Change Request |
Reference: | Change Request 315 |
Version No: | 1.9 |
Subject: | DG1126 - Review of KC65 - Colposcopy |
Type of Change: | Change to NHS data standards |
Effective Date: | 1 April 2003 |
Reason for Change: | Data Standards to support revisions to the KC65 return. |
For Part A of the return, the classification of COLPOSCOPY REFERRAL INDICATION has been updated to reflect the change to Clinical Indication.
For Part B, ATTENDED OR DID NOT ATTEND has been extended, and a new attribute APPOINTMENT TYPE introduced.
The description of COLPOSCOPY PRIME PROCEDURE TYPE has been modified to reflect Parts C1 and C2; and PATIENT INFORMED BIOPSY RESULT DATE has been changed to reflect Part D.
Minor changes have been made to BIOPSY REFERRAL OUTCOME and COLPOSCOPY PRIME PROCEDURE TYPE for Part E.
Changes have also been made to support the move from exclusively consultant activity, and to include nurse clinics.
Summary of changes:Class Definitions | |
CLINIC ATTENDANCE NURSE | Change to attributes |
OUT-PATIENT APPOINTMENT | Change to attributes |
Attribute Definitions | |
APPOINTMENT TYPE | New Attribute |
ATTENDED OR DID NOT ATTEND | Change to description |
BIOPSY REFERRAL OUTCOME | Change to description |
COLPOSCOPY PRIME PROCEDURE TYPE | Change to description |
COLPOSCOPY REFERRAL INDICATION | Change to description |
PATIENT INFORMED BIOPSY RESULT DATE | Change to description |
Central Return Forms | |
KC65 1 | Change guidance text |
KC65 2 | Change guidance text |
KC65 3 | Change guidance text |
KC65 4 | Change guidance text |
KC65 5 | Change guidance text |
KC65 6 | Change guidance text |
KC65 7 | New Form |
Diagrams | |
KC65 COLPOSCOPY CLINICS: REFERRALS, TREATMENTS AND OUTCOMES | Change to diagram contents |
Name: | Kevin Shine |
Date: | 11 March 2003 |
Sponsor: | Data Standards Team |
Attributes of this Class are:
COLPOSCOPY PRIME PROCEDURE TYPE | ||
colposcopy only | ||
FIRST ATTENDANCE |
Attributes of this Class are:
K | APPOINTMENT DATE | |
K | APPOINTMENT TIME | |
APPOINTMENT BOOKING SYSTEM TYPE | ||
APPOINTMENT TYPE | ||
colposcopy appointments only | ||
ATTENDED OR DID NOT ATTEND |
The type of an OUT-PATIENT APPOINTMENT for a colposcopy clinic. Note that there may be more than one appointment of type 'first appointment'.
Classification:
a. | First appointment : An appointment for a first attendance |
b. | Treatment: A follow-up appointment specifically for treatment |
c. | Follow-up/surveillance: All other follow-up appointments |
Context | Alias |
---|---|
plural | APPOINTMENT TYPES |
This indicates whether or not a PERSON or PATIENT attended for an appointment. If the
For colposcopy appointments only, code 2 is subdivided into:
(i) before the appointment date
(ii) on the appointment day
and code 3 is subdivided into:
(i) arrived, but did not wait to be seen
(ii) other
National Codes:
5 | Attended on time or, if late, before the relevant health care professional was ready to see the patient |
6 | Arrived late, after the relevant health care professional was ready to see the patient, but was seen |
7 | Patient arrived late and could not be seen |
2 | Appointment cancelled by, or on behalf of, the patient |
3 | Did not attend - no advance warning given |
4 | Appointment cancelled or postponed by the HEALTH CARE PROVIDER |
Note: The classification has been listed in logical sequence rather than alphanumeric order.
Context | Alias |
---|---|
plural | ATTENDED OR DID NOT ATTEND |
A code used to reference an outcome of a REFERRAL FOR BIOPSY. For cervical histology, biopsies are taken after a colposcopy has been performed.
For cervical histology for KC61 purposes, the classification is:
a. | Cervical Cancer (including micro-invasive) | |
| ||
b. | Adenocarcinoma in situ / CGIN | |
c. | CIN3 | |
d. | CIN2 | |
e. | CIN1 | |
f. | HPV only | |
g. | No CIN/No HPV | |
h. | Inadequate biopsy | |
i. | Colposcopy - Nothing Abnormal Detected (NAD)/no biopsy taken | |
j. | Results not known by laboratory | |
k. | Non cervical cancers detected |
For cervical histology for KC65 purposes, the classification is:
a. | Cancer (including micro-invasive) | |
b. | Adenocarcinoma in situ | |
c. | CIN3 | |
d. | CIN2 | |
e. | CIN1 | |
f. | HPV/cervicitus only | |
g. | No CIN/No HPV (normal) | |
h. | Inadequate/unsatisfactory biopsy | |
i. | Result not known by clinic |
For breast cancer screening for KC62 purposes,the classification is:
a. | Benign or negative | ||
b. | Inconclusive | ||
c. | Positive; i.e. cancer detected | ||
i. | non-invasice or possibly micro-invasive | ||
a. | low (DCIS only detected) | ||
b. | intermediate (DCIS only detected) | ||
c. | high (DCIS only detected) | ||
d. | grade not known (DCIS only detected) | ||
ii. | definitely micro-invasive | ||
a. | low (DCIS only detected) | ||
b. | intermediate (DCIS only detected) | ||
c. | high (DCIS only detected) | ||
d. | grade not known (DCIS only detected) | ||
iii. | invasive size not known | ||
a. | Grade I | ||
b. | Grade II | ||
c. | Grade III | ||
d. | grade not known | ||
iv. | invasive size known | ||
a. | Grade I | ||
b. | Grade II | ||
c. | Grade III | ||
d. | grade not known | ||
v. | invasive status not known | d. | Biopsy not done or result not yet know |
References:
KC65 - Colposcopy Clinics, Referrals, Treatments and Outcomes
KC61: Pathology Laboratories - Cervical Cytology and Outcome of Gynaecological Referrals
KC62: Adult Screening Programmes - Breast Screening
Context | Alias |
---|---|
plural | BIOPSY REFERRAL OUTCOMES |
The COLPOSCOPY PRIME PROCEDURE TYPESidentifies the prime PATIENT PROCEDURE undertaken during the first Colposcopy Clinic OUT-PATIENT ATTENDANCE CONSULTANT. The
Note where the PATIENT opts to defer treatment to a later time the classification e. No treatment; no treatment received and no biopsy taken, should be recorded.
Classification:
a. | Ablation; treatment method recorded as ablation. This will include cold coagulation, cryotherapy, cautery and diathermy. |
(i) biopsy result available | |
(ii) no biopsy taken, or biopsy result not known by clinic | |
b. | Loop/laser excision or knife cone; treatment method recorded as loop/laser excision or knife cone and biopsy type recorded as other than no biopsy. This will include LLETZ and NEEP. |
c. | Diagnostic biopsy (punch); no treatment received and biopsy type recorded as directed biopsy or multiple directed biopsy, or any other biopsy taken for diagnostic purposes only. |
d. | Other; treatment method recorded as other and biopsy type recorded as other than no biopsy. This will include polyp avulsion and treatment with silver nitrate. |
e. | No treatment; no treatment received and no biopsy taken. |
Context | Alias |
---|---|
plural | COLPOSCOPY PRIME PROCEDURE TYPES |
The referral indication of a REFERRAL REQUEST to a Colposcopy Clinic.
Classification:
a. | Screening smear | |
i. | Abnormal screening smear | |
ii. | Abnormal smear after colposcopy | |
b. | Clinical indication | |
i. | Urgent | |
ii. | Non-urgent |
Context | Alias |
---|---|
plural | COLPOSCOPY REFERRAL INDICATIONS |
The date the patient was informed of the result of a biopsy taken as a result of a colposcopy PATIENT PROCEDURE. The date the patient was informed in writing of the result of a biopsy taken as a result of a colposcopy PATIENT PROCEDURE.
Context | Alias |
---|---|
plural | PATIENT INFORMED BIOPSY RESULT DATES |
Central Return Form Guidance |
The Department, NHS Cervical Screening Programme (NHSCSP) and Regional Offices require information from NHS HEALTH CARE PROVIDERS on colposcopy clinic activity.
The KC65 will form part of the wider NHS Cancer Information Strategy which aims to improve the effectiveness and efficiency of care delivery for those with actual or suspected cancer, throughout the patient journey.
The information is used to monitor the process of achieving the Government's target to reduce the incidence of invasive cervical cancer and to monitor the performance of colposcopy clinics on local, regional and national levels.
Information on the return is also used in Public Expenditure Survey (PES) negotiations, resource allocation to the NHS and Departmental accountability.
Information based on the KC65 return is published annually by the Department in the Statistical Bulletin Cervical Screening Programme.
KC65 is a quarterly return with the first quarter starting on 1 April and the last quarter ending on 31 March. Returns must be submitted by the thirtieth working day after the end of the quarter.
The KC65 return requires the ORGANISATION CODE and ORGANISATION NAME of the NHS HEALTH CARE PROVIDER- NHS Trust or Primary Care Trust - as well as the name of a contact and the contact telephone number on the front page. It must be signed and dated by the person completing the return.
The British Society for Colposcopy and Cervical Pathology has agreed a Minimum Data Set (MDS) for colposcopy services, currently being introduced into Colposcopy Clinics. The MDS meets professional requirements for audit and quality improvement as well as departmental needs, and provides the information needed to complete the KC65.
Colposcopy is a PATIENT PROCEDURE carried out on a woman who has been referred to a Colposcopy Clinic following a SCREENING TEST carried out either as part of a SCREENING PROGRAMME or opportunistically. Alternatively the woman may be referred as a result of clinical indications.
Central Return Form Guidance |
Part A of the KC65 return is a count of the number of women referred for colposcopy. This information is used to monitor referral patterns to ensure that guidelines on referral are being followed.
A colposcopy is a PATIENT PROCEDURE carried out during a CLINIC ATTENDANCE CONSULTANT on a PATIENT. The PATIENTwill have been referred to the Colposcopy Clinic:
In cases where there is both a clinical indication and a SCREENING TESTreferral smear, the referral should be treated as clinical indication.
The data is based on the woman's first OUT-PATIENT APPOINTMENT CONSULTANT in the quarter regardless of whether she attended the clinic or not. Please note that the total number referred as recorded in Part A should equal the total number waiting as recorded in Part B as both parts relate to the same cohort of women.
- | following a SCREENING TEST carried out either as part of a SCREENING PROGRAMME or opportunistically. |
or | |
- | as a result of clinical indication |
In cases where there is both a clinical indication and a
This line counts all the women with a REFERRAL REQUEST for coloposcopy with a COLPOSCOPY REFERRAL INDICATION of Screening smear. These are PERSONS IN A SCREENING PROGRAMME who have been given a SCREENING TESTas part of a planned SCREENING PROGRAMME. It also includes women screened opportunistically, these women have had a SCREENING TESTwith the OPPORTUNISTIC SCREENING INDICATOR of Yes. In addition, if a PERSON IN A SCREENING PROGRAMMEhas been suspended from the SCREENING PROGRAMMEfollowing colposcopy and is currently having surveillance smears as indicated by SCREENED WHILE SUSPENDED INDICATOR of Yes, it may be that an abnormal smear will cause the woman to be re-referred to colposcopy. In this case the COLPOSCOPY REFERRAL INDICATIONshould be Screening smear, regardless of whether or not she has been discharged from colposcopy at this time.
This line counts all the women with a REFERRAL REQUESTfor coloposcopy with a COLPOSCOPY REFERRAL INDICATIONof Clinical indication.
Where a woman is referred with symptoms and is given a SCREENING TESTthe COLPOSCOPY REFERRAL INDICATIONshould still be Clinical indication and not Screening smear. Where no symptoms are present the COLPOSCOPY REFERRAL INDICATIONshould not be Clinical indication.
The information in columns 2-9 is based on the cervical screening test results, which led to the REFERRAL REQUEST. Classifications are those of CYTOLOGY RESULT TYPES of a REQUEST FOR PATHOLOGY INVESTIGATION and are in accordance with the categories shown in box 22 of HMR 101/5 Request/Report for Cervical or Vaginal Cytology. Entries recorded in Other (column 9) should only occur in exceptional circumstances. NHS Cervical Screening Programme (NHSCSP) guidelines state that all smears should be identified as belonging to one of the eight recognised category classifications of CYTOLOGY RESULT TYPE. Other (column 9) does not correspond to these recognised categories and should be used to record those rare cases in which a recognised category is not appropriate. Where an entry is present in Other (column 9) then supporting notes should be recorded in the available box on the first page of the KC65 form. Where the cervical screening test results which led to the REFERRAL REQUESTindicates more than one result type, the most severe result should recorded as the CYTOLOGY RESULT TYPE.
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Inadequate sample (cat.1). NHS Cervical Screening Programme guidelines state the recording of three cervical screening tests with a CYTOLOGY RESULT TYPEclassification of Inadequate sample (cat.1) indicates referral to colposcopy however, referral to colposcopy may occur following an inadequate smear for other reasons.
NHS Cervical Screening Programme guidelines state the recording of three cervical screening tests with a
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Borderline changes (cat.8).
NHS Cervical Screening Programme guidelines state the recording of three cervical screening tests with a CYTOLOGY RESULT TYPEclassification of Borderline changes (cat.8) indicates referral to colposcopy however, referral to colposcopy may occur following a borderline smear for other reasons.
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Mild dyskaryosis (cat.3).
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Moderate dyskaryosis (cat. 7), including abnormal, unclassifiable and ungraded smears.
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Severe dyskaryosis (cat.4).
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Severe dyskaryosis/?invasive carcinoma (cat.5).
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of ?Glandular neoplasia (cat.6), including adenocarcinoma.
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Other. This should only be used in the rare situations where usual categorisation is not appropriate. Examples include women with incomplete or missing records and women who have moved from abroad. Where an entry is present in Other (column 9) then supporting notes should be recorded in the available box on the first page of the KC65 form.
Where a woman is referred with symptoms and is given a
A count of the number of women who have been referred to the colposcopy clinic with a REFERRAL REQUESTwith a COLPOSCOPY REFERRAL INDICATIONof Clinical indication.
This is the total of women referred for colposcopy, split between with those referred with a COLPOSCOPY REFERRAL INDICATIONof Clinical indication and those referred with a COLPOSCOPY REFERRAL INDICATIONof Screening smear.
This is the total for all women counted in columns 2 to 11.
Central Return Form Guidance |
Part B of KC65 shows, for each referral, the waiting time before the first offered appointment. The NHS Cervical Screening Programme (NHSCSP) has issued guidance on waiting times, and the information is used to monitor whether clinics are meeting these standards.
The waiting time is the length of time between the date on the referral letter - the REFERRAL DATE of the REFERRAL REQUEST for colposcopy and the woman's first OUT-PATIENT APPOINTMENT CONSULTANT in the quarter, regardless of whether she attended the colposcopy clinic or not. Where there has been a direct referral from the cytology laboratory, the referral date is the date the smear was reported - the SCREENING RESULT SENT DATE. Please note that the total number referred as recorded in Part A should equal the total number waiting as recorded in Part B as both parts relate to the same cohort of women.
This counts the number of women whose waiting time was less than or equal to 14 days.
This counts the number of women whose waiting time was more than 14 days but less than or equal to 28 days.
This counts the number of women whose waiting time was more than 28 days but less than or equal to 56 days.
This counts the number of women whose waiting time was more than 56 days but less than or equal to 84 days.
This counts the number of women whose waiting time was more than 84 days.
The information in columns 2-6 is based on the cervical screening test result which led to the REFERRAL REQUESTand directly relates to the information recorded in columns 2-9 of Part A of this form. Classifications are those of CYTOLOGY RESULT TYPES of a REQUEST FOR PATHOLOGY INVESTIGATION and are in accordance with the categories shown in box 22 of HMR 101/5 Request/Report for Cervical or Vaginal Cytology. For Part B certain categories have been added together e.g. column 4 of Part B directly relates to column 5 and 6 of Part A.
A count of the number of women with a CYTOLOGY RESULT TYPESclassification of Inadequate sample (cat. 1).
A count of the number of women with a CYTOLOGY RESULT TYPESclassification of Borderline changes (cat. 8) or Mild dyskaryosis (cat. 3).
A count of the number of women with a CYTOLOGY RESULT TYPESclassification of Moderate dyskaryosis (cat. 7), including abnormal, unclassifiable and ungraded smears or Severe dyskaryosis (cat. 4).
A count of the number of women with a CYTOLOGY RESULT TYPESclassification of Severe dyskaryosis/?invasive carcinoma (cat. 5) or ?Glandular neoplasia (cat. 6), including adenocarcinoma.
A count of the number of women with a CYTOLOGY RESULT TYPESclassification of Other.
A count of the number of women who have been referred to the colposcopy clinic with a REFERRAL REQUESTwith a COLPOSCOPY REFERRAL INDICATION of Clinical indication.
This is the total of all women by length of time waiting.
This is the total for all women counted in columns 2 to 8.
The following data quality checks should be made:
Central Return Form Guidance |
Part C of the KC65 return is a count of procedures undertaken at coloposcopy clinics, showing the nature of the initial treatment by result of referral. The information is used to monitor treatment patterns at first attendance to ensure that treatment guidelines, such as on the number of biopsies taken, are met.
Data is collected on the woman's first OUT-PATIENT APPOINTMENT CONSULTANT in the quarter (with FIRST ATTENDANCE classified as First Attendance). Where a woman has a smear taken during the attendance the COLPOSCOPY PRIME PROCEDURE TYPE should be recorded as No treatment; no treatment received and no biopsy taken.
The procedures undertaken in the coloposcopy clinics are PATIENT PROCEDURES.Only one PATIENT PROCEDUREshould be counted for each woman's FIRST ATTENDANCE. If more than one procedure is carried out, the most severe should be recorded for KC65.
Lines 0001 to 0008 require data on the number of women referred for colposcopy by CYTOLOGY RESULT TYPES.
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Inadequate sample (cat. 1).
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Borderline changes (cat. 8).
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Mild dyskaryosis (cat. 3).
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Moderate dyskaryosis (cat. 7), including abnormal, unclassifiable and ungraded smears..
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Severe dyskaryosis (cat. 4).
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Severe dyskaryosis/invasive carcinoma (cat. 5).
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of ?Glandular neoplasia (cat. 6), including adenocarcinoma..
A count of the number of women with a CYTOLOGY RESULT TYPEclassification of Other. Entries recorded in Other (line 0008) should only occur in exceptional circumstances. NHS Cervical Screening Programme (NHSCSP) guidelines state that all smears should be identified as belonging to one of the eight recognised category classifications of CYTOLOGY RESULT TYPE. Other (line 0008) does not correspond to these recognised categories and should be used to record those rare cases in which a recognised category is not appropriate. Where an entry is present in Other (line 0008) then supporting notes should be recorded in the available box on the first page of the KC65 form.
A count of the number of women who have been referred to the colposcopy clinic with a REFERRAL REQUEST with a COLPOSCOPY REFERRAL INDICATION of Clinical indication. Note all procedures carried out on women who have been referred to the colposcopy clinic with a REFERRAL REQUESTwith a COLPOSCOPY REFERRAL INDICATIONof Clinical indication should be recorded in this line regardless of the result of any smear taken after the referral.
This is the total for all women counted in columns 2 to 7.
This counts the number of women who received no treatment and for whom was recorded a COLPOSCOPY PRIME PROCEDURE TYPE of No treatment; no treatment received and no biopsy taken.
This counts the number of women who received no treatment and for whom a COLPOSCOPY PRIME PROCEDURE TYPEof Diagnostic biopsy (punch); no treatment received and biopsy type recorded as directed biopsy or multiple directed biopsy was recorded.
This counts the number of women who for whom was recorded a COLPOSCOPY PRIME PROCEDURE TYPEof Ablation; treatment method recorded as ablation and biopsy type recorded as other than no biopsy. This will include cold coagulation, cryotherapy, cautery and diathermy.
This counts the number of women who for whom was recorded a COLPOSCOPY PRIME PROCEDURE TYPEof Loop/laser excision or knife cone; treatment method recorded as loop/laser excision or knife cone and biopsy type recorded as other than no biopsy. This will include LLETZ and NEEP.
This counts the number of women who for whom was recorded a COLPOSCOPY PRIME PROCEDURE TYPEof Other; treatment method recorded as other and biopsy type recorded as other than no biopsy. This will include polyp avulsion and treatment with silver nitrate.
This is the total of all first attendances (see paragraph 2), subdivided by the CYTOLOGY RESULT TYPEclassifications, except that the classification Other is included in with Clinical Indication No referral smear.
Central Return Form Guidance |
Part D of the KC65 return shows for each biopsy the time elapsing before the woman is informed of the result. The NHS Cervical Screening Programme (NHSCSP) has issued guidance on waiting times, and the information is used to monitor whether clinics are meeting these standards. The return is based upon those biopsies taken during the first month of the quarter.
The time measured in this part of the return is the interval between the PROCEDURE DATE of the colposcopy PATIENT PROCEDURE at which the biopsy was taken and the PATIENT INFORMED BIOPSY RESULT DATE.
Column 2 counts the number of biopsies taken during the first month of the quarter. These are subdivided by the waiting times in lines 0001-0005.
This counts the number of women whose waiting time was less than or equal to 14 days.
This counts the number of women whose waiting time was more than 14 days but less than or equal to 28 days.
This counts the number of women whose waiting time was more than 28 days but less than or equal to 56 days.
This counts the number of women whose waiting time was more than 56 days but less than or equal to 84 days.
This counts the number of women whose waiting time was more than 84 days.
This is the total for all women counted in column 2.
This is the total for all women counted in columns 2 to 8.
This counts the number of women who received no treatment and for whom was recorded a
This counts the number of women who for whom was recorded a COLPOSCOPY PRIME PROCEDURE TYPE of Ablation; treatment method recorded as ablation. This will include cold coagulation, cryotherapy, cautery and diathermy. (ii) no biopsy taken, or biopsy result not known by clinic.
Central Return Form Guidance |
Part E of KC65 shows the histological result for each biopsy, BIOPSY REFERRAL OUTCOME, which indicates whether cancer or a pre-cancerous condition has been identified from the sample taken. The information will help to monitor whether NHS Cervical Screening Programme (NHSCSP) guidance on the quality of biopsies and accuracy of diagnosis is being met.
This part of the KC65 return is based upon those biopsies taken during the first month of the quarter. Please note that the total number of biopsies recorded in Part E should equal the total number recorded in Part D as both parts relate to the same biopsies.
Column 4 counts the total number of BIOPSY REFERRAL OUTCOMES. These are analysed by biopsy type.
This counts the number of women for whom a COLPOSCOPY PRIME PROCEDURE TYPE of Diagnostic biopsy (punch); no treatment received and biopsy type recorded as directed biopsy or multiple directed biopsy was recorded.
This counts the number of women for whom a COLPOSCOPY PRIME PROCEDURE TYPEother than Diagnostic biopsy (punch); no treatment received and biopsy type recorded as directed biopsy or multiple directed biopsy was recorded.
These results are further sub-divided by BIOPSY REFERRAL OUTCOME.
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of Cancer (including micro-invasive).
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of Adenocarcinoma in situ.
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of CIN3.
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of CIN2.
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of CIN1.
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of HPV/cervicitus only.
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of No CIN/No HPV (normal).
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of Inadequate/unsatisfactory biopsy.
This counts women with a BIOPSY REFERRAL OUTCOMEclassification of Result not known by clinic.
This is the total for all women counted in columns 2, 3 and 4.
The following data quality checks should be made:
Central Return Form Guidance |
Part E of KC65 shows the histological result BIOPSY REFERRAL OUTCOME for each cervical biopsy, which indicates whether cancer or a pre-cancerous condition has been identified from the sample taken. The information will help to monitor whether NHS Cervical Screening Programme (NHSCSP) guidance on the quality of biopsies and accuracy of diagnosis is being met.
This part of the KC65 return is based upon those biopsies taken during the first month of the quarter. Please note that the total number of biopsies recorded in Part E should equal the total number recorded in Part D as both parts relate to the same biopsies.
Column 5 counts the total number of
This counts the number of women for whom a COLPOSCOPY PRIME PROCEDURE TYPE of Diagnostic biopsy (punch); no treatment received and biopsy type recorded as directed biopsy or multiple directed biopsy or any other biopsy taken for diagnostic purposes only was recorded.
This counts the number of women for whom a COLPOSCOPY PRIME PROCEDURE TYPE of Loop/laser excision or knife cone; treatment method recorded as loop/laser excision or knife cone and biopsy type recorded as other than no biopsy. This will include LLETZ and NEEP was recorded.
This counts the number of women for whom a
These results are further sub-divided by
This counts women with a
This counts women with a
This counts women with a
This counts women with a
This counts women with a
This counts women with a
This counts women with a
This counts women with a
This counts women with a
This is the total for all women counted in columns 2 to 5.
The following data quality checks should be made:
Part D | Part E |
Column 2 Line 006 | = Column 4 Line 010 |
KC65 Colposcopy Clinics: Referrals, Treatments and Outcomes