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/*==============================================*/
/* Project: PHD Maternal HEPC Analysis */
/* Author: Ryan O'Dea and Sarah Munroe */
/* Created: 4/27/2023 */
/* Updated: 03/2025 by SJM */
/*==============================================*/
/* Project Goal:
Characterize the HCV care cascade in women of reproductive age with OUD and Hepatitis C
Describe charateristics of the cohort and related Hepatitis C outcomes: linkage to care, loss-to-follow-up, relinkage to care, and DAA treatment initiation
Calculate rates of Hepatitis C outcomes: linkage to care, loss-to-follow-up, relinkage to care, and DAA treatment initiation
Part 1: Construct OUD cohort
Part 2: HCV Care Cascade
Part 3: Tables1 and 2 - Crude Analysis
Part 4: Calculate Rates
Detailed documentation of all datasets and variables:
https://www.mass.gov/info-details/public-health-data-warehouse-phd-technical-documentation */
/*===== SUPRESSION CODE =========*/
ods path(prepend) DPH.template(READ) SASUSER.TEMPLAT (READ);
proc format;
value supp010_ 1-10=' * ';
run ;
proc template;
%include "/sas/data/DPH/OPH/PHD/template.sas";
run;
/*==============================*/
/* Overall, the logic behind the known capture is fairly simple:
search through individual databases and flag if an ICD9, ICD10,
CPT, NDC, or other specialized code matches our lookup table.
If a record has one of these codes, it is 'flagged' for OUD.
The utilized databases are then joined onto the SPINE demographics
dataset and if the sum of flags is greater than zero, then the
record is flagged with OUD.
At current iteration, data being pulled through this method is
stratified by Year (or Year and Month), Race, Sex, and Age
(where age groups are defined in the table below). */
/*==============================*/
/* GLOBAL VARIABLES */
/*==============================*/
%LET year = (2014:2022);
%LET MOUD_leniency = 30;
%let today = %sysfunc(today(), date9.);
%let formatted_date = %sysfunc(translate(&today, %str(_), %str(/)));
/*===========AGE================*/
PROC FORMAT;
VALUE age_grps_five
low-14 = '999'
15-18 = '1'
19-25 = '2'
26-30 = '3'
31-35 = '4'
36-45 = '5'
46-high = '999';
/* ======= HCV TESTING CPT CODES ======== */
%LET AB_CPT = ('G0472','86803','86804','80074');
%LET RNA_CPT = ('87520','87521','87522');
%LET GENO_CPT = ('87902','3266F');
/* === HCV DIAGNOSIS CODES ====== */
%LET HCV_ICD = ('7051', '7054','707',
'7041', '7044','7071',
'B1710','B182','B1920',
'B1711','B1921');
/* HCV Direct Action Antiviral Codes */
%LET DAA_CODES = ('00003021301','00003021501','61958220101','61958180101','61958180301',
'61958180401','61958180501','61958150101','61958150401','61958150501',
'72626260101','00074262501','00074262528','00074262556','00074262580',
'00074262584','00074260028','72626270101','00074308228','00074006301',
'00074006328','00074309301','00074309328','61958240101','61958220101',
'61958220301','61958220401','61958220501','00006307402','51167010001',
'51167010003','59676022507','59676022528','00085031402');
/*========ICD CODES=============*/
%LET ICD = ('30400','30401','30402','30403',
'30470','30471','30472','30473',
'30550','30551','30552','30553', /* ICD9 */
'F1110','F1111','F11120','F11121',
'F11122','F11129','F1113','F1114',
'F11150','F11151','F11159','F11181',
'F11182','F11188','F1119','F1120',
'F1121','F11220','F11221','F11222',
'F11229','F1123','F1124','F11250',
'F11251','F11259','F11281','F11282',
'F11288','F1129','F1193','F1199', /* ICD10 */
'9701','96500','96501','96502',
'96509','E8500','E8501','E8502',
'T400X1A','T400X2A','T400X3A','T400X4A',
'T400X1D','T400X2D','T400X3D','T400X4D',
'T401X1A','T401X2A','T401X3A','T401X4A',
'T401X1D','T401X2D','T401X3D','T401X4D',
'T402X1A','T402X2A','T402X3A','T402X4A',
'T402X1D','T402X2D','T402X3D','T402X4D',
'T403X1A','T403X2A','T403X3A','T403X4A',
'T403X1D','T403X2D','T403X3D','T403X4D',
'T404X1A','T404X2A','T404X3A','T404X4A',
'T404X1D','T404X2D','T404X3D','T404X4D',
'T40601A','T40601D','T40602A','T40602D',
'T40603A','T40603D','T40604A','T40604D',
'T40691A','T40692A','T40693A','T40694A',
'T40691D','T40692D','T40693D','T40694D',
'T40411A','T40411D','T40412A','T40412D',
'T40413A','T40413D','T40414A','T40414D',
'T40421A','T40421D','T40422A','T40422D',
'T40423A','T40423D','T40424A','T40424D' /* Overdose Codes */);
%LET PROC = ('G2067','G2068','G2069','G2070',
'G2071','G2072','G2073','G2074',
'G2075', /* MAT Opioid */
'G2076','G2077','G2078','G2079',
'G2080', /*Opioid Trt */
'H0020','HZ81ZZZ','HZ84ZZZ','HZ91ZZZ','HZ94ZZZ',
'J0570','J0571','J0572','J0573',
'J0574','J0575','J0592', 'J2315','Q9991','Q9992''S0109'/* Naloxone*/);
/* Take NDC codes where buprenorphine has been identified,
insert them into BUP_NDC as a macro variable */
%LET bsas_drugs = (5,6,7,21,22,23,24,26);
proc sql;
create table bupndcf as
select distinct ndc
from PHDPMP.PMP
where BUP_CAT_PMP = 1;
quit;
proc sql noprint;
select quote(trim(ndc),"'") into :BUP_NDC separated by ','
from bupndcf;
quit;
/*============================ */
/* Part 1: Construct OUD cohort */
/*============================ */
/*====================*/
/* 1. Demographics */
/*====================*/
/* Using data from DEMO, take the cartesian coordinate of years
(as defined above) and months 1:12 to construct a shell table */
PROC SQL;
CREATE TABLE demographics AS
SELECT DISTINCT ID, FINAL_RE, FINAL_SEX, YOB, SELF_FUNDED
FROM PHDSPINE.DEMO
WHERE FINAL_SEX = 2 & SELF_FUNDED = 0;
QUIT;
/*====================*/
/* 2. APCD */
/*====================*/
/* The APCD consists of the Medical and Pharmacy Claims datasets and,
along with Casemix, are the datasets where we primarily search along
our ICD code list. We construct a variable named `OUD_APCD` within our
APCD Medical dataset using `MED_ICD1-25`, `MED_PROC1-7`, `MED_ECODE`, `MED_ADM_DIAGNOSIS`
and `MED_DIS_DIAGNOSIS`. We preform a rowwise search and add one to a
temporary `count` variable if they appear within our ICD code list.
At the end, if the `count` variable is strictly greater than one
then our `OUD_APCD` flag is set to 1.
The APCD medical dataset does not hold variables for searching
for NDC Codes, so we add in the APCD pharmacy dataset with
`PHARM_NDC` to search for applicable NDC codes.
If `PHARM_NDC` or `PHARM_ICD` is within our OUD Codes lists above,
then our `OUD_PHARM` flag is set to 1.*/
DATA apcd (KEEP= ID oud_apcd year_apcd);
SET PHDAPCD.MOUD_MEDICAL (KEEP= ID MED_ECODE MED_ADM_DIAGNOSIS MED_AGE
MED_ICD_PROC1-MED_ICD_PROC7
MED_ICD1-MED_ICD25
MED_FROM_DATE_YEAR MED_FROM_DATE_MONTH
MED_DIS_DIAGNOSIS
MED_PROC_CODE
WHERE= (MED_FROM_DATE_YEAR IN &year));
cnt_oud_apcd = 0;
oud_apcd = 0;
ARRAY vars1 {*} ID MED_ECODE MED_ADM_DIAGNOSIS
MED_ICD_PROC1-MED_ICD_PROC7
MED_ICD1-MED_ICD25
MED_DIS_DIAGNOSIS
MED_PROC_CODE;
DO i = 1 TO dim(vars1);
IF vars1[i] in &ICD THEN cnt_oud_apcd = cnt_oud_apcd+1;
END;
DROP= i;
IF cnt_oud_apcd > 0 THEN oud_apcd = 1;
IF oud_apcd = 0 THEN DELETE;
year_apcd = MED_FROM_DATE_YEAR;
RUN;
DATA pharm (KEEP= oud_pharm ID year_pharm);
SET PHDAPCD.MOUD_PHARM(KEEP= PHARM_NDC PHARM_FILL_DATE_MONTH PHARM_AGE
PHARM_FILL_DATE_YEAR PHARM_ICD ID);
IF PHARM_ICD IN &ICD OR
PHARM_NDC IN (&BUP_NDC) THEN oud_pharm = 1;
ELSE oud_pharm = 0;
IF oud_pharm = 0 THEN DELETE;
IF oud_pharm > 0 THEN year_pharm = PHARM_FILL_DATE_YEAR;
RUN;
/*====================*/
/* 3. CASEMIX */
/*====================*/
/* ### Emergency Department
Casemix.ED (Emergency Department) has three smaller internally
linked tables: ED, ED_DIAG, and ED_PROC; all linked together by
their internal `ED_ID`, which is only found in the ED tables
and should not be linked back to the PHD ID.
1. ED: Within the ED Dataset, we are interested in if `ED_DIAG1`
or `ED_PRINCIPLE_ECODE` are within our OUD Code list.
A temporary variable `OUD_ED_RAW` is created as a flag.
2. ED_DIAG: Within the ED_DIAG Dataset, we construct our flag,
`OUD_ED_DIAG` from the variable `ED_DIAG`
3. ED_PROC: Within the ED_PROC Dataset, we construct our flag,
`OUD_ED_PROC` from the variable `ED_PROC`
4. Datasets ED, ED_DIAG, and ED_PROC and joined along
their internal `ED_ID`. If the sum of created flags is
strictly greater than zero, then the overall `OUD_CM_ED`
flag is set to 1.
### Hospital Inpatient Discharge
Casemix.HD (Hospital Inpatient Discharge) follows the same pattern
as ED and has three smaller internally linked tables: HD, HD_DIAG,
and HD_PROC; all linked together by their internal `HD_ID`,
which is only found in the HD tables and should not be linked
back to the PHD ID.
1. HD: Within the HD Dataset, we are intersted in if `HD_PROC1` or
`HD_DIAG1` are within our OUD Code list. A temporary variable
`OUD_HD_RAW` is created as a flag.
2. HD_DIAG: Within the HD_DIAG Dataset, we construct our flag,
`OUD_HD_DIAG` from the variable `HD_DIAG`
3. HD_PROC: Within the HD_PROC Dataset, we construct our flag,
`OUD_HD_PROC` from the variable `HD_PROC`
4. Datasets HD, HD_DIAG, and HD_PROC and joined along their
internal `HD_ID`. If the sum of created flags is strictly
greater than zero, then the overall `OUD_CM_HD` flag is set to 1.
### Outpatient Observations
Casemix.OO (Outpatient Observations) breaks from the previous
pattern of HD and ED by only have one attributing table.
Within this table, we construct our flag `OUD_CM_OO` by searching
through `OO_DIAG1-16`, `OO_PROC1-4`, `OO_CPT1-10`, and
`OO_PRINCIPALEXTERNAL_CAUSECODE`. We preform a rowwise search and
add one to a temporary `count` variable if they appear within our
code lists. At the end, if the `count` variable is strictly greater
than one then our `OUD_CM_OO` flag is set to 1. */
/* ED */
DATA casemix_ed (KEEP= ID oud_cm_ed year_cm ED_ID);
SET PHDCM.ED (KEEP= ID ED_DIAG1 ED_PRINCIPLE_ECODE ED_ADMIT_YEAR ED_AGE ED_ID ED_ADMIT_MONTH
WHERE= (ED_ADMIT_YEAR IN &year));
IF ED_DIAG1 in &ICD OR
ED_PRINCIPLE_ECODE IN &ICD THEN oud_cm_ed = 1;
ELSE oud_cm_ed = 0;
IF oud_cm_ed > 0 THEN do;
year_cm = ED_ADMIT_YEAR;
end;
RUN;
/* ED_DIAG */
DATA casemix_ed_diag (KEEP= oud_cm_ed_diag ED_ID);
SET PHDCM.ED_DIAG (KEEP= ED_ID ED_DIAG);
IF ED_DIAG in &ICD THEN oud_cm_ed_diag = 1;
ELSE oud_cm_ed_diag = 0;
RUN;
PROC SQL;
CREATE TABLE casemix_ed_diag AS
SELECT a.ID, a.ED_ID, a.ED_ADMIT_YEAR, b.oud_cm_ed_diag
FROM PHDCM.ED AS a
RIGHT JOIN casemix_ed_diag AS b
ON a.ED_ID = b.ED_ID
WHERE a.ED_ADMIT_YEAR IN &year;
QUIT;
/* ED_PROC */
DATA casemix_ed_proc (KEEP= oud_cm_ed_proc ED_ID);
SET PHDCM.ED_PROC (KEEP= ED_ID ED_PROC);
IF ED_PROC in &PROC THEN oud_cm_ed_proc = 1;
ELSE oud_cm_ed_proc = 0;
RUN;
/* CASEMIX ED MERGE */
PROC SQL;
CREATE TABLE pharm AS
SELECT DISTINCT *
FROM pharm;
CREATE TABLE casemix_ed_proc AS
SELECT DISTINCT *
FROM casemix_ed_proc;
CREATE TABLE apcd AS
SELECT DISTINCT *
FROM apcd;
CREATE TABLE casemix_ed AS
SELECT DISTINCT *
FROM casemix_ed;
CREATE TABLE casemix_ed_diag AS
SELECT DISTINCT *
FROM casemix_ed_diag;
CREATE TABLE casemix AS
SELECT *
FROM casemix_ed
LEFT JOIN casemix_ed_diag ON casemix_ed.ED_ID = casemix_ed_diag.ED_ID
LEFT JOIN casemix_ed_proc ON casemix_ed_diag.ED_ID = casemix_ed_proc.ED_ID;
QUIT;
DATA casemix (KEEP= ID oud_ed year_cm);
SET casemix;
IF SUM(oud_cm_ed_proc, oud_cm_ed_diag, oud_cm_ed) > 0 THEN oud_ed = 1;
ELSE oud_ed = 0;
IF oud_ed = 0 THEN DELETE;
RUN;
/*====================*/
/* 4. HD */
/*====================*/
DATA hd (KEEP= HD_ID ID oud_hd_raw year_hd);
SET PHDCM.HD (KEEP= ID HD_DIAG1 HD_PROC1 HD_ADMIT_YEAR HD_AGE HD_ID HD_ADMIT_MONTH HD_ECODE
WHERE= (HD_ADMIT_YEAR IN &year));
IF HD_DIAG1 in &ICD OR
HD_PROC1 in &PROC OR
HD_ECODE IN &ICD THEN oud_hd_raw = 1;
ELSE oud_hd_raw = 0;
IF oud_hd_raw > 0 THEN do;
year_hd = HD_ADMIT_YEAR;
end;
RUN;
/* HD DIAG DATA */
DATA hd_diag (KEEP= HD_ID oud_hd_diag);
SET PHDCM.HD_DIAG (KEEP= HD_ID HD_DIAG);
IF HD_DIAG in &ICD THEN oud_hd_diag = 1;
ELSE oud_hd_diag = 0;
RUN;
PROC SQL;
CREATE TABLE hd_diag AS
SELECT a.ID, a.HD_ID, a.HD_ADMIT_YEAR, b.oud_hd_diag
FROM PHDCM.HD AS a
RIGHT JOIN hd_diag AS b
ON a.HD_ID = b.HD_ID
WHERE a.HD_ADMIT_YEAR IN &year;
QUIT;
/* HD PROC DATA */
DATA hd_proc(KEEP= HD_ID oud_hd_proc);
SET PHDCM.HD_PROC (KEEP = HD_ID HD_PROC);
IF HD_PROC IN &PROC THEN oud_hd_proc = 1;
ELSE oud_hd_proc = 0;
RUN;
/* HD MERGE */
PROC SQL;
CREATE TABLE pharm AS
SELECT DISTINCT *
FROM pharm;
CREATE TABLE hd_diag AS
SELECT DISTINCT *
FROM hd_diag;
CREATE TABLE casemix AS
SELECT DISTINCT *
FROM casemix;
CREATE TABLE hd AS
SELECT DISTINCT *
FROM hd;
CREATE TABLE hd_proc AS
SELECT DISTINCT *
FROM hd_proc;
CREATE TABLE hd AS
SELECT *
FROM hd
LEFT JOIN hd_diag ON hd.HD_ID = hd_diag.HD_ID
LEFT JOIN hd_proc ON hd.HD_ID = hd_proc.HD_ID;
QUIT;
DATA hd (KEEP= ID oud_hd year_hd);
SET hd;
IF SUM(oud_hd_diag, oud_hd_raw, oud_hd_proc) > 0 THEN oud_hd = 1;
ELSE oud_hd = 0;
IF oud_hd = 0 THEN DELETE;
RUN;
/*====================*/
/* 5. OO */
/*====================*/
DATA oo (KEEP= ID oud_oo year_oo);
SET PHDCM.OO (KEEP= ID OO_DIAG1-OO_DIAG16 OO_PROC1-OO_PROC4
OO_ADMIT_YEAR OO_ADMIT_MONTH OO_AGE
OO_CPT1-OO_CPT10
OO_PRINCIPALEXTERNAL_CAUSECODE
WHERE= (OO_ADMIT_YEAR IN &year));
cnt_oud_oo = 0;
ARRAY vars2 {*} OO_DIAG1-OO_DIAG16 OO_PROC1-OO_PROC4 OO_CPT1-OO_CPT10 OO_PRINCIPALEXTERNAL_CAUSECODE;
DO k = 1 TO dim(vars2);
IF SUBSTR(VNAME(vars2[k]), 1) IN ('OO_PROC', 'OO_CPT') THEN DO;
IF vars2[k] IN &PROC THEN
cnt_oud_oo = cnt_oud_oo + 1;
END;
ELSE IF vars2[k] IN &ICD THEN
cnt_oud_oo = cnt_oud_oo + 1;
END;
DROP k;
IF cnt_oud_oo > 0 THEN oud_oo = 1;
ELSE oud_oo = 0;
IF oud_oo = 0 THEN DELETE;
year_oo = OO_ADMIT_YEAR;
RUN;
/*====================*/
/* 6. CM OO MERGE */
/*====================*/
PROC SQL;
CREATE TABLE casemix AS
SELECT *
FROM casemix
FULL JOIN hd ON casemix.ID = hd.ID
FULL JOIN oo ON hd.ID = oo.ID;
QUIT;
PROC STDIZE DATA = casemix OUT = casemix reponly missing = 9999; RUN;
DATA casemix (KEEP = ID oud_cm year_cm);
SET casemix;
IF oud_ed = 9999 THEN oud_ed = 0;
IF oud_hd = 9999 THEN oud_hd = 0;
IF oud_oo = 9999 THEN oud_oo = 0;
IF sum(oud_ed, oud_hd, oud_oo) > 0 THEN oud_cm = 1;
ELSE oud_cm = 0;
IF oud_cm = 0 THEN DELETE;
year_cm = min(year_oo, year_hd, year_cm);
RUN;
/*====================*/
/* 7. BSAS */
/*====================*/
/* Like Matris, the BSAS dataset involves some PHD level encoding.
We tag a record with our flag, `OUD_BSAS`, if
`CLT_ENR_PRIMARY_DRUG`, `CLT_ENR_SECONDARY_DRUG`,
`CLT_ENR_TERTIARY_DRUG` are in the encoded list: (5,6,7,21,22,23,24,26)
or if `PHD_PRV_SERV_CAT = 7` (Opioid Treatment).
Descriptions of the BSAS drugs respective to
PHD level documentation
1. 5: Heroin
2. 6: Non-Rx Methadone
3. 7: Other Opiates
4. 21: Oxycodone
5. 22: Non-Rx Suboxone
6. 23: Rx Opiates
7. 24: Non-Rx Opiates
8. 26: Fentanyl */
DATA bsas (KEEP= ID oud_bsas year_bsas);
SET PHDBSAS.BSAS (KEEP= ID CLT_ENR_OVERDOSES_LIFE
CLT_ENR_PRIMARY_DRUG
CLT_ENR_SECONDARY_DRUG
CLT_ENR_TERTIARY_DRUG
PDM_PRV_SERV_CAT
ENR_YEAR_BSAS
ENR_MONTH_BSAS
AGE_BSAS
WHERE= (ENR_YEAR_BSAS IN &year));
IF (CLT_ENR_OVERDOSES_LIFE > 0 AND CLT_ENR_OVERDOSES_LIFE ^= 999)
OR CLT_ENR_PRIMARY_DRUG in &bsas_drugs
OR CLT_ENR_SECONDARY_DRUG in &bsas_drugs
OR CLT_ENR_TERTIARY_DRUG in &bsas_drugs
OR PDM_PRV_SERV_CAT = 7 THEN oud_bsas = 1;
ELSE oud_bsas = 0;
IF oud_bsas = 0 THEN DELETE;
year_bsas = ENR_YEAR_BSAS;
RUN;
/*====================*/
/* 8. MATRIS */
/*====================*/
/* The MATRIS Dataset depends on PHD level encoding of variables
`OPIOID_ORI_MATRIS` and `OPIOID_ORISUBCAT_MATRIS` to
construct our flag variable, `OUD_MATRIS`. */
DATA matris (KEEP= ID oud_matris year_matris);
SET PHDEMS.MATRIS (KEEP= ID OPIOID_ORI_MATRIS
OPIOID_ORISUBCAT_MATRIS
inc_year_matris
inc_month_matris
AGE_MATRIS
AGE_UNITS_MATRIS
WHERE= (inc_year_matris IN &year));
IF OPIOID_ORI_MATRIS = 1
OR OPIOID_ORISUBCAT_MATRIS in (1:5) THEN oud_matris = 1;
ELSE oud_matris = 0;
IF oud_matris = 0 THEN DELETE;
year_matris = inc_year_matris;
RUN;
/*====================*/
/* 9. DEATH */
/*====================*/
/* The Death dataset holds the official cause and manner of
death assigned by physicians and medical examiners. For our
purposes, we are only interested in the variable `OPIOID_DEATH`
which is based on 'ICD10 codes or literal search' from other
PHD sources.*/
DATA death (KEEP= ID oud_death year_death);
SET PHDDEATH.DEATH (KEEP= ID OPIOID_DEATH YEAR_DEATH AGE_DEATH
WHERE= (YEAR_DEATH IN &year));
IF OPIOID_DEATH = 1 THEN oud_death = 1;
ELSE oud_death = 0;
IF oud_death = 0 THEN DELETE;
year_death = YEAR_DEATH;
RUN;
/*====================*/
/* 10. PMP */
/*====================*/
/* Within the PMP dataset, we only use the `BUPRENORPHINE_PMP`
to define the flag `OUD_PMP` - conditioned on BUP_CAT_PMP = 1. */
DATA pmp (KEEP= ID oud_pmp year_pmp);
SET PHDPMP.PMP (KEEP= ID BUPRENORPHINE_PMP date_filled_year AGE_PMP date_filled_month BUP_CAT_PMP
WHERE= (date_filled_year IN &year));
IF BUPRENORPHINE_PMP = 1 AND
BUP_CAT_PMP = 1 THEN oud_pmp = 1;
ELSE oud_pmp = 0;
IF oud_pmp = 0 THEN DELETE;
year_pmp = date_filled_year;
RUN;
/*===========================*/
/* 11. MAIN MERGE */
/*===========================*/
/* As a final series of steps:
1. APCD-Pharm, APCD-Medical, Casemix, Death, PMP, Matris,
BSAS are joined together on the cartesian coordinate of Months
(1:12), Year (2015:2022), and SPINE (Race, Sex, ID)
2. The sum of the fabricated flags is taken. If the sum is strictly
greater than zero, then the master flag is set to 1.
Zeros are deleted
4. We select distinct ID, Age Bins, Race, Year, and Month and
output the count of those detected with OUD
5. Any count that is between 1 and 10 are suppressed and set to -1,
any zeros are true zeros */
PROC SQL;
CREATE TABLE oo AS
SELECT DISTINCT *
FROM oo;
CREATE TABLE bsas AS
SELECT DISTINCT *
FROM bsas;
CREATE TABLE matris AS
SELECT DISTINCT *
FROM matris;
CREATE TABLE death AS
SELECT DISTINCT *
FROM death;
CREATE TABLE pmp AS
SELECT DISTINCT *
FROM pmp;
PROC SQL;
CREATE TABLE oud AS
SELECT * FROM demographics
LEFT JOIN apcd ON apcd.ID = demographics.ID
LEFT JOIN casemix ON casemix.ID = demographics.ID
LEFT JOIN death ON death.ID = demographics.ID
LEFT JOIN bsas ON bsas.ID = demographics.ID
LEFT JOIN matris ON matris.ID = demographics.ID
LEFT JOIN pmp ON pmp.ID = demographics.ID
LEFT JOIN pharm ON pharm.ID = demographics.ID;
CREATE TABLE oud AS
SELECT DISTINCT *
FROM oud;
QUIT;
PROC STDIZE DATA = oud OUT = oud reponly missing = 9999; RUN;
DATA oud;
SET oud;
ARRAY oud_flags {*} oud_apcd oud_cm
oud_death oud_matris
oud_pmp oud_bsas
oud_pharm;
DO i = 1 TO dim(oud_flags);
IF oud_flags[i] = 9999 THEN oud_flags[i] = 0;
END;
oud_cnt = sum(oud_apcd, oud_cm, oud_death, oud_matris, oud_pmp, oud_bsas, oud_pharm);
IF oud_cnt > 0 THEN oud_master = 1;
ELSE oud_master = 0;
IF oud_master = 0 THEN DELETE;
oud_year = min(year_apcd, year_cm, year_matris, year_bsas, year_pmp);
IF oud_year = 9999 THEN oud_age = 999;
ELSE IF oud_year ne 9999 THEN oud_age = oud_year - YOB;
RUN;
PROC SORT data=oud;
by ID oud_age;
RUN;
data oud;
set oud;
by ID;
if first.ID;
run;
data oud;
set oud;
age_grp_five = put(oud_age, age_grps_five.);
IF age_grp_five = 999 THEN DELETE;
run;
PROC SQL;
CREATE TABLE oud_distinct AS
SELECT DISTINCT ID, YOB, oud_age, age_grp_five as agegrp, FINAL_RE FROM oud;
QUIT;
PROC SQL;
SELECT COUNT(DISTINCT ID) AS Number_of_Unique_IDs
INTO :num_unique_ids
FROM oud_distinct;
QUIT;
%put Number of unique IDs in oud_distinct table: &num_unique_ids;
/*============================ */
/* 12. ADD PREGANANCY */
/*============================ */
DATA all_births (keep = ID BIRTH_INDICATOR YEAR_BIRTH AGE_BIRTH);
SET PHDBIRTH.BIRTH_MOM (KEEP = ID YEAR_BIRTH AGE_BIRTH
WHERE= (YEAR_BIRTH IN &year));
BIRTH_INDICATOR = 1;
RUN;
data fetal_deaths_renamed;
set PHDFETAL.FETALDEATH;
rename FETAL_DEATH_YEAR = YEAR_BIRTH
MOTHER_AGE_FD = AGE_BIRTH;
run;
DATA fetal_deaths_renamed (keep = ID BIRTH_INDICATOR YEAR_BIRTH AGE_BIRTH);
SET fetal_deaths_renamed (KEEP = ID YEAR_BIRTH AGE_BIRTH
WHERE= (YEAR_BIRTH IN &year));
BIRTH_INDICATOR = 1;
RUN;
DATA all_births;
SET all_births fetal_deaths_renamed;
RUN;
proc SQL;
CREATE TABLE births AS
SELECT ID,
SUM(BIRTH_INDICATOR) AS TOTAL_BIRTHS,
min(YEAR_BIRTH) as FIRST_BIRTH_YEAR,
max(BIRTH_INDICATOR) as BIRTH_INDICATOR FROM all_births
GROUP BY ID;
run;
PROC SQL;
SELECT COUNT(DISTINCT ID) AS Number_of_Unique_IDs
INTO :num_unique_ids
FROM births;
QUIT;
%put Number of unique IDs in births table: &num_unique_ids;
PROC SQL;
CREATE TABLE oud_preg AS
SELECT * FROM oud_distinct
LEFT JOIN births ON oud_distinct.ID = births.ID;
QUIT;
DATA oud_preg;
SET oud_preg;
IF BIRTH_INDICATOR = . THEN BIRTH_INDICATOR = 0;
run;
proc sort data=all_births;
by ID AGE_BIRTH;
run;
data birthsmoms_first;
set all_births;
by ID AGE_BIRTH;
if first.ID;
run;
proc sql;
create table oud_preg as
select oud_preg.*,
birthsmoms_first.AGE_BIRTH
from oud_preg
left join birthsmoms_first
on oud_preg.ID = birthsmoms_first.ID;
quit;
/* ========================================================== */
/* 13. Extract AB/RNA/GENOTYPE Testing Data */
/* ========================================================== */
/* Extract antibody/rna/genotype testing records (CPT codes) from the PHDAPCD.MOUD_MEDICAL dataset.
Then, remove duplicate testing records based on unique combinations of ID and testing date and sort by ID and testing date in ascending order.
Transpose the testing dates for each individual into wide format to create multiple columns for testing dates.
Extract the year from the testing records for each ID and creates a new dataset that includes distinct IDs, testing years, and age at testing.
Select the earliest testing year for each ID and output the frequency of tests occurring in infants under the age of 4. */
/* AB */
DATA ab;
SET PHDAPCD.MOUD_MEDICAL (KEEP = ID MED_FROM_DATE MED_PROC_CODE MED_FROM_DATE_YEAR
WHERE = (MED_PROC_CODE IN &AB_CPT));
run;
proc sql;
create table AB1 as
select distinct ID, MED_FROM_DATE, *
from AB;
quit;
PROC SORT data=ab1;
by ID MED_FROM_DATE;
RUN;
PROC TRANSPOSE data=ab1 out=ab_wide (KEEP = ID AB_TEST_DATE:) PREFIX=AB_TEST_DATE_;
BY ID;
VAR MED_FROM_DATE;
RUN;
PROC SQL;
create table AB_YEARS as
SELECT DISTINCT ID, MED_FROM_DATE_YEAR as AB_TEST_YEAR
FROM AB1;
quit;
PROC SQL;
create table AB_YEARS_COHORT as
SELECT *
FROM OUD_DISTINCT
LEFT JOIN AB_YEARS on OUD_DISTINCT.ID = AB_YEARS.ID;
quit;
/* RNA */
DATA rna;
SET PHDAPCD.MOUD_MEDICAL (KEEP = ID MED_FROM_DATE MED_PROC_CODE
WHERE = (MED_PROC_CODE IN &RNA_CPT));
run;
PROC SORT data=rna;
by ID MED_FROM_DATE;
RUN;
PROC TRANSPOSE data=rna out=rna_wide (KEEP = ID RNA_TEST_DATE:) PREFIX=RNA_TEST_DATE_;
BY ID;
VAR MED_FROM_DATE;
RUN;
/* GENOTYPE */
DATA geno;
SET PHDAPCD.MOUD_MEDICAL (KEEP = ID MED_FROM_DATE MED_PROC_CODE
WHERE = (MED_PROC_CODE IN &GENO_CPT));
run;
PROC SORT data=geno;
by ID MED_FROM_DATE;
RUN;
PROC TRANSPOSE data=geno out=geno_wide (KEEP = ID GENO_TEST_DATE:) PREFIX=GENO_TEST_DATE_;
BY ID;
VAR MED_FROM_DATE;
RUN;
PROC FREQ data = AB;
title "AB CPT CODES";
table MED_PROC_CODE;
run;
PROC FREQ data = RNA;
title "RNA CPT CODES";
table MED_PROC_CODE;
run;
PROC FREQ data = geno;
title "GENOTYPE CPT CODES";
table MED_PROC_CODE;
run;
title;
/* ========================================================== */
/* 14. Join All Testing Data with OUD Cohort and Create HCV Testing Indicators */
/* ========================================================== */
/* This step joins antibody, RNA, and genotype testing data to the main OUD dataset based on the ID and
creates indicators for whether ID had antibody, RNA, and any HCV testing. */
PROC SQL;
CREATE TABLE OUD_HCV AS
SELECT * FROM oud_preg
LEFT JOIN ab_wide ON ab_wide.ID = oud_preg.ID
LEFT JOIN rna_wide ON rna_wide.ID = oud_preg.ID
LEFT JOIN geno_wide ON geno_wide.ID = oud_preg.ID;
QUIT;
DATA OUD_HCV;
SET OUD_HCV;
AB_TEST_INDICATOR = 0;
RNA_TEST_INDICATOR = 0;
GENO_TEST_INDICATOR = 0;
IF AB_TEST_DATE_1 = . THEN AB_TEST_INDICATOR = 0; ELSE AB_TEST_INDICATOR = 1;
IF RNA_TEST_DATE_1 = . THEN RNA_TEST_INDICATOR = 0; ELSE RNA_TEST_INDICATOR = 1;
IF GENO_TEST_DATE_1 = . THEN GENO_TEST_INDICATOR = 0; ELSE GENO_TEST_INDICATOR = 1;
run;
DATA OUD_HCV;
SET OUD_HCV;
ANY_HCV_TESTING_INDICATOR = 0;
IF AB_TEST_INDICATOR = 1 OR RNA_TEST_INDICATOR = 1 THEN ANY_HCV_TESTING_INDICATOR = 1;
run;
/* ========================================================== */
/* 15. Extract HCV Status from MAVEN Database */
/* ========================================================== */
/* This section retrieves the HCV diagnosis status for each ID from the MAVEN database,
calculates the age at diagnosis, and creates indicators for HCV seropositivity and confirmed HCV. */
PROC SORT DATA=PHDHEPC.HCV;
BY ID EVENT_DATE_HCV;
RUN;
DATA HCV_STATUS;
SET PHDHEPC.HCV;
BY ID EVENT_DATE_HCV;
IF FIRST.ID AND EVENT_YEAR_HCV >= 2014 THEN DO;
HCV_SEROPOSITIVE_INDICATOR = 1;
CONFIRMED_HCV_INDICATOR = (DISEASE_STATUS_HCV = 1);
OUTPUT;
END;
KEEP ID AGE_HCV EVENT_MONTH_HCV EVENT_YEAR_HCV EVENT_DATE_HCV HCV_SEROPOSITIVE_INDICATOR CONFIRMED_HCV_INDICATOR RES_CODE_HCV;
RUN;
PROC SQL;
CREATE TABLE IDU_STATUS AS
SELECT ID,
CASE
WHEN SUM(EVER_IDU_HCV = 1) > 0 THEN 1
WHEN SUM(EVER_IDU_HCV = 0) > 0 AND SUM(EVER_IDU_HCV = 1) <= 0 THEN 0
WHEN SUM(EVER_IDU_HCV = 9) > 0 AND SUM(EVER_IDU_HCV = 0) <= 0 AND SUM(EVER_IDU_HCV = 1) <= 0 THEN 9
ELSE 9
END AS EVER_IDU_HCV_MAT
FROM PHDHEPC.HCV
WHERE EVENT_YEAR_HCV >= 2014
GROUP BY ID;
QUIT;
PROC SQL;
CREATE TABLE HCV_STATUS AS
SELECT A.*, B.EVER_IDU_HCV_MAT
FROM HCV_STATUS A
LEFT JOIN IDU_STATUS B ON A.ID = B.ID;
QUIT;
PROC SQL;
CREATE TABLE OUD_HCV_STATUS AS
SELECT * FROM OUD_HCV
LEFT JOIN HCV_STATUS ON HCV_STATUS.ID = OUD_HCV.ID;
QUIT;
/* ========================================================== */
/* 16. Linkage to HCV Care */
/* ========================================================== */
/* This section retrieves medical records related to HCV care from the MOUD_MEDICAL dataset,
filters based on relevant ICD codes, and creates a dataset for infants linked to HCV care. */
DATA HCV_LINKED_SAS;
SET PHDAPCD.MOUD_MEDICAL (KEEP = ID MED_FROM_DATE MED_FROM_DATE_MONTH MED_FROM_DATE_YEAR MED_ADM_TYPE MED_ICD1
WHERE = (MED_ICD1 IN &HCV_ICD));
RUN;
PROC SORT DATA=HCV_LINKED_SAS;
BY ID MED_FROM_DATE;
RUN;
DATA HCV_LINKED;
SET HCV_LINKED_SAS;
BY ID MED_FROM_DATE;
IF FIRST.ID THEN DO;
HCV_PRIMARY_DIAG = 1;
OUTPUT;
END;
KEEP ID MED_FROM_DATE_MONTH MED_FROM_DATE_YEAR HCV_PRIMARY_DIAG;
RUN;
PROC SQL;
CREATE TABLE OUD_HCV_LINKED AS
SELECT * FROM OUD_HCV_STATUS
LEFT JOIN HCV_LINKED ON HCV_LINKED.ID = OUD_HCV_STATUS.ID;
QUIT;
DATA OUD_HCV_LINKED; SET OUD_HCV_LINKED;
IF HCV_PRIMARY_DIAG = . THEN HCV_PRIMARY_DIAG = 0;
IF HCV_SEROPOSITIVE_INDICATOR = . THEN HCV_SEROPOSITIVE_INDICATOR = 0;
run;
/* ========================================================== */
/* 17. DAA (Direct-Acting Antiviral) Treatment Starts */
/* ========================================================== */
/* This section identifies IDs who started DAA treatment, retains the first DAA start, calculates the age at DAA start,
and creates indicators for DAA initiation. */
DATA DAA; SET PHDAPCD.MOUD_PHARM (KEEP = ID PHARM_FILL_DATE PHARM_FILL_DATE_MONTH PHARM_FILL_DATE_YEAR PHARM_NDC PHARM_AGE
WHERE = (PHARM_NDC IN &DAA_CODES));
RUN;
PROC SORT DATA=DAA;
BY ID PHARM_FILL_DATE;
RUN;
DATA DAA_STARTS;
SET DAA;
BY ID PHARM_FILL_DATE;
IF FIRST.ID THEN DO;
DAA_START_INDICATOR = 1;
OUTPUT;
END;
KEEP ID PHARM_AGE PHARM_FILL_DATE PHARM_FILL_DATE_MONTH PHARM_FILL_DATE_YEAR DAA_START_INDICATOR;
RUN;
PROC SQL;
CREATE TABLE OUD_HCV_DAA AS
SELECT * FROM OUD_HCV_LINKED
LEFT JOIN DAA_STARTS ON DAA_STARTS.ID = OUD_HCV_LINKED.ID;
QUIT;
DATA OUD_HCV_DAA; SET OUD_HCV_DAA;
IF DAA_START_INDICATOR = . THEN DAA_START_INDICATOR = 0;
run;