Other Neonatal Disorders
Cause description
Other neonatal disorders is a label defined by GBD, which refers to a specific collection of causes of neonatal health loss.
This collection of causes is defined by a collection of ICD 9 and 10 codes. We list the ICD 10 codes below. The complete lists can be found at:
Notably, GBD estimates fatal and nonfatal burden separately, and defines other neonatal disorders differently in the nonfatal and fatal models. In particular, they differ on codes P04, P05, and P07:
Category code |
Category definition |
Specific code |
Fatal |
Nonfatal |
|---|---|---|---|---|
P00 |
Newborn affected by maternal conditions that may be unrelated to present pregnancy |
P00.0 P00.1 P00.2 P00.3 P00.4 P00.5 P00.6 P00.7 P00.8 P00.81 P00.89 P00.9 |
||
P01 |
Newborn affected by maternal complications of pregnancy |
P01.2 P01.3 P01.4 P01.5 P01.6 P01.8 P01.9 |
||
P04 |
Newborn affected by noxious substances transmitted via placenta or breast milk |
P04.0 P04.1 P04.2 P04.5 P04.6 P04.8 P04.9 |
Excl. |
|
P05 |
Disorders of newborn related to slow fetal growth and fetal malnutrition |
P05.0 P05.00 P05.01 P05.02 P05.03 P05.04 P05.05 P05.06 P05.07 P05.08 P05.1 P05.10 P05.11 P05.12 P05.13 P05.14 P05.15 P05.16 P05.17 P05.18 P05.2 P05.9 |
Excl. |
|
P07 |
Disorders of newborn related to short gestation and low birth weight, not elsewhere classified |
P07.0 P07.10 P07.14 P07.15 P07.16 P07.17 P07.18 |
Excl. |
|
P08 |
Disorders of newborn related to long gestation and high birth weight |
P08.0 P08.1 P08.2 P08.21 P08.22 |
||
P09 |
Abnormal findings on neonatal screening |
P09 |
||
P19 |
Metabolic acidemia in newborn |
P19.0 P19.1 P19.2 P19.9 |
||
P29 |
Cardiovascular disorders originating in the perinatal period |
P29.0 P29.1 P29.11 P29.12 P29.2 P29.3 P29.4 P29.8 P29.81 P29.89 P29.9 |
||
P50 |
Newborn affected by intrauterine (fetal) blood loss |
P50.0 P50.1 P50.2 P50.3 P50.4 P50.5 P50.8 P50.9 |
||
P51 |
Umbilical hemorrhage of newborn |
P51.0 P51.8 P51.9 |
||
P52 |
Intracranial nontraumatic hemorrhage of newborn |
P52.0 P52.1 P52.2 P52.21 P52.22 P52.3 P52.4 P52.5 P52.6 P52.8 P52.9 |
||
P53 |
Hemorrhagic disease of newborn |
P53.0 |
||
P54 |
Other neonatal hemorrhages |
P54.0 P54.1 P54.2 P54.3 P54.4 P54.5 P54.6 P54.8 P54.9 |
||
P60 |
Disseminated intravascular coagulation of newborn |
P60.0 |
||
P61 |
Other perinatal hematological disorders |
P61.0 P61.1 P61.3 P61.4 P61.5 P61.6 P61.8 P61.9 |
||
P70 |
Transitory disorders of carbohydrate metabolism specific to newborn |
P70.3 P70.4 P70.8 P70.9 |
||
P71 |
Transitory neonatal disorders of calcium and magnesium metabolism |
P71.0 P71.1 P71.2 P71.3 P71.4 P71.8 P71.9 |
||
P72 |
Other transitory neonatal endocrine disorders |
P72.0 P72.1 P72.2 P72.8 P72.9 |
||
P74 |
Other transitory neonatal electrolyte and metabolic disturbances |
P74.0 P74.1 P74.2 P74.3 P74.4 P74.5 P74.6 P74.8 P74.9 |
||
P76 |
Other intestinal obstruction of newborn |
P76.0 P76.1 P76.2 P76.8 P76.9 |
||
P78 |
Other perinatal digestive system disorders |
P78.0 P78.1 P78.2 P78.3 P78.8 P78.81 P78.82 P78.83 P78.89 P78.9 |
||
P80 |
Hypothermia of newborn |
P80.0 P80.8 P80.9 |
||
P81 |
Other disturbances of temperature regulation of newborn |
P81.0 P81.8 P81.9 |
||
P83 |
Other conditions of integument specific to newborn |
P83.0 P83.1 P83.2 P83.3 P83.30 P83.39 P83.4 P83.5 P83.6 P83.8 P83.9 |
||
P84 |
Other problems with newborn |
P84.0 |
||
P92 |
Feeding problems of newborn |
P92.0 P92.01 P92.09 P92.1 P92.2 P92.3 P92.4 P92.5 P92.6 P92.8 P92.9 |
||
P93 |
Reactions and intoxications due to drugs administered to newborn |
P93.0 P93.8 |
||
P94 |
Disorders of muscle tone of newborn |
P94.0 P94.1 P94.2 P94.8 P94.9 |
||
P96 |
Other conditions originating in the perinatal period |
P96.3 P96.4 P96.8 P96.81 P96.82 P96.83 P96.89 |
It is important to note that “Other neonatal disorders” is precisely the ICD codes listed above (plus their ICD 9 counterparts), and does not refer to “all causes of neonatal health loss excluded from other cause models within the GBD framework”.
Modeling Other Neonatal Disorders in GBD 2017
Fatal model
Other neonatal disorders contribute to both fatal and nonfatal health burden. The fatal model is a standard CoDEM model, which runs on vital registration and surveillance data to estimate the proportion of deaths coded to the “neonatal other” ICD codes, listed above.
Within the context of GBD, “neonatal disorders comprises five causes: preterm birth complications, neonatal encephalopathy and birth trauma, neonatal sepsis and other infections, hemolytic disease and neonatal jaundice, and other neonatal disorders. These five CoDEM models are run, in addition to a “parent” model, to which the children models are all squeezed.
Nonfatal estimates
The nonfatal burden of “other neonatal disorders” is not explicitly modeled by GBD. We here include the complete content of the “Other neonatal disorders” writeup in the 2017 [YLD] Appendix:
In addition to the neonatal disorders described above, there are many diverse types of neonatal disorders with a range of severities and associated sequelae. Because these other neonatal disorders are diverse in their underlying causes and risk factors as well as in their associated health outcomes, modelling them together in a DisMod-MR model would not produce reliable estimates of prevalence or excess mortality. Instead, we calculated the YLDs caused by other neonatal disorders directly using a YLD/YLL ratio.
We calculated the ratio of YLDs to YLLs across the specified neonatal disorders for which non-fatal outcomes were modelled, using YLL estimates from the GBD 2017 cause of death (CoD) analysis. We then multiplied this YLD/YLL ratio by the YLL estimates for other chronic respiratory diseases from the GBD 2017 CoD analysis, providing us with an estimate of the YLDs associated with other neonatal disorders.
Model Assumptions and Limitations
Todo
Finalize this section once we’ve come to conclusion on a modeling strategy
The lack of a nonfatal model within the GBD framework poses a significant challenge to the project of incorporating neonatal disorders, and thus interventions with impacts on neonatal disorders, into a vivarium simulation.
To model “other neonatal disorders” within the vivarium framework, we would need to know:
prevalence, in order to correctly initialize the right proportion of the population with other neonatal disorders;
birth prevalence, in order to be able to correctly initialize new simulants throughout the simulation;
incidence, in order for susceptible simulants to appropriately become prevalent cases;
remission, in order for prevalent cases to appropriately remit;
excess mortality rate (EMR), in order to appropriately calculate YLLs attributable to other neonatal disorers
We have EMR from GBD’s fatal other neonatal model. Then, most of the conditions encapsulted by neonatal other have no incidence (other than birth prevalence) or remission, so we can reasonably model these conditions to have niether incidence nor remission.
However, GBD does not produce estimates of birth prevalence or prevalence of other neonatal disorders. As other neonatal YLDs are calculated as a ratio based on other neonatal YLLs, this also means that other neonatal disorders also lacks any associated disability weights.
If we could determine birth prevalence, we could then concievably use EMR to calculate prevalence. Then, we should be able to back-calculate the correct disability weights per age/sex/location/year to get back the YLDs estimated by GBD, as YLDs for a given individual are calculated by multiplying {years lived with disability x} by {disability weight associated with disability x}.
However, the issue of birth prevalence remains. As the “other neonatal” conditions are so heterogenous, our preliminary efforts to find data have not returned anything useable.
We note that if we were to run our model with a too-high birth prevalence, “other neonatal disorders” would fill a disproportionatley large ratio of other neonatal disorders, and we would choose a set of too-low disability weights.
If we were to run our model with a too-low birth prevalence, “other neonatal disorders” would fill too small a proportion of other neonatal disorders, and we would choose an set of inaccurately high disability weights. In both of these scenarios this could significantly skew calculation of YLDs, depending on how incorrect our birth prevalence inputs are.
Todo
Include Lu’s calculation of % of avoidable burden that is attributed to other neonatal
Todo
Describe cause model
Restrictions
Restriction type |
Value |
Notes |
|---|---|---|
Male only |
False |
|
Female only |
False |
|
YLL only |
False |
|
YLD only |
False |
|
YLL age group start |
Early neonatal |
age_group_id = 2; [0-7 days) |
YLL age group end |
Post neonatal |
age_group_id = 4; [28 days-1 year) |
YLD age group start |
Early neonatal |
age_group_id = 2; [0-7 days) |
YLD age group end |
95 plus |
age_group_id = 235; 95 years + |
References
2017 YLD appendix https://ars.els-cdn.com/content/image/1-s2.0-S0140673618322037-mmc1.pdf