Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Prevalence and burden of illness of treated hemolytic neonatal hyperbilirubinemia in a privately insured population in the United States

BMC Pediatrics volume 19, Article number: 53 (2019) Cite this article

Abstract

Background

Prevalence of hemolytic neonatal hyperbilirubinemia (NHB) is not well characterized, and economic burden at the population level is poorly understood. This study evaluated the prevalence, clinical characteristics, and economic burden of hemolytic NHB newborns receiving treatment in U.S. real-world settings.

Methods

This cohort study used administrative claims from 01/01/2011 to 08/31/2017. The treated cohort had hemolytic NHB diagnosis and received phototherapy, intravenous immunoglobulin, and/or exchange transfusions. They were matched with non-NHB newborns who had neither NHB nor related treatments on the following: delivery hospital/area, gender, delivery route, estimated gestational age (GA), health plan eligibility, and closest date of birth within 5 years. Inferential statistics were reported.

Results

The annual NHB prevalence was 29.6 to 31.7%; hemolytic NHB, 1.8 to 2.4%; treated hemolytic NHB, 0.46 to 0.55%, between 2011 and 2016. The matched analysis included 1373 pairs ≥35 weeks GA. The treated hemolytic NHB cohort had significantly more birth trauma and hemorrhage (4.5% vs. 2.4%, p = 0.003), vacuum extractor affecting newborn (1.9% vs. 0.8%, p = 0.014), and polycythemia neonatorum (0.8% vs. 0%, p = 0.001) than the matched non-NHB cohort. The treated hemolytic NHB cohort also had significantly longer mean birth hospital stays (4.5 vs. 3.0 days, p < 0.001), higher level 2–4 neonatal intensive care admissions (15.7% vs. 2.4, 15.9% vs. 2.8 and 10.6% vs. 2.5%, respectively, all p < 0.001) and higher 30-day readmission (8.7% vs. 1.7%, p < 0.001).

One-month and one-year average total costs of care were significantly higher for the treated hemolytic NHB cohort vs. the matched non-NHB cohort, $14,405 vs. $5527 (p < 0.001) and $21,556 vs. $12,986 (p < 0.001), respectively. The average costs for 30-day readmission among newborns who readmitted were $13,593 for the treated hemolytic NHB cohort and $3638 for the matched non-NHB cohort, p < 0.001. The authors extrapolated GA-adjusted prevalence of treated hemolytic NHB in the U.S. newborn population ≥ 35 weeks GA and estimated an incremental healthcare expenditure of $177.0 million during the first month after birth in 2016.

Conclusions

The prevalence of treated hemolytic NHB was 4.6–5.5 patients per 1000 newborns. This high-risk hemolytic NHB imposed substantial burdens of healthcare resource utilization and incremental costs on newborns, their caregivers, and the healthcare system.

Peer Review reports

Background

Neonatal hyperbilirubinemia (NHB), a common condition in newborn infants, results from elevated blood bilirubin levels. The excessive bilirubin manifests as yellowing of the skin and the normally white outer layer of the eyeballs [1,2,3]. While most cases resolve quickly without intervention, NHB is a common reason for inpatient readmissions, and admission to the neonatal intensive care unit (NICU) [4, 5]. The prevalence of NHB is not precisely known, however, estimates suggest that approximately 50% full-term and 80% preterm [6] newborns develop some form of NHB. High-risk NHB occurs in 8–9% of neonates during the first week after birth [5, 7].

The origin of NHB may be physiologic or pathologic. Physiologic NHB may be caused by neonate immaturity and the resulting inability to cope with elevated levels of bilirubin [8]. This benign form resolves itself in 2–3 weeks following birth, and usually without treatment [1, 2]. Pathologic NHB may be caused by hemolytic disease of the newborn (HDN), red blood cell (RBC) enzyme deficiency, or impaired bilirubin excretion [9]. HDN results from incompatibilities between maternal and fetal blood types (Rh, ABO or a minor blood group), which may cause ruptures in fetal RBCs and elevated bilirubin levels. Hemolytic NHB usually appears within 24 h after birth [1, 2, 4].

The American Academy of Pediatrics (AAP) clinical practice guidelines address the assessment, screening, and treatment of NHB among infants at ≥35 weeks of gestation [10]. Risk assessment and treatment nomograms based on total serum bilirubin level, postnatal age in hours, and gestational age of the newborn with the presence or absence of risk factors are available to guide patient management [10]. Similar guidelines are not available for neonates at less than 35 weeks of gestation because of scant evidence-based data, differences in clinical manifestations and unclear treatment outcomes [11].

When treatment is indicated, AAP guidelines recommend phototherapy as the initial treatment [6, 10]. In cases where bilirubin levels continue to increase despite phototherapy, the guidelines recommend adding exchange transfusion of whole blood to the treatment regimen, typically in the NICU [2, 10]. For hemolytic cases, AAP guidelines recommend the administration of intravenous immunoglobulin (IVIg) as adjunctive therapy when bilirubin levels continue to rise despite intensive phototherapy [2, 10]. These challenges in management of high-risk hyperbilirubinemia substantially increase the urgency for safer and more effective screening and/or treatment options, especially when viewed against the knowledge that the permanent sequelae of kernicterus spectrum disorders (KSDs) might be prevented.

To the best of our knowledge, the prevalence of hemolytic NHB newborns receiving treatment has not been well characterized, and economic burden at the population level is poorly understood. Our study aimed to address this knowledge gap. We focused on newborns with hemolytic NHB who received treatment because the receipt of intervention indicated that those neonates met the AAP guideline for the recommendation of intervention in order to prevent severe NHB and the spectrum of associated complications [10, 12,13,14].

Methods

Design and data source

This retrospective matched cohort study used the HealthCore Integrated Research Database (HIRDSM), a geographically dispersed managed-care repository with claims data on more than 45 million enrollees residing across all 50 states, to identify infants born from 01/01/2011 through 08/31/2017. The HIRD is one of the largest privately insured population databases in the U.S [15]. This observational study was exempt from informed consent stipulations as researchers accessed a limited data set without individual enrollee identifiers and only summary statistics were reported. The study complied with all relevant provisions of the Health Insurance Portability and Accountability Act.

Study population

Newborns were linked to their birth mothers via shared health plan subscriber identification (ID) numbers. Mothers’ delivery dates were verified within 32 days of newborns’ dates of birth using delivery codes (Appendix: Table 7). Infants with 30-day or longer continuous enrollment after birth and mothers with at least 12 months of continuous health plan enrollment before delivery were included. All newborns, regardless of their estimated gestational age (GA), were included for NHB prevalence estimation. The treated hemolytic NHB and matched non-NHB cohorts were selected among newborns ≥35 weeks GA. We excluded newborns < 35 weeks GA as there was no clinical practice guidelines available for this group due to lack of evidence-based data, variabilities in clinical manifestations, and uncertainties about treatment benefits [11].

NHB population was defined as newborns with ≥1 International Classification of Diseases (ICD)-9/10-CM diagnostic codes of NHB (ICD-9-CM = 773.0, 773.1, 773.2, 773.4, 774.x and ICD-10-CM = P55.x, P57.x, P58.x, P59.x) during the first 30 days after birth. Newborns with ≥1 ICD-9/10-CM diagnosis codes of ICD-9-CM = 773.0, 773.1, 773.2, 773.4, 774.0, 774.1, 774.7 and ICD-10-CM = P55.x, P57.x, P58.0, P58.1, P58.8, P58.9 were selected for the population of NHB with hemolysis indicators or hemolytic NHB (Appendix: Table 8).

Treated hemolytic NHB cohort

Treated hemolytic NHB cohort were selected from the hemolytic NHB population if they were ≥ 35 weeks GA and received at least one NHB intervention including: phototherapy (Healthcare Common Procedure Coding System [HCPCS] = E0202, S9098; ICD-9-CM procedure = 99.83; ICD-10-PCS = 6A600ZZ, 6A601ZZ), IVIg treatment along with NHB diagnosis code on the same claim (CPT = 90283, 90284; Generic Product Identifier [GPI] =19100020x; HCPCS = J1459, J1556, J1557, J1559, J1561, J1562, J1566, J1568, J1569, J1572, J1599), or exchange transfusions (CPT = 36450, 36456; ICD-9-CM procedure = 99.01; ICD-10-PCS = 30233H1, 30243H1).

Non-NHB cohort

A non-NHB cohort was established using 1:1 matching with newborns in the treated hemolytic NHB cohort ≥35 weeks GA. Inclusion in the non-NHB cohort required the absence of NHB diagnostic codes, no NHB treatment and a minimum of 30-day health plan enrollment after birth. Exact matching was performed based on delivery hospital/provider, gender, delivery route (C-section or vaginal), estimated GA, and post-index health plan continuous enrollment. When the matching of delivery hospital/provider was not possible, residence zip code (5-digit) was used instead. After all factors of interest were matched, newborns with the closest date of birth within 5 years were selected.

Gestational age

We calculated the GA of a newborn from prenatal procedure testing dates, from a range of common prenatal tests in the mother’s medical claims, using the weighted procedure date-based average methodology, as described by Wallace et al. [16]. This method demonstrated that 67% of all deliveries and 60% of preterm deliveries had estimated GA staying within one week of the actual GA [16].

Outcomes

Prevalence of NHB

The annual prevalence of NHB, hemolytic NHB and treated hemolytic NHB were estimated for 2011 through 2016 as the number of newborns diagnosed with a disease divided by the total number of newborns after mother-infant linkage and health plan eligibility requirement during a particular calendar year.

Hospitalization and healthcare resource utilization

All-cause hospital measures included birth hospitalization, length of stay, NICU admissions, receipt of NHB treatments, and readmissions. The use of emergency department (ED) visits, physician office visits, other outpatient visits, and prescription fills were also presented. All healthcare resource utilization during the first 30 days and first year after birth were summarized.

Clinical characteristics and outcomes

The effects of hyperbilirubinemia on the brain and neurodevelopmental status were examined by evaluating occurrences of kernicterus, cerebral palsy, encephalopathy, hearing and vision loss, motor dysfunction, and neurodevelopmental delay during the first year after birth. These clinical outcomes were identified using ICD-9/10-CM diagnosis codes, requiring ≥1 diagnosis for inpatient/ED settings or ≥ 2 diagnoses on distinct dates for physician office settings (Appendix: Table 9).

Costs of care

Total all-cause costs during the first 30 days and first year after birth were reported. Since newborn care during birth hospitalization could be billed under their mothers’ plan ID, mothers’ delivery hospitalization costs were included to avoid any potential unequal underestimation between the newborn cohorts. These costs were the sum of the total paid amount by health plans, members’ out-of-pocket costs, and coordination of benefits. Total costs consisted of expenses incurred in inpatient, ED, office visits, other outpatient settings and pharmacy costs. Costs were adjusted for inflation using the Medical Care Consumer Price Index, and calculated in terms of 2017 U.S. dollars [17].

Extrapolation to the U.S. newborn population

Using U.S. Centers for Disease Control and Prevention (CDC) 2016 birth data by gestational age [18] and the estimated prevalence from our study, we applied a direct standardization method to extrapolate the 2016 U.S. GA-adjusted treated hemolytic NHB prevalence [19]. We then calculated population-level total healthcare expenditure based on our extrapolated prevalence and costs estimates.

Statistical analysis

All outcome measures were compared between the treated hemolytic NHB and matched non-NHB cohorts. Statistical differences between groups were assessed using McNemar or McNemar-Bowker tests for categorical variables and paired t-tests or Wilcoxon signed-rank tests for continuous variables, respectively. A conventional alpha of 0.05 with two-tailed level of significance was used to interpret statistical significance. Statistical analyses were performed with SAS EG 7.1 (SAS Institute, Cary, NC).

Results

Study population

Of the 1.4 million identified newborns, 365,937 were successfully linked to their birth mothers (Fig. 1). A total of 1673 newborns with hemolytic NHB received treatment and were of ≥35 weeks GA. Among those, 1373 treated hemolytic NHB newborns were matched with non-NHB newborns; the matching rate was 82.1%.

Fig. 1
figure 1

Flow chart of the study population. Treated hemolytic NHB newborns were exactly matched to non-NHB newborns on delivery hospital/provider, gender, delivery route (Csection or vaginal), estimated GA, and post-index health plan continuous enrollment. When the matching of delivery hospital/provider was not possible, residence zip code (5-digit) was used instead. After all of the above factors were matched, newborn with the closest DOB within 5 years was selected. DOB: date of birth; GA: gestational age; NHB: neonatal hyperbilirubinemia

Full size image

Prevalence of NHB

The annual prevalence of NHB ranged from 29.6 to 31.7% during 2011 to 2016. The prevalence of hemolytic NHB during that period ranged from 1.8 to 2.4%, while the range for treated hemolytic NHB was 0.46 to 0.55% (Fig. 2). Upon stratification by estimated GA, the prevalence (95% Confidence Interval (CI)) of NHB among newborns < 35 weeks GA was 49.4% (95% CI: 48.6–50.1%), 38.4% (95% CI: 37.9–38.8%) of those 35–37 weeks GA, and 27.9% (95% CI: 27.7–28.1%) of those > 37 weeks GA during 2011 to 2016. Hemolytic NHB was reported in 2.8% (95% CI: 2.5–3.0%) of newborns < 35 weeks GA, 2.3% (95% CI: 2.1–2.4%) of those 35–37 weeks GA, and 2.0% (95% CI: 1.9–2.0%) of those > 37 weeks GA. The prevalence of treated hemolytic NHB among newborns < 35 weeks GA was 1.09% (95% CI: 0.93–1.25%), 0.70% (95% CI: 0.62–0.77%) of those 35–37 weeks GA, and 0.44% (95% CI: 0.41–0.46%) of those > 37 weeks GA (Table 1).

Fig. 2
figure 2

Prevalence of NHB, hemolytic NHB and treated hemolytic NHB stratified by GA from 2011 to 2016

Full size image
Table 1 Prevalence of NHB, hemolytic NHB and treated hemolytic NHB stratified by gestational age (GA) from 2011 to 2016
Full size table

Mother and newborn demographic and clinical characteristics

The mean age of mothers of treated hemolytic NHB and matched non-NHB (32.2 vs. 32.1 years, p = 0.40), region of residence, type of health plan, comorbidity and gestational diabetes were similar at time of delivery. Slightly less than one-third (29.1%) of births was delivered by C-section, and 18.2% of newborns were of 35–37 weeks GA in each cohort (Table 2).

Table 2 Mother and newborn demographic and clinical characteristics
Full size table

NHB treatment

During birth hospitalizations, 69.1% of the treated hemolytic NHB cohort received treatment. During the first 30 days after birth, 98.9% received phototherapy only, 0.3% received exchange transfusion only, 0.1% received phototherapy plus IVIg, and 0.7% received phototherapy plus exchange transfusion (Table 3).

Table 3 NHB treatment pattern during 30 days after birth
Full size table

Newborn clinical conditions and neurodevelopmental disorders

Newborns in the treated hemolytic NHB cohort had significantly higher proportions of birth trauma and hemorrhage (4.5% vs. 2.4%, p = 0.003), delivery by vacuum extractor affecting newborn (1.9% vs. 0.8%, p = 0.014), and polycythemia neonatorum (0.8% vs. 0.0%, p = 0.001) compared to the matched non-NHB cohort (Table 4). No difference was observed in neurodevelopmental disorders during the first year after birth between cohorts. Nine (1.2%) of the treated hemolytic NHB newborns had kernicterus.

Table 4 Newborn clinical conditions and neurodevelopmental disorders
Full size table

Healthcare resource utilization and costs during 30 days after birth

Treated hemolytic NHB newborns had longer average length of stay during birth hospitalization (4.5 days vs. 3.0 days; p < 0.001), and a greater proportion were admitted to NICU (82.6% vs. 70.0%; p < 0.001) compared to matched non-NHB newborns (Table 5). Significantly higher proportions of treated hemolytic NHB newborns were admitted to NICU levels 2–4 (15.7% vs. 2.4%; 15.9% vs. 2.8%; and 10.6% vs. 2.5%, respectively; all p < 0.001). Hospital readmissions and physician office visits were significantly higher for treated hemolytic NHB newborns than the matched non-NHB cohort, 8.7% vs. 1.7% (p < 0.001) and 90.8% vs. 82.6% (p < 0.001), respectively. No difference was reported for ED visits (1.7% vs. 1.4%, p = 0.54) and prescription fills (6.3% vs. 6.0%, p = 0.81) between the groups.

Table 5 Healthcare resource utilization and costs during 30 days after birth
Full size table

Mean (SD) total 30-day all-cause costs for the newborns were $14,405 ($43,918) for the treated hemolytic NHB group and $5,527 ($50,079) for the matched non-NHB cohort (p < 0.001). The treated hemolytic NHB group incurred mean (SD) total inpatient hospitalization costs of $13,794 ($43,949) compared to $5,216 ($50,083) in the matched non-NHB group, p < 0.001. The average costs of readmissions among those readmitted to the hospitals were $13,593 ($34,524) and $3,638 ($5,685) for the treated hemolytic NHB and non-NHB groups, respectively. The mean (SD) 30-day incremental total all-cause costs associated with treated hemolytic NHB newborns was $9,381 ($63,558) composed of $8,878 ($59,943) from newborns plus $503 ($19,969) from mothers’ delivery hospitalization.

Healthcare resource utilization and costs during one year after birth

Of 1,373 pairs, 765 (55.7%) matched pairs with one-year follow-up were included in the analysis. There was no statistically significant difference between the two cohorts in inpatient admissions and ED visits during the period from 31 days to 1 year after birth. Physician office visits and prescription fills were slightly higher in the treated hemolytic NHB group compared to the matched non-NHB group (99.7% vs. 97.4%, p < 0.001 and 69.7% vs. 63.5%, p = 0.009, respectively). The mean (SD) total one-year all-cause costs incurred by the treated hemolytic NHB cohort were $21,556 ($60,823) compared to $12,986 ($72,164) in the matched non-NHB cohort, p < 0.001. The average (SD) one-year incremental total all-cause costs associated with treated hemolytic NHB was $9,383 ($84,478), consisting of $813 ($12,922) from mother’s delivery hospitalization and $8,570 ($82,379) from newborns (Table 6).

Table 6 Healthcare resource utilization and costs during one year after birth
Full size table

Extrapolation to the U.S. population

The extrapolation of 2016 U.S. GA-adjusted treated hemolytic NHB prevalence was 0.53%, 20,854 newborns (95% CI, 18,398-23,311) among 3.9 million newborns in the U.S. in 2016. Among newborns ≥35 weeks GA, the GA-adjusted prevalence of treated hemolytic NHB was 0.50% resulting in 18,872 newborns (95% CI, 16,523 - 21,221). The 18,872 treated hemolytic NHB newborns represent an estimated total healthcare expenditure of $271.9 million and incremental costs of $177.0 million compared with their counterparts without NHB during the first month after birth in the U.S. in 2016.

Discussion

To the best of our knowledge, this is the first study to estimate the prevalence of high-risk hemolytic NHB newborns receiving intervention, and to quantify the burden of hemolytic NHB in the US. The proportions of newborns with hemolytic NHB who received treatment were 0.46 to 0.55% in a privately insured population in the US. Although not prevalent, those high-risk hemolytic NHB neonates who received treatment were associated with substantial healthcare resource utilization and incremental economic burden.

NHB research in the U.S. has been limited, and prevalence estimates vary markedly in the handful of studies in the literature. In a systematic review that included 14 studies to examine the effects and outcomes of phototherapy, Woodgate and Jardine noted that about 50% of full-term and 80% preterm newborns developed jaundice [6]. In a survey at medical centers that practiced universal pre-discharge total serum bilirubin (TSB) screening, Bhutani et al. reported jaundice in 84% of healthy newborns ≥35 weeks GA [20]. Another study, which used inpatient data from the Healthcare Costs and Utilization Project (HCUP), reported 15.6% of newborns had jaundice [21]. These variations could, in part, be due to differences in the study population, case definitions (e.g., TSB level vs. visible jaundice), data sources, and underdiagnosis or underreporting of mild cases. Mild NHB typically resolves without intervention, and may not be fully captured in administrative claims (used in our study) and hospital discharge data (HCUP). Such cases may not be reflected in reimbursements because of bundled payments, which could result in an underestimation of general NHB prevalence.

Our study focused on NHB specifically with etiology of hemolytic diseases, and we found that approximately 7% of the NHB cases were hemolytic NHB. Our estimated prevalence of treated hemolytic NHB (ranging from 0.46–0.55%) was comparable to < 1% of significant hemolysis reported by Wagle and Deshpande [22]. Chang et al. estimated that about 6% of newborns ≥35 weeks GA received phototherapy at Kaiser Permanente hospitals [23]. Using our estimate that 7% of the NHB newborns in this study had hemolytic NHB along with the assumption that all the newborns in the Chang et al. study had NHB, we inferred that approximately 0.42% of newborns in Chang et al. were phototherapy-treated hemolytic NHB — which is close to our estimate. Treatment rates could vary remarkably as treatment practice across hospitals/institutions differ in how cases are identified and when treatment should be initiated [24, 25]. Additionally, prior literature suggested that NHB patients could be under-treated. One U.S. study showed that only approximately half (54%) of healthy term newborns for whom AAP clinical practice guidelines recommended phototherapy received treatment [26].

We found that treated hemolytic NHB newborns had significantly longer length of stay during their birth hospitalization, higher 30-day readmission rates, higher NICU use and slightly higher rates of physician office visits, compared to their matched counterparts. Length of stay of mothers’ delivery hospitalizations were also slightly longer in the treated hemolytic NHB cohort (2.9 days vs 2.5 days, data not shown). These findings suggest significant burden to patients, their caregivers, and the healthcare system. Prior studies have shown that NHB was as major cause of readmission. Approximately half (51%) of all readmissions occurring 2 weeks after birth were attributable to NHB [27]. The increase in physician office visits we reported was also consistent with available literature, which found that NHB was associated with increased parental awareness, and newborns receiving phototherapy had higher rates of outpatient visits [28].

We also found that hemolytic NHB newborns who received treatment incurred 2.6 times the average costs of their matched non-NHB counterparts during the first 30 days after birth. The majority of the incremental cost was derived from birth hospitalizations. Indirect costs associated with patients’ and caregivers’ quality of life as well as caregivers’ loss of productivity could not be evaluated using claims data. As of now, no prior study has examined the economic burden of hemolytic NHB. One earlier study estimated the average cost of childbirth via vaginal or caesarian at $18,329 or $27,866, respectively, in a private health plan [29]. Those estimates were close to the average costs, $20,568, of the sum of maternal delivery (mean (SD) = $15,413 ($20,010), data not shown) and newborn birth hospitalization ($5,155 ($50,080), Table 5) in the non-NHB cohort in our study. Such comparability might warrant the representativeness and generalizability of our study results to other privately insured populations. In this study, we found that the majority of treated hemolytic NHB newborns received phototherapy. A total of 15 (1%) newborns received IVIg or ET, which are recommended by AAP when bilirubin levels continue to rise despite intensive phototherapy. This group imposed even greater economic burden with average (SD) total one-month all-cause costs of $81,065 ($133,767) (data not shown).

We extrapolated our findings to the entire U.S. newborn population in 2016. The extrapolation estimated total healthcare expenditure of $271.9 million and incremental costs of $177.0 million among 18,872 treated hemolytic NHB newborns as compared with their counterparts without NHB during the first month after birth. Our extrapolation assumed our estimates were applicable to the U.S. newborn population mainly insured by private insurance plans or Medicaid. This projection should be interpreted with caution as privately insured populations tend to have higher socioeconomic status and healthcare expenditures than the Medicaid population [30]. Further research in the Medicaid newborn population is warranted to examine our assumptions and estimates.

We did not observe significant difference in neurodevelopment delay, language disorders, motor dysfunction, cerebral palsy, abnormal behavior, encephalopathy, hearing and vision loss between treated hemolytic NHB newborns and the matched non-NHB cohort during the first year of birth. However, the observation period was likely too short as many of these conditions might not be identifiable nor noticeable in the first year of life. Kernicterus, a brain injury resulting from severe NHB, was found in nine newborns, approximately 1.2% of all treated hemolytic NHB newborns during the one-year follow up. Kernicterus has been reported from 1.0 to 3.7 cases per 100,000 live birth in the literature [31, 32], but these incidence rates were estimated for the general population in contrast to the high-risk hemolytic NHB population (treated) in this study. As hemolytic NHB was strongly correlated with higher incidences of birth trauma, polycythemia, and other subsequent morbidities which could also cause neurodevelopment disorders, neurodevelopment disorders in this population could be due to a combination of hemolytic NHB and other morbidities, rather than hemolytic NHB alone.

Effective management of high-risk hemolytic NHB is critical to reduce the impact of disease burden on patients, their caregivers, and the healthcare system. Several studies have investigated comprehensive approaches, such as pre-discharge bilirubin screening for all newborns [25], or the implementation of a standard pathway including treatment algorithms (e.g., requiring irradiance compliance to ensure consistent delivery of effective phototherapy) and education to increase awareness among clinicians [33]. These comprehensive approaches have demonstrated success in reducing costs, length of stay [33] and hospital readmission rates [25]. In addition, new treatment options are needed. For example, an investigational treatment – stannsoporfin (SnMP, a heme oxygenase inhibitor) with or without phototherapy was studied for use in the management of NHB or hemolytic NHB [34, 35].

Limitations

Our results should be interpreted in light of certain limitations. Known risk factors such as family history, race and ethnicity, and breastfeeding status are not available in administrative claims data. Cases of mild NHB do not usually require intervention, and can be underdiagnosed and/or under-coded in administrative data leading to underestimation of NHB and hemolytic NHB. The use of phototherapy during hospitalization might not have been observed due to bundled payments and/or under-coding. Duration on phototherapy was also not captured. This study population was from a U.S. privately insured population, which may limit the generalizability of these results to other population segments, such as Medicaid.

Conclusions

This is likely the first study estimating the prevalence of newborns with hemolytic NHB who received intervention in the U.S. This high-risk population imposes a substantial burden of healthcare resource utilization and incremental costs on newborns, their caregivers, and the healthcare system. Effective management protocols and emerging new treatments may help to mitigate the overall burden of hemolytic NHB.

Abbreviations

AAP:

American Academy of Pediatrics

CI:

Confidence Interval

GA:

Gestational age

HCRU:

Healthcare resource utilization

HDN:

Hemolytic disease of the newborn

ICD-9/10-CM:

The international classification of diseases, 9/10th Revision, clinical modification

ICD-9-CM/10-PCS:

The international classification of diseases, 9/10th Revision, procedure coding system

IVIg:

Intravenous immunoglobulin

KSDs:

Kernicterus spectrum disorders

NHB:

Neonatal hyperbilirubinemia

NICU:

Neonatal intensive care unit

RBC:

Red blood cell

SD:

Standard deviation

TSB:

Total serum bilirubin

References

  1. Cohen RS, Wong RJ, Stevenson DK. Understanding neonatal jaundice: a perspective on causation. Pediatr Neonatol. 2010;51(3):143–8.

    Article  Google Scholar 

  2. Ullah S, Rahman K, Hedayati M. Hyperbilirubinemia in neonates: types, causes, clinical examinations, preventive measures and treatments: a narrative review article. Iran J Public Health. 2016;45(5):558–68.

    PubMed  PubMed Central  Google Scholar 

  3. Kaplan M, Hammerman C. Understanding and preventing severe neonatal hyperbilirubinemia: is bilirubin neurotoxity really a concern in the developed world? Clin Perinatol. 2004;31(3):555–75 x.

    Article  Google Scholar 

  4. Porter ML, Dennis BL. Hyperbilirubinemia in the term newborn. Am Fam Physician. 2002;65(4):599–606.

    PubMed  Google Scholar 

  5. Woodgate P, Jardine LA. Neonatal jaundice. BMJ Clin Evid. 2011;2011.

  6. Woodgate P, Jardine LA. Neonatal jaundice: phototherapy. BMJ Clin Evid. 2015;2015.

  7. Smitherman H, Stark AR, Bhutani VK. Early recognition of neonatal hyperbilirubinemia and its emergent management. Semin Fetal Neonatal Med. 2006;11(3):214–24.

    Article  Google Scholar 

  8. Memon N, Weinberger BI, Hegyi T, Aleksunes LM. Inherited disorders of bilirubin clearance. Pediatr Res. 2016;79(3):378–86.

    Article  CAS  Google Scholar 

  9. Murray NA, Roberts IA. Haemolytic disease of the newborn. Arch Dis Child Fetal Neonatal Ed. 2007;92(2):F83–8.

    Article  Google Scholar 

  10. American Academy of Pediatrics Subcommittee on H. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics. 2004;114(1):297–316.

    Article  Google Scholar 

  11. Maisels MJ, Watchko JF, Bhutani VK, Stevenson DK. An approach to the management of hyperbilirubinemia in the preterm infant less than 35 weeks of gestation. J Perinatol. 2012;32(9):660–4.

    Article  CAS  Google Scholar 

  12. Amin SB, Bhutani VK, Watchko JF. Apnea in acute bilirubin encephalopathy. Semin Perinatol. 2014;38(7):407–11.

    Article  Google Scholar 

  13. Muchowski KE. Evaluation and treatment of neonatal hyperbilirubinemia. Am Fam Physician. 2014;89(11):873–8.

    PubMed  Google Scholar 

  14. Watchko JF, Tiribelli C. Bilirubin-induced neurologic damage--mechanisms and management approaches. N Engl J Med. 2013;369(21):2021–30.

    Article  CAS  Google Scholar 

  15. Wasser T, We B, Ycas J, Tunceli O. Applying Weighting Methodologies to a Commercial Database to Project US Census Demographic Data. Am J Account Care. 2015;3:33–8.

    Google Scholar 

  16. Wallace AE, Le BK, Selvam N, et al. Estimation of gestional age at birth using claims-based algorithms in a commercially insured US population. Presented at the International Society for Pharmacoepidemiolkogy (ISPE) 32nd international conference on Pharmacoepidemiology (ICPE) and therapeutic risk management. 2016;Dublin, Ireland Astract available at https://onlinelibrary.wiley.com/doi/full/10.1002/pds.4070#. Accessed 23 Apr 2018.

  17. Consumer Price Index for Medical Care. Available at https://www.hrsa.gov/get-health-care/affordable/hill-burton/cpi.html. Accessed 23 Apr 2018.

  18. United States Department of Health and Human Services (US DHHS), Centers for Disease Control and Prevention (CDC), National Center for Health Statistics (NCHS), Division of Vital Statistics, Natality public-use data 2007-2016, on CDC WONDER Online Database, February 2018. Available at http://wonder.cdc.gov/natality-current.html . Accessed 29 May 2018.

  19. Curtin LR, Klein RJ. Direct standardization. Statistical Notes. 1995;Available at https://www.cdc.gov/nchs/data/statnt/statnt06rv.pdf . Accessed 29 May 2018.

  20. Bhutani VK, Stark AR, Lazzeroni LC, Poland R, Gourley GR, Kazmierczak S, et al. Predischarge screening for severe neonatal hyperbilirubinemia identifies infants who need phototherapy. J Pediatr. 2013;162(3):477–82 e1.

    Article  Google Scholar 

  21. Burke BL, Robbins JM, Bird TM, Hobbs CA, Nesmith C, Tilford JM. Trends in hospitalizations for neonatal jaundice and kernicterus in the United States, 1988-2005. Pediatrics. 2009;123(2):524–32.

    Article  Google Scholar 

  22. Wagle S, Deshpande PG. Hemolytic Disease of the Newborn. Medspace. 2017.

  23. Chang PW, Kuzniewicz MW, McCulloch CE, Newman TB. A Clinical Prediction Rule for Rebound Hyperbilirubinemia Following Inpatient Phototherapy. Pediatrics. 2017;139(3).

  24. Bhutani VK, Johnson LH, Schwoebel A, Gennaro S. A systems approach for neonatal hyperbilirubinemia in term and near-term newborns. J Obstet Gynecol Neonatal Nurs. 2006;35(4):444–55.

    Article  Google Scholar 

  25. Eggert LD, Wiedmeier SE, Wilson J, Christensen RD. The effect of instituting a prehospital-discharge newborn bilirubin screening program in an 18-hospital health system. Pediatrics. 2006;117(5):e855–62.

    Article  Google Scholar 

  26. Atkinson LR, Escobar GJ, Takayama JI, Newman TB. Phototherapy use in jaundiced newborns in a large managed care organization: do clinicians adhere to the guideline? Pediatrics. 2003;111(5 Pt 1):e555–61.

    Article  Google Scholar 

  27. Maisels MJ, Kring E. Length of stay, jaundice, and hospital readmission. Pediatrics. 1998;101(6):995–8.

    Article  CAS  Google Scholar 

  28. Usatin D, Liljestrand P, Kuzniewicz MW, Escobar GJ, Newman TB. Effect of neonatal jaundice and phototherapy on the frequency of first-year outpatient visits. Pediatrics. 2010;125(4):729–34.

    Article  Google Scholar 

  29. Truven Health Analytics. The cost of having a baby in the United Sates. Marketscan study prepared for childbirth connection, Catalyst for Payment Reform and Center for Healthcare Quality and Payment Reform; 2013. Available at https://transform.childbirthconnection.org/wp-content/uploads/2013/01/Cost-of-Having-a-Baby-Executive-Summary.pdf. (Accessed 29 May 2018).

  30. Ku L, Broaddus M. Public and private health insurance: stacking up the costs. Health Aff (Millwood). 2008;27(4):w318–27.

    Article  Google Scholar 

  31. Brooks JC, Fisher-Owens SA, Wu YW, Strauss DJ, Newman TB. Evidence suggests there was not a "resurgence" of kernicterus in the 1990s. Pediatrics. 2011;127(4):672–9.

    Article  Google Scholar 

  32. Bhutani VK, Johnson L. Kernicterus in the 21st century: frequently asked questions. J Perinatol. 2009;29(Suppl 1):S20–4.

    Article  Google Scholar 

  33. Romero HM, Ringer C, Leu MG, Beardsley E, Kelly K, Fesinmeyer MD, et al. Neonatal Jaundice: Improved Quality and Cost Savings After Implementation of a Standard Pathway. Pediatrics. 2018.

  34. Hudak ML, Rosenfeld W, Ruiz N. Tin Mesoporphyrin (SnMP) as Adjunctive Treatment to Phototherapy (PT) in Neonates with Hyperbilirubinemia (HB) and Hemolysis. Pediatric Academic Societies Meeting; Toronto, ON, CanadaMay 5–8, 2018.

  35. Bhutani VK, Poland R, Meloy LD, Hegyi T, Fanaroff AA, Maisels MJ. Clinical trial of tin mesoporphyrin to prevent neonatal hyperbilirubinemia. J Perinatol. 2016;36(7):533–9.

    Article  CAS  Google Scholar 

  36. Beyrer J, Nolot S, Haldane D, Johnston J. Developing an ICD-10-CM Version of Charlson Comorbidities for United States Real-world Healthcare Data. ISPOR 22nd Annual International Meeting; Boston, MA; May 20–24, 2017. 2017.

Download references

Acknowledgements

The authors thank B. Bernard Tulsi for writing and editorial support and Nianya Liu for data programming and querying. We also would like to thank Dr. Joseph Singer, Chief Medical Officer, for providing clinical input and perspectives to the study. Thanks to Dr. Holly Romero, Andrew Rava, Ruixin Tan, and all reviewers of the protocol or manuscript for their helpful feedback. All errors or omissions remain the responsibility of the authors.

Funding

The study was funded by Mallinckrodt Pharmaceuticals. Authors T-CY, NR, and EAB, employees of Mallinckrodt at the time of the study, participated in study design, data interpretation, and revising different versions of this article, and approved it for submission.

Availability of data and materials

The corresponding author has direct access to the dataset used for this study, clarification could be provided upon reasonable request.

Author information

Authors and Affiliations

  1. Mallinckrodt Pharmaceuticals, Bedminster, NJ, 07921, USA

    Tzy-Chyi Yu, Nancy Ruiz & Elaine A. Böing

  2. HealthCore, Inc., An Independent Subsidiary of Anthem, Inc, Wilmington, DE, 19801, USA

    Chi Nguyen, Siting Zhou, Xian Zhang & Hiangkiat Tan

Authors
  1. Tzy-Chyi Yu
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Chi Nguyen
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Nancy Ruiz
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Siting Zhou
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Xian Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Elaine A. Böing
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Hiangkiat Tan
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

All the authors contributed substantially to the conceptualization and design of this study. Authors CN, SZ, XZ and HT, employees of HealthCore, engaged in data acquisition and analysis. Authors T-CY, NR, and EAB, were/are employees of Mallinckrodt Pharmaceuticals, along with all the other authors CN, NR, SZ, XZ, and HT were involved in study design, data interpretation and participated in drafting and revising the different versions of this article. The final version of the article was approved by all authors.

Corresponding author

Correspondence to Chi Nguyen.

Ethics declarations

Ethics approval and consent to participate

This non-experimental observational study was exempt from Institutional Review Board (IRB) informed consent stipulations. The researchers accessed a limited dataset without individual enrollee identifiers, and only summary statistics were reported. This work complied with all relevant provisions of the US federal Health Insurance Portability and Accountability Act of 1996 (HIPAA).

Consent for publication

Not applicable. The study does not contain data from any individual person.

Competing interests

The authors declare the following: T-CY is an employee and a stockholder of Mallinckrodt Pharmaceuticals, Bedminster, New Jersey 07921, USA. NR was an employee and is a stockholder of Mallinckrodt Pharmaceuticals, Bedminster, New Jersey 07921, USA. EAB is an employee of Mallinckrodt Pharmaceuticals, Bedminster, New Jersey 07921, USA. CN, SZ, XZ, HT are employees of HealthCore, Inc Wilmington, Delaware 19,801, USA whose activities on research projects are funded by various pharmaceutical/biotech/medical device companies.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Appendix

Appendix

Table 7 Codes to identify delivery
Full size table
Table 8 Codes to identify neonatal hyperbilirubinemia
Full size table
Table 9 Codes to identify NICU admission, gestational age estimation and newborn clinical conditions
Full size table

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yu, TC., Nguyen, C., Ruiz, N. et al. Prevalence and burden of illness of treated hemolytic neonatal hyperbilirubinemia in a privately insured population in the United States. BMC Pediatr 19, 53 (2019). https://doi.org/10.1186/s12887-019-1414-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12887-019-1414-x

Keywords

BMC Pediatrics

ISSN: 1471-2431

Contact us