infants after transfer, but recognize that this may be an oversimplification for the continuing care and discharge planning that may be required by these high-risk infants.

In this VLBW cohort, the overall rates of TFC, TFC failure, and death among infants transferred for convalescence were low. Infants who were transferred for convalescence and discharged from the hospital had an LOS similar to infants who were not transferred for convalescence. Future studies should weigh the cost-effectiveness, risks, and benefits of TFC that might differ on the basis of geography and the capabilities of surrounding community hospitals that would accept these high-risk infants for continuing care.

We thank our colleagues who submit data to Vermont Oxford Network on behalf of infants and their families. Participating centers are listed in Supplemental Table 6.

Dr Boghossian participated in the conception and design of the study, including the analysis plan and in the interpretation of the data, and wrote all drafts of the manuscript, and helped to revise it critically for important intellectual content; Ms Greenberg participated in designing the analysis plan, was responsible for the data management and data analysis, participated in the interpretation of the data, and helped to revise the manuscript critically for important intellectual content; Dr Edwards participated in the conception of the study and the interpretation of the data and revised the manuscript critically for important intellectual content; Dr Horbar participated in the conception of the study, is the chief executive and scientific officer of the Vermont Oxford Network, from which the data were drawn, participated in the interpretation of the data, and helped to revise the manuscript critically for important intellectual content; and all authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

FUNDING: Supported by the Eunice Kennedy Shriver National Institute of Child Health & Human Development of the National Institutes of Health under award #R03HD097305 and by the National Institute on Minority Health and Health Disparities under award #R01MD016012. Funded by the National Institutes of Health (NIH).

CONFLICT OF INTEREST DISCLAIMER: Ms Greenberg reported receiving compensation from Vermont Oxford Network for serving as a statistician. Dr Horbar is an employee of Vermont Oxford Network and Dr Edwards receives salary support from Vermont Oxford Network. The other authors have indicated they have no conflicts of interest relevant to this article to disclose.

DR

delivery room

LOS

length of stay

NEC

necrotizing enterocolitis

ROP

retinopathy of prematurity

TFC

transfer for convalescence

VLBW

very low birth weight

VON

Vermont Oxford Network

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Supplementary data