Placenta Accreta
Conditions
Keywords
Pregnancy outcomes, Topographic classification, Placenta accreta
Brief summary
The present study is a prospective multicenter study consisting of a cohort of patients with prenatal or intraoperative diagnosis of PAS, evaluating the clinical outcomes of the group of patients found in each category of the topographic classification. In addition, an approach to evaluate the acceptability of this classification among the obstetrician-gynecologists of the participating medical centers will be included.
Detailed description
The aim of this study is to describe the demographic and clinical characteristics of patients with a diagnosis of placenta accreta spectrum, and to determine the correlation between the topographic classification and the clinical outcomes found in the study. Finally, to evaluated whether the proposed classification is accepted by the obstetrician-gynecologists of the participating centers that manage placenta accreta spectrum patients. It is an observational, multicentric study of a prospective cohort, in which data will be obtained from the medical records and other documents in each participating center, which are considered to be of routine use in day-to-day clinical practice. The study of the outcomes proposed in this protocol will be limited to those recorded in the clinical records and will be taken into account until the participant is discharged from the hospital, during which a surgical intervention was performed due to the suspicion or diagnosis of PAS. It is projected that the period of patient enrollment will last 2 years, counting on from the first participant included. The study population is pregnant patients with a diagnosis of placenta accreta spectrum who visits any of the participating medical centers, and also obstetrician-gynecologists working in participating medical centers. The centers invited to participate are hospitals or clinics that already have knowledge in how to apply the surgical staging of PAS, and the topographic classification and have experience using it.
Interventions
None listed
Sponsors
Fundacion Clinica Valle del Lili
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* Pregnant woman over 18 years old. * Prenatal diagnosis by ultrasound or MRI of Placenta Accreta Spectrum (PAS), regardless of the suspected degree of severity of the disease. * Case requiring surgical management, either as scheduled or emergent procedure. * Application of the topographic classification of placenta accreta spectrum during laparotomy.
Exclusion criteria
* None.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Days of postoperative hospitalization | From the day the surgery is performed until the day of discharge or the date of death from any cause, whichever occurs first, evaluated up to 42 days. | Number of days the patient was hospitalized from the day of surgery to the day of discharge |
| Volume of intraoperative blood loss | During surgery | Surgical bleeding calculated in milliliters |
| Bladder injury | Up to 42 days postpartum | Number of patients who had Bladder injuries |
| Surgical reintervention | Up to 42 days postpartum | Number of patients who need surgical reoperation after index surgery |
| Complications associated with vascular interventions | Up to 42 days postpartum | The patient presented thrombosis or other complication during post-surgery associated with vascular interventions. |
| Maternal death | 24 months | Does the patient die during this study |
Countries
Colombia
Contacts
Primary ContactAlbaro J Nieto-Calvache, MD
Backup ContactDaniela Sarria-Ortiz, MD
Outcome results
None listed