Introduction
Stillbirth (SB) is a reproductive tragedy not only related to immediate maternal risks
inherent to clinical management but also to psychosocial problems, such as depression,
posttraumatic stress, social stigmatization, and difference in the quality of live
of families.[1]
Each year, at least 2.6 million SBs occur worldwide, especially in poor or developing
countries.[2] According to the Ministry of Health of Brazil, a total of 351,912 SBs was registered
during the period from 2006 to 2016. From this total, 129,173 occurred in the Southeast
region, with a monthly average of 11,000 occurrences.[3] Additionally, many epidemiological studies have registered that most SBs would be
susceptible to prevention.[4]
Despite the negative impacts they produce, SBs are unattractive from the point of
view of clinical research, and most of the time, investigations are very superficial
and have a very limited extent, affecting their understanding and implications. Promoting
the educational audit of SB cases, performed by a technically qualified team and with
availability of resources, such as laboratory evaluations, placenta study, and necropsies,
can produce consistent information to understand the factorswith SB and to support
prevention strategies.[5]
The assessment of the causes associated with SB remains a major challenge for understanding
the problem at a population scale. The recurrent diagnosis of intrauterine hypoxia
as a cause of death hardly contributes to understanding the phenomenon. In addition,
many studies do not specify whether hypoxia occurred before or during birth.[6]
Thus, SB rates are valuable indicators related to the quality of obstetric care globally,
and they contribute to the support of public health planning processes. The more precise
the identification of the associated causes, the better strategies can be planned
to improve the quality of prenatal care.[7]
Considering that, in Brazil, more than 98.0% of deliveries are performed in hospitals,
the amount of information produced by the local mortality investigation committees
allows the identification of factors associated with SB and provides guidelines for
more effective prevention in the coverage area.[8]
Therefore, in view of its relevance, our objective is to describe the conditions associated
with SB in a maternity hospital school located in the North zone of the city of São
Paulo and the epidemiological trends in the last 15 years.
Methods
This is a cross-sectional observational study conducted at Hospital e Maternidade-escola
Vila Nova Cachoeirinha (HMEC), located in the North zone of the city of São Paulo.
The design of the study followed the Strenghtening the Reporting of Observational
Studies in Epidemiology (STROBE)[9] statement, and it included 1,139 cases of SB attended in the period from 2003 to
2017. In view of some registry failures during the data collection, the total number
of cases will be different in some variables.
The evaluation of all SBs was based on data from the perinatal mortality committee
of the HMEC, using clinical information, notes available in the prenatal folder, maternal
laboratory tests and necropsy in SB fetuses, and studies of placenta. The SB definition
is according Brazil Ministry of Health based on weight, which defines SB as a death
that occurs in any fetus weighing 500 g or more. To allow for international comparisons,
we divided the general population according to the birth weight in two groups: intermediate
stillbirths (ISBs), those with birth weight between 500 and 999 g, and late stillbirths
(LSBs), which consider fetus with 1,000 g or more.[7]
The following variables were selected: age group; number of pregnancies, prenatal
care; number of prenatal visits, presence of fetal vitality at admission in hospital;
characteristics of birth (site and type of birth), onset of labor, placenta study
and necropsy of fetus. The associated causes related to SB were evaluated in addition
to the historical evolution of the most frequent reasons, and SB coefficients.
All data was stored in Windows Excel (Microsoft Corp., Redmond, WA, USA) worksheets,
and graphs and tables were then constructed based on them. We used the statistical
software SPSS for Windows, version 18.0 (SPSS Inc., Chicago, IL, USA) to estimate
the prevalence ratio (PR) and odds ratio (Odds), considering the 95% confidence interval
(95% CI).
The project was approved by the Ethics and Research Committee of HMEC (Reference No.
787.747), according to Resolution No. 466/2012 of the National Health Council (CONEP,
in the Portuguese acronym).
Results
During the study period, the total number of live births in the HMEC was 95,650, and
the number of SBs was 1,139, resulting in a stillbirth rate (SBR) of 11.9 per 1,000.
Taking into account only the cases of fetal deaths that occurred after hospitalization,
the coefficient of in-hospital stillbirth (IHSR) was 2.8 per 1,000. ([Table 1]).
Table 1
Annual distribution of live births, total number of stillbirths, general stillbirth
rate and in-hospital stillbirth rate (Maternity School of Vila Nova Cachoeirinha 2003-2017)
YEAR
|
LIVE BIRTHS (n)
|
STILLBIRTHS (n)
|
SBR[*]
|
IHSR[*]
|
2003
|
4,596
|
88
|
18.8
|
6.0
|
2004
|
5,973
|
87
|
14.3
|
3.1
|
2005
|
5,129
|
75
|
14.4
|
4.2
|
2006
|
5,180
|
52
|
9.9
|
2.8
|
2007
|
5,980
|
61
|
10.1
|
3.0
|
2008
|
5,973
|
73
|
12.1
|
3.8
|
2009
|
6,053
|
83
|
13.5
|
3.2
|
2010
|
6,205
|
51
|
8.1
|
1.4
|
2011
|
7,022
|
63
|
8.9
|
1.7
|
2012
|
7,763
|
79
|
10.1
|
1.6
|
2013
|
7,592
|
95
|
12.3
|
1.7
|
2014
|
7,189
|
82
|
11.2
|
1.8
|
2015
|
6,867
|
92
|
13.2
|
2.9
|
2016
|
6,820
|
78
|
11.3
|
2.9
|
2017
|
7,308
|
80
|
10.8
|
1.9
|
TOTAL
|
95,650
|
1,139
|
11.93
|
2.8
|
Abbreviations: SBR, general stillbirth rate; IHSR, in-hospital stillbirth rate.
* per 1,000
in this table, it is also possible to observe that, over the years, the demand for
HMEC care has been increasing. When comparing numbers from 2003 to those of 2017,
there was a 59.9% increase in the number of live births. Over the years, despite of
the expansion in the number of live births, we can see stable institutional trends
in both SBR and IHSR ([Graphic 1]).
Graphic 1 Annual distribution of live births, general stillbirth coefficient (GSBC) and intrahospitalar
stillbirth coefficient (IHSBC). (Maternity School of Vila Nova Cachoeirinha 2003-2017)
When analyzing maternal and perinatal variables ([Table 2]), we observed that patients younger than 16 years and over 40 years represented
2.2% and 4.4% of the general population, respectively. However, pregnant women younger
than 16 years old were more likely to have ISB (OR of 0.32, 0.15–0.75), while patients
over 40 years of age presented a higher chance of LSB (PR 0.85, 0.72–0.99). Women
at first pregnancy comprised 37.5% of the population, and this group showed greater
chances of ISB (PR 0.79; 0.67- 0.93), while women with more than 5 pregnancies represented
13.4% of the total population with a higher probability of presenting LSB (PR 0.87,
0.78–0.97). Regarding prenatal care, we found that 25.7% of the population had no
prenatal visits, a similar distribution for both groups. However, when evaluating
the number of visits performed between the patients who had prenatal care, 31.2% presented
at least 6 visits, and this possibility was more frequent among the patients who had
LSB (OR 4.56, 3.23- 6.44).
Table 2
Maternal and perinatal characteristics related to stillbirth. Prevalence rates and
odds ratio (Maternity School of Vila Nova Cachoeirinha 2003-2017)
|
ISB
|
LSB
|
TOTAL
|
OR
|
|
N
|
%
|
PR ISB
|
N
|
%
|
PR ISB
|
N
|
%
|
|
Age group
|
|
|
|
|
|
|
|
|
|
< 16 years
|
15
|
3.9
|
0.55[*] (0.39–0.77)
|
10
|
1.3
|
1,67[*] (1.03–2.70)
|
25
|
2.2
|
0.32[*] (0.15–0.757)
|
≥ 16 years
|
366
|
96.1
|
|
734
|
98.7
|
|
1,100
|
97.8
|
|
Total
|
381
|
100.0
|
|
744
|
100.0
|
|
1,125
|
100.0
|
|
< 40 years
|
370
|
97.1
|
1.53 (0.90–2.59)
|
706
|
94.9
|
0.85[*] (0.72–0.99)
|
1,076
|
95.6
|
1.81 (0.92–3.58)
|
≥ 40 years
|
11
|
2.9
|
|
38
|
5.1
|
|
49
|
4.4
|
|
Total
|
381
|
100.0
|
|
744
|
100.0
|
|
1,125
|
100.0
|
|
Number of gestations
|
|
|
|
|
|
|
|
|
|
1
|
166
|
43.1
|
0.79[*] (0.67–0.93)
|
257
|
34.6
|
1.13[*] (1.04–1.24)
|
423
|
37.5
|
0.69[*] (0.54–0.89)
|
≥ 2
|
219
|
56.9
|
|
486
|
65.4
|
|
705
|
62.5
|
|
Total
|
385
|
100.0
|
|
743
|
100.0
|
|
1,128
|
100.0
|
|
< 5
|
346
|
89.9
|
1.37[*] (1.03–1.82)
|
631
|
84.9
|
0.87[*] (0.78–0.97)
|
977
|
86.6
|
1.57[*] (1.07–2.32)
|
≥ 5
|
39
|
10.1
|
|
112
|
15.1
|
|
151
|
13.4
|
|
Total
|
385
|
100.0
|
|
743
|
100.0
|
|
1,128
|
100.0
|
|
Prenatal care
|
|
|
|
|
|
|
|
|
|
No
|
92
|
25.8
|
1.01 (0.83–1.22)
|
181
|
25.6
|
0.99 (0.90–1.10)
|
789
|
74.3
|
1.01 (0.75–1.35)
|
Yes
|
264
|
74.2
|
|
525
|
74.4
|
|
273
|
25.7
|
|
Total
|
356
|
100.0
|
|
706
|
100.0
|
|
1,062
|
100.0
|
|
Appointments
|
|
|
|
|
|
|
|
|
|
< 6
|
310
|
87.1
|
3.05[*] (2.30–4.04)
|
421
|
59.6
|
0.67[*] (0.62–0.72)
|
731
|
68.8
|
4.56[*] (3.23–6.44)
|
≥ 6
|
46
|
12.9
|
|
285
|
40.4
|
|
331
|
31.2
|
|
Total
|
356
|
100.0
|
|
706
|
100.0
|
|
1,062
|
100.0
|
|
Fetal heartrate at admission
|
|
|
|
|
|
|
|
|
|
Absent
|
259
|
67.3
|
0.61[*] (0.52–0.72)
|
612
|
82.2
|
1.37[*] (1.21–1.55)
|
871
|
77.1
|
0.45[*] (0.34–0.59)
|
Present
|
126
|
32.7
|
|
133
|
17.8
|
|
259
|
22.9
|
|
Total
|
385
|
100.0
|
|
745
|
100.0
|
|
1,130
|
100.0
|
|
Place of birth
|
|
|
|
|
|
|
|
|
|
Non-hospital
|
25
|
6.5
|
0.61[*] (0.46–0.80)
|
21
|
2.8
|
1.46[*] (1.07–2.01)
|
46
|
4.0
|
0.42[*] (0.23–0.75)
|
In hospital
|
362
|
93.5
|
|
731
|
97.2
|
|
1,093
|
96.0
|
|
Total
|
387
|
100.0
|
|
752
|
100.0
|
|
1,139
|
100.0
|
|
Onset of labor
|
|
|
|
|
|
|
|
|
|
Spontaneous
|
261
|
67.4
|
1.05 (0.88–1.25)
|
494
|
65.8
|
0.97 (0.89–1.06)
|
755
|
66.3
|
1.08 (0.83–1.40)
|
Induction[**]
|
126
|
32.6
|
|
257
|
34.2
|
|
383
|
33.7
|
|
Total
|
387
|
100.0
|
|
751
|
100.0
|
|
1,138
|
100.0
|
|
Type of birth[#]
|
|
|
|
|
|
|
|
|
|
Normal
|
330
|
91.2
|
1.98[*] (1.43–2.74)
|
587
|
80.3
|
0.78[*](0.72–0.85)
|
917
|
83.9
|
2.53[*] (1.68–3.79)
|
Cesarean
|
32
|
8.8
|
|
144
|
19.7
|
|
176
|
16.1
|
|
Total
|
362
|
100.0
|
|
731
|
100.0
|
|
1,093
|
100.0
|
|
Necropsy
|
|
|
|
|
|
|
|
|
|
Yes
|
362
|
95.5
|
0.77 (0.51–1.17)
|
690
|
93.6
|
1.12 (0.96–1.31)
|
1,052
|
94.2
|
0.69 (0.39–1.22)
|
No
|
17
|
4.5
|
|
47
|
6.4
|
|
64
|
5.8
|
|
Total
|
379
|
100.0
|
|
737
|
100.0
|
|
1,116
|
100.0
|
|
Study of placenta
|
|
|
|
|
|
|
|
|
|
Yes
|
291
|
98.0
|
0.75 (0.38–1.50)
|
514
|
97.0
|
1.14 (0.88–1.48)
|
805
|
97.3
|
0.66 (0.26–1.71)
|
No
|
6
|
2.0
|
|
16
|
3.0
|
|
22
|
2.7
|
|
Total
|
297
|
100.0
|
|
530
|
100.0
|
|
827
|
100.0
|
|
Abbreviations: ISB, immediate stillbirth; LSB, late stillbirth; N, number; OR, odds
ratio; PR, prevalence ratio.
* Significance (95% confidence interval)
# Only in hospital.
** Misoprostol was the option to ripening cervix in 81.7% of cases.
As for the presence of fetal vitality at hospital admission, 77.1% of the cases already
presented fetal death in the initial care, and this possibility was more likely to
occur among the LSB group (OR 0.45, 0.34–0.59). In 96.0% of the cases, the births
have occurred at the hospital, but ISB cases were more likely to occur at home (OR
0.42, 0.23–0.75). The labor was already installed in 66.3% of the general population,
and this distribution was similar in both groups. Among the patients who underwent
induction of labor, vaginal misoprostol was the most commonly used method. Regarding
the type of delivery, cesarean section was performed in 16.1% of the cases, and the
LSB group had a higher chance of this type of delivery (OR 2.53, 1.68–3.79).
Regarding the possibility of research support being complemented by necropsy and/or
placenta study, both the ISB and LSB groups had a similar distribution, with 94.2%
and 97.3%, respectively. When we observe the factors associated with fetal deaths,
[Table 3] shows the main causes according to frequencies. Despite the research methods used,
in 22.1% of the study population, the possible cause of fetal death was not identified.
This distribution was similar for both ISB and LSB groups. In the same table we can
identify the main causes associated with fetal deaths:: infections of the amniotic
sac and membranes (27.9%), fetal malformations (12.5%), placental abruption (11.2%),
hypertensive syndromes (8.5%), and syphilis (3.9%).
Table 3
Frequencies and causal factors attributed to intermediate stillbirth and late stillbirth
(Maternity School of Vila Nova Cachoeirinha 2003-2017)
ATTRIBUTED FACTORS
|
ISB
|
LSB
|
TOTAL
|
|
|
N
|
%
|
PR ISB
|
N
|
%
|
PR LSB
|
N
|
%
|
OR
|
Infections (amniotic sac and membranes)
|
122
|
32.0
|
0.82[*] (0.69–0.98)
|
193
|
25.8
|
1.11 (1.01–1.23)
|
315
|
27.9
|
0.74[*] (0.56–0.97)
|
Indeterminate
|
89
|
23.4
|
0.93 (0.77–1.12)
|
160
|
21.4
|
1.04 (0.94–1,15)
|
249
|
22.1
|
0,89 (0.67–1.20)
|
Fetal malformation
|
44
|
11.5
|
1.09 (0.84–1,42)
|
97
|
13.0
|
0.96 (0.85–1.08)
|
141
|
12.5
|
1.14 (0.78–1.67)
|
Placental abruption
|
30
|
7.9
|
1.47[*] (1.06 - 2.03)
|
96
|
12.9
|
0.85[*] (0.77–0,95)
|
126
|
11.2
|
1.72[*] (1.12–2,65)
|
Hypertensive syndrome
|
47
|
12.3
|
0,66[*] (0,53 - 0.83)
|
49
|
6.6
|
1,32[*] (1,08 - 1.62)
|
96
|
8.5
|
0.49[*] (0.27–0.83)
|
Syphilis
|
9
|
2.4
|
1.68 (0.93–3.02)
|
35
|
4.7
|
0.83[*] (0.71–0.96)
|
44
|
3.9
|
2.03 (0.97–4.27)
|
Umbilical cord changes
|
12
|
3.1
|
1.19 (0.73–1.93)
|
30
|
4.,9
|
0.92 (0.76–1.12)
|
42
|
3.7
|
1.29 (0.65–2.54)
|
Other placentary disorders
|
14
|
3.7
|
0.96 (0.63–1.48)
|
26
|
3.5
|
1.02 (0.81–1,28)
|
40
|
3.5
|
0.94 (0.49–1.83)
|
Fetal-fetal transfusion syndrome
|
6
|
1.6
|
1.42 (0.70–2.86)
|
19
|
2.5
|
0,87 (0.69–1.09)
|
25
|
2.2
|
1.63 (0.65–4.12)
|
Diabetes mellitus
|
1
|
0.3
|
6.51 (0.96–43.94)
|
18
|
2.4
|
0.69[*] (0.62–0.78)
|
19
|
1.7
|
9.38[*](1.25–70.55)
|
Other causes
|
5
|
1.3
|
1.36 (0.63–2.91)
|
15
|
2.0
|
0.88 (0.68–1.14)
|
20
|
1.8
|
1.54 (0.54–4,27)
|
TOTAL
|
381
|
100.0
|
|
747
|
100.0
|
|
1,128
|
100.0
|
|
Abbreviation: ISB, immediate stillbirth; LSB, late stillbirth; N, number; OR, odds
ratio; PR, prevalence ratio.
* Significance (95% confidence interval)
The comparison between the groups showed that the ISB group had higher chances for
infection (OR 0.74, 0.56–0.97) and hypertensive syndromes (OR 0.49, 0.27–0.83). On
the other hand, the LSB group had higher chances for placental abruption (1.72, 1.12–2.65)
and diabetes mellitus (9.38; 1.25–70.55). Regarding syphilis, we found a similar distribution
in the groups; however, with a higher prevalence ratio among the LSB patients (0.83;
0.71–0.96).
Trends concerning the five main causes associated with SB, related to the period of
the present study, show some stability, despite of alternations over time (Fig. 2),
except for amniotic sac and membranes infections, which shows a decresing trend when
comparing the initial evaluation from the first years of the study to the evaluation
of the last years. The most important aspect to highlight is the increase in maternal
syphilis from the year 2013 on, remaining at an outstanding level compared with the
previous years (Fig. 2).
Discussion
According to the Ministry of Health of Brazil, SB remains an important public health
problem, with stagnant numbers. From 1996 to 2006, the GSBC remained above 10.0%,
with regional disparities and worse results in the North and Northeast regions.[7]
Data available in the Tabnet system of the Municipal Health Department of the city
of São Paulo shows that, between 2010 and 2016, the total number of fetal deaths in
the Northern region of São Paulo is still stable, with around 250 SBs every year.
It is important to mention that HMEC attends 25.8% of all cases in the region.[9]
[10] The set of information provided in this study may be useful for understanding the
key factors associated with fetal deaths occurring in this region and supporting strategic
measures to reduce their impact on public health.
Maternal age is a single factor associated with adverse pregnancy outcomes, including
intrauterine growth restriction (IUGR), preeclampsia, and placental abruption.[11]
[12] A study performed in the Northeast region of Brazil showed that advanced maternal
age persists as an independent factor related to SB.[13]
In the present study, the total number of cases occurred in women of the age group
considered adequate for gestation. Although the extremes of age may be a risk factor,
the attributable contribution of this population to SB is relatively small. However,
the age group under 16 years old presented a higher ISB than LSB rate, suggesting
an earlier exposure to risk factors. At the other extreme age group, we observed that
pregnant women older than 40 years were more likely to develop LSB, a fact that is
possibly associated with a greater range of exposure to factors associated with fetal
death, such as maternal diseases and fetal malformations.Therefore, family planning
programs could add this message for both age groups.
The number of pregnancies seems to be a risk factor associated with SB, as documented
in a multinational study that identified higher risks related to both the first pregnancy
and to pregnant women with more than five previous deliveries.[14]
Our population follows the same pattern, but first pregnancy showed a higher ISB rate,
while patients with five or more pregnancies are associated to higher LSB risk. Despite
these findings, the association of maternal parity and the risk of fetal death should
be interpreted with caution, considering that confounding factors may limit this conclusion.[4]
[14] It should be added that the higher the number of pregnancies, the greater the chance
of exposure, following the same logic applied to maternal age.
Regarding prenatal care, the literature is unanimous in considering the qualification
of this follow-up of pregnancy as essential for the reduction of maternal and perinatal
risks in order to achieve good results. According to the Brazilian Program for Humanization
of Prenatal and Childbirth, and to the World Health Organization, the occurrence of
SBs is higher among women whose prenatal care was considered inadequate.[15]
[16]
This statement is confirmed by one study conducted in the Southern region of Brazil,
where inadequate prenatal was associated with the occurrence of SB.[17] In the present study, we found that among the total number of cases, 25.7% did not
attend any prenatal visits. This expressive rate reveals that many opportunities for
intervention probably were lost in order to reduce the risk of fetal death. This concerning
situation was similar in both groups.
Regarding the number of prenatal care visits, it seems reasonable that the ISB group
would have fewer consultations, since fetal death occurred in the earlier stages of
pregnancy. However, even in the LSB group, 68.8% of the cases had less than 6 visits.
Perhaps, the same logic applies in this case, and it is reasonable to assume that
the number of visits, per se, does not seem to be associated with the occurrence of
SB cases but rather their initial qualification. This aspect deserves special attention
because the notes in the prenatal cards are essential for identifying possible factors
related to SB. Therefore, strategic actions directed to ensure accessibility to medical
care as soon as possible, their initial qualification. In addition, in many cases,
the quality of the information available in the prenatal records presented at the
time of hospitalization does not help to elucidate the causes of SB.
Although it is possible to understand that the risk of SB is reduced by means of qualified
care actions, it should be considered that identifying the moment of the fetal death
is a very difficult task. Biological determinisms are complex and, often, not identified
in a timely manner. In addition, SB may be the result of different etiologies and
not of a single disorder, and it is unlikely that any individual test will be able
to predict fetal death and identify all causes.[18] In any case, the SB among hospitalized patients is important to identify possible
assistance failures in situations that can be prevented.
We identified that, in the total population, fetal heartbeats were absent at the time
of hospital admission in 77.1% of the cases. When comparing the groups, we found out
that the ISB group had higher chances of fetal death occurring during hospitalization.
We believe that this fact may be associated with institutional characteristics, since
HMEC is a reference center to high-risk pregnancies, where several patients remain
under institutional care until reaching viable gestational age. Although this phenomenon
may occur, it did not significantly affect the evolution of IHSR (in-hospital stillbirth
rate) throughout our historical series ([Graphic 1]).
Regarding delivery care, in 96.0% of all cases, births have occurred in the hospital
environment, and, among them, 66.3% of the cases were admitted in spontaneous labor.
Cases requiring cervix ripening received intravaginal misoprostol or endocervix Foley
catheter, but misoprostol was the more common method used in 81.7% of the cases.
However, a notable fact is that non-hospital births occurred in 4.0% of the population,
and the ISB group had greater chances of this type of occurrence. The dramaticity
of these situations must be emphasized considering the additional exposure of these
women to the risks of severe bleeding and infection. These occurrences were more frequent
among the ISB group, but we did not identify a related factor other than the possibility
of a smaller fetal volume facilitating their expulsion.
For the care of pregnant women with SB, the indication of cesarean section only makes
sense when maternal risks outweigh the benefits, such as instability imposed by placental
abruption or risks of uterine rupture.[14]
When evaluating the overall cesarean section rates, it is verified that this occurred
in 15.4% of the cases, which allows us to state that they are within the guidelines
of care. It is necessary to consider that the main cases of cesarean section were
placental abruption, and patients with scars, in whose case the risks of uterine rupture
were not negligible. The characteristics of labor assistance verified in our series
can provide two topics for obstetric practice: the first is a strong recommendation
that vaginal birth is the preferential option for these situations, considering maternal
risks. The second refers to the use of misoprostol in adequate doses, and the respect
to the time necessary for the onset of labor.[19]
The task of investigating and identifying factors associated with SB remains as an
important point to understand this dramatic outcome and to provide alternatives for
prevention and counseling.[20] Even with several alternatives available for research, many causes remain unknown.[21] In this scenario, the anatomopathological evaluation of the fetus and placenta may
be valuable in elucidating the case. This practice is still not widely adopted and
is identified by some authors in only 30.0 to 35.0% of occurrences.[17]
[20]
In our study, both placenta and fetal studies were performed in expressive percentage
([Table 2]) and assisted in the definition of the associated cause. Nevertheless, 22.1% of
the cases remained as unidentified etiology, with this aspect being similar between
the groups. Not having the answer that clarifies a SB is a frustrating experience
for the family and the medical staff. Thus, the entire diagnostic arsenal (clinical,
imaging, laboratory and pathological anatomy) should be used to elucidate the cause
of fetal death.[22] However, in many cases, severe fetal maceration limits a more detailed study of
the corpse.
During the study period, there were many factors associated with SB, with some alternations
occurring during the years of study (Fig. 2). Amniotic sac and membranes infections
had an expressive participation in our sample and was often identified only by the
placenta study, in which we can identify chorioamnionitis, frequently associated with
funisitis.
Infections can cause SB through several mechanisms, including direct fetal infection,
placental injury, and severe maternal illness. Many bacteria, viruses and protozoa
have been associated with SBs. In developed countries, up to 24.0% of the cases of
SB were attributed to some infection. Thus, screening of maternal infectious processes
at sites such as the urinary tract, teeth, and vagina would possibly reduce their
impact on the causes of SB. However, to implement these actions is not an easy task
in our health system. Regarding fetal anomalies, all conditions were grouped. This
group of reasons was associated in 12.5% of the general population, with a similar
distribution between ISB and LSB ([Table 3]). Differently from our results, a study in Southern Brazil that reviewed autopsy
records of all SBs (n = 111) in one hospital reported that 26.0% of SBs were caused by congenital anomalies.
Although studies that evaluate risks indicate that fetal anormalities have strong
association with SB, frequencies are very diverse in the literature, ranging from
2.1 to 33.3%. Such differences are most likely related to the various clinical profiles
of the institutions where the cases are studied. Centers with a high concentration
of this type of problem may have relevant rates in their indicators, but this cannot
be transferred to the general population.[4]
[23]
[24]
[25]
[26]
[27]
[28]
Placental abruption is recognized as one of the main causes of fetal death, with a
percentage attribution between 7.5 and 42.0%.[4] Moreover, it is worth mentioning that this condition imposes a higher maternal risk,
given its emergency character, with a quick hemodynamic failure of the woman. Besides,
there is a very frequent need for cesarean delivery due to the uncertainty of fetal
vitality, adding more risks to the care of these patients. The higher chances of this
serious obstetric condition were associated with LSB cases. In view of the dramatic
condition of placental abruption and uterine hypertonia, evaluation of fetal conditions
is a very difficult task. Therefore, it is understandable that in this singular situation,
the rate of cesarean section is higher in view of the uncertainty of fetal death.
This is why cesarean birth is the best option when facing such dramatic situations.
The risk of fetal death increases in hypertensive patients, with chronic hypertension
and preeclampsia being included in this category, due to varying degrees of placental
insufficiency and IUGR in addition to acute events, such as placental abruption.[23]
On a global scale, it is estimated that 2.6 million SBs occur annually around the
world and ∼ 16.0% of them occur in pregnancies complicated by gestational hypertension.[24] In the present study, 8.5% of the SB cases had hypertensive syndrome as their main
cause. It is added that placental abruption, often associated with patients with hypertensive
disorders, was also an important cause during the study period ([Table 3]).
The highest chances of this association were identified among cases of ISB. Possibly,
this fact could be explained by the presence of patients in the high-risk unit in
the very early stages of gestation, when the expectant management is adopted to improve
the prognosis of the newborn in view of extreme prematurity.
Considering that when it comes to hypertension, maternal and perinatal outcomes are
directly related to the quality of prenatal care, it would be important to adopt prevention
and early detection actions. This would have a positive impact on the reduction of
severe cases and on early identification of placental insufficiency, thus allowing
more timely actions.
A very concerning condition was the identification of syphilis as responsible for
3.9% of SBs in our population, with a more significant prevalence among the LSB group.
In addition, we noticed an increasing trend in its prevalence since 2013 (Fig. 2).
It is estimated that, each year, between 1 and 2 million pregnancies are affected
by syphilis in the world. Among the adverse perinatal outcomes in infected pregnant
women, we highlight fetal death, which may occur in 30.0 to 40.0% of the cases. A
study related to syphilis, conducted in the Americas, has shown that positive sorology
has a 6.8-fold higher chance of SB compared with healthy women.[29]
From 2005 to June 2017, 200,253 cases of syphilis were reported in pregnant women
in Brazil, 44.2% of whom were residents of the Southeast region.[30] The increase in the number of cases recorded in our study probably runs parallel
with the syphilis epidemic detected by the national health authorities.
This constant increase in cases of syphilis in pregnant women may be related to several
factors, such as greater coverage of testing, reduction of condom use, resistance
of health professionals to the administration of penicillin in primary care, and shortages
of penicillin.[30]
Preventing SB attributable to syphilis should be easier in contexts of high prevalence,
considering that the diagnosis and treatment of the disease during pregnancy occurred
effectively.[29] Unfortunately, this does not seem to be happening.
Regarding the set of factors associated with SB, when evaluating the behavior of the
frequencies over the period studied, we found that five factors concentrated the majority
of the cases. [Graphic 2] illustrates that, over the years, amniotic sac and membranes infections defined
as chorioamnionitis have tended to decline: in 2003, they accounted for 36.9% of the
cases, and, in 2017, this portion reached 25.0%. We considered it a complex task to
identify the reasons for this behavior, considering that we did not detect global
assistance actions that could reduce the risks of maternal infection and its consequences.
Graphic 2 Frequency of the main factors related to fetal deaths and trends. Maternity School
of Vila Nova Cachoeirinha 2003–2017. (Maternity School of Vila Nova Cachoeirinha 2003-2017)
Despite the persistence of the investigation criteria, indeterminate causes accounted
for 22.1% of the cases, revealing difficulties in refining the research. Even with
the resources currently available, we are far from a more advanced level of research
that may include cytogenetic studies, fetal tissue cultures, including viral research,
screening for hereditary deficiencies, evaluation of fetal and/or placental hemorrhage,
dosage of heavy metals and environmental pollutants, among others.
A standardized universal definition of SBs and their causes is a key issue, so that
the methodological quality of SB research is improved. In addition, adopting international
standardization for the classification of fetal deaths could facilitate comparisons
between different regions and guide actions to reduce this phenomenon.[22] More studies about SBs should be further explored by official statistics in view
of their undoubted importance in terms of public health and valuable sentinel event
of prenatal care quality. Limitations related to more diagnostic methodologies justify
the maintenance of expressive rates of undiagnosed fetal deaths.