Data dictionary: Breast Implants - DBIR
From Beacon
Go back to Dutch Institute for Clinical Auditing Databases (DICA) (The Netherlands) page.
This is a summary of the variables available in the database. You can download the complete data dictionary. Click here to learn more.
Patient Identification
- Hospital
- Local patient identification number
- Unique patient number, clinic
Patient Demographics
- Date of birth
- Sex
Cosmetic Surgery Information
- First bilateral cosmetic augmentation? If you select “yes”, some answers will be prefilled. Please check carefully if these answers apply to your patient and complete remaining questions.
- Is this a first cosmetic augmentation where a new implant is inserted bilaterally?
- Side of operation
- Operation date
- Indication of surgery
- Previous radiotherapy
- First implant surgery of this breast
Medical and Surgical Details
- What is the ASA classification before operation
- Nicotine abuse
- Height in centimeters
- Weight in kilograms
- BMI
- Intervention
- Replacement of device with autologous tissue
Implant Information
- Incision site
- Plane (of re-insertion)
- Capsulectomy
- Manufacturer ADM
- Manufacturer MESH
- Mastopexy
- Autologous flap cover
- Fat grafting
- Preoperative antibiotics
- Postoperative antibiotics
- Rinse of the pocket
- Rinse of the pocket type
- Sleeve/funnel
- Nipple guards
- Glove change for insertion
- Drains
- Planned replacement of TE with permanent implant
- Planned replacement of TE for autologous reconstruction
Postoperative Complications
- Problem at contralateral side (no complications on this side)
- Deep wound infections
- Skin necrosis or dehiscence
- Seroma
- Hematoma
- Autologous flap problem (e.g., LD)
- Skin scarring problems
- Capsular contracture
- Capsular contracture grade
- Breast pain
- Patient dissatisfied with volume
- Asymmetry
- Newly diagnosed breast cancer
- Suspicion of BIA-ALCL
- PA confirmed BIA-ALCL
- Patient's request without health complaints
- Suspicion of breast implant-associated illness (previously ASIA)
- Device rupture or Device deflation
- Silicone extravasation
- Silicone extravasation type
- Device Malposition
- Recall
- Other (describe)
- Seroma/Hematoma
Device Details
- Is the device inserted or removed?
- Is the current device already registered by this hospital in the DBIR?
- Insertion type
- Year of implantation (yyyy)
- Medical records or device passport
- Identifiable markers on implant
- Reference No
- Manufacturer
- Device type
- Texture
- Coating
- Fill
- Shape
- (Maximum) weight/volume of implant (cc or gr)
- Manufacturer supports barcode
- Using GS1 barcode scanner?
- GS1 barcode. Code starts with (01)
- Barcode Processing Status
- GTIN (= global trade item number)
- Expiry Date (YYMMDD)
- Lot Number
- Serial Number
SARS-CoV-2 Infection Information
- Was there (clinical) suspicion of or a test performed for a SARS-CoV-2 infection in the period before admission up until 30 days after admission?
- Date of admission or, if not available, date of treatment
- Has the patient been tested for SARS-CoV-2 infection using a chest CT, RT-PCR or another specific lab test?
- On what date was the first suspicion of SARS-CoV-2 infection? [ICD-10: U07.2 date]
- If unknown: Was this before treatment or during / after treatment?
- On what date was the first specific test performed for SARS-CoV-2 infection? [ICD-10: U07.1 or U07.2 date]
- If unknown: Was this before treatment or during / after treatment?
- On what date was the first positive lab test on SARS-CoV-2? [ICD-10: U07.1 date]
- If unknown: Was this before treatment or during / after treatment?
- Date and time of admission to ICU
- Date and time of discharge from ICU
- Destination after discharge from ICU
- What was the final status regarding SARS-CoV-2?