Data dictionary: Breast Implants - DBIR: Difference between revisions

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<span style="display:none">forresearchers</span>
<span style="display:none">thenetherlandscountry</span>
Go back to [[Dutch Institute for Clinical Auditing Databases (DICA) (The Netherlands)]] page.
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. [https://dica.nl/data-aanvragen/ Click here to learn more].
This is a summary of the variables available in the database. You can download the complete data dictionary. [https://dica.nl/data-aanvragen/ Click here to learn more].


'''Patient Identification'''
'''Table 1:''' Patient Identification.
* Hospital
{| class="wikitable"
* Local patient identification number
! Variables
* Unique patient number, clinic
|-
| Hospital
|-
| Local patient identification number
|-
| Unique patient number, clinic
|}


'''Table 2:''' Patient Demographics.
{| class="wikitable"
! Variables
|-
| Date of birth
|-
| Sex
|}


'''Patient Demographics'''
'''Table 3:''' Cosmetic Surgery Information.
* Date of birth
{| class="wikitable"
* Sex
! Variables
|-
| 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
|}


'''Table 4:''' Medical and Surgical Details.
{| class="wikitable"
! Variables
|-
| What is the ASA classification before operation
|-
| Nicotine abuse
|-
| Height in centimeters
|-
| Weight in kilograms
|-
| BMI
|-
| Intervention
|-
| Replacement of device with autologous tissue
|}


'''Cosmetic Surgery Information'''
'''Table 5:''' Implant Information.
* <b>First bilateral cosmetic augmentation?</b> If you select “yes”, some answers will be prefilled. Please check carefully if these answers apply to your patient and complete remaining questions.
{| class="wikitable"
* Is this a first cosmetic augmentation where a new implant is inserted bilaterally?
! Variables
* Side of operation
|-
* Operation date
| Incision site
* Indication of surgery
|-
* Previous radiotherapy
| Plane (of re-insertion)
* First implant surgery of this breast
|-
| 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
|}


'''Table 6:''' Postoperative Complications.
{| class="wikitable"
! Variables
|-
| 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
|}


'''Medical and Surgical Details'''
'''Table 7:''' Device Details.
* What is the ASA classification before operation
{| class="wikitable"
* Nicotine abuse
! Variables
* Height in centimeters
|-
* Weight in kilograms
| Is the device inserted or removed?
* BMI
|-
* Intervention
| Is the current device already registered by this hospital in the DBIR?
* Replacement of device with autologous tissue
|-
| 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
|}


 
'''Table 8:''' SARS-CoV-2 Infection Information.
'''Implant Information'''
{| class="wikitable"
* Incision site
! Variables
* Plane (of re-insertion)
|-
* Capsulectomy
| 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?
* Manufacturer ADM
|-
* Manufacturer MESH
| Date of admission or, if not available, date of treatment
* Mastopexy
|-
* Autologous flap cover
| Has the patient been tested for SARS-CoV-2 infection using a chest CT, RT-PCR or another specific lab test?
* Fat grafting
|-
* Preoperative antibiotics
| On what date was the first suspicion of SARS-CoV-2 infection? [ICD-10: U07.2 date]
* Postoperative antibiotics
|-
* Rinse of the pocket
| If unknown: Was this before treatment or during / after treatment?
* Rinse of the pocket type
|-
* Sleeve/funnel
| On what date was the first specific test performed for SARS-CoV-2 infection? [ICD-10: U07.1 or U07.2 date]
* Nipple guards
|-
* Glove change for insertion
| If unknown: Was this before treatment or during / after treatment?
* Drains
|-
* Planned replacement of TE with permanent implant
| On what date was the first positive lab test on SARS-CoV-2? [ICD-10: U07.1 date]
* Planned replacement of TE for autologous reconstruction
|-
 
| If unknown: Was this before treatment or during / after treatment?
 
|-
'''Postoperative Complications'''
| Date and time of admission to ICU
* Problem at contralateral side (no complications on this side)
|-
* Deep wound infections
| Date and time of discharge from ICU
* Skin necrosis or dehiscence
|-
* Seroma
| Destination after discharge from ICU
* Hematoma
|-
* Autologous flap problem (e.g., LD)
| What was the final status regarding SARS-CoV-2?
* 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?

Latest revision as of 17:42, 4 December 2025

forresearchers thenetherlandscountry 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.

Table 1: Patient Identification.

Variables
Hospital
Local patient identification number
Unique patient number, clinic

Table 2: Patient Demographics.

Variables
Date of birth
Sex

Table 3: Cosmetic Surgery Information.

Variables
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

Table 4: Medical and Surgical Details.

Variables
What is the ASA classification before operation
Nicotine abuse
Height in centimeters
Weight in kilograms
BMI
Intervention
Replacement of device with autologous tissue

Table 5: Implant Information.

Variables
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

Table 6: Postoperative Complications.

Variables
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

Table 7: Device Details.

Variables
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

Table 8: SARS-CoV-2 Infection Information.

Variables
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?