Partheeban Muruganandam1, Deepa Shanmugam2, Niranjjan Ramachandran3. 1. Dept. of Psychiatry, Mahatma Gandhi Medical College & Research Institute, Puducherry, India. 2. Dept. of Obstetrics and Gynaecology, Aarupadai Veedu Medical College, Puducherry, India. 3. Dept. of Community Medicine, Vinayaga mission medical College, Karaikal, India.
We would like to thank the above authors for their interest in our article and for raising
relevant points. Our response is as follows:As our study was initiated during the postpartum period, we were not sure about antenatal
mood symptoms as no structured assessment was done during the antenatal period. However,
during our assessment, we had considered the history of treatment for depression. Hence, we
mentioned the term “postpartum” as a specifier in view of uncertainty about the antepartum
period.We also acknowledge that the possibility of postpartum blue cannot be ruled out in our study.
We mentioned it as postpartum depression (PPD) as there is no definitive diagnostic entity for
postpartum blues in the DSM-5. Our findings support the view that mothers
with a history of depression are at risk of PPD.[1] However, we took the score of 10 based on previous literature.[2] We considered a lower score to cover patients who have mild symptoms. Patients who were
screened positive during the initial assessment were referred to a psychiatry outpatient
clinic for psychological intervention; details of treatment intervention were not mentioned as
it was not our primary study objective.Possible reasons for the increased rate of LSCS in our sample are the tertiary care setting
where patients with high-risk pregnancies were often involved, which is not comparable to the
general population, and early discharge from inpatient care following vaginal delivery. A
meta-analysis had found an inconsistent association of elective and emergency caesarian
section with PPD.[3] As we did not categorize the type of lower segment cesarean section (LSCS), our
findings might not be comparable to their result. However, future studies should explore the
type of LSCS with PPD in this special population, to consider it as a potential confounder. We
acknowledge the typological error “Assisted Delivery” which should have been “Assisted
Reproductive Technologies.”We used a validated screening instrument (Edinburgh Depression Rating Scale) for assessing
perinatal depression. All interviews were done by a qualified psychiatrist who did both the
initial interview and the assessments during baseline and follow-up.We acknowledge that a family history of PPD could have been considered as a potential
confounder that might have influenced the result.This discussion highlights the importance of research in this interesting and important
area.
Authors: Sumitra Devi Shrestha; Rina Pradhan; Thach D Tran; Rosa C Gualano; Jane R W Fisher Journal: BMC Pregnancy Childbirth Date: 2016-04-04 Impact factor: 3.007