| Literature DB >> 34552149 |
Dana Anaïs Muin1, Anke Scharrer2, Alex Farr3, Herbert Kiss3, Helmuth Haslacher4.
Abstract
The effect of timing of hospital admission for stillbirth delivery following late intrauterine fetal death (IUFD) has not yet been described. By this study, we aimed to gain an understanding of the impact of "immediate" (i.e., on the same day of IUFD diagnosis) versus "delayed" hospital admission (i.e., on the subsequent day or two days after IUFD diagnosis) on maternal and delivery outcome parameters. This retrospective cohort study comprised all women who suffered a singleton IUFD ≥ 21 gestational weeks and delivered the stillborn at our tertiary referral center between 2003 and 2019. We excluded all terminations of pregnancy and women presenting with acute symptoms on the day of IUFD diagnosis. In total, 183 women were included of whom 69.4% (n = 127) were immediately admitted and 30.6% (n = 56) had delayed admission. Median gestational age of IUFD was 30+3 (21+0-41+3) weeks. Whilst women with early signs of labor were more frequently admitted immediately (87.5%; 14/16), neither maternal demographic and obstetric parameters, nor day of the week or presenting symptoms influenced the timing of hospital admission. 77.6% (142/183) of women after IUFD diagnosis delivered within the first 3 days after admission. Women after immediate admission equally often delivered on admission day and the day after (26.0%; 33/127 each), women after delayed admission most commonly delivered the day after admission (39.3%; 22/56). Stillbirth delivery on the day of diagnosis was more common upon immediate admission (p = 0.006), especially in early gestational weeks (p = 0.003) and with small fetal weight (p < 0.001), requiring less induction of labor. No significant difference regarding delivery mode, labor duration, use of intrapartum analgesia, need for episiotomy and risk of perineal injury was observed between the groups. Also rate of intrapartum hemorrhage was independent of admission timing, although immediately admitted women experienced greater median blood loss after vaginal delivery. Maternal laboratory parameters (hemoglobin, thrombocytes and CRP) were independent of admission timing, except for higher levels of leucocytes, neutrophils and lymphocytes in immediately admitted women. Our study shows no clinical superiority of immediate hospital admission for stillbirth delivery. Under stable medical circumstances, it, therefore, seems feasible to allow the woman delayed admission for labor and delivery.Entities:
Mesh:
Year: 2021 PMID: 34552149 PMCID: PMC8458494 DOI: 10.1038/s41598-021-98229-9
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
Figure 1Flowchart on the selection of the study population following fetal death at the Department of Obstetrics and Gynecology, Medical University of Vienna, Austria, between 2003 and 2019.
Study sample characteristics (n = 183) after hospital admission for stillbirth delivery at the Department of Obstetrics and Gynecology, Medical University of Vienna between 2003 and 2019.
| Maternal characteristics | n | % | |
|---|---|---|---|
| Age at stillbirth (years)a | 31 ± 7 | ||
| Ethnicity | Middle European | 86 | 47 |
| Eastern European | 48 | 26.2 | |
| Turkish | 26 | 14.2 | |
| Middle Eastern | 10 | 5.5 | |
| African | 7 | 3.8 | |
| South Asian, Indian | 3 | 1.6 | |
| American | 2 | 1.1 | |
| Chinese | 1 | 0.5 | |
| Gravida ( | 2 (1–12) | ||
| Para ( | 1 (0–9) | ||
| Body mass index (kg/m2)b | 24.5 (14.6–43.3) | ||
| BMI categories | Underweight | 4 | 2.9 |
| Normal | 71 | 51.1 | |
| Pre-obese | 44 | 31.7 | |
| Obesity class I | 9 | 6.5 | |
| Obesity class II | 8 | 5.8 | |
| Obesity class III | 3 | 2.2 | |
| Nicotine consumption | 36 | 23.5 | |
| Hypertensive disorders in pregnancy | Pre-existing hypertension | 12 | 6.6 |
| Pre-eclampsia | 14 | 7.7 | |
| Pregnancy induced hypertension | 7 | 3.8 | |
| HELLP | 4 | 2.2 | |
| Diabetes | Insulin-dependent gestational diabetes | 17 | 9.3 |
| Pre-existing diabetes | 4 | 2.2 | |
| Gestational diabetes (diet only) | 3 | 1.6 | |
| Co-morbidities | Other medical | 35 | 19.1 |
| Hemostatic | 15 | 8.2 | |
| Auto-immune disorder | 11 | 6 | |
| Antiphospholipid Syndrome | 6 | 3.3 | |
| Gynecological | 5 | 2.7 | |
| Cardiac | 3 | 1.6 | |
| Neurological | 2 | 1.1 | |
| Mental | 2 | 1.1 | |
| Respiratory | 0 | 0 | |
| Total number of co-morbidities ( | 0 | 105 | 57.4 |
| 1 | 61 | 33.3 | |
| 2 | 13 | 7.1 | |
| 3 | 2 | 1.1 | |
| 4 | 2 | 1.1 | |
| Social restriction/domestic violence | 5 | 2.7 | |
BMI body mass index, HELLP hemolysis, elevated liver enzymes, low platelets.
aMean ± standard deviation.
bMedian (minimum – maximum).
Comparison of fetomaternal characteristics and obstetric variables after stillbirth delivery between immediate and delayed admission groups.
| Total (n = 183) | Immediate admission (n = 127) | Delayed admission (n = 56) | ||||
|---|---|---|---|---|---|---|
| Maternal | Maternal age (years)a | 31 ± 7 | 31 ± 6 | 32 ± 7 | 0.094d | |
| Body mass index (kg/m2)b | 24.5 (15.6–43.3) | 25.1 (15.6–43.3) | 24.2 (18.6–37.6) | 0.669e | ||
| Para ( | 1 (0–9) | 0 (0–9) | 1 (0–9) | 0.529e | ||
| Previous LSCS ( | None | 144 (78.7%) | 99 (78.0%) | 45 (80.4%) | 0.847f | |
| 1 | 30 (16.4%) | 21 (16.5%) | 9 (16.1%) | |||
| 2 | 9 (4.9%) | 7 (5.5%) | 2 (3.6%) | |||
| Presenting symptoms | None | 103 (56.6%) | 71 (56.3%) | 32 (57.1%) | 0.473f | |
| Fetal | 51 (28.0%) | 31 (24.6%) | 20 (35.7%) | |||
| Maternal | 12 (6.6%) | 10 (7.9%) | 2 (3.6%) | |||
| Labor | 16 (8.8%) | 14 (11.1%) | 2 (3.6%) | |||
| Not reported | 0 (0.0%) | 1 (0.1%) | 0 (0.0%) | |||
| Fetal | Gestational age (days)b | 213 (147–290) | 209 (147–290) | 221 (152–288) | 0.331e | |
| Maceration grade | 0 | 17 (11.6%) | 16 (15.1%) | 1 (2.5%) | < 0.001f | |
| I | 20 (13.7%) | 17 (16.0%) | 3 (7.5%) | |||
| II | 43 (29.5%) | 34 (32.1%) | 9 (22.5%) | |||
| III | 66 (45.2%) | 39 (36.8%) | 27 (67.5%) | |||
| Obstetrics | Delivery modec | Vaginal cephalic | 110 (60.1%) | 78 (61.4%) | 32 (57.1%) | 0.465f |
| Vaginal breech | 53 (29.0%) | 35 (27.6%) | 18 (32.1%) | |||
| Ventouse | 3 (1.6%) | 1 (0.8%) | 2 (3.6%) | |||
| LSCS | 17 (9.3%) | 13 (10.3%) | 4 (7.1%) | |||
| Robson classification of LSCS | 10C | 8 (47.1%) | 7 (53.8%) | 1 (25%) | 0.130f | |
| 10B | 2 (11.8%) | 2 (15.4%) | 0 (0.0%) | |||
| 5C | 2 (11.8%) | 2 (15.4%) | 0 (0.0%) | |||
| 6C | 2 (11.8%) | 1 (7.7%) | 1 (25.0%) | |||
| 4B | 1 (5.9%) | 0 (0.0%) | 1 (25.0%) | |||
| 6B | 1 (5.9%) | 1 (7.7%) | 0 (0.0%) | |||
| 7C | 1 (5.9%) | 0 (0.0%) | 1 (25.0%) | |||
| Time length of vaginal delivery (h)b | 3 (0–28) | 3 (0–28) | 4 (0–26) | 0.231e | ||
| 2nd stage of labor (min)b | 10 (0–376) | 10 (0–289) | 18 (0–376) | 0.197e | ||
| 3rd stage of labor (min)b | 10 (0–90) | 10 (0–78) | 10 (0–90) | 0.323e | ||
| Blood loss (ml)b | 200 (30–2500) | 200 (30–2500) | 150 (50–1000) | 0.064e | ||
| Anesthesiac | None | 100 (54.6%) | 63 (49.6%) | 37 (66.1%) | 0.089f | |
| Peridural | 36 (19.7%) | 26 (20.5%) | 10 (17.9%) | |||
| Epidural | 21 (11.5%) | 19 (20.5%) | 2 (3.6%) | |||
| Spinal | 14 (7.7%) | 10 (7.9%) | 4 (7.1%) | |||
| Intubation | 11 (6.0%) | 9 (7.1%) | 2 (3.6%) | |||
| Local | 1 (0.5%) | 0 (0.0%) | 1 (1.8%) | |||
| Episiotomyc | None | 181 (98.9%) | 126 (99.2%) | 55 (98.2%) | 0.549f | |
| Mediolateral | 2 (1.1%) | 1 (0.8%) | 1 (1.8%) | |||
| Perineal injuryc | None | 154 (84.2%) | 107 (84.3%) | 47 (83.9%) | 0.358f | |
| Vaginal tear | 9 (4.9%) | 8 (6.3%) | 1 (1.8%) | |||
| 1st degree tear | 7 (3.8%) | 5 (3.9%) | 2 (3.6%) | |||
| Labial tear | 6 (3.3%) | 2 (1.6%) | 4 (7.1%) | |||
| 2nd degree tear | 4 (2.2%) | 3 (2.4%) | 1 (1.8%) | |||
| Cervical tear | 3 (1.6%) | 2 (1.6%) | 1 (1.8%) | |||
LSCS lower segment caesarean section.
aMean ± Standard deviation.
bMedian (minimum − maximum).
cFrequency (proportion).
dUnpaired t-test with level of significance < 0.05.
eMann–Whitney U test with level of significance < 0.05.
fFishers’s exact test with level of significance < 0.05.
Robson classification: 10C: All singleton cephalic, ≤ 36 weeks (including previous LSCS): LSCS before labor; 10B: All singleton cephalic, ≤ 36 weeks (including previous LSCS): induced labor; 5C: Previous LSCS, singleton cephalic, ≥ 37 weeks: LSCS before labor; 6C: All nulliparous breeches: LSCS before labor; 4B: Multipara, singleton cephalic, ≥ 37 weeks: induced labor; 6B: All nulliparous breeches: induced labor; 7C: All multiparous breeches (including previous LSCS): LSCS before labor.
Figure 2Forest plot illustrating the odds ratios (and 95% Confidence Intervals) from multivariate logistic regression to identify the relationship between timing of hospital admission and possible predictors (i.e., weekday, parity, presenting symptom at diagnosis) following intrauterine fetal death (n = 183; level of significance p < 0.05, two-tailed). IUFD intrauterine fetal death, OR odds ratio, CI confidence interval. Figure software: Prism 9 for macOS, Version 9.2.0.
Figure 3Time to stillbirth delivery after immediate (n = 127) and delayed (n = 56) hospital admission (nested scatter dot plot; width of distribution of points proportional to the number of delivered women; Day 0 = hospital admission day). Stillbirth delivery occurred in 20.8% (38/183) on Day 0; in 30.1% (55/183) on Day 1, and in 20.2% (37/183) on Day 3. Figure software: Prism 9 for macOS, Version 9.2.0.
Figure 4Presenting symptoms on day of IUFD diagnosis in women who delivered on the same day of hospitalization (n = 33 immediate admission; n = 5 delayed admission). Figure software: Prism 9 for macOS, Version 9.2.0.
Figure 5Methods of induction of labor following fetal death at the Department of Obstetrics and Gynecology, Medical University of Vienna, Austria, between 2003 and 2019 (“Dinoprostone only” includes Propess, Prostin E2; “Misoprostol only” includes Cytotec, Misodel, Cyprostol). Figure software: Prism 9 for macOS, Version 9.2.0.
Figure 6Comparison of maternal laboratory values between immediate versus delayed admission (n = 166, excluding all women who delivered by caesarean section; Scatter dot plot with line at median; Mann–Whitney U test; two-tailed Exact p-value with 99% confidence interval). Figure software: Prism 9 for macOS, Version 9.2.0.