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Postnatal depression screening in a paediatric primary care setting in Italy

  • Antonio Clavenna1Email authorView ORCID ID profile,
  • Elena Seletti1,
  • Massimo Cartabia1,
  • Anna Didoni2,
  • Filomena Fortinguerra1,
  • Teresa Sciascia3,
  • Luca Brivio3,
  • Daniela Malnis4,
  • Maurizio Bonati1 and
  • on behalf of the Postnatal Depression Study Group
BMC PsychiatryBMC series – open, inclusive and trusted201717:42

https://doi.org/10.1186/s12888-017-1205-6

Received: 22 February 2016

Accepted: 11 January 2017

Published: 25 January 2017

Abstract

Background

Postnatal depression is a non-psychotic depressive disorder that begins within 4 weeks of childbirth and occurs in 13% of mothers and 10% of fathers.

A prospective study with the aim to evaluate the prevalence of postnatal depression by screening parents with the Edinburgh Postnatal Depression Scale (EPDS) in the Italian paediatric primary care setting was performed.

Methods

Mothers and fathers of infants born between 1 February and 31 July 2012, living in Italy’s Milan-1 local health unit area, represented the target population of this pilot study. Parents attending well-child visits at any of the family paediatricians’ offices between 60 to 90 days postpartum were asked to participate in the screening and to fill out the EPDS questionnaire. A cut-off score of 12 was used to identify parents with postnatal depression symptoms.

Maternal and paternal socio-demographic variables and information concerning pregnancy and delivery were also collected.

To investigate the association between screening positivity (dependent variable) and socio-demographic variables and factors related to pregnancy and delivery, a Pearson’s χ2 test was used.

Moreover, a stepwise multivariate logistic regression was carried out to evaluate the risk factors that most influence the probability of suffering from postnatal depression.

Results

In all, 126 out of 2706 (4.7%, 95% CI 3.9–5.5%) mothers and 24 out of 1420 (1.7%, 95% CI 1.0–2.4%) fathers were found to be positive for depressive symptoms. Women with mood disorders and anxiety during pregnancy were at increased risk of postpartum depression (OR 22.9, 95% CI 12.1–43.4).

Only 11 mothers (8.7%) positive to EPDS screening attended a psychiatric service, and for 8 of them the diagnosis of postnatal depression was confirmed.

Conclusions

The prevalence of postnatal depression was lower than previously reported. Routine screening resulted ineffective, since few mothers found positive for depression symptoms decided to attend psychiatric services.

Keywords

DepressionPostpartumScreeningPediatricsPhysiciansPrimary Care

Background

Postpartum depression (PPD) is a non-psychotic depressive disorder that the Diagnostic and Statistical Manual of Mental Disorders classifies as an Episode of Major Depressive Disorder that begins within 4 weeks of childbirth [1]. The international prevalence of maternal PPD was estimated at 13%, but the data are influenced by several factors such as screening tools, screening period, and country in which the study was conducted [2, 3]. While maternal depression and its influence on child development is well studied [4, 5], there are few studies on paternal depression, whose estimated prevalence is 10.4% [6].

In Italy few studies have been carried out and are characterized by large variability. Their estimates of maternal PPD range from 1.8% to 38.9% [715]. Only one study evaluated the prevalence of paternal PDD in Italy, with an estimate of 12.6% in the first month after the birth of the neonate. [10]

Postpartum depression adversely affects mothers, infants, and families [1620], and the early recognition of PPD symptoms is crucial for the health of the mother and neonate [21].

Several tools were developed for this purpose, and the most widely used is the Edinburgh Postnatal Depression Scale (EPDS) [22]. This is a 10-item, self-reported questionnaire in which women are asked to rate how they have felt in the previous 7 days. Each question is scored 0–3 (resulting range 0–30) [23].

The cut-off score of 12/13 was considered the best threshold for identifying women at risk of PPD, with a sensitivity of 86% and a specificity of 78% [23].

To improve identification of the disease, programmes providing universal screening in the primary care setting have been proposed, but their effectiveness has been debated [2428].

In Italy, no study has ever evaluated the feasibility of EPDS screening in the paediatric primary care setting. In this regard, a pilot study was performed to evaluate the feasibility of routine screening with EPDS by family paediatricians, to estimate the prevalence of PPD symptoms in mothers and fathers, and to evaluate the influence of maternal and paternal characteristics on the risk of PPD.

Methods

Study design and procedures

An observational prospective study was performed in the area covered by the Milan-1 local health unit (ASL Milano 1, now part of the ATS della Città Metropolitana di Milano), in northern Italy’s Lombardy Region.

Postnatal depression screening was proposed to the parents of infants born between 1 February and 31 July 2012 who attended the second well-child visit performed by the family paediatrician (FP).

Italian FPs routinely perform periodic well-child visits to monitor the growth and wellbeing of children. The first visit is usually scheduled around 30–45 days after birth, and the second between 60 and 90 days afterwards. The timing of the second well-child visit coincides with the period in which the risk of postpartum depression is greatest [2], it is consistent with the period chosen for questionnaire administration by Benvenuti et al in the validation study of the Italian version of EPDS [8], and therefore represents an adequate time frame for screening, without implying an additional burden for FPs and parents.

During the first well-child visit FPs explained the aim of the study to parents, provided them with an information leaflet, and asked them to attend the following visit.

The EPDS questionnaire was given to mothers or fathers, or both, during the 2nd well-child visit. Parents were asked to self-complete the questionnaire in the FP’s waiting room and to return it to the FP. Privacy was guaranteed to parents when filling in the questionnaire and parents were asked to complete the questionnaire separately. The Italian version of EPDS, for which the cross-cultural equivalence with the original one was established [8], was used in the study. It was first validated by Carpiniello et al in 1997 [9], and, subsequently, by Benvenuti et al, who estimated the maximum positive predictive value (PPV) using 12/13 points as a threshold (PPV = 90.9%), with a specificity of 98.9% and a sensitivity of 55.6% [8].

Socio-demographic variables of the mothers and fathers (age, educational level, employment, marital status) were collected. Mothers were also asked if they perceived delivery as difficult or problematic, if they had mood disorders and/or excessive anxiety during pregnancy, if they attended antenatal courses, and if they received information on PPD during the course.

Data on the child (date of birth, gestational age at birth, birth weight, and type of pregnancy and delivery) were collected by the FP on his/her case report form.

Mothers and fathers were considered positive for postpartum depression if the EPDS score was 13 or more. These parents were referred to one of three of the LHU’s referral psychiatric services for postpartum depression care, using a protocol defined before the start of the study.

Mothers and fathers who were negative at the time of EPDS screening, and who subsequently developed depressive symptoms, had the possibility to attend psychiatric services through referral by general practitioners or through self-referral.

Psychiatrists and psychologists of the psychiatric services were asked to inform the FP and the coordinating centre of whether the diagnosis of PPD was confirmed or not.

Before the start of the study, FPs received specific training on the symptoms and effects of postpartum depression, on the use of the EPDS, and on the referral protocol.

The study was approved by the Milan LHU’s Ethics Review Board. Data were analysed using an anonymous patient code.

Written consent was obtained by all parents participating in the study.

Data analysis

Prevalence was estimated as the number of positive mothers and fathers over the number of mothers/fathers screened.

To investigate the association between screening positivity (dependent variable) and socio-demographic variables and factors related to pregnancy and delivery, a Pearson’s χ2 test was used and odds ratios (OR) with 95% CIs were calculated.

Moreover, a stepwise multivariate logistic regression was carried out in order to evaluate the risk factors that most influence the probability of having PPD symptoms. All variables with at least 10% significance (p < 0.10) with the univariate analysis were included in the model.

Results

During the 6 month observation period, 4206 infants were born in the Milan-1 LHU area, 3705 of whom were cared for by one of the 117 FPs involved in the study. Mothers and/or fathers of 2727 (74%) newborns agreed to participate in the study. The mean number of infants per FP with at least one parent who underwent screening with the EPDS was 23 (range 4–53).

Parent characteristics are reported in Table 1. The mean age was 33.5 years (SD 4.8) for the mothers and 36.3 years (SD 5.8) for the fathers. In all, 68% of mothers and 62% of fathers were 30–39 years old, and 7% were single-parents.
Table 1

Characteristics of mothers and fathers participating in the study

Variable

Mothers

N (%)

Fathers

N (%)

Age (years)

  ≤ 24

144 (5.7)

26 (1.9)

 25–29

468 (18.3)

155 (11.3)

 30–34

896 (35.1)

386 (28.2)

 35–39

839 (33.0)

465 (34.0)

  ≥ 40

202 (7.9)

336 (24.6)

Education

 Primary school

466 (17.4)

424 (30.1)

 Secondary School

1354 (50.5)

681 (48.4)

 Degree/PhD

861 (32.1)

303 (21.5)

Occupation

 Yes

2247 (84.1)

1387 (98.2)

 No

424 (15.9)

25 (1.8)

Marital status

 Married

2492 (92.5)

1319 (93.1)

 Single

202 (7.5)

98 (6.9)

Primiparous

 Yes

1407 (52.7)

569 (40.7)

 No

1262 (47.3)

828 (59.3)

Pregnancy Course

 Normal

2441 (91)

1278 (90.5)

 Pathological

241 (9)

134 (9.5)

Delivery Course

 Regular

2056 (77)

715 (74.8)

 Difficult

433 (16.2)

161 (16.9)

 Problematic

183 (6.8)

79 (8.3)

Type of delivery

 Vaginal

1834 (68.9)

960 (69.1)

 Caesarean

827 (31.1)

429 (30.9)

Weight

  ≤ 2500 g

168 (6.2)

87 (6.1)

  > 2500 g

2532 (93.8)

1333 (93.9)

Weeks of gestation

  < 37

180 (6.7)

89 (6.3)

  ≥ 37

2513 (93.3)

1327 (93.7)

Antenatal course

 Yes

1717 (64.6)

n.a.

 No

942 (35.4)

 

Information about PPD

 Yes

1272 (74.0)

n.a.

 No

445 (26.0)

 

Mood changes

 Yes

1199 (45.0)

n.a.

 No

1465 (55.0)

 

Excessive Anxiety

 Yes

343 (13.5)

n.a.

 No

2190 (86.5)

 

n.a.: not applicable

A total of 126 out of 2706 (4.7%, 95% CI 3.9–5.5%) mothers and 24 out of 1420 (1.7%, 95% CI 1.0–2.4%) fathers resulted positive to the EPDS test.

In 8 out of 1410 parent couples (0.6%) both mother and father were positive to the questionnaire.

Results of univariate analyses evaluating the effect of maternal characteristics, and of variables related to the neonate, pregnancy, and delivery, on the risk of having PPD symptoms are shown in Table 2. An increased risk of maternal depressive symptoms was strongly associated with a history of mood (OR 7.2, 95% CI 4.5–12.15, p < 0.001) and/or anxiety disorder (OR 9.6, 95% CI 6.5–14.3, p < 0.001) during pregnancy.
Table 2

Characteristics of mothers with PPD symptoms

 

N (%)

crude O.R.

95% CI

p-value

Age (years)

  ≤ 24

14 (9.7)

1

  

  ≥ 25

105 (4.4)

0.47

0.26 to 0.91

0.006

Education

 Primary School

29 (6.2)

1

  

 Secondary School/Degree

94 (4.2)

0.67

0.43 to1.03

0.06

Employment

 Yes

83 (3.6)

1

  

 No

37 (8.7)

2.49

1.65 to 3.71

<0.0001

Marital status

 Married

109 (4.3)

1

  

 Single

17 (8.4)

2.00

1.18 to 3.42

0.009

Primiparous

 Yes

71 (5.0)

1

  

 No

53 (4.2)

0.82

0.57 to 1.19

0.30

Pregnancy Course

 Normal

107 (4.4)

1

  

 Pathological

18 (7.4)

1.76

1.02 to 2.91

0.03

Delivery Course

 Regular

69 (3.3)

1

  

 Difficult/Problematic

55 (8.9)

2.82

1.96 to 4.07

<0.0001

Type of delivery

 Vaginal

74 (4.0)

1

  

 Caesarean

51 (6.1)

1.56

1.08 to 2.91

0.02

Weight

  ≤ 2500 g

10 (5.9)

1

  

  > 2500 g

115 (4.5)

1.33

0.65 to 2.51

0.40

Weeks of gestation

  < 37

2 (1.1)

1

  

  ≥ 37

113 (4.5)

4.19

1.03 to 17.10

0.03

Antenatal course

 Yes

81 (4.7)

1

  

 No

44 (4.7)

0.99

0.68 to 1.44

0.97

Information about PPD

 Yes

49 (3.8)

1

  

 No

32 (7.2)

1.93

1.22 to 3.06

0.0615

Mood changes

 No

19 (1.3)

1

  

 Yes

104 (8.6)

7.22

4.48 to 12.15

<0.0001

Excessive Anxiety

 No

50 (2.3)

1

  

 Yes

63 (18.3)

9.6

6.50 to 14.28

<0.0001

Other variables found to be associated with the possibility of presenting symptoms were young age, being a single parent, unemployment, and factors related to the pregnancy such as type of delivery, the course of pregnancy, and the maternal perception of the delivery.

In the logistic regression model the combined presence of mood disorders and anxiety during pregnancy was associated with an OR of 22.9 (95% CI 12.1–43.4) of developing PPD symptoms, while having only one of them decreased the OR to 4.7 (95% CI 2.5–8.9).

The risks for unemployed women and for single parents were, respectively, 2.4 (95% CI 1.5–3.8) and 1.8 (95% CI 1.0–3.4) times greater than the respective reference categories. Having perceived the delivery as difficult or problematic was associated with an OR of 2.3 (95% CI 1.2–4.5).

The univariate analyses found that the variables associated with an increased risk of PPD symptoms in fathers were being a single parent (OR 4.5; 95% CI 1.7–11.6), having a low education level (OR 3.4; 95% CI 1.5–7.6), not becoming father for the first time (OR 2.9; 95% CI 1.3–7.4), and having a partner with both mood and anxiety disorders during pregnancy (OR 5.9; 95% CI 2.1–16.6) (Table 3).
Table 3

Characteristic of fathers with PPD symptoms

 

N (%)

crude O.R.

95% CI

p-value

Age (years)

  ≤ 29

6 (3.3)

2.2

0.8–5.6

0.12

  ≥ 30

18 (1.5)

1

  

Education

 Primary School

13 (3.1)

3.4

1.5–7.6

0.013

 Secondary School/Degree

11 (1.1)

1

  

Employment

 Yes

23 (1.7)

1

  

 No

1 (5.9)

3.9

0.2–23.6

0.36

Marital status

 Married

18 (1.4)

1

  

 Single

6 (6.1)

4.5

1.3–7.4

0.005

First child

 Yes

8 (1.0)

1

  

 No

16 (2.8)

2.9

1.3–7.4

0.011

Pregnancy Course*

 Normal

21 (1.6)

1

  

 Pathological

3 (2.2)

1.4

0.3–4.3

0.49

Delivery Course*

 Regular

14 (1.3)

1

  

 Difficult/Problematic

10 (2.9)

2.2

0.9–5.0

0.10

Type of delivery*

 Vaginal

16 (1.9)

1

  

 Caesarean

8 (1.7)

0.9

0.4–2.2

0.77

Birth weight (newborn)

  ≤ 2500 g

2 (2.3)

1.4

0.2–5.2

0.65

  > 2500 g

22 (1.7)

1

  

Weeks of gestation

  < 37

1 (1.1)

0.6

0.03–3.5

1.00

  ≥ 37

23 (1.7)

1

  

Antenatal course*

 Yes

13 (1.4)

1

  

 No

11 (2.3)

1.7

0.6–3.7

0.35

Information about PPD*

 Yes

10 (1.5)

1

  

 No

3 (1.3)

0.9

0.2–3.0

1.00

Mood changes*

 No

15 (1.2)

1

  

 Yes

9 (2.3)

1.9

0.8–5.0

0.17

Excessive Anxiety*

 No

16 (1.4)

1

  

 Yes

8 (4.4)

3.2

1.3–7.7

0.02

*information provided by the partner (mother)

The adjusted OR for paternal PPD symptoms associated with having a partner who reported “changes in mood and excessive anxiety” during pregnancy was 4.4 (95% CI 1.6–12.5). Moreover, being a single parent increased the risk 4.3 fold (95% CI 1.6–11.9). Becoming fathers not for the first time was associated with an adjusted OR for PPD of 2.7 (95% CI 1.1–6.6).

Of the 126 mothers who resulted positive to the EPDS screening, only 11 (8.7%) attended the LHU’s psychiatric services: for 8 of them the diagnosis of postpartum depression was confirmed.

Eight mothers who resulted negative to the EPDS screening attended the psychiatric services and were all diagnosed with postpartum depression.

In all, for 8 out of the 19 (42%) mothers seen by a mental health professional, the results of the EPDS screening and the clinical evaluation matched.

None of the 24 fathers positive to EPDS screening attended the LHU’s psychiatric services.

Discussion

This study had the largest number of participating parents in Italy, and was the first to evaluate the routine screening of mothers and fathers with the EPDS in the Italian paediatric primary care setting.

The prevalence observed in our sample (4.7% of mothers) was generally lower than that reported at the national and international levels [2, 715]. In Italy, the prevalence of PPD at 3 months, estimated with the EPDS with a cut-off ≥13, ranged between 2.7% and 38.9% [7, 8, 11, 14, 15].

These differences may be related to the characteristics of the women (e.g. socio-demographic, economic, and cultural factors), the setting (geographical or urban versus rural), or the study design (e.g. sample size, inclusion criteria, timing of the screening, and observation period).

A study that screened a cohort of women between the 6th and 12th week after birth in the Bergamo Province (about 60 km away from the Milan-1 LHU area) found a slightly greater prevalence (7.1%) than that found in the Milan-1 LHU area [15]. The screening performed in the Bergamo Province enrolled only women who attended antenatal courses in three hospitals, and included also migrant mothers. These factors may partly explain the different estimates between two closely located settings, with similar socioeconomic and demographic characteristics.

The prevalence of depressive symptoms in fathers was very low. Only one Italian study evaluated the prevalence of PPD in fathers, with an estimate of 12.6% [10]. It should, however, be underlined that the screening was performed between 15 and 20 days after the birth of the newborn, and an EPDS cut-off score of 7 was used. Several factors could explain the low prevalence of symptoms in fathers, for example the greater reluctance in reporting distress, gender differences in manifesting depressive symptoms, and, consequently, the potential need for different screening tools or cut-off scores for mothers and fathers, and differences in the onset of depressive symptoms, which may be delayed in fathers [29].

The presence of mood disorders and/or anxiety during pregnancy resulted as the main determinant of the risk of depressive symptoms in mothers. Other factors that increased the risk of PPD symptoms were unemployment, the lack of partner support, and the perception of delivery as a problematic event. These findings are consistent with previous studies [10, 15, 30, 31].

A partner who had mood disorder and/or anxiety during pregnancy is a major risk factor also for paternal PPD. Several studies reported that having a partner with elevated depressive symptoms or depression was the most common correlate of paternal depression [32], and a positive, and moderate in size (r = 0.308; 95% CI, 0.228–0.384), correlation between paternal and maternal depression was found in the meta-analysis by Paulson and Dazemore [6].

Taking into account that family paediatricians in Italy are the guardians of the health of children and their families, well-child visits (in particular the second one) could represent a good occasion to perform universal screening with the EPDS. The percentage of mothers (73%) and fathers (38%) who participated in the screening supports this possibility. This percentage is estimated using the total number of infants in the cohort (3705) as the denominator. In this regard, a lower rate of paternal participation in the screening is expected, since only 10% of fathers usually attend the second well-child visit (data provided by the FPs before the start of the study).

The effectiveness of universal screening in the primary care setting is widely debated [2628, 33].

The usefulness of screening has been advocated in the United States [26, 33, 34], while a universal screening programme was found not to be effective in one Australian rural shire [24], and routine screening was reported as not cost-effective in the UK, mainly due to the potential additional costs of managing women incorrectly diagnosed as depressed [27].

In particular, the lack of sound evidence regarding the cost-effectiveness of EPDS screening is a relevant barrier to its adoption in universal screening programmes in primary care, and more research is needed in this area [35]. Unfortunately, we cannot provide any information on the costs of the screening, but the costs related to the management of false positives do not seem to represent a major problem in the Italian setting.

In our study, few mothers and no fathers agreed to attend a psychiatric service dedicated to the management of postpartum depression. Our findings indicate that the most relevant problem of a PPD screening performed in the Italian paediatric primary care setting could be the scant access to specialist evaluation.

From this point of view, routine screening of parents, alone, does not seem useful: it should be part of a wider initiative involving the target population, psychiatric services, and primary care family physicians and paediatricians.

Strengths and limitations

The main strength of our pilot study was the possibility to screen a significant number of parents of a cohort of newborns in a homogeneous setting, covering 73% of mothers.

There were, however, some limitations. Only parents with a good comprehension of the Italian language were included, and results may not be applicable to migrant parents. Moreover, the primary aim of the study was not to evaluate the predictors of PPD, so only a few socio-demographic variables were collected, and data concerning self esteem, childcare stress, life stress, parental expectations, parental relationships, and infant temperament were not recorded or analysed.

Unfortunately, we were not able to collect data on why parents who resulted positive to the screening did not attend psychiatric services or how mothers who were negative to the screening attended them (e.g. referral by general practitioner versus self-referral).

Finally, it is possible that a few parents positive to EPDS screening attended a private psychiatric service and could therefore not be monitored for confirmation of the diagnosis, resulting in an underestimation of the percentage of mothers and fathers who seek help from a mental health professional.

Conclusions

In conclusion, this pilot study indicates that a routine screening with EPDS by family paediatricians is feasible and can cover a significant proportion of mothers and fathers. This screening, however, does not seem to be effective in identifying parents with postpartum depression, if not as a part of a wider initiative involving the target population and psychiatric services.

Abbreviations

EPDS: 

Edinburgh postnatal depression scale

FP: 

Family paediatrician

LHU: 

Local health unit

NHS: 

National health service

PPD: 

Postpartum depression

Declarations

Acknowledgements

We are grateful to Chiara Pandolfini for language editing.

The composition of the Postnatal depression study group was as follows (affiliations at the time of the study are reported here):*

Scientific Committee: Antonio Clavenna, Filomena Fortinguerra, Elena Seletti, Maurizio Bonati, Laboratorio per la Salute Materno Infantile, IRCCS - Istituto di Ricerche Farmacologiche “Mario Negri”, Milano; Anna Didoni, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Milan, Italy; Daniela Malnis, ASL Milano 1; Luca Brivio, Mariella Dana, Teresa Sciascia, family pediatricians, ASL Milano 1; Valeria Brenna, Farida Ferrato, Claudio Montresor, Mauro Percudani Azienda Ospedaliera G. Salvini, Garbagnate Milanese (MI), Allegra Fisogni, Lorena Vergani, Azienda Ospedaliera Ospedale di Legnano (MI), Alessandro Grecchi, Azienda Ospedaliera San Carlo (MI).

Family pediatricians: Francesca Amman, Hakam Asi, Antonella Avisani, Patrizio Banfi, Maria Pia Battilana, Carla Berardi, Giuseppina Beretta, Paola Beniamina Beretta, Maria Enrica Bertoglio, Lucia Bigalli, Emilio Bognetti, Marzia Boschetti, Dorella Bricalli, Luca Brivio, Pietro Buratti, Sonia Buzzi, Daniela Caccia, Gloria Caldarulo, Marina Irene Camiletti, Maria Luisa Cappuccilli, Maria Maura Carcano, Valentina Carmine, Antonio Cenci, Alberto Civardi, Daniela Cofano, Giuseppina Colavita, Francesca Colletta, Marzia Colombo, Mirella Colombo, Annalisa Cordoni, Anna Corno, Lina Crupi, Andrea Dall’Oglio, Beatrice Damiani, Mariella Dana, Monica De Angelis, Debora De Biase, Marina De Sanctis, Maria Elisabetta Di Cosimo, Laura Di Francesco, Mirella Di Leo, Massimiliano Dozzi, Maria Teresa Elicio, Patrizia Elli, Giuseppe Felice, Loredana Ferrari, Valentina Finizio, Paola Flumine, Cinzia Foschi, Mariacarla Garavaglia, Patrizia Gaslini, Riccardo Ghezzi, Maria Grazia Giuliani, Anna Immacolata Giurgola, Marco Giussani, Angela Rossana Grassi, Emanuela Gualdoni, Tiziana Guidi, Simonetta Gulli, Jarir Hussein Hamade, Talal Jaber, Gudrun Jischke, Roberto Lambiase, Maria Cristina Libretti, Maria Luisa Lodi, Maria Teresa Lovallo, Monica Lukezic, Giovanna Mancuso, Ermenegildo Marciante, Edgardo Marziani, Maria Gabriella Metta, Giovanna Miotto, Marco Moioli, Silvia Angela Monti, Anna Cinthia Morello, Rosanna Moretto, Gloria Nicolini, Patrizia Oldani, Paolo Paganuzzi, Marina Palmieri, Laura Pedrotti, Maria Gabriella Pellegrini, Elena Piacentini, Luisa Maria Poggi, Norberto Porta, Paola Portioli, Alfiero Prandoni, Barbara Ramenghi, Carla Rampini, Patrizia Rossi, Barbara Letizia Saccani, Moris Sahran, Vincenzo Saitta Salanitri, Laura Saleri, Mariam Nabil Sayegh, Teresa Sciascia, Elena Secco, Fabrizio Seidita, Silvia Senaldi, Stefania Signori, Stefania Soardo, Maria Giovanna Stabile, Patrizia Stasi, Marinella Strada, Angela Natalia Tagliati, Kadher Tamini, Maria Vittoria Tiranzi, Marta Travaini, Carla Tulipano, Antonio Usala, Mauro Villa, Giorgio Villa, Emilia Viola, Agnesita Viola, Cristina Volpe, Marco Giuseppe Volpi, Maria Zingales.

The authors would like to thank all parents and pediatricians who agreed to participate in the study.

Funding

The study was partly funded by the Milan-1 local health unit (ASL Milano 1), Italy.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Authors’ contributions

All the authors contributed equally to the design of the study and in writing the protocol. AC and MB coordinated and supervised the study. AC and ES drafted the first version of the manuscript. ES and MC conducted the statistical analysis. AC, AD, and MB interpreted the data. FF, LB, TS; DM coordinated and supervised data collection. All authors substantially contributed to and have approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Ethics approval and consent to participate

The study was approved by the Milan LHU’s Ethics Review Board. Written consent was obtained by all parents participating in the study.

Consent for publication

Not Applicable.

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Authors’ Affiliations

(1)
Laboratory for Mother and Child Health, Department of Public Health, IRCCS- Istituto di Ricerche Farmacologiche “Mario Negri”
(2)
Child and Adolescent Neuropsychiatry Unit, Fondazione IRCCS Ca’ Granda - Ospedale Maggiore Policlinico
(3)
ATS Città Metropolitana di Milano
(4)
Direzione Socio Sanitaria, ASST Santi Paolo e Carlo

References

  1. American Psychiatric Association. Diagnostic and statistical manual of mental disorders:DSM-5. 5th ed. Washington D.C: American Psychiatric Publishing; 2013.View ArticleGoogle Scholar
  2. Gavin NI, Gaynes BN, Lohr KN, Meltzer-Brody S, Gartlehner G, Swinson T. Perinatal depression: a systematic review of prevalence and incidence. Obstet Gynecol. 2005;106:1071–83.View ArticlePubMedGoogle Scholar
  3. O’Hara MW, Swain AM. Rates and risk of postpartum degression - a meta-analysis. Int Rev Psychiatry. 1996;8:37–54.View ArticleGoogle Scholar
  4. Kingston D, Tough S, Whitfield H. Prenatal and postpartum maternal psychological distress and infant development: a systematic review. Child Psychiatry Hum Dev. 2012;43:683–714.View ArticlePubMedGoogle Scholar
  5. Davalos DB, Yadon CA, Tregellas HC. Untreated prenatal maternal depression and the potential risks to offspring: a review. Arch Womens Ment Health. 2012;15:1–14.View ArticlePubMedGoogle Scholar
  6. Paulson JF, Bazemore SD. Prenatal and postpartum depression in fathers and its association with maternal depression: a meta-analysis. JAMA. 2010;303:1961–9.View ArticlePubMedGoogle Scholar
  7. Banti S, Mauri M, Oppo A, Borri C, Rambelli C, Ramacciotti D, et al. From the third month of pregnancy to 1 year postpartum. Prevalence, incidence, recurrence, and new onset of depression. Results from the perinatal depression-research & screening unit study. Compr Psychiatry. 2011;52:343–51.View ArticlePubMedGoogle Scholar
  8. Benvenuti P, Ferrara M, Niccolai C, Valoriani V, Cox JL. The Edinburgh postnatal depression scale: validation for an Italian sample. J Affect Disord. 1999;53:137–41.View ArticlePubMedGoogle Scholar
  9. Carpiniello B, Pariante CM, Serri F, Costa G, Carta MG. Validation of the Edinburgh postnatal depression scale in Italy. J Psychosom Obstet Gynaecol. 1997;18:280–5.View ArticlePubMedGoogle Scholar
  10. Curro V, De RE, Maulucci S, Maulucci ML, Silvestri MT, Zambrano A, et al. The use of Edinburgh postnatal depression scale to identify postnatal depression symptoms at well child visit. Ital J Pediatr. 2009;35:32.View ArticlePubMedPubMed CentralGoogle Scholar
  11. Elisei S, Lucarini E, Murgia N, Ferranti L, Attademo L. Perinatal depression: a study of prevalence and of risk and protective factors. Psychiatr Danub. 2013;25 Suppl 2:S258–62.PubMedGoogle Scholar
  12. Girardi P, Pompili M, Innamorati M, Serafini G, Berrettoni C, Angeletti G, et al. Temperament, post-partum depression, hopelessness, and suicide risk among women soon after delivering. Women Health. 2011;51:511–24.View ArticlePubMedGoogle Scholar
  13. Mauri M, Oppo A, Montagnani MS, Borri C, Banti S, Camilleri V, et al. Beyond “postpartum depressions”: specific anxiety diagnoses during pregnancy predict different outcomes: results from PND-ReScU. J Affect Disord. 2010;127:177–84.View ArticlePubMedGoogle Scholar
  14. Monti F, Agostini F, Marano G, Lupi F. The course of maternal depressive symptomatology during the first 18 months postpartum in an Italian sample. Arch Womens Ment Health. 2008;11:231–8.View ArticlePubMedGoogle Scholar
  15. Piacentini D, Leveni D, Primerano G, Cattaneo M, Volpi L, Biffi G, et al. Prevalenza e fattori di rischio della depressione post parto tra le donne che partecipano ai corsi pre parto. Epidemiol Psichiatr Soc. 2009;18:214–20.PubMedGoogle Scholar
  16. Avan B, Richter LM, Ramchandani PG, Norris SA, Stein A. Maternal postnatal depression and children’s growth and behaviour during the early years of life: exploring the interaction between physical and mental health. Arch Dis Child. 2010;95:690–5.View ArticlePubMedGoogle Scholar
  17. Feldman R, Granat A, Pariente C, Kanety H, Kuint J, Gilboa-Schechtman E. Maternal depression and anxiety across the postpartum year and infant social engagement, fear regulation, and stress reactivity. J Am Acad Child Adolesc Psychiatry. 2009;48:919–27.View ArticlePubMedGoogle Scholar
  18. 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;119:116–23.View ArticlePubMedGoogle Scholar
  19. Murray L, Arteche A, Fearon P, Halligan S, Goodyer I, Cooper P. Maternal postnatal depression and the development of depression in offspring up to 16 years of age. J Am Acad Child Adolesc Psychiatry. 2011;50:460–70.View ArticlePubMedGoogle Scholar
  20. Stein A, Pearson RM, Goodman SH, Rapa E, Rahman A, McCallum M, et al. Effects of perinatal mental disorders on the fetus and child. Lancet. 2014;384:1800–19.View ArticlePubMedGoogle Scholar
  21. Sharma V, Sharma P. Postpartum depression: diagnostic and treatment issues. J Obstet Gynaecol Can. 2012;34:436–42.View ArticlePubMedGoogle Scholar
  22. Boyd RC, Le HN, Somberg R. Review of screening instruments for postpartum depression. Arch Womens Ment Health. 2005;8:141–53.View ArticlePubMedGoogle Scholar
  23. 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.View ArticlePubMedGoogle Scholar
  24. Armstrong S, Small R. Screening for postnatal depression: not a simple task. Aust N Z J Public Health. 2007;31:57–61.View ArticlePubMedGoogle Scholar
  25. Chaudron LH, Szilagyi PG, Kitzman HJ, Wadkins HI, Conwell Y. Detection of postpartum depressive symptoms by screening at well-child visits. Pediatrics. 2004;113:551–8.View ArticlePubMedGoogle Scholar
  26. Chaudron LH, Szilagyi PG, Campbell AT, Mounts KO, McInerny TK. Legal and ethical considerations: risks and benefits of postpartum depression screening at well-child visits. Pediatrics. 2007;119:123–8.View ArticlePubMedGoogle Scholar
  27. Paulden M, Palmer S, Hewitt C, Gilbody S. Screening for postnatal depression in primary care: cost effectiveness analysis. BMJ. 2009;339:b5203.View ArticlePubMedPubMed CentralGoogle Scholar
  28. Yawn BP, Dietrich AJ, Wollan P, Bertram S, Graham D, Huff J, et al. TRIPPD: a practice-based network effectiveness study of postpartum depression screening and management. Ann Fam Med. 2012;10:320–9.View ArticlePubMedPubMed CentralGoogle Scholar
  29. Goodman JH. Paternal postpartum depression, its relationship to maternal postpartum depression, and implications for family health. J Adv Nurs. 2004;45:26–35.View ArticlePubMedGoogle Scholar
  30. Beck CT. A meta-analysis of predictors of postpartum depression. Nurs Res. 1996;45:297–303.View ArticlePubMedGoogle Scholar
  31. Beck CT. Predictors of postpartum depression: an update. Nurs Res. 2001;50:275–85.View ArticlePubMedGoogle Scholar
  32. Wee KY, Skouteris H, Pier C, Richardson B, Milgrom J. Correlates of ante- and postnatal depression in fathers: a systematic review. J Affect Disord. 2011;130:358–77.View ArticlePubMedGoogle Scholar
  33. O’Connor E, Rossom RC, Henninger M, Groom HC, Burda BU. Primary care screening for and treatment of depression in pregnant and postpartum women: evidence report and systematic review for the US preventive services task force. JAMA. 2016;315:388–406.View ArticlePubMedGoogle Scholar
  34. Yogman MW. Postpartum depression screening by pediatricians: time to close the gap. J Dev Behav Pediatr. 2016;37:157.View ArticlePubMedGoogle Scholar
  35. Hewitt C, Gilbody S, Brealey S, Paulden M, Palmer S, Mann R, Green J, Morrell J, Barkham M, Light K, Richards D. Methods to identify postnatal depression in primary care: an integrated evidence synthesis and value of information analysis. Health Technol Assess. 2009;13(36):1–145, 147–230.Google Scholar

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© The Author(s). 2017

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