Abstract
Purpose
To evaluate the burden of illness caused by hyperemesis gravidarum (HG) and association of readmissions due to HG with maternal, environmental and pregnancy-related factors, and different pregnancy outcomes.
Methods
Data of women with HG diagnosis in Finland, 2005–2017, were retrieved from health-care registers. Associations between readmissions due to HG and age, gravidity, parity, pre-pregnancy body mass index (BMI), smoking, marital status, socioeconomic status, municipality population, assisted reproductive technology (ART), and number and sex of fetuses were analyzed in pregnancies resulting in delivery. Admissions and readmissions due to HG in deliveries, gestational trophoblastic disease, ectopic pregnancies, miscarriages and pregnancy terminations were calculated.
Results
10,381 pregnancies with HG diagnosis were identified: 9518 live births, 31 stillbirths, 8 cases of gestational trophoblastic disease, 16 ectopic pregnancies, 299 miscarriages, and 509 pregnancy terminations. Both outpatients and inpatients were included. Readmission occurred in 60% of pregnancies, inpatient readmission in 17%. Parity of ≥ 5, multiple gestation and female sex of fetus were associated with higher odds of readmission, maternal age 36–40 years, BMI ≥ 35 kg/m2, smoking and ART with lower odds of readmission. Of the 9549 pregnancies resulting in delivery, 33% involved at least one outpatient visit or inpatient episode after the first trimester, and 8% in the third trimester.
Conclusion
The majority of women suffering from HG needed repeated medical care, often persisting after the first trimester. Our results provide practical information allowing clinicians to prepare for symptom duration beyond the first trimester and emphasize the importance of planning for eventual long-term treatment.
Keywords: Hyperemesis gravidarum, Pregnancy, Miscarriage, Pregnancy termination, Ectopic pregnancy, Gestational trophoblastic disease
Introduction
Hyperemesis gravidarum (HG) is the most common cause of hospitalization in the first trimester of pregnancy in pregnancies resulting in delivery [1], and sometimes continues even until birth [2–4]. Universally accepted definition of HG remains to be formulated, and an international collaborative group is working on a consensus definition. The first version was presented in the International Colloquium on Hyperemesis Gravidarum in 2019 and contained the following criteria: pregnant woman; other causes of nausea and vomiting were excluded; beginning of symptoms in early pregnancy; symptoms: nausea and vomiting (at least one of these severe); inability to eat/drink normally; strong effect on daily activity; signs of dehydration. Register studies, the present included, rely on clinical diagnoses as defined in the health-care system, which may differ according to local practices. Commonly cited definitions of HG include symptoms of nausea and vomiting, weight loss and dehydration [5–7]. In Finland, HG is diagnosed according to the ICD-10 classification of diseases, which titles the HG-related O21 diagnoses as “excessive vomiting in pregnancy” [8, 9]. HG is a relatively rare condition, estimated to occur in 0.3–3.6% of pregnancies [10, 11]. In Finland, HG hospitalization rate of 0.7% [12] and overall incidence of 1.3% have been reported [11]. Readmission rates from 13 to 34% have been observed [4, 7, 13–15], and average length of hospitalization has been reported to be 2–5 days [1, 7, 13, 16, 17]. Curative treatment for HG has not been discovered, and current treatment strategies aim at relieving symptoms and alleviating complications of HG, such as dehydration and malnutrition [18–20]. There are currently no official guidelines for diagnosis or treatment of HG in Finland, but hospitalization criteria and protocols regarding antiemetic medication, as well as hydration and nutrition have recently been described [21]. As women suffering from HG are keenly looking forward to their symptoms resolving, they would welcome a realistic estimation of how long the need of medical care is likely to continue. However, knowledge about symptom duration and risk factors for readmission due to HG is sparse. Young maternal age, low socioeconomic status, Asian or Black ethnicity, female fetus and multiple pregnancy have been found to be associated with higher risk of readmission [4]. In some studies, nulliparous women had higher readmission risk [4, 22], but in others, neither age nor parity were associated with readmission risk [7, 13]. In one study, rehospitalization risk increased if the first hospitalization occurred before 9 weeks’ gestation, was longer than 2 days, and if the woman had had a previous HG pregnancy [23].
Data about pregnancies not resulting in live birth in association with HG are limited as well. In one study, stillbirth was more common among HG patients [17], but in another, no association was found [24], and in one large study, women with HG had lower risk of stillbirth [25]. Symptoms of HG occur in gestational trophoblastic disease [26–28], whereas in ectopic pregnancy they are not typical [29, 30]. Nausea and vomiting appear to be associated with lower risk of miscarriage [31–34]. In some cases, HG has led to pregnancy termination [15, 35].
Our objectives were to estimate the number and duration of admissions and readmissions due to HG, to assess factors associated with readmissions, and to evaluate the associations between pregnancy outcomes and readmissions. These objectives all aimed at helping physicians to advise and treat HG patients concerning the course of HG symptoms and to understand the burden of illness due to HG in medical care.
Materials and methods
STROBE guidelines [36] were followed in research and reporting of this study. The study plan was evaluated and approved by the Ethical committee of Hospital District of Southwest Finland (43/180/2011). Our data sources were the Hospital Discharge Register, the Medical Birth Register and the Register of Induced Abortions, used with permission of the Finnish Institute for Health and Welfare (THL/658/5.05.00/2012; THL/372/5.05.00/2018) as in our earlier study [11]. Data linkage between registers was performed using each woman’s unique personal identity code which is given to all citizens and permanent residents at birth or immigration and included in all Finnish health-care registers.
All pregnancies (N = 10,381) with an HG discharge diagnosis (ICD-10 diagnosis codes used in Finland for clinical diagnosing of HG during the study period: O21, O21.0, O21.1, O21.2, O21.8 and O21.9) [8, 9] in the Hospital Discharge Register between years 2005 and 2017 were included in the study, regardless of the outcome. Both outpatient visits and inpatient episodes were included. The outcomes were determined by combining the HG diagnosis data with other register data: information about live births and stillbirths was drawn from the Medical Birth Register, pregnancy termination data from the Register of Induced Abortions, and diagnoses related to gestational trophoblastic disease, ectopic pregnancy and miscarriage were retrieved from the Hospital Discharge Register. Five pregnancies with another cause of vomiting than HG (four cases of gallstones and one case of pancreatitis) were excluded (Fig. 1).
Fig. 1.
Flowchart of the study
The numbers of outpatient visits and inpatient episodes due to HG were calculated per 10,000 woman-years. Duration of inpatient episodes was calculated as days. An overnight inpatient episode was calculated as 2 days. The numbers of outpatient and inpatient episodes, and the total number of days spent in a hospital, were calculated per pregnancy. To account for the duration of pregnancy, the number of admissions were calculated per total number of pregnancy weeks in those pregnancies for which the information was available, i.e., pregnancies resulting in delivery and pregnancy terminations, as gestational week is not recorded in the Hospital Discharge Register in miscarriages, and duration of the condition in gestational trophoblastic disease or ectopic pregnancy is not recorded. Trimester-specific numbers of outpatient visits and inpatient episodes were calculated in pregnancies resulting in delivery and pregnancy terminations. Readmission rates in stillbirths, gestational trophoblastic disease, ectopic pregnancies, miscarriages and pregnancy terminations were compared to the readmission rate in live births.
In pregnancies for which the data were available, i.e., pregnancies resulting in delivery, the associations between readmissions and maternal, environmental and pregnancy-related factors were evaluated: maternal age in years (≤ 20; 21–25; 26–30; 31–35; 36–40 and ≥ 41), gravidity (number of pregnancies, including the present), parity (number of deliveries, including the present), pre-pregnancy body mass index (BMI) (< 18.5 kg/m2; 18.5–24.9 kg/m2; 25–29.9 kg/m2; 30–34.9 kg/m2 and ≥ 35 kg/m2), smoking (no; yes, but quit during the first trimester; yes, continued smoking after the first trimester), marital status (living/not living with partner), socioeconomic status based on standard classification of maternal occupation by Statistics Finland (upper-level white-collar workers, e.g., specialists and management level; lower-level white-collar workers, e.g., office staff; blue-collar workers, e.g., manual laborers; at home; other), municipality population (< 10,000 inhabitants; 10,000–99,999 inhabitants; ≥ 100,000 inhabitants), assisted reproductive technology (ART) (no/yes), number of fetuses (one; two or more) and sex of fetuses in singleton pregnancies (one male; one female) and multiple pregnancies (all male; all female; both sexes). Pregnancies involving only one outpatient visit or inpatient episode (no readmission) were compared to pregnancies involving more than one outpatient visit or inpatient episode (Table 1).
Table 1.
Readmissions due to hyperemesis gravidarum according to pregnancy outcomes
| Outcome | HG pregnancies, total | HG pregnancies, readmissiona | Readmission rate, % | OR (95% CI) Compared to live birth |
|---|---|---|---|---|
| Live birth | 9518 | 5803 | 61 | Ref |
| Stillbirthb | 31 | 19 | 61 | 1.02 (0.50–2.09) |
| Gestational trophoblastic disease | 8 | 3 | 38 | 0.45 (0.13–1.60) |
| Ectopic pregnancy | 16 | 4 | 25 | 0.21 (0.07–0.64) |
| Spontaneous abortion | 299 | 121 | 40 | 0.44 (0.34–0.55) |
| Pregnancy termination | 509 | 230 | 45 | 0.51 (0.43–0.61) |
| Total | 10,381 | 6180 | 60 |
HG hyperemesis gravidarum, OR odds ratio, CI confidence interval, Ref reference
aReadmission: more than one outpatient visit or hospitalization due to hyperemesis gravidarum during one pregnancy. The effect of duration of pregnancy in those pregnancies for which the information was available, i.e., pregnancies resulting in delivery and pregnancy terminations, is presented in Fig. 5
bStillbirth: includes pregnancies with at least one stillborn fetus: 26 singleton stillbirths, four pregnancies with one live and one stillborn fetus, and one pregnancy with two live and one stillborn fetus
The associations of maternal, environmental and pregnancy-related factors in pregnancies resulting in delivery with readmission were analyzed using univariable and multivariable binary logistic regression: factors with a p value < 0.10 in the univariable analysis were included in the multivariable model. Socioeconomic status was excluded from the multivariable model due to large amount of missing data. Otherwise, missing data were rare and not imputed. Pregnancy outcome comparisons were analyzed with binary logistic regression. Generalized estimating equations were used to account for the repeated pregnancies of the women. Results are presented using odds ratios (OR) with 95% confidence intervals (CI). The change in the number of outpatient visits/10,000 woman-years and inpatient episodes/10,000 woman-years during the study period was tested using Poisson regression. Statistical analysis was performed with SAS System for Windows, version 9.4 (SAS Institute Inc., Cary, NC).
Results
During the study period, there were altogether 16,853 outpatient visits (on average 1296 outpatient visits/year, equaling 4.7 outpatient visits/year/10,000 woman-years) and 9101 inpatient episodes (on average 700 inpatient episodes/year, equaling 2.6 inpatient episodes/10,000 woman-years) due to HG (Fig. 2). Altogether, 10,381 pregnancies involved at least one outpatient visit or inpatient episode. Of them, 9549 pregnancies resulted in delivery (9518 live births and 31 stillbirths). In pregnancies resulting in delivery in Finland, the incidence of HG was 1.3% and the recurrence rate of HG was 22%, as previously reported [11]. Of pregnancies diagnosed with HG, 832 did not result in delivery, and of these, 8 cases were gestational trophoblastic disease, 16 ectopic pregnancies, 299 miscarriages, and 509 pregnancy terminations.
Fig. 2.
Outpatient visits and inpatient episodes due to hyperemesis gravidarum in Finland, 2005–2017
Out of the 10,381 pregnancies diagnosed with HG, there were more than one outpatient visit and/or inpatient episode in 6180 pregnancies (60%). Inpatient readmission occurred in 1728 pregnancies (17%). Readmissions were most common in pregnancies resulting in live birth (61%) or stillbirth (61%) and lowest in ectopic pregnancies (25%) (Table 1).
Frequencies of outpatient care and inpatient episodes are presented in Fig. 2. An increase in outpatient visits and decrease in inpatient episodes were observed: from 2005 to 2017, the number of outpatient visits increased from 3.9/10,000 woman-years to 5.7/10,000 woman-years (p < 0.0001), whereas the number of inpatient episodes decreased from 3.2/10,000 woman-years to 1.9/10,000 woman-years (p < 0.0001) (Fig. 2). Of the pregnancies resulting in delivery, 41% involved only outpatient visits, 51% involved both outpatient visits and inpatient episodes, and 8% only inpatient episodes. Of the pregnancies not resulting in delivery, 56% involved only outpatient visits, 35% involved both outpatient and inpatient care, and 9% only inpatient episodes (Fig. 3). The median number of outpatient visits or inpatient episodes was two per pregnancy, range 1–35. Separately, the median number of outpatient visits per pregnancy was 1, range 0–32, and the median number of inpatient episodes per pregnancy was 1, range 0–17. The median length of inpatient episodes was 3 days, range 1–129 days.
Fig. 3.
Admissions and readmissions due to hyperemesis gravidarum in 2005–2017
The majority of outpatient visits and inpatient episodes occurred in the first trimester (Fig. 4). Of the 9549 pregnancies resulting in delivery, HG diagnosis was recorded only in the first trimester in 6351 pregnancies (67%), in the first and second trimesters in 921 pregnancies (10%) and from the first to third trimester in 262 pregnancies (3%); 1514 pregnancies (16%) had an HG diagnosis only in the second trimester, 389 pregnancies (4%) only in the third trimester and 112 pregnancies (1%) in the second and third but not in the first trimester. Most of the pregnancy terminations, 427 of 509, took place in the first trimester. Of the 82 pregnancies terminated in the second trimester, HG diagnosis was recorded only in the first trimester in 56 pregnancies (68%), in the first and second trimesters in 5 pregnancies (6%) and only in the second trimester in 21 pregnancies (26%). The number of admissions per gestational week was higher in terminated pregnancies compared to pregnancies resulting in delivery (Fig. 5).
Fig. 4.
Timing of outpatient and inpatient care due to hyperemesis gravidarum per pregnancy week in pregnancies resulting in delivery (a) and in terminated pregnancies (b)
Fig. 5.

Number of hyperemesis gravidarum diagnoses per pregnancy week in pregnancies resulting in delivery and terminated pregnancies
In multivariable analysis of maternal, environmental and pregnancy-related factors in pregnancies resulting in delivery, parity of five or more, multiple gestation and female sex of the fetus were associated with higher odds of readmission, whereas maternal age of 36–40 years, pre-pregnancy BMI of 35 or more, smoking during pregnancy and ART were associated with lower odds of readmission (Table 2). Compared to upper-level white-collar, white-collar and blue-collar workers had slightly lower odds of readmission in the univariable analysis (Table 2), but due to high number of missing data, the variable was excluded from the multivariable model. Gravidity, marital status and municipality population did not show any association with readmission (Table 2).
Table 2.
Results of univariable and multivariable analysis: associations between readmission due to HG and maternal, environmental and pregnancy-related factors in pregnancies resulting in delivery
| Characteristic | Readmissiona, all health-care services | OR, univariable | OR, multivariableb | |
|---|---|---|---|---|
| Yes (N = 5822) | No (N = 3727) | |||
| N (%) | N (%) | (95% CI) | (95% CI) | |
| Age, years | ||||
| ≤ 20 | 337 (5.8) | 231 (6.2) | 0.90 (0.75–1.08) | 1.04 (0.85–1.27) |
| 21–25 | 1321 (22.7) | 907 (24.3) | Ref | Ref |
| 26–30 | 1975 (33.9) | 1201 (32.2) | 0.88 (0.79–0.99) | 0.92 (0.82–1.04) |
| 31–35 | 1526 (26.2) | 923 (24.8) | 1.01 (0.91–1.12) | 0.97 (0.87–1.09) |
| 36–40 | 563 (9.7) | 397 (10.7) | 0.87 (0.75–1.01) | 0.81 (0.70–0.95) |
| ≥ 41 | 100 (1.7) | 68 (1.8) | 0.90 (0.65–1.23) | 0.86 (0.60–1.21) |
| Gravidity (number of pregnancies, current pregnancy included) | ||||
| 1 | 1870 (32.1) | 1265 (33.9) | Ref | |
| 2 | 1686 (29.0) | 1043 (28.0) | 1.07 (0.97–1.19) | |
| 3 | 1011 (17.4) | 658 (17.7) | 1.02 (0.91–1.15) | |
| 4 | 567 (9.7) | 358 (9.6) | 1.04 (0.90–1.21) | |
| ≥ 5 | 687 (11.8) | 403 (10.8) | 1.13 (0.98–1.30) | |
| Unknown | 1 | |||
| Parity (number of pregnancies resulting in delivery, current pregnancy included) | ||||
| 1 | 2545 (43.7) | 1720 (46.2) | Ref | Ref |
| 2 | 1864 (32.0) | 1183 (31.8) | 1.04 (0.95–1.14) | 1.03 (0.93–1.14) |
| 3 | 851 (14.6) | 516 (13.9) | 1.09 (0.96–1.23) | 1.12 (0.98–1.28) |
| 4 | 292 (5.0) | 181 (4.9) | 1.05 (0.87–1.27) | 1.14 (0.93–1.40) |
| ≥ 5 | 268 (4.6) | 126 (3.4) | 1.39 (1.–1.72) | 1.41 (1.11–1.78) |
| Unknown | 2 | 1 | ||
| Pre-pregnancy BMI, kg/m2 | ||||
| < 18.5 | 266 (4.7) | 166 (4.6) | 1.02 (0.83–1.25) | 1.05 (0.85–1.29) |
| 18.5–24.9 | 3286 (58.3) | 2077 (57.7) | Ref | Ref |
| 25–29.9 | 1277 (22.7) | 799 (22.2) | 1.01 (0.91–1.12) | 1.01 (0.91–1.13) |
| 30–34.9 | 552 (9.8) | 353 (9.8) | 0.98 (0.85–1.13) | 1.01 (0.87–1.17) |
| ≥ 35 or more | 254 (4.5) | 208 (5.8) | 0.77 (0.63–0.93) | 0.77 (0.63–0.93) |
| Unknown | 187 | 124 | ||
| Smoking during pregnancy | ||||
| No | 5213 (91.7) | 3137 (86.6) | Ref | Ref |
| Yes, but quit in first trimester | 236 (4.1) | 212 (5.9) | 0.67 (0.56–0.82) | 0.67 (0.55–0.81) |
| Yes, continued after first trimester | 238 (4.2) | 273 (7.5) | 0.53 (0.45–0.64) | 0.54 (0.44–0.65) |
| Unknown | 135 | 105 | ||
| Marital status | ||||
| Living with partner | 5220 (93.5) | 3296 (94.1) | Ref | |
| Not living with partner | 361 (6.5) | 205 (5.9) | 1.12 (0.94–1.34) | |
| Unknown | 241 | 226 | ||
| Socioeconomic status | ||||
| Upper-level white collar | 634 (17.4) | 325 (15.4) | Ref | |
| White collar | 1450 (39.8) | 927 (43.9) | 0.80 (0.68–0.94) | |
| Blue collar | 518 (14.2) | 334 (15.8) | 0.80 (0.66–0.97) | |
| At homec | 287 (7.9) | 135 (6.4) | 1.08 (0.85–1.38) | |
| Otherc | 751 (20.6) | 392 (18.6) | 0.98 (0.82–1.18) | |
| Unknown | 2182 | 1614 | ||
| Municipality population | ||||
| < 10,000 inhabitants | 799 (13.7) | 534 (14.4) | Ref | |
| 10,000–99,999 inhabitants | 2471 (42.6) | 1591 (42.9) | 1.03 (0.91–1.17) | |
| ≥ 100 000 inhabitants | 2536 (43.7) | 1582 (42.7) | 1.05 (0.93–1.20) | |
| Unknown | 16 | 20 | ||
| Assisted reproductive technology (ART)d | ||||
| No | 5640 (96.9) | 3583 (96.1) | Ref | Ref |
| Yes | 182 (3.1) | 144 (3.9) | 0.81 (0.65–1.02) | 0.77 (0.61–0.97) |
| Number of fetuses | ||||
| One fetus | 5612 (96.4) | 3632 (97.4) | Ref | Ref |
| Two or three fetuses | 210 (3.6) | 95 (2.6) | 1.46 (1.14–1.86) | 1.64 (1.27–2.12) |
| Sex of fetus, all pregnanciese | ||||
| Male | 2612 (44.9) | 1776 (47.6) | Ref | Ref |
| Female | 3210 (55.1) | 1951 (52.4) | 1.12 (1.03–1.21) | 1.13 (1.04–1.23) |
| Sex of fetus, singleton pregnanciesf | ||||
| One fetus, male | 2531 (45.1) | 1735 (47.8) | Ref | |
| One fetus, female | 3081 (54.9) | 1897 (52.2) | 1.12 (1.03–1.21) | |
| Sex of fetuses, multiple gestationf | ||||
| All male | 45 (21.4) | 26 (27.4) | Ref | |
| All female | 86 (41.0) | 36 (37.9) | 1.31 (0.71–2.44) | |
| Both sexes | 79 (37.6) | 33 (34.7) | 1.32 (0.70–2.48) | |
OR odds ratio, CI confidence interval, Ref reference
aReadmission: more than one outpatient visit or inpatient episode due to HG during one pregnancy
bAge, parity, BMI, smoking, ART, number of fetuses and sex of the fetus were included in the multivariable model
cSocioeconomic status, at home: unemployed, retired, stay-at-home mother; other: including, e.g., entrepreneurs, farmers and students, for which socioeconomic status cannot be determined
dART: yes = insemination, follicle stimulation or embryo transfer, or a combination of these
eIn twin pregnancies, the sex of the firstborn fetus was included in the analysis
fAdditional analyses, not included in the multivariable model due to collinearity with the sex and number of fetuses
Discussion
The burden of illness due to HG was substantial: in the scale of Finland, with a population of 5.5 million inhabitants and 50,000–61,000 births/year in 2005–2017, more than a thousand outpatient visits and several hundred inpatient episodes each year present a considerable load for health services and strain for the pregnant women. In one-third of pregnancies, the need of care due to HG continued after the first trimester, and in nearly one-tenth of pregnancies in the third trimester, highlighting the value of preparing for long-term treatment of HG.
In line with previous studies, outpatient visits were more common than inpatient episodes [37, 38]. The inpatient readmission rate, 17%, is likely to correspond to more severe HG symptoms, as outpatient visits occurring after inpatient episodes may also include follow-up visits with diminished HG symptoms. However, as the total number of outpatient visits and inpatient episodes remained at the same level throughout the study, the observed increase of outpatient care and decrease of inpatient care may reflect current objectives of early and accessible treatment in health-care units near the patients rather than changes in overall severity of HG symptoms during the study period [38–40].
In our study, repeated care was needed in 60% of HG pregnancies. Earlier studies have reported lower readmission rates: 13% (14 of 109 women) [15], 20% (38 of 192 women) [13], 28% (34,704 of 121 885 women) [4], 32% (62 of 191 women) [7] and 34% (38 of 113 women) [14]. The differences are likely to result from methodological diversity: in most studies, only inpatient hospitalizations [4, 7, 13, 15] or emergency department visits [14] were analyzed, and the sources of data varied: single hospital [13–15], several hospitals [7] or nation-wide hospitalization data [4]. Our inpatient readmission rate, 17%, fell in the lower end of the readmission rates observed earlier [4, 7, 13–15], highlighting the effect of different inclusion and exclusion criteria between studies.
Young maternal age has been associated with higher risk of readmission due to HG [4], in line with our observation of a lower risk in the older age groups, although the difference was statistically significant only in the age group of 36–40 years. Earlier studies have been inconsistent concerning the effect of parity [4, 41–43], and in our study, only parity of five or more was associated with higher risk of readmission. ARTs have been shown to be associated with risk of HG in general [42], and in our earlier study, we found the same result when comparing pregnancies diagnosed with HG to pregnancies not diagnosed with HG [11]. In the present study, the novel finding of inverse association of ART with readmissions can imply that the symptoms may not persist a long time in these cases. The small number of ART pregnancies did not permit distinguishing between different ART techniques, limiting our ability to interpret possible effect of different biological reasons for use of ARTs. Our results about smoking matched earlier results: smoking has been associated with lower risk of HG in general [41]. In a large study by Fiaschi et al. [4], low socioeconomic status, Asian or Black ethnicity, female fetus and multiple pregnancy were found to be risk factors for readmission, and our results confirmed these results regarding the number and sex of fetuses. The observed higher number of admissions per gestational week in terminated pregnancies compared to pregnancies resulting in delivery may reflect the strain of HG as one factor affecting the pregnancy termination decision, but as register data does not permit analyzing women’s motives in such decisions, these results should be interpreted with caution. Furthermore, in previous studies, nausea and vomiting in pregnancy and HG have been inversely associated with miscarriage [32, 33], in line with our observation of lower readmission rate due to HG in pregnancies resulting in miscarriage.
Although nausea and vomiting are often considered to resolve after the first trimester and studies tend to focus on the first trimester [14, 44], previous studies have shown that symptoms frequently persist past mid-pregnancy or even until birth [2–4]. In interview studies, women suffering from HG have expressed frustration when their symptoms continue longer than expected, highlighting the value of realistic evaluation of duration of HG [45, 46]. Our results provide helpful information regarding this question allowing clinicians to reflect the readmission risk and symptom duration in each woman’s individual situation. As many of the above-mentioned risk factors are not influenceable, these results cannot be employed for diminishing an individual woman’s readmission risk due to HG, but rather as tools for evaluating if her symptoms will be likely to persist and need repeated care.
The Finnish health-care registers’ high coverage and reliability are valuable assets for register-based studies [47]. We used nation-wide register data of outpatient visits and inpatient episodes of women admitted for HG, permitting admissions in different services to be merged. In Finland, primary health care is publicly funded and organized in health-care centers, including prenatal care units for pregnancy follow-up [48]. Virtually, all pregnant women attend routine pregnancy care organized by specialized maternity health-care nurses and midwives, with regular check-ups by physicians. Mild nausea and vomiting can be treated in primary care, and women with HG are referred to specialized obstetric clinics, led by specialists in obstetrics, where they can receive outpatient care or be admitted to a hospital. Registering a diagnosis following national guidelines is obligatory, and verified discharge diagnoses are systematically collected into centralized registers organized by the Finnish Institute of Health and Welfare [49]. Data linkage between registers enabled us to connect HG diagnoses to varied pregnancy outcomes. Analyzing both outpatient visits and inpatient episodes in the entire population allowed us to get a comprehensive picture of need of care due to HG, not limited to hospitalizations or certain service providers. The most important limitation to consider when assessing need of care using register data is the possible underestimation, as those women suffering from HG symptoms who did not contact health care or did not receive diagnosis were absent in the data. For some research questions, registers are not optimal. For instance, estimation of the number of miscarriages is limited by the extent to which they are recorded in health-care registers, and as not all miscarriages are clinically recognized [50], their number is likely to be underestimated. Also, the data structure did not permit adjustment for pre-existing or gestational comorbidities, symptom severity or treatment modalities, and assessing these questions requires a different study design. The small number of gestational trophoblastic disease and ectopic pregnancies diagnosed with HG suggest that results regarding these outcomes are to be interpreted with caution.
Definition of HG is essential for comparability of results, and different diagnostic and treatment practices may limit generalizability of findings. In Finland, HG is diagnosed according to the 10th version of the International Statistical Classification of Diseases and Related Health Problems (ICD). Different inclusion and exclusion criteria in HG studies have been common due to lack of consensus about the definition [51, 52]. The first consensus definition of HG presented in the Third International Colloquium on Hyperemesis Gravidarum is primarily intended for prospective clinical studies and cannot be retrospectively implemented in register research. There are currently no official hospitalization criteria or clinical guidelines for diagnosis or treatment of HG in Finland, but current practices and recommendations have been described in the primary Finnish Medical Journal Duodecim [21]. Women with HG can receive treatment, such as intravenous hydration or medication, in both outpatient and hospital settings, and the dichotomy turned out to be somewhat artificial: our analysis showed that in Finland, the majority of women with HG were treated in both settings.
In conclusion, our results reveal that readmissions due to HG are common and the need of medical care often continues after the first trimester of pregnancy. These findings emphasize the importance of planning for eventual long-term treatment of HG.
Author contributions
MN: manuscript writing, data analysis, data collection, manuscript editing, project development. PR: manuscript editing, project development. MG: manuscript editing, project development. TV: statistical analyses, manuscript editing. PP-K: manuscript editing, project development. All authors contributed to the writing process of the manuscript and approved the final version.
Funding
Open Access funding provided by University of Turku (UTU) including Turku University Central Hospital. This study was financially supported by the research funds from specified government transfers to MN, PR and PP-K, allocated by the Finnish Government, Hospital District of Southwest Finland.
Availability of data and material (data transparency)
Adhering to the EU General Data Protection Regulation (GDPR) and Finnish legislation concerning sensitive data such as health-related information, the authors are not authorized to share the data. The Finnish Institute for Health and Welfare (THL) can, on a case-by-case basis, grant permission to use the registers for purposes of scientific research.
Code availability (software application or custom code)
Not applicable.
Declarations
Conflict of interest
The authors report no conflicts of interest.
Ethics approval
The study plan was evaluated and approved by the Ethical committee of Hospital District of Southwest Finland (43/180/2011).
Consent to participate
Not applicable; our research data are based on mandatory health registers, which are collected on the basis of Finnish health register legislation without informed consent. The use of register data is possible after the data keeping organizations have authorized the use of their data.
Consent for publication
Not applicable.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Gazmararian JA, Petersen R, Jamieson DJ, Schild L, Adams MM, Deshpande AD, Franks AL. Hospitalizations during pregnancy among managed care enrollees. Obstet Gynecol. 2002;100:94–100. doi: 10.1016/s0029-7844(02)02024-0. [DOI] [PubMed] [Google Scholar]
- 2.Mullin PM, Ching C, Schoenberg F, MacGibbon K, Romero R, Goodwin TM, Fejzo MS. Risk factors, treatments, and outcomes associated with prolonged hyperemesis gravidarum. J Matern Fetal Neonatal Med. 2012;25:632–636. doi: 10.3109/14767058.2011.598588. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Fejzo MS, Poursharif B, Korst LM, Munch S, MacGibbon KW, Romero R, Goodwin TM. Symptoms and pregnancy outcomes associated with extreme weight loss among women with hyperemesis gravidarum. J Womens Health (Larchmt) 2009;18:1981–1987. doi: 10.1089/jwh.2009.1431. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Fiaschi L, Nelson-Piercy C, Tata LJ. Hospital admission for hyperemesis gravidarum: a nationwide study of occurrence, reoccurrence and risk factors among 8.2 million pregnancies. Hum Reprod. 2016;31:1675–1684. doi: 10.1093/humrep/dew128. [DOI] [PubMed] [Google Scholar]
- 5.Niemeijer MN, Grooten IJ, Vos N, Bais JM, van der Post JA, Mol BW, Roseboom TJ, Leeflang MM, Painter RC. Diagnostic markers for hyperemesis gravidarum: a systematic review and meta analysis. Am J Obstet Gynecol. 2014;211:15e1. doi: 10.1016/j.ajog.2014.02.012. [DOI] [PubMed] [Google Scholar]
- 6.Havnen GC, Truong MB, Do MH, Heitmann K, Holst L, Nordeng H. Women's perspectives on the management and consequences of hyperemesis gravidarum—a descriptive interview study. Scand J Prim Health Care. 2019;37:30–40. doi: 10.1080/02813432.2019.1569424. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Koot MH, Grooten IJ, van der Post JAM, Bais JMJ, Ris-Stalpers C, Leeflang MMG, Bremer HA, van der Ham DP, Heidema WM, Huisjes A, Kleiverda G, Kuppens SM, van Laar JOEH, Langenveld J, van der Made F, van Pampus MG, Papatsonis D, Pelinck MJ, Pernet PJ, van Rheenen-Flach L, Rijnders RJ, Scheepers HCJ, Vogelvang TE, Mol BW, Roseboom TJ, Painter RC. Determinants of disease course and severity in hyperemesis gravidarum. Eur J Obstet Gynecol Reprod Biol. 2020;245:162–167. doi: 10.1016/j.ejogrb.2019.12.021. [DOI] [PubMed] [Google Scholar]
- 8.World Health Organization The International Statistical Classification of Diseases and Related Health Problems, Version: 2010. http://apps.who.int/classifications/icd10/browse/2010/en#/O21. Accessed 21 Nov 2012
- 9.World Health Organization (2016) The International Statistical Classification of Diseases and Related Health Problems, Version 10. https://icd.who.int/browse10/2016/en#/O21. Accessed 2 June 2021
- 10.Einarson TR, Piwko C, Koren G. Quantifying the global rates of nausea and vomiting of pregnancy: a meta analysis. J Popul Ther Clin Pharmacol. 2013;20:e171–e183. [PubMed] [Google Scholar]
- 11.Nurmi M, Rautava P, Gissler M, Vahlberg T, Polo-Kantola P. Incidence and risk factors of hyperemesis gravidarum: a national register-based study in Finland, 2005–2017. Acta Obstet Gynecol Scand. 2020;99:1003–1013. doi: 10.1111/aogs.13820. [DOI] [PubMed] [Google Scholar]
- 12.Koot MH, Grooten IJ, Sebert S, Koiranen M, Jarvelin MR, Kajantie E, Painter RC, Roseboom TJ. Hyperemesis gravidarum and cardiometabolic risk factors in adolescents: a follow-up of the Northern Finland Birth Cohort 1986. BJOG. 2017;124:1107–1114. doi: 10.1111/1471-0528.14534. [DOI] [PubMed] [Google Scholar]
- 13.Tan PC, Jacob R, Quek KF, Omar SZ. Readmission risk and metabolic, biochemical, haematological and clinical indicators of severity in hyperemesis gravidarum. Aust N Z J Obstet Gynaecol. 2006;46:446–450. doi: 10.1111/j.1479-828X.2006.00632.x. [DOI] [PubMed] [Google Scholar]
- 14.Sharp BR, Sharp KM, Patterson B, Dooley-Hash S. Treatment of nausea and vomiting in pregnancy: factors associated with ED revisits. West J Emerg Med. 2016;17:585–590. doi: 10.5811/westjem.2016.6.29847. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Chraibi Z, Ouldamer L, Body G, Bacq Y. Hyperemesis gravidarum: a ten-year French retrospective study of 109 patients. Presse Med. 2015;44:e13–22. doi: 10.1016/j.lpm.2014.04.028. [DOI] [PubMed] [Google Scholar]
- 16.Bacak SJ, Callaghan WM, Dietz PM, Crouse C. Pregnancy-associated hospitalizations in the United States, 1999–2000. Am J Obstet Gynecol. 2005;192:592–597. doi: 10.1016/j.ajog.2004.10.638. [DOI] [PubMed] [Google Scholar]
- 17.Bailit JL. Hyperemesis gravidarum: epidemiologic findings from a large cohort. Am J Obstet Gynecol. 2005;193:811–814. doi: 10.1016/j.ajog.2005.02.132. [DOI] [PubMed] [Google Scholar]
- 18.Bottomley C, Bourne T. Management strategies for hyperemesis. Best Pract Res Clin Obstet Gynaecol. 2009;23:549–564. doi: 10.1016/j.bpobgyn.2008.12.012. [DOI] [PubMed] [Google Scholar]
- 19.McParlin C, O'Donnell A, Robson SC, Beyer F, Moloney E, Bryant A, Bradley J, Muirhead CR, Nelson-Piercy C, Newbury-Birch D, Norman J, Shaw C, Simpson E, Swallow B, Yates L, Vale L. Treatments for hyperemesis gravidarum and nausea and vomiting in pregnancy: a systematic review. JAMA. 2016;316:1392–1401. doi: 10.1001/jama.2016.14337. [DOI] [PubMed] [Google Scholar]
- 20.American College of Obstetrics and Gynecology ACOG practice bulletin 189: nausea and vomiting of pregnancy. Obstet Gynecol. 2018;131:935. doi: 10.1097/AOG.0000000000002604. [DOI] [PubMed] [Google Scholar]
- 21.Laitinen L, Polo-Kantola P. Hyperemesis gravidarum. Duodecim; lääketieteellinen aikakauskirja. 2019;135:1385–1392. [Google Scholar]
- 22.Godsey RK, Newman RB. Hyperemesis gravidarum. A comparison of single and multiple admissions. J Reprod Med. 1991;36:287–290. [PubMed] [Google Scholar]
- 23.Morris ZH, Azab AN, Harlev S, Plakht Y. Developing and validating a prognostic index predicting re-hospitalization of patients with hyperemesis gravidarum. Eur J Obstet Gynecol Reprod Biol. 2018;225:113–117. doi: 10.1016/j.ejogrb.2018.04.028. [DOI] [PubMed] [Google Scholar]
- 24.Tan PC, Jacob R, Quek KF, Omar SZ. Pregnancy outcome in hyperemesis gravidarum and the effect of laboratory clinical indicators of hyperemesis severity. J Obstet Gynaecol Res. 2007;33:457–464. doi: 10.1111/j.1447-0756.2007.00552.x. [DOI] [PubMed] [Google Scholar]
- 25.Fiaschi L, Nelson-Piercy C, Gibson J, Szatkowski L, Tata LJ. Adverse maternal and birth outcomes in women admitted to hospital for hyperemesis gravidarum: a population-based cohort study. Paediatr Perinat Epidemiol. 2018;32:40–51. doi: 10.1111/ppe.12416. [DOI] [PubMed] [Google Scholar]
- 26.Soto-Wright V, Bernstein M, Goldstein DP, Berkowitz RS. The changing clinical presentation of complete molar pregnancy. Obstet Gynecol. 1995;86:775–779. doi: 10.1016/0029-7844(95)00268-V. [DOI] [PubMed] [Google Scholar]
- 27.Hou JL, Wan XR, Xiang Y, Qi QW, Yang XY. Changes of clinical features in hydatidiform mole: analysis of 113 cases. J Reprod Med. 2008;53:629–633. [PubMed] [Google Scholar]
- 28.Mangili G, Giorgione V, Gentile C, Bergamini A, Pella F, Almirante G, Candiani M. Hydatidiform mole: age-related clinical presentation and high rate of severe complications in older women. Acta Obstet Gynecol Scand. 2014;93:503–507. doi: 10.1111/aogs.12357. [DOI] [PubMed] [Google Scholar]
- 29.ACOG ACOG Practice Bulletin No. 193: Tubal Ectopic Pregnancy. Obstet Gynecol. 2018;131:e91–e103. doi: 10.1097/AOG.0000000000002560. [DOI] [PubMed] [Google Scholar]
- 30.Downey LV, Zun LS. Indicators of potential for rupture for ectopics seen in the emergency department. J Emerg Trauma Shock. 2011;4:374–377. doi: 10.4103/0974-2700.83867. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Bashiri A, Neumann L, Maymon E, Katz M. Hyperemesis gravidarum: epidemiologic features, complications and outcome. Eur J Obstet Gynecol Reprod Biol. 1995;63:135–138. doi: 10.1016/0301-2115(95)02238-4. [DOI] [PubMed] [Google Scholar]
- 32.Chan RL, Olshan AF, Savitz DA, Herring AH, Daniels JL, Peterson HB, Martin SL. Severity and duration of nausea and vomiting symptoms in pregnancy and spontaneous abortion. Hum Reprod. 2010;25:2907–2912. doi: 10.1093/humrep/deq260. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Hinkle SN, Mumford SL, Grantz KL, Silver RM, Mitchell EM, Sjaarda LA, Radin RG, Perkins NJ, Galai N, Schisterman EF. Association of nausea and vomiting during pregnancy with pregnancy loss: a secondary analysis of a randomized clinical trial. JAMA Intern Med. 2016;176:1621–1627. doi: 10.1001/jamainternmed.2016.5641. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Morgan SR, Long L, Johns J, Angwin C, Maitra S, Ross JA. Are early pregnancy complications more common in women with hyperemesis gravidarum? J Obstet Gynaecol. 2017;37:355–357. doi: 10.1080/01443615.2016.1256955. [DOI] [PubMed] [Google Scholar]
- 35.Poursharif B, Korst LM, Macgibbon KW, Fejzo MS, Romero R, Goodwin TM. Elective pregnancy termination in a large cohort of women with hyperemesis gravidarum. Contraception. 2007;76:451–455. doi: 10.1016/j.contraception.2007.08.009. [DOI] [PubMed] [Google Scholar]
- 36.Vandenbroucke JP, von Elm E, Altman DG, Gotzsche PC, Mulrow CD, Pocock SJ, Poole C, Schlesselman JJ, Egger M, Initiative STROBE. Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): explanation and elaboration. Int J Surg. 2014;12:1500–1524. doi: 10.1016/j.ijsu.2014.07.014. [DOI] [PubMed] [Google Scholar]
- 37.Attard CL, Kohli MA, Coleman S, Bradley C, Hux M, Atanackovic G, Torrance GW. The burden of illness of severe nausea and vomiting of pregnancy in the United States. Am J Obstet Gynecol. 2002;186:S220–S227. doi: 10.1067/mob.2002.122605. [DOI] [PubMed] [Google Scholar]
- 38.Fiaschi L, Nelson-Piercy C, Deb S, King R, Tata LJ. Clinical management of nausea and vomiting in pregnancy and hyperemesis gravidarum across primary and secondary care: a population-based study. BJOG. 2019;126:1201–1211. doi: 10.1111/1471-0528.15662. [DOI] [PubMed] [Google Scholar]
- 39.McParlin C, Carrick-Sen D, Steen IN, Robson SC. Hyperemesis in pregnancy study: a pilot randomised controlled trial of midwife-led outpatient care. Eur J Obstet Gynecol Reprod Biol. 2016;200:6–10. doi: 10.1016/j.ejogrb.2016.02.016. [DOI] [PubMed] [Google Scholar]
- 40.Murphy A, McCarthy FP, McElroy B, Khashan AS, Spillane N, Marchocki Z, Sarkar RK, Higgins JR. Day care versus inpatient management of nausea and vomiting of pregnancy: cost utility analysis of a randomised controlled trial. Eur J Obstet Gynecol Reprod Biol. 2016;197:78–82. doi: 10.1016/j.ejogrb.2015.10.022. [DOI] [PubMed] [Google Scholar]
- 41.Fell DB, Dodds L, Joseph KS, Allen VM, Butler B. Risk factors for hyperemesis gravidarum requiring hospital admission during pregnancy. Obstet Gynecol. 2006;107:277–284. doi: 10.1097/01.AOG.0000195059.82029.74. [DOI] [PubMed] [Google Scholar]
- 42.Roseboom TJ, Ravelli AC, van der Post JA, Painter RC. Maternal characteristics largely explain poor pregnancy outcome after hyperemesis gravidarum. Eur J Obstet Gynecol Reprod Biol. 2011;156:56–59. doi: 10.1016/j.ejogrb.2011.01.010. [DOI] [PubMed] [Google Scholar]
- 43.Vilming B, Nesheim B. Hyperemesis gravidarum in a contemporary population in Oslo. Acta Obstet Gynecol Scand. 2001;79:640–643. [PubMed] [Google Scholar]
- 44.Young NR, La Rosa M, Mehr SA, Krasnow MM. Does greater morning sickness predict carrying a girl? Analysis of nausea and vomiting during pregnancy from retrospective report. Arch Gynecol Obstet. 2021;303:1161–1166. doi: 10.1007/s00404-020-05839-1. [DOI] [PubMed] [Google Scholar]
- 45.O'Brien B, Evans M, White-McDonald E. Isolation from "being alive": coping with severe nausea and vomiting of pregnancy. Nurs Res. 2002;51:302–308. doi: 10.1097/00006199-200209000-00006. [DOI] [PubMed] [Google Scholar]
- 46.Munch S. Women's experiences with a pregnancy complication: causal explanations of hyperemesis gravidarum. Soc Work Health Care. 2002;36:59–76. doi: 10.1300/J010v36n01_05. [DOI] [PubMed] [Google Scholar]
- 47.Sund R. Quality of the Finnish Hospital Discharge Register: a systematic review. Scand J Public Health. 2012;40:505–515. doi: 10.1177/1403494812456637. [DOI] [PubMed] [Google Scholar]
- 48.Laitinen L, Nurmi M, Ellilä P, Rautava P, Koivisto M, Polo-Kantola P. Nausea and vomiting of pregnancy: associations with personal history of nausea and affected relatives. Arch Gynecol Obstet. 2020;302:947–955. doi: 10.1007/s00404-020-05683-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Gissler M, Mohangoo AD, Blondel B, Chalmers J, Macfarlane A, Gaizauskiene A, Gatt M, Lack N, Sakkeus L, Zeitlin J. Perinatal health monitoring in Europe: results from the EURO-PERISTAT project. Inform Health Soc Care. 2010;35:64–79. doi: 10.3109/17538157.2010.492923. [DOI] [PubMed] [Google Scholar]
- 50.Linnakaari R, Helle N, Mentula M, Bloigu A, Gissler M, Heikinheimo O, Niinimaki M. Trends in the incidence, rate and treatment of miscarriage-nationwide register-study in Finland, 1998–2016. Hum Reprod. 2019;34:2120–2128. doi: 10.1093/humrep/dez211. [DOI] [PubMed] [Google Scholar]
- 51.Koot MH, Boelig RC, Van't Hooft J, Limpens J, Roseboom TJ, Painter RC, Grooten IJ. Variation in hyperemesis gravidarum definition and outcome reporting in randomised clinical trials: a systematic review. BJOG. 2018;125:1514–1521. doi: 10.1111/1471-0528.15272. [DOI] [PubMed] [Google Scholar]
- 52.Grooten IJ, Roseboom TJ, Painter RC. Barriers and challenges in hyperemesis gravidarum research. Nutr Metab Insights. 2016;8:33–39. doi: 10.4137/NMI.S29523. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Adhering to the EU General Data Protection Regulation (GDPR) and Finnish legislation concerning sensitive data such as health-related information, the authors are not authorized to share the data. The Finnish Institute for Health and Welfare (THL) can, on a case-by-case basis, grant permission to use the registers for purposes of scientific research.
Not applicable.




