GMRAIAD1 ;BPOIFO/JG - BUILD HL7 ORU^R01 MESSAGE FOR ADVERSE REACTION - PART 1 ; 18 Feb 2005 2:54 PM ;;4.0;Adverse Reaction Tracking;**22,23**;Mar 29, 1996 VALID ;;VDEF HL7 MESSAGE BUILDER ; Creates HL7 V2.4 ORU^R01 message for allergy adverse reaction ; ; This routines uses the following IAs: ; #4248 - VDEFEL calls (controlled) ; #3630 - VAFCQRY calls (controlled) ; #2196 - ^PS(50.416,IEN,0) (controlled) ; #4571 - ERR^VDEFREQ (controlled) ; ; This routine is called at tag EN as a Function by VDEFREQ1 ; ; This routine calls GMRAIAD2 for a portion of message ; Q ; EN(EVIEN,KEY,VFLAG,OUT,MSHP) ; ; ; Inputs: EVIEN = IEN of message in file 577 ; KEY - IEN of file to create message from ; VFLAG - "V" for VistA HL7 destination (default) ; OUT - target array, passed by reference ; MSHP - Piece 4 contains message subtype ; ; Output: Two part string with parts separated by "^" ; Part 1: "LM" - output in local array passed in "OUT" parameter ; "GM" - output in ^TMP("HLS",$J) ; Part 2: No longer used ; N DFN,HLFS,HLCM,HLSC,HLRP,HLES,HLQ,ALRDATA,DTE,DTP,ADD N DATA,VAL,I,S,X,Y,Z,X1,X2,HL7RC,IEN,OUTX,LIKE,LIKERSP,GMRAPID,SEQ N SEPF,SEPC,SEPR,SEPE,SEPS,ARRAY,PTC,CMP,GMRAHL ; ; Initialize stuff K ^TMP("HLS",$J) S S=0,ARRAY="OUT("_"""HLS"""_",S)",TARGET="LM^" M GMRAHL=VDEFHL ; ; Set up HL7 delimiters S HLCM=$E(GMRAHL("ECH")),HLRP=$E(GMRAHL("ECH"),2),HLSC=$E(GMRAHL("ECH"),4),HLES=$E(GMRAHL("ECH"),3) S HLFS=GMRAHL("FS"),HLQ=GMRAHL("Q"),HL7RC=HLES_HLFS_HLCM_HLRP_HLSC D SETDLMS^VDEFEL ; ; Get allergy data & patient ID S ALRDATA=$G(^GMR(120.85,KEY,0)) I ALRDATA="" D ERR^VDEFREQ("No data in file GMR(120.85) for IEN "_KEY) S ZTSTOP=1 G EXIT S DFN=$P(ALRDATA,U,2) I $G(^DPT(DFN,0))="" D ERR^VDEFREQ("No data in file DPT for DFN "_DFN) S ZTSTOP=1 G EXIT ; ; Build segments for message in OUT, $P # = HL7 field # ; ; PID - Use MPI PID builder PID K GMRAPID S OUTX="",S=1,SEQ="" D BLDPID^VAFCQRY(DFN,1,SEQ,.GMRAPID,.GMRAHL) F I=2:1 Q:$G(GMRAPID(I))="" S GMRAPID(1,I-1)=GMRAPID(I) K GMRAPID(I) M OUTX=GMRAPID(1) K GMRAPID D SAVE ; ; OBR OBR S S=S+1,OUTX="",$P(OUTX,HLFS)=1,$P(OUTX,HLFS,25)="F" S VAL=KEY_HLCM_$P(SITEPARM,U,6)_"_120.85",$P(OUTX,HLFS,3)=VAL S $P(OUTX,HLFS,4)="ADVERSE REACTION REPORT"_HLCM_HLCM_"L" ; ;Date/time reaction occured S $P(OUTX,HLFS,7)=$$TS^VDEFEL($P(ALRDATA,U,1)) ; ; Entering User S VAL=$$XCN200^VDEFEL($P(ALRDATA,U,19)),$P(VAL,HLCM,8)="ENT",$P(OUTX,HLFS,32)=VAL ; ; Observer (Witness) S VAL=$$XCN200^VDEFEL($P(ALRDATA,U,13)),$P(VAL,HLCM,8)="OBS" ; ; Reporter S X=$P($G(^GMR(120.85,KEY,"RPT")),U,1) S X=HLCM_$P(X,",",1)_HLCM_$P($P(X,",",2)," ",1)_HLCM_$P($P(X,",",2)," ",2) S $P(X,HLCM,8)="RPT",$P(OUTX,HLFS,34)=VAL_HLRP_X ; ; Related Reaction S X=$P(ALRDATA,U,15)_HLCM_$P($G(^GMR(120.8,$P(ALRDATA,U,15),0)),U,2)_HLCM_"L" S $P(OUTX,HLFS,47)=X S OUTX="OBR"_HLFS_OUTX D SAVE ; ; OBX 1 - Symptoms OBX1 S S=S+1,OUTX=1_HLFS_"CE"_HLFS_"SYMPTOM"_HLFS ; ; Get the reactions S X=0,(Y,Z)="" F S X=$O(^GMR(120.85,KEY,2,X)) Q:X'?1N.N D . S Y=^GMR(120.85,KEY,2,X,0),VAL=$P(Y,U,3) . I $P(Y,U,2)'="" S Z=Z_$P(Y,U,2)_HLRP . E S Z=Z_$P(^GMRD(120.83,+Y,0),U,1)_HLRP S $P(OUTX,HLFS,5)=$E(Z,1,$L(Z)-1) ; ; Severity S $P(OUTX,HLFS,8)=$$GET1^DIQ(120.85,KEY_",",14.5) ; ; Reaction entered by S $P(OUTX,HLFS,16)=$$XCN200^VDEFEL(VAL) S $P(OUTX,HLFS,11)="F" S OUTX="OBX"_HLFS_OUTX D SAVE ; ; RXA/RXE/RXR/OBX Suspected Agent Group G OBX2:$G(^GMR(120.85,KEY,3,1,0))="" S IEN=0 RXAGRP1 F S IEN=$O(^GMR(120.85,KEY,3,IEN)) Q:IEN'?1N.N D . S S=S+1,OUTX="0"_HLFS_"1" K ALRDATA M ALRDATA=^GMR(120.85,KEY,3,IEN) . ; . ; RXA . ; Start & Stop dates . S VAL=$P($G(ALRDATA(1)),U) I VAL S $P(OUTX,HLFS,3)=$$TS^VDEFEL(VAL) . S VAL=$P($G(ALRDATA(1)),U,2) I VAL S $P(OUTX,HLFS,4)=$$TS^VDEFEL(VAL) . ; . ; Suspected agent & daily dose . S VAL=$P(ALRDATA(0),U),$P(OUTX,HLFS,5)=$$HL7RC(VAL) . S VAL=$P(ALRDATA(0),U,2),$P(OUTX,HLFS,6)=$$HL7RC(VAL) . ; . ; Lot number, Exp. Date, Manufacturer . S VAL=$P(ALRDATA(0),U,8) S:VAL $P(OUTX,HLFS,15)=$$HL7RC(VAL) . S VAL=$P($G(ALRDATA(1)),U,3) I VAL S $P(OUTX,HLFS,16)=$$TS^VDEFEL(VAL) . S VAL=$P(ALRDATA(0),U,7) S:VAL $P(OUTX,HLFS,17)=$$HL7RC(VAL) . ; . ; Indication for use . S VAL=$P(ALRDATA(0),U,4) S:VAL $P(OUTX,HLFS,19)=$$HL7RC(VAL) . ; . ; Set into array . S OUTX="RXA"_HLFS_OUTX D SAVE . ; . ; RXE . S S=S+1,OUTX="",CMP="" . ; . ; Previous doses . S $P(CMP,HLCM,1)=$$HL7RC($P(ALRDATA(0),U,9)) . ; . ; Duration . S X1=$P($G(ALRDATA(1)),U,2),X2=$P($G(ALRDATA(1)),U) D ^%DTC S:X="" X=0 S $P(CMP,HLCM,3)=X . ; . ; Last date given . S VAL=$P(ALRDATA(0),U,10) I VAL S $P(CMP,HLCM,5)=$$TS^VDEFEL(VAL) . S $P(OUTX,HLFS)=CMP,CMP="" . ; . ; Give codes . S VAL=$P(ALRDATA(0),U),$P(CMP,HLCM,1)=$$HL7RC(VAL) . S $P(CMP,HLCM,4)=$P($G(ALRDATA(1)),U,4),$P(CMP,HLCM,6)="NDC" . S $P(OUTX,HLFS,2)=CMP,$P(OUTX,HLFS,3)=0 . ; . ; SIG . S $P(OUTX,HLFS,7)=$$HL7RC($P($G(ALRDATA(1)),U,5)) . ; . ; Daily dose . S $P(OUTX,HLFS,19)=$$HL7RC($P(ALRDATA(0),U,2)) . S OUTX="RXE"_HLFS_OUTX D SAVE . ; . ; RXR . ; Route of administration . S OUTX="",VAL=$P(ALRDATA(0),U,3) S:VAL="" VAL="UNKNOWN" S $P(OUTX,HLFS,1)=$$HL7RC(VAL) . S S=S+1,OUTX="RXR"_HLFS_OUTX D SAVE . ; . ; OBX - LIKES . S LIKERSP=$G(ALRDATA("LIKE")) I LIKERSP'="" F LIKE=1:1:6 D . . S S=S+1,OUTX=1_HLFS_"CE"_HLFS . . S VAL="LIKE "_LIKE_HLCM_$P($T(LIKEQ+(LIKE)),";",3),$P(OUTX,HLFS,3)=VAL . . S X=$P(LIKERSP,U,LIKE),X=$S(X="y":"Y",X="n":"N",1:""),VAL=X_HLCM . . S X=$S(X="Y":"YES",X="N":"NO",1:"") . . S VAL=VAL_X_HLCM_"HL70136",$P(OUTX,HLFS,5)=VAL,$P(OUTX,HLFS,11)="F" . . S OUTX="OBX"_HLFS_OUTX D SAVE . . ; . ; Likelihood . S S=S+1,OUTX=1_HLFS_"CE"_HLFS_"LIKELIHOOD" . S VAL=$P(LIKERSP,U,7) S:VAL="" VAL=5 . S X=VAL_HLCM_$P("REMOTE,POSSIBLE,PROBABLE,HIGHLY PROBABLE, ",",",VAL) . S $P(OUTX,HLFS,5)=X,$P(OUTX,HLFS,11)="F" . S OUTX="OBX"_HLFS_OUTX D SAVE ; ; OBX2 - Lab Results OBX2 S X=$G(^GMR(120.85,KEY,4,0)) G CALL:X="" S IEN=0 F S IEN=$O(^GMR(120.85,KEY,4,IEN)) Q:IEN'?1N.N D . S S=S+1,OUTX=1_HLFS_"CE"_HLFS . S X=^GMR(120.85,KEY,4,IEN,0),$P(OUTX,HLFS,3)=$$HL7RC($P(X,U,1)) . S $P(OUTX,HLFS,5)=$$HL7RC($P(X,U,2)),$P(OUTX,HLFS,11)="F" . S $P(OUTX,HLFS,14)=$$TS^VDEFEL($P(X,U,3)) . S OUTX="OBX"_HLFS_OUTX D SAVE ; ; Call GMRAIAD2 CALL D ENTRY^GMRAIAD2 ; ; OBX10 - IND/NDA Info OBX10 S X=$G(^GMR(120.85,KEY,"MFR2")) G RXAGRP2:X="" S S=S+1,OUTX=1_HLFS_"ST",$P(OUTX,HLFS,5)=$P(X,U,1) S OUTX="OBX"_HLFS_OUTX D SAVE ; ; RXA/RXE Concommitant Drugs Group RXAGRP2 S X=$G(^GMR(120.85,KEY,13,0)) G EXIT:X="" S IEN=0 F S IEN=$O(^GMR(120.85,KEY,13,IEN)) Q:IEN'?1N.N D . ; . ; RXA . S X=^GMR(120.85,KEY,13,IEN,0),S=S+1,OUTX=0_HLFS_1 . ; . ; Start Date, Stop Date . I $P(X,U,2)'="" S $P(OUTX,HLFS,3)=$$TS^VDEFEL($P(X,U,2)) . I $P(X,U,3)'="" S $P(OUTX,HLFS,4)=$$TS^VDEFEL($P(X,U,3)) . ; . ; Drug Name . S $P(OUTX,HLFS,5)=$$HL7RC($P(X,U,1)),$P(OUTX,HLFS,6)=0 . S OUTX="RXA"_HLFS_OUTX D SAVE . ; . ; RXE . ; Stop Date . S S=S+1,OUTX="",VAL=$$TS^VDEFEL($P(X,U,3)) . S Y="",$P(Y,HLCM,5)=VAL,$P(OUTX,HLFS,1)=Y . ; . ; Drug Name . S $P(OUTX,HLFS,2)=$$HL7RC($P(X,U,1)),$P(OUTX,HLFS,3)=0 . ; . ; SIG if known . S $P(OUTX,HLFS,5)="UNK",$P(OUTX,HLFS,7)=$$HL7RC($P(X,U,5)) . S OUTX="RXE"_HLFS_OUTX D SAVE ; ; Done building segments EXIT Q TARGET ; ; ; Place current string into message array ; Turn string into array if length >245. ; Move local array to global if needed SAVE N I I $P(OUTX,HLFS)'="PID",$L(OUTX)>245 D . K ADD S ADD=$E(OUTX,1,245),OUTX=$E(OUTX,246,$L(OUTX)) . F I=1:1 S ADD(I)=$E(OUTX,1,245),OUTX=$E(OUTX,246,$L(OUTX)) Q:OUTX="" . K OUTX M OUTX=ADD M @ARRAY=OUTX ; ; Move local array to global if it's getting big. I $P(TARGET,U)="LM",$S<16000 D . K ^TMP("HLS",$J) M ^TMP("HLS",$J)=OUT("HLS") K OUT("HLS") . S $P(TARGET,U)="GM",ARRAY="^TMP("_"""HLS"""_",$J,S)" K OUTX,ADD Q ; ; Replace any HL7 coding chars. in strings with HL7 escape sequence ; Input: X = data string HL7RC(X) N OCHR,RCHR,RCHRI,TYPE,I F TYPE="E","F","C","R","S" D . S RCHRI=$S(TYPE="E":1,TYPE="F":2,TYPE="C":3,TYPE="R":4,TYPE="S":5) . S OCHR=$E(HL7RC,RCHRI),RCHR=$E("EFSRT",RCHRI) . Q:'$F(X,OCHR) . F I=1:1 Q:$E(X,I)="" I $E(X,I)=OCHR S X=$E(X,1,I-1)_HLES_RCHR_HLES_$E(X,I+1,999),I=I+2 Q X ; LIKEQ ; LIKE set ;;1. Reaction normally occurs with this reactant? ;;2. Administration of the reactant was stopped? ;;3. Reaction stopped when the administration of the reactant was terminated? ;;4. Reactant was re-administered? ;;5. Reaction could be due to the patient current clinical condition? ;;6. Reaction reappeared after the reactant was re-administered?