Skip to main content
Erschienen in: BMC Pregnancy and Childbirth 1/2019

Open Access 01.12.2019 | Research article

Trajectories of maternal depressive and anxiety symptoms from pregnancy to five years postpartum and their prenatal predictors

verfasst von: Asma Ahmed, Angela Bowen, Cindy Xin Feng, Nazeem Muhajarine

Erschienen in: BMC Pregnancy and Childbirth | Ausgabe 1/2019

Abstract

Background

Maternal depression and anxiety have distinct constellations of symptom trajectories, which are associated with factors that may vary between different groups of women. The aim of this study was to identify subgroups of women who exhibit unique longitudinal trajectory patterns of depressive and anxiety symptoms from pregnancy to 5 years postpartum and the antenatal predictors associated with these maternal groups.

Methods

The study used a longitudinal data collected from 615 women in Saskatchewan from pregnancy to 5 years postpartum. Semiparametric group-based models were used to identify latent maternal depressive and anxiety trajectory groups. Multinomial logit models were then used to assess the association between maternal characteristics and the identified latent trajectory groups.

Results

We identified four trajectory groups of maternal depressive symptoms: low-stable (35%); moderate-stable (54%); moderate-increasing (5%); and high-decreasing (6%), and three trajectory groups of maternal anxiety symptoms: very low-stable (13%); low-stable (58%); and moderate-stable (29%). We also identified several risk factors, most notably history of depression and stress, that were significantly associated with these trajectories.

Conclusion

History of depression and increased stress are significant risk factors that can be identified during regular perinatal visits; therefore, clinicians should inquire about these risk factors to identify women at high risk of ongoing depression or anxiety.
Begleitmaterial
Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1186/​s12884-019-2177-y) contains supplementary material, which is available to authorized users.
Abkürzungen
aOR
Adjusted odds ratio
BIC
Bayesian Information Criterion
CI
Confidence interval
CNORM
Censored normal distribution
EPDS
Edinburgh Postnatal Depression Scale
EPDS-A
Edinburgh Postnatal Depression Scale-Anxiety subscale
FIP
The Feeling in Pregnancy and Motherhood study

Background

Depression and anxiety disorders are highly prevalent among childbearing women, with rates as high as 30% [1, 2]. Maternal depression and anxiety are associated with poor health outcomes for the woman and her entire family [3, 4], which may have serious implications for the child’s developmental and psychological outcomes if untreated [5, 6]. Moreover, chronic depression affects long-term maternal health, with increased psychiatric morbidity (most notably more frequent and severe depressions) as well as physical and cognitive decline [7].
There is a growing evidence that maternal depressive and anxiety symptoms are heterogeneous, highly diversified with their onset, course, duration, and severity [812]. Nandi et al., reviewed population-based studies of depression and anxiety trajectories and concluded that research in this area is still in its infancy; nonetheless, they found studies which confirm distinct groups of symptom trajectories for depression and anxiety (i.e., clusters of women who follow similar symptom patterns s over time), and that these trajectories are associated with risk factors that may vary between groups [9]. A more recent systematic review of perinatal depressive symptom trajectories found a similar pattern of depressive trajectories across studies and emphasized the need for further research within different settings [13].
Different methods have been used to model the developmental trajectories of maternal mental health symptoms over time. Both longitudinal mixed-effects and latent growth curve models model individual variabilities of these symptoms over time using a single growth curve, assuming that all individuals belong to the same underlying population [13]. Hence, these models may oversimplify the underlying complexity and heterogeneity of symptoms [13]. Alternatively, group-based trajectory modeling can be used to identify clusters of individuals who follow a similar evolution of behaviour [14]. This method is particularly important in the case of maternal depression and anxiety, as it allows for capturing the diversity of these symptoms in terms of onset, course, timing, and severity [15]. Furthermore, these models do not require prior information on the number and shape of groups, and they allow the magnitude and direction of change of depressive or anxiety symptoms to vary between different trajectories [14].
Previous research on the trajectories of maternal depression has examined the period between late pregnancy up to 1 to 2 years postpartum [1618]. Very few studies have examined maternal anxiety trajectories with most up to 1–2 years postpartum, with mixed results [16, 17, 19]. These studies provide evidence for longitudinal trajectories of maternal depression and anxiety; but, findings vary with the study population, location, and start and length of follow-up. Moreover, whereas the predictors for maternal depression and anxiety are well documented, there remains a paucity of research that links longitudinal trajectories of maternal depression and anxiety to their risk factors. This is particularly important as some risk factors may be associated with certain subgroups of women with maternal depression or anxiety, which would allow for targeted interventions. Early intervention directed towards at high risk women has been shown to reduce the risk of developing major depression [20]. Thus, it is essential to explore the trajectories of maternal depressive and anxiety symptoms beyond the perinatal period not only to recognize which women target by early mental health interventions but also to identify modifiable risk factors.
This study sought to identify maternal depressive and anxiety symptoms’ trajectory groups and their antenatal predictors and answer the following questions: 1. What are the distinct trajectory patterns for maternal depressive symptoms from pregnancy to 5 years postpartum, and what are the antenatal predictors associated with these trajectory groups? and 2. What are the distinct trajectory patterns for maternal anxiety symptoms from pregnancy to 5 years postpartum, and what are the antenatal predictors associated with these trajectory groups?

Methods

Sample

This study uses data from the Feelings in Pregnancy and Motherhood Study and follow up study of child and maternal outcomes (FIP), a longitudinal epidemiological study of maternal depression and associated factors [21, 22]. In brief, in 646 women recruited from the community. Women were eligible to participate in the study if they were: 1. within the first 20 weeks of pregnancy, 2. able to speak English, and 3. residing in one of two regional health authorities in Saskatchewan (Saskatoon Health Region and Five Hills Health Region). Data was collected via face-to-face individual interviews by trained research assistants five times; early pregnancy (17.4 +/− 4.9 weeks gestation) and late pregnancy (30.6 +/− 2.7 weeks gestation), once in early postpartum (4.2 +/− 2.1 weeks), and again at 36 and 60 months postpartum. A detailed description of the FIP study is published elsewhere [21, 22].
Missing data was managed using the PROC TRAJ maximum likelihood estimation to estimate model parameters when there are at least two observations per individual [8, 23]. Nagin indicates that it is reasonable to exclude cases with very incomplete assessment histories [14], which was also done by other researchers who used the same methodology [8]. For this study, we excluded cases with more than three missing values, and thus our sample included 615 participants at time 1 (early pregnancy), 601 women at time 2 (late pregnancy), 592 women at time 3 (early postpartum), 337 women at time 4 (36 months postpartum), and 308 women at time 5 (60 months postpartum). Written consent was informed and ethical approval was received from the Office of Research Ethics at the University of Saskatchewan.

Measures

Antenatal predictors

Selection of antenatal predictors was based on those reported in the literature, such as age, marital status, ethnicity, education, employment, income, parity, whether the pregnancy was planned or not, level of satisfaction with their relationship with the partner, if they have one, any history of depression, as well as behavioural factors (smoking, alcohol, recreational drug use, and exercise level). Social support was measured by asking participants about people who provide them with emotional support. Responses were summed into a summary variable that indicates the level of social support as low-level (0–1 support) and high-level of support (two or more supports). Women were asked to indicate sources of stress from a list of stressors, their responses were combined into one summary variable that was dichotomized as low stress level (0–2 stressors) or high stress level (more than two stressors).

Outcome variables

Perinatal depressive symptoms
The Edinburgh Postnatal Depression Scale (EPDS) was used to assess women for depressive symptoms [24]. The EPDS is one of the most commonly validated screening tools for detection of perinatal depression with sensitivity of 59–100%, specificity of 49–100%, and good internal consistency (Cronbach’s Alpha> 0.80) [25, 26]. It is a 10-item self-rated questionnaire, and responses are reported on a Likert scale from zero to three with a maximum score of 30.
Perinatal anxiety symptoms
The three-item anxiety subscale (EDPS-A) was used to screen for anxiety symptoms [27]. Bowen and colleagues have confirmed an EPDS anxiety subscale (Items 3–5) during pregnancy (Cronbach’s alpha coefficient = 0.71) [28], while Ross et al., confirmed the same factors in postpartum women [29]. Responses are reported on a Likert scale from zero to three with a maximum score of nine [30].

Data analysis

The semiparametric, group-based approach for modeling developmental trajectories [14] was used to identify trajectories of maternal depressive symptoms based on their total EPDS scores and anxiety symptoms based on their EPDS-A scores from early pregnancy to 5 years postpartum. The PROC TRAJ procedure in SAS was used to estimate group-based trajectories models [31, 32]. In our study, we chose to use the censored normal distribution (CNORM) distribution as depression and anxiety scores tend to cluster at their respective minimum values depicted as a right-skewed distribution.
A two-stage model selection strategy was used to find the optimum number of groups and shape of trajectories that best fit the data [14]. In the first stage, we started to test models that consisted of two-six groups with cubic degree polynomial, guided by previous literature [8, 10, 16, 33]. Once the number of groups was identified based on a series of model selection criteria, i.e., Bayesian Information Criterion (BIC), Bayes factor, and the probability of being the correct model, a backward elimination method was used to select the order of trajectories. Non-significant cubic, quadratic, and linear terms were removed consecutively until all terms in the model were significant. Theoretical considerations such as the expected number and shape of trajectories, as well as the interpretability of these trajectories, were also considered [8]. To check whether the model fits the data well, several model diagnostic methods were used, including the average posterior probability of assignment, the odds of correct classification, the estimated group probability versus proportion of sample assigned to the group, and the confidence intervals for group membership probability.
Due to significant attrition, especially at the 36th and 60th months postpartum, we included the dropout statement extension in the PROC TRAJ SAS procedure to account for missing data [23]. We then compared models with and without the dropout statement to check the magnitude of change in the trajectory shape parameter estimates, as well as group membership probabilities.
Multinomial regression models were then used to assess the effects of various maternal characteristics at baseline on the probability of belonging to a specific trajectory group compared to a reference group [14, 34]. All analyses were performed using SAS software version 9.4.

Results

Over 50% of participants were primiparous, and most were Caucasian women living in a stable relationship with a moderately high socioeconomic status (see Table 1).
Table 1
Sociodemographic, psychosocial, and behavioral characteristics of FIP cohort study participants (n = 615) at different latent trajectory groups of maternal depression and anxiety symptoms [n (%)]
 
Depression trajectories
 
Anxiety trajectories
 
Maternal characteristics
Total (n = 615)
Low-stable (n = 215)
Moderate-stable (n = 332)
Moderate-increasing (n = 32)
High-decreasing (n = 36)
p-value
Very low-stable (n = 80)
Low-stable (n = 357)
Moderate-stable (n = 178)
p-value
Mother’s age
     
0.025
   
< 0.001
 < 25 years
96 (15.6)
27 (12.6)
50 (15.1)
8 (25.0)
11 (30.6)
 
7 (8.8)
44 (12.3)
45 (25.3)
 
 ≥ 25 years
519 (84.4)
188 (87.4)
282 (84.9)
24 (75.0)
25 (69.4)
 
73 (91.3)
313 (87.7)
133 (74.7)
 
Parity
     
0.438
   
0.850
 0
327 (53.3)
121 (56.3)
171 (51.6)
19 (59.4)
16 (44.4)
 
42 (52.5)
187 (52.5)
98 (55.1)
 
 ≥ 1
287 (46.7)
94 (43.7)
160 (48.3)
13 (40.6)
20 (55.6)
 
38 (47.5)
169 (47.5)
80 (44.9)
 
Education
     
0.022
   
0.147
 < grade 12
24 (3.9)
5 (2.3)
12 (3.6)
2 (6.3)
5 (13.9)
 
1 (1.3)
12 (3.4)
11 (6.2)
 
 ≥ grade 12
590 (96.1)
209 (97.6)
320 (96.4)
30 (93.8)
31 (86.1)
 
79 (98.8)
344 (96.6)
167 (93.8)
 
Ethnicity
     
0.004
   
0.036
 Caucasian
522 (85.0)
193 (89.8)
280 (84.6)
25 (78.1)
24 (66.7)
 
73 (91.3)
308 (86.3)
141 (79.7)
 
 Non-Caucasian
92 (15.0)
22 (10.2)
51 (15.4)
7 (21.9)
12 (33.3)
 
7 (8.8)
49 (13.7)
36 (20.3)
 
Marital status
     
0.001
   
0.029
 Non-partnered
57 (9.3)
10 (4.7)
33 (9.9)
4 (12.5)
10 (27.8)
 
4 (5.0)
28 (7.8)
25 (14.0)
 
 Partnered
558 (90.7)
205 (95.4)
299 (90.1)
28 (87.5)
26 (72.2)
 
76 (95.0)
329 (92.2)
153 (86.0)
 
Employment
     
0.001
   
0.050
 Yes
487 (79.5)
185 (86.1)
259 (78.3)
22 (68.8)
21 (60.0)
 
68 (85.0)
289 (81.2)
130 (73.5)
 
 No
126 (20.6)
30 (14.0)
72 (21.8)
10 (31.3)
14 (40.0)
 
12 (15.0)
67 (18.8)
47 (26.6)
 
Income
     
< 0.001
   
< 0.001
 < $20,000
75 (12.5)
14 (6.5)
40 (12.4)
5 (16.1)
16 (45.7)
 
2 (2.5)
36 (10.3)
37 (21.6)
 
 20-$40,000
109 (18.1)
33 (15.4)
64 (19.9)
8 (25.8)
4 (11.4)
 
15 (18.8)
57 (16.2)
37 (21.6)
 
 40-$60,000
129 (21.4)
41 (19.2)
76 (23.6)
6 (19.4)
6 (17.1)
 
15 (18.8)
70 (19.9)
44 (25.7)
 
 > $60,000
289 (48.0)
126 (58.9)
142 (44.1)
12 (38.7)
9 (25.7)
 
48 (60.0)
188 (53.6)
53 (31.0)
 
Past depression
     
< 0.001
   
< 0.001
 Yes
217 (35.3)
35 (16.3)
136 (41.0)
18 (56.3)
28 (77.8)
 
12 (15.0)
99 (27.7)
106 (59.6)
 
 No
398 (64.7)
180 (83.7)
196 (59.0)
14 (43.8)
8 (22.2)
 
68 (85.0)
258 (72.3)
72 (40.5)
 
Stress level
     
< 0.001
   
< 0.001
 Low (0–2)
362 (59.4)
170 (80.6)
174 (52.7)
14 (43.8)
4 (11.1)
 
66 (84.6)
223 (63.0)
73 (41.2)
 
 High (> 2)
247 (40.6)
41 (19.4)
156 (47.3)
18 (56.3)
32 (88.9)
 
12 (15.4)
131 (37.0)
104 (58.8)
 
Support level
     
0.043
   
0.105
 Low (0–1)
104 (16.9)
25 (11.6)
63 (19.0)
6 (18.8)
10 (27.8)
 
8 (10.0)
59 (16.6)
37 (20.8)
 
 High (> 1)
510 (83.1)
190 (88.4)
268 (81.0)
26 (81.3)
26 (72.2)
 
72 (90.0)
297 (83.4)
141 (79.2)
 
Relationship satisfaction
     
< 0.001
   
0.009
 Not satisfied
75 (12.3)
14 (6.5)
38 (11.6)
6 (18.8)
17 (48.6)
 
7 (8.8)
35 (9.9)
33 (18.8)
 
 Satisfied
536 (87.7)
201 (93.5)
291 (88.5)
26 (81.3)
18 (51.4)
 
73 (91.3)
320 (90.1)
143 (81.3)
 
Planned pregnancy
     
0.001
   
0.030
 Yes
366 (59.5)
147 (68.4)
190 (57.2)
16 (50.0)
13 (36.1)
 
55 (68.8)
218 (61.1)
93 (52.3)
 
 No
249 (40.5)
68 (31.6)
142 (42.8)
16 (50.0)
23 (63.9)
 
25 (31.3)
139 (38.9)
85 (47.8)
 
Smoking
     
< 0.001
   
0.011
 No or quit
548 (89.3)
203 (94.4)
293 (88.5)
27 (84.4)
25 (69.4)
 
76 (95.0)
324 (90.8)
148 (83.6)
 
 Yes
66 (10.8)
12 (5.6)
38 (11.5)
5 (15.6)
11 (30.6)
 
4 (5.0)
33 (9.2)
29 (16.4)
 
Alcohol
     
0.321
   
0.402
 No or quit
573 (93.2)
202 (94.0)
309 (93.1)
31 (96.9)
31 (86.1)
 
77 (96.3)
329 (92.2)
167 (93.8)
 
 Yes
42 (6.8)
13 (6.1)
23 (6.9)
1 (3.1)
5 (13.9)
 
3 (3.8)
28 (7.8)
11 (6.2)
 
Drugs
     
0.310
   
0.250
 No or quit
596 (97.1)
208 (97.2)
324 (97.6)
31 (96.9)
33 (91.7)
 
80 (100.0)
343 (96.4)
173 (97.2)
 
 Yes
18 (2.9)
6 (2.8)
8 (2.4)
1 (3.1)
3 (8.3)
 
0.00 (0.0)
13 (3.7)
5 (2.8)
 
Exercise
     
0.103
   
0.248
 Never or occasional
284 (46.2)
90 (41.9)
155 (46.7)
16 (50.0)
23 (63.9)
 
33 (41.3)
160 (44.8)
91 (51.1)
 
 Regular
331 (53.8)
125 (58.1)
177 (53.3)
16 (50.0)
13 (36.1)
 
47 (58.8)
197 (55.2)
87 (48.9)
 

Maternal depression trajectory groups

Candidate models containing two to six groups were analyzed. The BIC score increased from the two-group to the four-group model, and then it started to decrease as further groups were added. The Bayes Factor showed strong evidence in support of the four-group model compared to the three-group and five-group model; the probability of being the correct model was the highest for the four-group model (0.984). Therefore, we chose the four-group model as the best fitting and most parsimonious model (see Additional file 1 for model fit indices). Figure 1 depicts the four maternal depression groups with 95% confidence limits. The average posterior probability ranged from 0.83 for the moderate-increasing group to 0.91 for the high-decreasing group (mean = 0.86), indicating a very good model fit. In addition, the model met the other three indicators of model adequacy (Additional file 2).
The first depression group “low-stable” (n = 215, 35.0%) included women whose EPDS scores were consistently low throughout the follow-up period. Women in the largest group “moderate-stable” (n = 332, 54.0%) reported a moderate level of depressive symptoms across the period of follow-up that minimally decreased over time. More fluctuations were seen in the other two groups (moderate-increasing and high-decreasing), as evident from the significant cubic term for both groups. Depression scores for women assigned to the moderate-increasing group (n = 32, 5.2%) were slightly higher than those of the moderate-stable group during pregnancy; however, their EPDS scores increased significantly postpartum. Women in the high-decreasing group (n = 36, 5.9%) experienced high levels of depressive symptoms during pregnancy which started to decrease gradually after giving birth, except for a slight increase between the third and fifth year of follow-up (EPDS scores are summarized by time and depressive trajectory group in Additional file 3).
Comparison of the basic model and the extended model that accounts for participants’ attrition revealed that parameter estimates and group membership probabilities for the low-stable and moderate-stable groups were almost identical between both models. However, the estimates for the linear, quadratic, and cubic terms, as well as group membership probabilities of the other two groups were different (see Additional file 4).

Maternal anxiety trajectory groups

To determine the best number of anxiety groups, we compared BIC values of the two-group to six-group models. The BIC score increased from the two-group model to the three-group model, but they started to decrease as further groups were added (see Additional file 5). Hence, we concluded the three-group model as the best fitting and most parsimonious model. Figure 2 illustrates the three maternal anxiety groups with their 95% confidence limits. The average posterior probability ranged from 0.87 to 0.88 for the very low-stable group (mean = 0.87), indicating a very good model fit. Other model fit diagnostics also indicated a good model fit (Additional file 6).
The first and the smallest group “very low-stable” (n = 80, 13.0%) was composed of women whose anxiety symptoms were the lowest of the sample and were relatively stable over the whole period of follow-up. More than half the sample (n = 357, 58.1%) belonged to the second group “low-stable”, and their anxiety scores were fairly constant at levels that were higher than those of the very low-stable group. The third group “moderate-stable” included women with moderate to high anxiety scores throughout the period of follow-up, but with a slight decrease over time; one-third of the sample (n = 178, 29.0%) fell into this group. EPDS-A scores are summarized by time and anxiety trajectory group in Additional file 7. Comparison of the model with and without dropout extension revealed that trajectory shape parameter estimates, as well as group membership probabilities for both models, were almost identical (refer to Additional file 4).

Multinomial regression

For depression trajectory groups, risk factors of membership in the moderate-stable compared with the low-stable group included a history of depression, high stress level, and non-Caucasian ethnicity. Compared to the low-stable group, membership in the moderate-increasing group was associated with a history of depression and high stress level. For the high-decreasing group, significant associations compared to the low-stable group included a history of depression, high stress level, being a tobacco user, and non-Caucasian ethnicity (see Table 2).
Table 2
Sociodemographic, psychosocial, and behavioral predictors of the latent trajectory group membership for the maternal depressive symptom based on the multivariate multinomial regression model
 
Moderate-stable
Moderate-increasing
High-decreasing
Determinants
aOR
95% CI
aOR
95% CI
aOR
95% CI
Ethnicity: non-Caucasian
1.91*
1.03–3.54
2.37
0.77–7.35
3.87*
1.30–11.53
Past depression: yes
3.09***
1.97–4.85
4.67***
2.01–10.82
8.57***
3.29–22.30
Stress level: high
3.16***
2.05–4.85
4.28***
1.85–9.87
18.96***
5.99–59.96
Smoking: yes
1.72
0.82–3.59
1.63
0.45–5.92
3.58*
1.17–10.97
Reference group is the low-stable trajectory group; variables included in the model: ethnicity, past depression, income, stress level, and smoking
aOR adjusted odds ratio, CI confidence interval
*p-value < 0.05. ***p-value < 0.001; n = 607 after removing the missing data in the covariates
Results of multinomial regression for anxiety groups showed that compared to the very low-stable group, the only variable associated with the low-stable group was the high stress level. Higher stress level, history of depression, and low income were associated with the moderate-stable group, relative to the very low-stable group (refer to Table 3).
Table 3
Sociodemographic, psychosocial, and behavioral predictors of the latent trajectory group membership for the maternal anxiety symptom based on the multivariate multinomial regression model
 
Low-stable
Moderate-stable
aOR
95% CI
aOR
95% CI
Income
 <$20,000/assistance
2.69
0.59–12.29
6.00*
1.2528.81
 $20,000 – $40,000
0.75
0.378–1.51
1.47
0.67–3.24
 $40,000 - $60,000
1.25
0.64–2.43
2.87**
1.34–6.16
Past depression: yes
1.70
0.87–3.36
6.01***
2.91–12.40
Stress level: high
2.91**
1.49–5.68
4.83***
2.34–9.98
The reference group is the very low-stable trajectory group; variables included in the model: ethnicity, past depression, income, and stress level
aOR adjusted odds ratio, CI confidence interval
*p-value < 0.05. **p-value < 0.01. ***p-value < 0.001; n = 596 after removing the missing data in the covariates

Discussion

We identified four trajectory groups of maternal depression and three trajectory groups of maternal anxiety. The four depression trajectory groups were: low-stable (35.0%), moderate-stable (54.0%), moderate-increasing (5.2%), and high-decreasing (5.9%). Women who belonged to the low-stable and moderate-stable had EPDS scores that were below the cutoff point of clinical significance throughout the period of follow-up. Our findings are consistent with other studies, such as van der Waerden et al. [10], Denckla et al. [11], Campbell et al. [35] and Luoma et al. [33], which identified trajectory groups with no symptoms, low symptoms, and/or moderate symptoms of depression that were relatively stable across the period of follow-up and had the highest proportion of participants.
Like our high-decreasing group, van der Waerden and colleagues identified a prenatal group (5%) with high symptoms during pregnancy that decreased after giving birth and increased again between 36 and 60 months postpartum [10]. The slight increase in EPDS scores seen between the 36th and 60th months postpartum could possibly be related to a subsequent pregnancy, although this information was not readily available from the FIP data. Whereas previous studies concluded a small group of high symptoms that were relatively stable over time (also referred to as “chronic”) [10, 11, 33, 35], groups with high depressive symptoms in the present study displayed more fluctuation over time. Nonetheless, caution is required when comparing our results to these studies because of the variation in the period of follow-up and the tool used to assess depression.
We also identified three anxiety trajectory groups, very low-stable (13.0%), low-stable (58.1%), and moderate-stable (29.0%). Bayrampour et al. [16], documented five trajectory groups of maternal anxiety among 1445 women in Canada, who were followed from pregnancy to 1 year postpartum. Around 70% of the women in our sample experienced very low or low anxiety symptoms throughout the period of follow-up, which is comparable to Bayrampour’s results [16]. Almost a third of our sample had moderate-high anxiety symptoms that were stable across pregnancy to 5 years postpartum, whereas Bayrampour et al., concluded two groups of high anxiety symptoms that varied over time; antepartum and postpartum groups. They also concluded a very small group (1.5%) with chronic anxiety symptoms [16]. Likewise, the three trajectories (decreasing, increasing, and transient groups) with moderate-high anxiety symptoms in Barthel’s study showed fluctuation across the perinatal period [19].
We identified maternal risk factors associated with maternal depression and/or anxiety trajectory groups; high stress level and history of depression consistently predicted groups with moderate to high depressive or anxiety symptoms, and as the severity of symptom increases the magnitude of the impact of these factors increase, suggesting a dose-response relationship. As Britton [2] documented, women who have experienced depression in the past are vulnerable to both depression and anxiety during pregnancy, postpartum, as well as to persistent symptoms that extend well beyond the perinatal period. The present study concludes that stress is a major determinant of women’s mental health, especially during childbearing period, which is also consistent with van der Waerden and Bayrampour’s results [10, 16]. Researchers report that stress can invoke hormonal changes including increased activity of the HPA axis, and reduced levels of norepinephrine [36, 37], which can trigger maternal depressive and/or anxiety symptoms. Being non-Caucasian emerged as a significant predictor of trajectory groups with high depressive symptoms, which is consistent with van der Waerden et al.’s [10], conclusions. Low income has been documented to increase the risk of both depression and anxiety [2, 38], as it was for the trajectory group with moderate anxiety symptoms but, this factor was not significantly associated with distinct trajectory groups for depressive symptoms. This could be related to the small sample size of groups with high depressive symptoms, and the small number of low-income participants in our sample. The only behavioural factor that significantly predicted high depressive symptoms groups was tobacco use, which is in keeping with the literature that showed a significant association between prenatal smoking and perinatal depression [3941].
Strengths of the present study are the longitudinal nature and the repeated assessments during pregnancy, postpartum and up to 5 years postpartum and the use of validated screening tools for maternal depression and anxiety. Our sample included women who may be at low risk of maternal mental disorders (mostly Caucasian women with relatively high socioeconomic status), and thus the generalizability of our results may be limited to women of similar circumstance. The high attrition rates, particularly of those who could be at high risk of being depressed or anxious (such as non-Caucasian women, women with low socioeconomic status), which may have led to the underestimation of the severity of these disorders, and may have affected the significance and magnitude of association with maternal risk factors. We considered baseline covariates in our analysis, as information about some time varying covariates (stress, income, etc.) was not collected at each assessment wave. The size of some trajectory groups was small, which may have affected the power to detect true associations and their precision in relation to some of the risk factors.

Conclusion

Our results have shown that while some women with perinatal mental health symptoms may recover quickly, for others, these symptoms may be chronic. This heterogeneity of symptoms may necessitate multiple assessments for depressive and anxiety during pregnancy and the postpartum period, and beyond to recognize women at high risk of ongoing depression or anxiety. Furthermore, recognizing these women may allow for preventative and treatment interventions, which may alter symptom progress over time. Healthcare providers for women in the perinatal period should inquire about past psychiatric illness, as it appears to be a major predictor of perinatal depression and anxiety [2, 38, 42], and about stress levels, particularly during pregnancy and around birth, which can be major transitional periods in a woman’s life. Public health interventions that target some of the modifiable risk factors (e.g. smoking) specifically designed for women in the perinatal period may reduce the burden of these illnesses at the population level. Further research is recommended to examine the evolution of depressive and anxiety symptoms over longer periods and among different populations, particularly high-risk populations of women.

Acknowledgements

We thank the women who participated in the study. We also appreciate the funding support from the Canadian Institutes of Health Research.

Funding

The FIP study was supported by the Canadian Institutes of Health Research (Grant 145179 and 220896). The funding body had no role in the design, collection, analysis, or interpretation of data nor in the writing or submission of the manuscript for publication.

Availability of data and materials

The datasets generated and/or analyzed during the current study are available in the Research Advancement through Cohort Cataloguing and Harmonization (ReACH) repository at https://​www.​maelstrom-research.​org/​mica/​network/​reach. Sociodemographic questions, as well as questions about past psychiatric history, sources of stress, and sources of support have been utilized within our research group through various studies. The Edinburgh Postnatal Depression Scale (EPDS) is one of the most validated screening tools for the detection of perinatal depression and has been translated into many languages. A three-item anxiety subscale of the EPDS (EDPS-A, items 3, 4, 5) has also been confirmed as a screen for perinatal anxiety symptoms.
After providing all necessary details, informed written consent was obtained from all participants prior to commencing data collection.
Ethical approval was received from the Research Ethics Board at the University of Saskatchewan (BEH 16–159).
Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Anhänge

Additional files

Literatur
1.
Zurück zum Zitat Wang L, Wu T, Anderson JL, Florence JE. Prevalence and risk factors of maternal depression during the first three years of child rearing. J Women’s Health. 2011;20(5):711–8.CrossRef Wang L, Wu T, Anderson JL, Florence JE. Prevalence and risk factors of maternal depression during the first three years of child rearing. J Women’s Health. 2011;20(5):711–8.CrossRef
2.
Zurück zum Zitat Britton JR. Maternal anxiety: course and antecedents during the early postpartum period. Depress Anxiety. 2008;25(9):793–800.CrossRef Britton JR. Maternal anxiety: course and antecedents during the early postpartum period. Depress Anxiety. 2008;25(9):793–800.CrossRef
3.
Zurück zum Zitat Letourneau NL, Dennis C-L, Benzies K, Duffett-Leger L, Stewart M, Tryphonopoulos PD, et al. Postpartum depression is a family affair: addressing the impact on mothers, fathers, and children. Issues Ment Health Nurs. 2012;33(7):445–57.CrossRef Letourneau NL, Dennis C-L, Benzies K, Duffett-Leger L, Stewart M, Tryphonopoulos PD, et al. Postpartum depression is a family affair: addressing the impact on mothers, fathers, and children. Issues Ment Health Nurs. 2012;33(7):445–57.CrossRef
4.
Zurück zum Zitat Buist A, Gotman N, Yonkers KA. Generalized anxiety disorder: course and risk factors in pregnancy. J Affect Disord. 2011;131(1):277–83.CrossRef Buist A, Gotman N, Yonkers KA. Generalized anxiety disorder: course and risk factors in pregnancy. J Affect Disord. 2011;131(1):277–83.CrossRef
5.
Zurück zum Zitat Turney K. Pathways of disadvantage: explaining the relationship between maternal depression and children’s problem behaviors. Soc Sci Res. 2012;41(6):1546–64.CrossRef Turney K. Pathways of disadvantage: explaining the relationship between maternal depression and children’s problem behaviors. Soc Sci Res. 2012;41(6):1546–64.CrossRef
6.
Zurück zum Zitat Fihrer I, McMahon CA, Taylor AJ. The impact of postnatal and concurrent maternal depression on child behaviour during the early school years. J Affect Disord. 2009;119(1):116–23.CrossRef Fihrer I, McMahon CA, Taylor AJ. The impact of postnatal and concurrent maternal depression on child behaviour during the early school years. J Affect Disord. 2009;119(1):116–23.CrossRef
7.
Zurück zum Zitat Goveas J, Espeland M, Hogan P, Tindle H, Shih R, Kotchen J, et al. Depressive symptoms and longitudinal changes in cognition: Women’s health initiative study of cognitive aging. J Geriatr Psychiatry Neurol. 2014;27(2):94–102. Goveas J, Espeland M, Hogan P, Tindle H, Shih R, Kotchen J, et al. Depressive symptoms and longitudinal changes in cognition: Women’s health initiative study of cognitive aging. J Geriatr Psychiatry Neurol. 2014;27(2):94–102.
8.
Zurück zum Zitat Campbell SB, Matestic P, von Stauffenberg C, Mohan R, Kirchner T. Trajectories of maternal depressive symptoms, maternal sensitivity, and children’s functioning at school entry. Dev Psychol. 2007;43(5):1202–15.CrossRef Campbell SB, Matestic P, von Stauffenberg C, Mohan R, Kirchner T. Trajectories of maternal depressive symptoms, maternal sensitivity, and children’s functioning at school entry. Dev Psychol. 2007;43(5):1202–15.CrossRef
9.
Zurück zum Zitat Nandi A, Beard JR, Galea S. Epidemiologic heterogeneity of common mood and anxiety disorders over the lifecourse in the general population: a systematic review. BMC Psychiatry. 2009;9(1):31.CrossRef Nandi A, Beard JR, Galea S. Epidemiologic heterogeneity of common mood and anxiety disorders over the lifecourse in the general population: a systematic review. BMC Psychiatry. 2009;9(1):31.CrossRef
10.
Zurück zum Zitat van der Waerden J, Galera C, Saurel-Cubizolles MJ, Sutter-Dallay AL, Melchior M, Group EM-CCS. Predictors of persistent maternal depression trajectories in early childhood: results from the EDEN mother-child cohort study in France. Psychol Med. 2015;45(9):1999–2012.CrossRef van der Waerden J, Galera C, Saurel-Cubizolles MJ, Sutter-Dallay AL, Melchior M, Group EM-CCS. Predictors of persistent maternal depression trajectories in early childhood: results from the EDEN mother-child cohort study in France. Psychol Med. 2015;45(9):1999–2012.CrossRef
11.
Zurück zum Zitat Denckla C, Mancini A, Consedine N, Milanovic S, Basu A, Seedat S, et al. Distinguishing postpartum and antepartum depressive trajectories in a large population-based cohort: the impact of exposure to adversity and offspring gender. Psychol Med. 2018;48(7):1139–47.CrossRef Denckla C, Mancini A, Consedine N, Milanovic S, Basu A, Seedat S, et al. Distinguishing postpartum and antepartum depressive trajectories in a large population-based cohort: the impact of exposure to adversity and offspring gender. Psychol Med. 2018;48(7):1139–47.CrossRef
12.
Zurück zum Zitat Putnam K, Robertson-Blackmore E, Sharkey K, Payne J, Bergink V, Munk-Olsen T, et al. Heterogeneity of postpartum depression: a latent class analysis. Lancet Psychiatry. 2015;2(1):59–67.CrossRef Putnam K, Robertson-Blackmore E, Sharkey K, Payne J, Bergink V, Munk-Olsen T, et al. Heterogeneity of postpartum depression: a latent class analysis. Lancet Psychiatry. 2015;2(1):59–67.CrossRef
13.
Zurück zum Zitat Baron E, Bass J, Murray SM, Schneider M, Lund C. A systematic review of growth curve mixture modelling literature investigating trajectories of perinatal depressive symptoms and associated risk factors. J Affect Disord. 2017;223:194–208.CrossRef Baron E, Bass J, Murray SM, Schneider M, Lund C. A systematic review of growth curve mixture modelling literature investigating trajectories of perinatal depressive symptoms and associated risk factors. J Affect Disord. 2017;223:194–208.CrossRef
14.
Zurück zum Zitat Nagin DS. Group-based modeling of development. Cambridge: Harvard University Press; 2005.CrossRef Nagin DS. Group-based modeling of development. Cambridge: Harvard University Press; 2005.CrossRef
15.
Zurück zum Zitat Gross HE, Shaw DS, Burwell RA, Nagin DS. Transactional processes in child disruptive behavior and maternal depression: a longitudinal study from early childhood to adolescence. Dev Psychopathol. 2009;21(01):139–56.CrossRef Gross HE, Shaw DS, Burwell RA, Nagin DS. Transactional processes in child disruptive behavior and maternal depression: a longitudinal study from early childhood to adolescence. Dev Psychopathol. 2009;21(01):139–56.CrossRef
16.
Zurück zum Zitat Bayrampour H, Tomfohr L, Tough S. Trajectories of perinatal depressive and anxiety symptoms in a community cohort. J Clin Psychiatry. 2016;77(11):e1467.CrossRef Bayrampour H, Tomfohr L, Tough S. Trajectories of perinatal depressive and anxiety symptoms in a community cohort. J Clin Psychiatry. 2016;77(11):e1467.CrossRef
17.
Zurück zum Zitat Kuo S-Y, Chen S-R, Tzeng Y-L. Depression and anxiety trajectories among women who undergo an elective cesarean section. PLoS ONE [Electronic Resource]. 2014;9(1):e86653.CrossRef Kuo S-Y, Chen S-R, Tzeng Y-L. Depression and anxiety trajectories among women who undergo an elective cesarean section. PLoS ONE [Electronic Resource]. 2014;9(1):e86653.CrossRef
18.
Zurück zum Zitat Sutter-Dallay AL, Cosnefroy O, Glatigny-Dallay E, Verdoux H, Rascle N. Evolution of perinatal depressive symptoms from pregnancy to two years postpartum in a low-risk sample: the MATQUID cohort. J Affect Disord. 2012;139(1):23–9.CrossRef Sutter-Dallay AL, Cosnefroy O, Glatigny-Dallay E, Verdoux H, Rascle N. Evolution of perinatal depressive symptoms from pregnancy to two years postpartum in a low-risk sample: the MATQUID cohort. J Affect Disord. 2012;139(1):23–9.CrossRef
19.
Zurück zum Zitat Barthel D, Kriston L, Barkmann C, Appiah-Poku J, Te Bonle M, Doris KYE, et al. Longitudinal course of ante-and postpartum generalized anxiety symptoms and associated factors in West-African women from Ghana and Côte d’Ivoire. J Affect Disord. 2016;197:125–33.CrossRef Barthel D, Kriston L, Barkmann C, Appiah-Poku J, Te Bonle M, Doris KYE, et al. Longitudinal course of ante-and postpartum generalized anxiety symptoms and associated factors in West-African women from Ghana and Côte d’Ivoire. J Affect Disord. 2016;197:125–33.CrossRef
20.
Zurück zum Zitat Dennis C. Hodnett e. Psychosocial and psychological interventions for treating postpartum depression. Cochrane Database Syst Rev. 2007;4:CD006116. Dennis C. Hodnett e. Psychosocial and psychological interventions for treating postpartum depression. Cochrane Database Syst Rev. 2007;4:CD006116.
21.
Zurück zum Zitat Bowen A, Bowen R, Butt P, Rahman K, Muhajarine N. Patterns of depression and treatment in pregnant and postpartum women. Can J Psychiatr. 2012;57(3):161–7. Bowen A, Bowen R, Butt P, Rahman K, Muhajarine N. Patterns of depression and treatment in pregnant and postpartum women. Can J Psychiatr. 2012;57(3):161–7.
22.
Zurück zum Zitat Rahman K, Bowen A, Muhajarine N. Examining the factors that moderate and mediate the effects on depression during pregnancy and postpartum. J Pregnancy Child Health. 2014;1(116):2. Rahman K, Bowen A, Muhajarine N. Examining the factors that moderate and mediate the effects on depression during pregnancy and postpartum. J Pregnancy Child Health. 2014;1(116):2.
23.
Zurück zum Zitat Haviland AM, Jones BL, Nagin DS. Group-based trajectory modeling extended to account for nonrandom participant attrition. Sociol Methods Res. 2011;40(2):367–90. Haviland AM, Jones BL, Nagin DS. Group-based trajectory modeling extended to account for nonrandom participant attrition. Sociol Methods Res. 2011;40(2):367–90.
24.
Zurück zum Zitat Cox JL, Holden JM, Sagovsky R. Detection of postnatal depression. Development of the 10-item Edinburgh postnatal depression scale. Br J Psychiatry. 1987;150:782–6.CrossRef Cox JL, Holden JM, Sagovsky R. Detection of postnatal depression. Development of the 10-item Edinburgh postnatal depression scale. Br J Psychiatry. 1987;150:782–6.CrossRef
25.
Zurück zum Zitat Teissedre F, Chabrol H. A study of the Edinburgh Postnatal Depression Scale (EPDS) on 859 mothers: detection of mothers at risk for postpartum depression. L’Encephale. 2004;30(4):376–81.CrossRef Teissedre F, Chabrol H. A study of the Edinburgh Postnatal Depression Scale (EPDS) on 859 mothers: detection of mothers at risk for postpartum depression. L’Encephale. 2004;30(4):376–81.CrossRef
26.
Zurück zum Zitat The American College of Obstetricians and Gynecologists. Screening for perinatal depression: Committee Opinion No. 630. Obstet Gynecol. 2015;125(630):1268–71. The American College of Obstetricians and Gynecologists. Screening for perinatal depression: Committee Opinion No. 630. Obstet Gynecol. 2015;125(630):1268–71.
27.
Zurück zum Zitat Matthey S, Fisher J, Rowe H. Using the Edinburgh postnatal depression scale to screen for anxiety disorders: conceptual and methodological considerations. J Affect Disord. 2013;146(2):224–30.CrossRef Matthey S, Fisher J, Rowe H. Using the Edinburgh postnatal depression scale to screen for anxiety disorders: conceptual and methodological considerations. J Affect Disord. 2013;146(2):224–30.CrossRef
28.
Zurück zum Zitat Bowen A, Bowen R, Maslany G, Muhajarine N. Anxiety in a socially high-risk sample of pregnant women in Canada. Can J Psychiatr. 2008;53(7):435–40.CrossRef Bowen A, Bowen R, Maslany G, Muhajarine N. Anxiety in a socially high-risk sample of pregnant women in Canada. Can J Psychiatr. 2008;53(7):435–40.CrossRef
29.
Zurück zum Zitat Ross LE, Evans SG, Sellers E, Romach M. Measurement issues in postpartum depression part 1: anxiety as a feature of postpartum depression. Arch Womens Ment Health. 2003;6(1):51–7.CrossRef Ross LE, Evans SG, Sellers E, Romach M. Measurement issues in postpartum depression part 1: anxiety as a feature of postpartum depression. Arch Womens Ment Health. 2003;6(1):51–7.CrossRef
30.
Zurück zum Zitat Matthey S, Valenti B, Souter K, Ross-Hamid C. Comparison of four self-report measures and a generic mood question to screen for anxiety during pregnancy in English-speaking women. J Affect Disord. 2013;148(2):347–51.CrossRef Matthey S, Valenti B, Souter K, Ross-Hamid C. Comparison of four self-report measures and a generic mood question to screen for anxiety during pregnancy in English-speaking women. J Affect Disord. 2013;148(2):347–51.CrossRef
31.
Zurück zum Zitat Jones BL, Nagin DS, Roeder K. A SAS procedure based on mixture models for estimating developmental trajectories. Sociol Methods Res. 2001;29(3):374–93.CrossRef Jones BL, Nagin DS, Roeder K. A SAS procedure based on mixture models for estimating developmental trajectories. Sociol Methods Res. 2001;29(3):374–93.CrossRef
32.
Zurück zum Zitat Jones BL, Nagin DS. Advances in group-based trajectory modeling and an SAS procedure for estimating them. Sociol Methods Res. 2007;35(4):542–71.CrossRef Jones BL, Nagin DS. Advances in group-based trajectory modeling and an SAS procedure for estimating them. Sociol Methods Res. 2007;35(4):542–71.CrossRef
33.
Zurück zum Zitat Luoma I, Korhonen M, Salmelin RK, Helminen M, Tamminen T. Long-term trajectories of maternal depressive symptoms and their antenatal predictors. J Affect Disord. 2015;170:30–8.CrossRef Luoma I, Korhonen M, Salmelin RK, Helminen M, Tamminen T. Long-term trajectories of maternal depressive symptoms and their antenatal predictors. J Affect Disord. 2015;170:30–8.CrossRef
34.
Zurück zum Zitat Agresti A. Categorical data analysis. Hoboken: Wiley; 2003. Agresti A. Categorical data analysis. Hoboken: Wiley; 2003.
35.
Zurück zum Zitat Campbell SB, Morgan-Lopez AA, Cox MJ, McLoyd VC. A latent class analysis of maternal depressive symptoms over 12 years and offspring adjustment in adolescence. J Abnorm Psychol. 2009;118(3):479–93.CrossRef Campbell SB, Morgan-Lopez AA, Cox MJ, McLoyd VC. A latent class analysis of maternal depressive symptoms over 12 years and offspring adjustment in adolescence. J Abnorm Psychol. 2009;118(3):479–93.CrossRef
36.
Zurück zum Zitat Anand A, Charney DS. Norepinephrine dysfunction in depression. J Clin Psychiatry. 2000;61(Suppl10):16–24. Anand A, Charney DS. Norepinephrine dysfunction in depression. J Clin Psychiatry. 2000;61(Suppl10):16–24.
37.
Zurück zum Zitat Oshima A, Miyano H, Yamashita S, Owashi T, Suzuki S, Sakano Y, et al. Psychological, autonomic and neuroendocrine responses to acute stressors in the combined dexamethasone/CRH test: a study in healthy subjects. J Psychiatr Res. 2001;35(2):95–104.CrossRef Oshima A, Miyano H, Yamashita S, Owashi T, Suzuki S, Sakano Y, et al. Psychological, autonomic and neuroendocrine responses to acute stressors in the combined dexamethasone/CRH test: a study in healthy subjects. J Psychiatr Res. 2001;35(2):95–104.CrossRef
38.
Zurück zum Zitat O’Hara MW, Swain AM. Rates and risk of postpartum depression - a meta-analysis. Int Rev Psychiatry. 1996;8:37–54.CrossRef O’Hara MW, Swain AM. Rates and risk of postpartum depression - a meta-analysis. Int Rev Psychiatry. 1996;8:37–54.CrossRef
39.
Zurück zum Zitat Le Strat Y, Dubertret C, Le Foll B. Prevalence and correlates of major depressive episode in pregnant and postpartum women in the United States. J Affect Disord. 2011;135(1):128–38.CrossRef Le Strat Y, Dubertret C, Le Foll B. Prevalence and correlates of major depressive episode in pregnant and postpartum women in the United States. J Affect Disord. 2011;135(1):128–38.CrossRef
40.
Zurück zum Zitat Salimi S, Terplan M, Cheng D, Chisolm MS. The relationship between postpartum depression and perinatal cigarette smoking: an analysis of PRAMS data. J Subst Abus Treat. 2015;56:34–8.CrossRef Salimi S, Terplan M, Cheng D, Chisolm MS. The relationship between postpartum depression and perinatal cigarette smoking: an analysis of PRAMS data. J Subst Abus Treat. 2015;56:34–8.CrossRef
41.
Zurück zum Zitat Smedberg J, Lupattelli A, Mårdby A-C, Øverland S, Nordeng H. The relationship between maternal depression and smoking cessation during pregnancy—a cross-sectional study of pregnant women from 15 European countries. Arch Womens Ment Health. 2015;18(1):73–84.CrossRef Smedberg J, Lupattelli A, Mårdby A-C, Øverland S, Nordeng H. The relationship between maternal depression and smoking cessation during pregnancy—a cross-sectional study of pregnant women from 15 European countries. Arch Womens Ment Health. 2015;18(1):73–84.CrossRef
42.
Zurück zum Zitat Lancaster CA, Kj G, Flynn HA, Yoo H, Marcus SM, Davis MM. Risk factors depressive symptoms during pregnancy: a systematic review. Am J Obstet Gynecol. 2010;202(1):5–14.CrossRef Lancaster CA, Kj G, Flynn HA, Yoo H, Marcus SM, Davis MM. Risk factors depressive symptoms during pregnancy: a systematic review. Am J Obstet Gynecol. 2010;202(1):5–14.CrossRef
Metadaten
Titel
Trajectories of maternal depressive and anxiety symptoms from pregnancy to five years postpartum and their prenatal predictors
verfasst von
Asma Ahmed
Angela Bowen
Cindy Xin Feng
Nazeem Muhajarine
Publikationsdatum
01.12.2019
Verlag
BioMed Central
Erschienen in
BMC Pregnancy and Childbirth / Ausgabe 1/2019
Elektronische ISSN: 1471-2393
DOI
https://doi.org/10.1186/s12884-019-2177-y

Weitere Artikel der Ausgabe 1/2019

BMC Pregnancy and Childbirth 1/2019 Zur Ausgabe

Hirsutismus bei PCOS: Laser- und Lichttherapien helfen

26.04.2024 Hirsutismus Nachrichten

Laser- und Lichtbehandlungen können bei Frauen mit polyzystischem Ovarialsyndrom (PCOS) den übermäßigen Haarwuchs verringern und das Wohlbefinden verbessern – bei alleiniger Anwendung oder in Kombination mit Medikamenten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Weniger postpartale Depressionen nach Esketamin-Einmalgabe

Bislang gibt es kein Medikament zur Prävention von Wochenbettdepressionen. Das Injektionsanästhetikum Esketamin könnte womöglich diese Lücke füllen.

Bei RSV-Impfung vor 60. Lebensjahr über Off-Label-Gebrauch aufklären!

22.04.2024 DGIM 2024 Kongressbericht

Durch die Häufung nach der COVID-19-Pandemie sind Infektionen mit dem Respiratorischen Synzytial-Virus (RSV) in den Fokus gerückt. Fachgesellschaften empfehlen eine Impfung inzwischen nicht nur für Säuglinge und Kleinkinder.

Update Gynäkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert – ganz bequem per eMail.