{"aaData": [["100", "SMAC I", "", "", "", "", "", "", "", "", "", "", "", "", "", "", "", "
\nMust use a load list, Cross link by ID or CUP. Param 3 must have the\ntest code. Example 01A for SODIUM\n\n
\nLAEKT7 is used to process output taken from the instrument interface.\nParam 3 should contain the abbreviation of the test that is transmitted.\n(exp. Ca for Calcium, Cl- for Chloride, etc).\n\n
\nASTRA 4,6,8/8E,IDEAL have the same output format.\nThe program, LASTRA, must have consecutive entries in the CHEM TEST fields\nand will not permit the processing of calculated results (ANION GAP, etc).\nThe program, LAASTRA, allows calculated results. Param 3 requires the\nchemistry code (01A for Na, 06A for Glucose, etc) or\ndescription (01 for Anion Gap, 03 for Osmolality, etc.).\n\n
\nTest # in Auto instrument file should match Ektachem test #.\n\n
\nUses the SP-120 interface.\n\n
\nWBC count is internal numbers 1 - 27.\nPARAM 3 stores the character on the keyboard used for entry.\nRBC MORPHOLOGY is internal numbers 31 - 58, layed out the same as the WBC\n (31 - 39), (40 - 48), (49 - 58), The '\\' is used to display the WBC values.\nThere can be 3 rows of keys displayed, location is by internal number.\nROW 1 (1 - 9)\nROW 2 (10 - 18)\nROW 3 (19 - 27)\nPARAM 1 can change the value of V.\nThe keys '-' (MINUS), '!' (Comment), '?' (show values) are reserved functions.\nPARAM 2 is set to 1 if the test is included in the total count, or to 2\nif not included in the total count e.g. NRBC set to 2, SEGS set to 1.\n\n
\nProgram LAS790 can also be used with Coulter S880, but you must enter in \nENTRY FOR LAGEN: IDE,LOG=+$E(Y(2),8,10) and CROSS LINK BY: Accession.\n\n
\nThe ACA needs to run in the terminal interface mode.\nThe aca routine doesn't use any parameters.\n\n
\nNeed to turn off the ACK/NAK.\n\n
\nNeeds to have Handshake Response S OUT=$C(6)\nParam 3 should include the test name that is transmited from the\ninstrument. Example: RBC is for URINE RBC/HPF, <4 spaces>RBC is\nfor URINE RBC CASTS, Sp. Gravity is for SPECIFIC GRAVITY.\n\n
\nCross link by tray cup, entry: cup. Use a loadlist of sequence, cups/tray\n(absolute value (sample 1 - sample 2)) / average <= Param 2 / 100\nFor a PT with results of 9.5, 10.5, and Param 2 of 20,\nthe result is stored (.1 is < .2).\nIf Param 2 is left blank, the average will always be stored.\nParam 3 needs to include the transmitted test name (PT for prothrobin\ntime, APT for partial thromboplastin time)\n \nExecute code for SKIP: (namespaced for > Version 3)\nS LRCUP=LRCUP+1 S:LRCUP'=1 LRCUP=LRCUP+1 I LRCUP>LRMAXCUP S LRTRAY=\nLRTRAY+1,LRCUP=1\n= to # cups/tray. If you wish to run samples in duplicate you must\nhave in the loadlist a load transform called "SKIP". This will only place\nsamples on odd numbered cups, leaving the even numbers to run the same\nsamples ie. 1,2 are duplicates, 3,4 etc. The result stored will be the\naverage of the two samples. If you wish to not store results that do not\ncorrelate, enter in Param 2 the % of variation allowed.\nExample\n The result will be stored if\n\n
\nUses PARAM 1 with the format: I SEL=# S V=$E(Y(##),###,####) D NUM\nwhere \n# is the number of lines transmitted depending on the selectivity\n(selectivity 0 transmits 4 lines, 1 transmits 8, otherwise 2 lines).\n## is the line number the test is transmitted on.\n### is the starting position of the test.\n#### is the ending position of the test.\nExample: for WBC I SEL'=2 S V=$E(Y(2),1,5) D NUM\n for MONO% I SEL=8 S V=$E(Y(5),14,19) D NUM\n\n
\nThese are notes for the American dade PARAMAX.\nThe test are NUMBERED in the file with the same number that the \nparamax uses to indcate the test. (ie. 1=albumin, 36=chloride).\nCross link by IDE for manually entered accession numbers, or ID if\nyou are matching the barcode # to the accession #.\nIf you are matching the last 3 numbers of the barcode to the accession\nnumber use ID,LOG=+$E(ID,$L(ID)-2,$L(ID))\n\n
\nUses Param 3 to identify test which must match the test name that\nis transmited.\n\n
\nUses Param 3 to identify test, which must match the test name that is\n \nThe accession number may be entered in the sample ID field along with\nthe patient's name. Example: 132 or DOE, JOHN 132.\nThe instrument may also be run by tray/cup.\ntransmitted. Param 3 should not contatin any spaces. Exp. BILI D\nshould be BILID in Param 3. The program, LASPEC, is used by Abbott's\nsoftware version M2.0.\n \nParam 2 is used to determine the number of decimal places the test\nwill be reported with. No entry in Param 2 will round off to a whole\nnumber. Example: NA with Param 2 blank or Param 2 as 0 will report\n143.7000 as 144. K with Param 2 as 1 will report 3.6800 as 3.7.\n\n
\nParam 3 must contain the test name that is transmitted for that test.\nThe tests correcting for patient temp must be preceded by a '.\nExample. PCO2 would have pCO2 for param 3; whereas, PCO2 AT PT.TEMP would\nhave 'pCO2. Instrument transmits a 7 data bits only.\n\n
\nParam 3 must contain the test abbreviation or identifier that is\ntransmitted with the results. Param 2 determines the # of decimal\nplaces for the test result. No entry in Param 2 will default the\nresult to a whole number.\n\n
\nTransmits at 7 data bits, 2 stop bits, even or odd parity and selectable\nbaud rate. Must use a loadlist to link patient data.\n\n
\nParam 3 should be the test identifier. Param 2 will set the number of\ndecimal places for the result, if it is 0 or no entry, the result will\nbe a whole number.\n\n
\nThe program LATDX1 is used with TDX instruments that have V10.1 of\nAbbott's software which allows the input of a specimen identifier.\nThis allows running the instrument to be run by accession or by\na load list. Param 3 should include the name of the test with no\nspaces. Example: VALPOIC ACID should be VALPOICACID.\nParam 2 is used to determine the number of decimal places the result\nwill be reported as. If Param 2 is not entered or is 0 the result\nwill be reported as a whole number, if 1 is entered the result will\nhave 1 decimal place, etc.\n\n
\nHematrak 360,480,590 can all use the program, LAH480.\n\n
\nThis instrument only transmits at 110 baud rate and since the LSI may only\nbe configured down to 150 baud rate, a modification must be made to the\nhardware. The internal number of the test in the auto instrument file must\nmatch the test id #. Example: PT - entry 1, PTT - entry 3.\n\n
\nHematrak 360,480,590 can all use the program, LAH480.\n\n
\nCoulter S+4,S+5,S+6 all may use the program, LACOLT5.\nvalue will be 1 less, and should be cross linked by ID.\nThe ticket flag transmission mode should be set to OFF on the instrument.\n \nThe COUTLER JT3 will run with either the LACOLT5 or the LACOLT6 routines.\nIf you are not running the EO# and BA# tests you can use the LACOLT5.\nIf you are running these tests you will need to use LACOLT6 as when\nthese tests are activated the "," is not used between the test name\nand the result.\nInstruments using DT WITH DH INTERFACE and Coulter S+ Jr. (the format \nin ^LA will not have a ',' between the test name and the results) use \nLACOLT6. \nParameters will depend on wether a patient id # is transmitted\n(this is controlled by a dip switch setting inside the Coulter's CRT).\nIf a patient id is transfered, WBC will have for Param 1: S V=Y(5)\nand should be cross linked by IDE.\nIf a patient id is not transfered, Param 1: S V=Y(4) ie. the subscript\n\n
\nIf this instrument is interfaced to a keypad instrument, the file entry\nand program for the keypad instrument should be used.\n \nMust use a load list. Param 1 is used to extract the value for the test.\nParam 3 is used to identify the test.\n\n
\nMust use the 4B format.\nParam 3 must contain the test # transmitted by the instrument (exp.\nBUN transmits 04=17 where 04 is the test #, 17 is the result. In this\ncase 04 would be entered in Param 3 for the test BUN.).\nThis instrument may need to be transmitted as 7 data bits, regardless of\nwhat the instrument says it is set at.\n\n
\nThe routine is setup to use the following values for the KDA's controls:\nA1='::',A2=':/',A3=<CR>,B1=<CR>,B2=':',B3='\\',B4=':',B5=<CR>\n\n
\nUse format option 3.\n\n
\nThe program LAMODU is used with the Modulus Urocomp keypads with or without\nwhere a degree of 1 would give the result Few.\n \nThe field 'LOAD CHEM TESTS' should be set to 'U' if you have many comments.\nThis will avoid possible store errors.\nthe keypad being interfaced to a urinalysis instrument. Param 1 is used\nto extract the results for the test. The position of the results on the\ndata stream will be dependent on being interfaced to a Clinitek 200, 2000,\nor used as a seperate workstation.\n \nCoded comments can be done similar to the Biovation keypads\n(explained in the INTERFACE NOTES field).\nIf Param 3 is not used the default is 'None$Few$Mod$Many$Profuse$Noted'\n\n
\nThe program LAMODH is used with the Modulus Comp-U-Diff. The results are\n(explained in the INTERFACE NOTES field). If Param 3 is not used the\ndefault is '$1+$2+$3+$4+$Slight$Occ$Few$Mod$Marked'\nwhere a degree of 1 would give the result 1+.\n \nThe field 'LOAD CHEM TESTS' should be set to 'U' if you have many comment\nentries. This will avoid possible store errors.\nextracted from the line of data that is transmitted using Param 1.\n \nExample: for the test LYMPHS (in this case Channel 4)\nParam 1: S V=$E(Y(1),20,22)\nwhere the value is assigned the 20th thru 22nd characters of the results \ntransmitted.\n \nCoded comments can be done similar to the Biovation Hematology keypads\n\n
\nTest # in auto instrument file must match SMA II test code.\n\n
\nThe program LABIOH is used with the Biovation keypads with or without\nParam 1: S V=$E(Y(2),4,5) D NUM S:'V V=""\nThis value is assigned the 4th thru 5th characters of the\n2nd line of the transmitted results.\n \nMorphology results may be assigned to tests or may be put in as comments.\nExample: for the test HYPOCHROMIA.\nParam 1: S V="" I $D(TY(140)) S V=TY(140) D CODE\nwhere 14 is the first 2 digits of the code for the test HYPOCHROMIA.\nThe 3rd digit of the entered code will determine the degree of the result.\nIf there is no entry in Param 3 the default will use\nthe keypad being interfaced to a hematology instrument.\n'Noted$1+$2+$3+$4+$Rare$Occ$Few$Mod$Many'\n(degree 0 gives a result of 'Noted', 1 gives a result of 1+, ...)\n \nExample: if the code entered is '143' and Param 3 is\nNoted$Slight$Mod$Marked the result would be 'Marked'. If Param 3 did not\nhave an entry the result would be '3+'.\n \nCoded Comments: Comments may be entered by using the test, 'OTHER'.\n(to enter more than one test, 'OTHER', enter it in quotes)\n \nUse Model 1300 format #6 if not interfaced to a cell counter.\nComment without degrees:\nExample (Param 1): S V="" I $D(TY(5)) S RMK=RMK_"CLOTTED; " K V\nwhere 5 is the code for the comment 'CLOTTED; '. The code # must be <99\nand may be dependent on what the instrument is able to transmit. The\ncomment will string together any other comments, hence the reason for\nending the comment with a "; ". Since a value is not being assigned to\nthe test 'OTHER', the variable 'V' is killed.\n \nComment with a degree:\nExample:\nUse Model 1320 format #3 if interfaced to a cell counter.\nParam 1:\nI $D(TY(250)) S V=TY(250) D CODE S RMK=RMK_"Dohle Bodies, "_V_"; " K V\nParam 3:\nRare$Occ$Sl$Mk\nwhere 25 is the first 2 digits of the code for the comment 'Dohle Bodies'\nand V is the degree of the comment. If 252 was entered, the comment\nwould be 'Dohle Bodies, Sl; '. If Param 3 was not entered, the comment\nwould be 'Dohle Bodies, 2+; '.\n \nThe field 'LOAD CHEM TESTS' should be set to 'U' if you have many comment\nParam 1 is used to extract the results for the test.\nentries. This will avoid possible store errors.\nParam 3 is optional and may be used to define the vocabulary for reporting.\n \nExample:\nfor the test MONOS\n\n
\nTest # in auto instrument file must match DEMAND test #.\n\n
\nParam 3 contains test # transmitted by instrument.\n\n
\nTest # in auto instrument file must match RA1000 test #.\n\n
\nLAEKT7P is used to process output taken from the printer port.\nParam 1 is used to extract the test values from their postion on the\nprinted report.\n\n
\nParam 3 contains the test name that is transmitted.\n\n
\nInternal # of CHEM TEST field should match the test code # that the\ninstrument transmits. No parameters needed.\nThis instrument must be run by tray-cup. Instrument should not be run\non tray 0.\n\n
\nUses Param 1 to extract the data.\nS X="TEST",V=$S($D(Y(X)):$E(Y(X),7,14),1:"") S:Y(#)["?" V=""\nwhere TEST is the test name transmitted by the instrument.\n\n
\nThe program LABIOU is used with the Biovation keypads with or without\nIf the value is ":" it is reported as "TRACE", otherwise it uses calls\nthe subroutine 'CODE' to determine how it is to be reported.\nThe value is used to select the result from a character string either\non the line CODE or in Param 3. If Param 3 has an entry it will be used,\notherwise it uses 'None$Few$Mod$Many$Profuse$Noted' (value 0 gives a\nresult of 'None', 1 gives a result of 'Few', ...).\n \nExample: if the value transmited is '3'\nand Param 3 is Neg$30$100$300$>200\nthe result would be '300'.\nthe keypad being interfaced to a urinalysis instrument (exp. Clinitek 200).\nIf Param 3 did not have an entry, the result would be 'Many'.\n \nNote: The '$' is used as a delimiter instead of the usual '^' to avoid\nconflicting with file definitions.\n \nCoded Comments:\nComments may be entered by using the test 'OTHER'.\n(to enter more than one test, 'OTHER', enter it in quotes)\n \nComment without degrees:\nThe 1 line format should be used - model 3500b format #1.\nExample (Param 1): I $D(TY(1)) S RMK=RMK_"QUANTITY NOT SUFFICIENT; " K V\nwhere 1 is the code for the comment 'QUANTITY NOT SUFFICIENT; '.\nThe code # must be <99 and may be dependent on what the instrument is\nable to transmit. The comment will string together any other comments,\nhence the reason for ending the comment with a "; ". Since a value is not\nbeing assigned to the test 'OTHER', the variable 'V' is killed.\n \nComment with a degree:\nExample:\nParam 1:\nParam 1 is used to extract the results for the test. Param 3 is optional\nI $D(TY(160)) S V=TY(160) D CODE S RMK=RMK_"Trip Phos Cr, "_V_"; " K V\nParam 3:\n$1+$2+$3+$4+\nwhere 16 is the first 2 digits of the code for the comment 'Trip Phos Cr'\nand V is the degree of the comment.\nIf 164 was entered, the comment would be 'Trip Phos Cr, 4+; '.\nIf Param 3 was not entered, the comment would be 'Trip Phos Cr, Profuse; '.\n \nThe field 'LOAD CHEM TESTS' should be set to 'U' if you have many comment\nentries. This will avoid possible store errors.\nand may be used to define the vocabulary for reporting.\n \nExample: for the test URINE PROTEIN\nParam 1: S V=$E(Y(1),7) D:V'=":" CODE S:V=":" V="TRACE"\nThe value is assigned the 7th character of the transmitted results.\n\n
\nParam 2 may be used to divide value. Example: If RBC is 504 and param 2\nis 100 the value will be 5.04. The variables RBC, HCT, and HGB are\navailable to calculate indices.\n\n
\nInternal # of CHEM TEST field should match the the TEST ID #.\nNo parameters needed.\n\n
\nMust use a load list.\n\n
\nMust use a load list. Cross link by CUP. Test # in auto instrument\nfile must match test # also need Param 1 set up.\n\n
\nTest # in auto instrument file must match Hitachi 737 #.\nUse output format 2 on revision 2.1.\n\n
\nThe electrical connection of the VITEK can be done with the following.\n 20--|\nup the Autoinstrument node (62.4). See lab installation guide for\nprocedures on adding a new organism to the etiology file.\n \nSTEP 3.\nStep thru the beginning fields and fill them in as you would normally\ndo. Several fields will need to be set up differently depending on\nwhether you are running unidirectionally or bidirectionally.\nThese fields are:\nProgram Name uni = LAMIVTK bi = LAMIVTKU\nHandshake response uni = S OUT=$C(6) bi = D ^LAMIVTKC\n \n \nSTEP 4.\nThe entry comes with 10 card types already started for you. These entries\nare never to be deleted as other entries will refer back to them.\nUsing your VITEK interface documentation enter the card type you will\nwant to enter organisms or drugs for. Step thru the prompts until you\ncome to the Select Organism prompt. Enter the organism name and its\ncard code for each organism for this card type. Once you have organisms\nentered for the intitial 10 entries you do not have to enter organisms for\nany of the following card types as the code will refer back to these\n 7------------------------7\ninitial entries.\n \nWhen entering a new card the process card call field needs to be filled\nin with the MUMPS code listed below for PRocessing call. For example\nif you want to process a GNS-F1 card which has a card code of 54 you\nwould enter 'D ^LAMIV12'.\n \nCard Ref. \nCode Spec. Name Processing call\n 01 5.1 GPS-A D ^LAMIV11\n \n 02 5.3 GPSSA D ^LAMIV11\n 03 5.5 GPSTA D ^LAMIV11\n 04 NOT USED\n 05 5.4 YBC D 54^LAMIV11\n 06-0A CARD TYPES NOT USED\n 0B 5.10 UID-1 D ^LAMIV10\n 0C 5.2 BACIL D 52^LAMIV10\n 0D XXX BIOLD NOT SUPPORTED BY VITEK\n 0E 5.12 GNI D 512^LAMIV12\n 0F 5.11 GPI D 511^LAMIV11\nTo set up the VITEK unidirectionally you will need to run the program\n 0FB 5.11 GPI-2 Mate to '0F' which holds 2nd organism table.\n Called from '0F' card if needed.\n 10 5.13 GPS-M D ^LAMIV11\n 11 XXX SCC NOT SUPPORTED BY VITEK\n 12 5.10 UID-3 D 510^LAMIV10\n 13 5.14 GNS D ^LAMIV12\n 14 5.15 GNU D ^LAMIV12\n 15 5.16 GNS-T D ^LAMIV12\n 16 5.17 GNU-T D ^LAMIV12\n 17-A4 GNS FLEX D ^LAMIV12\nCIEP on the VITEK to configure the instrument. If you are running with\n \nSince so many of the cards have the same organisms identified they are\nentered only once on one type of card. The Gram Positive cards\nuse 1 of 2 tables of organisms which are listed under card types '0F'\nand '0FB' and these tables are used for lookup of the organism for all\ngram positive identifications whether it is on an GPI card or on a \nGPS flex card. The Gram Negative codes are handled by a single table\nidentified under the GNI card and is used for all flex panals also.\nGram Negative flex cards can list up to 5 organisms on one card and\nwhen this occurs the organism list is found on the GNS card.\nbidirectional you will need to run the program BCIEP to accomplish this.\n \nThe following is a list of where the organisms will be found for \nthe different cards.\n \nCard '0F' is the main GPI card, and is used by all GPS cards for\n Org ID lookup.\nCard '0FB' is the secondary GPI card used to hold second table of\n organisms. It is used by processing routine when needed.\n This card is a Pseudo card and therefore does not have a call.\nCard '0E' is the main GNI card, and is used by all GNS cards for\n \n Org ID lookup.\nCARD '10' is the main GPS flex card and is used by all other flex cards\n for Organism lookup when multiple organisms are identified.\nCARD '05' is the main card used for identifying yeasts.\nCARD '0B' is used to identify urines\nCARd '12' is also used to identify urines.\nCARD '13' is the GNS flex card and is used by all other flex cards\n for organism lookup when multiple organisms are identified.\nCARD '14' is the GNU flex card and is used by all other flex cards\n for organism lookup when multiple organisms are identified.\nTo set up the VITEK for unidirectional the following paramaters should\nCARD '0C' is used for Bacillus identification.\n \nSTEP 5\nNow step to the Select drug prompt for the card type. If the\ndocumentation has a list of drugs for that card type then enter the\ndrug name, its param 1, its card code, and the print order.\n \nMany of the drugs listed for a card type have more than one code\nassociated with the drug. When this occurs you will add the drug\nname to the listing once for each code associated with that drug.\nbe set as:\n \nThe VITEK data is processed by a set of routines that start LAMIV.\n LAMIV00 is routine used to determine MIC value for the drug.\n The routine is called from the param1 field of the drug\n subfield of the micro card type field. The param1 is in\n the form: "S RUN="x"_U_LARTN D @RUN where "x" is the line\n tag to enter the routine LAMIV00.. The Tag line in the\n routine LAMIV00 for each entry point tells which drug codes\n and type of card (pos, neg) are valid for this entry point.\n For example if you are using a gram negative card which\n VITEK LSI\n \n reports out the drug code as 'C' for tetracycline you \n would find by looking at the routine LAMIV00 that the \n proper entry point would be at 'I' and the entry in param1\n would then be 'S LARTN="I"_U_"LAMIV00" D @LARTN'.\n LAMIV10 is routine used for processing bacillus and urine ID cards\n LAMIV11 is routine for processing Gram Positive identification,\n flex cards and Yeast cards.\n LAMIV12 is routine for processing Gram Negative identification\n and Gram Negative flex cards cards.\n \nON/OFF SWITCH: OFF\nThe above routines will convert the VITEK coded data to an organism\nname, a drug name, a raw MIC value, and an interpretation which will\nall be shown to you upon verification.\n \nCertain drugs have codes which can not be entered thru fileman. These\ndrug codes are "^@?". These characters have special meaning to FILEMAN\nand cannot be entered directly. To get around this problem the routine\nLAMICRA is included. This routine will prompt for the autoinstrument\nentry, the card type and then walk thru the drug nodes displaying the\nentered code. You can enter the code or enter a return at this time.\nRETRY WAIT: 10 SECONDS (SET TO MAX ALLOWED)\nThe routine will either continue when a return is entered or enter the\ncode into the file and build the "C" cross reference entry for you.\n \n****NOTE**** If the autoinstrument file is ever recross referenced you\nwill have to reenter these codes as they will be lost.\n \nThe last field here is the print order field. This field is used by\nthe verify code to display the list of drugs in whatever order you\nchose. This was primarily added so that the organisms and drugs would\ndisplay in the same order as the printed VITEK form.\nACK WAIT: 3 SECONDS (SET TO MAX ALLOWED)\n \nOccasionally VITEK will start producing a new card type. These cards will\nusually have a card code above A4. If you want to use the new card be\nsure of the type of card it is and use the process card call that is used\nfor a similar card.\n \nWhen running in bidirectional mode some additional fields need to be\nfilled in.\n \nThe FILE BUILD ROUTINE field needs to have the program name LAMIVTKD\nNACKS BEFORE AUTO DISABLE: 3\nwhich builds and stores the download records from the load list file.\n \nIn the Lab Site Parameter file you will need to respond to the new field\nDOWNLOAD FULL DATA. If you answer YES the routines will download all\nof the data available about the patient and test. If you answer NO the\nroutines will only download the minimum information needed by the \ninstrument to run the test.\n \nIn the LAB TEST file those tests that are to be downloaded will need a\nunique number assigned to it (0-9) in the field MICRO PREFIX CODE.\nSTX/ETX PROTOCOL: "SSS"/<CR><LF>\n \nThe auto instrument file has 3 additional fields to fill in.\nSend tray/cup - which is a yes/no answer and is the default display\nwhen you start generating the download file.\nQueue build - is a yes/no answer that is the default display when\nstarting to generate a download file and determines if the file is\nbuilt while you wait or is queued out to run by itself giving you\nyou terminal back immediately.\n \nBe very aware that the verify routines used by the rest of the LAB will\nHOST PROTOCAL CHARACTERISTICS: 1200 BAUD, NO PARITY, 8 BIT/CHAR,\nNOT work for microbiology. Use only the verify routines for micro\nwhich will be supplied.\n 2 STOP BITS\nXON TIME-OUT VALUE: 10\nDELAY BETWEEN CHARACTERS: 50\n 2---------\\/-------------2\nDISPLAY DATA OPTION: OFF\nAMS COMPUTER INTERFACE: ENABLED\n \nFor bidirectional you have the following parameters.\nBIDIRECTIONAL INTERFACE (UPLOAD) IS : ENABLED\nBIDIRECTIONAL INTERFACE (DOWNLOAD) IS: ENABLED\nDOWNLOAD PORT: /dev/tty1\nUPLOAD PORT: /dev/tty1\nTIMEOUTS:\n CHECKSUM <ACK>: default is 3 set as high as possible\n 3---------/\\-------------3\n HOST RESPONSE: defalut is 3 set as high as possible\n XON/XOFF: default is 10 set higher if having problems\nRETRY LIMITS:\n CHECKSUM ERROR: 3\n <ENQ>: 3\nRETRY INTERVALS:\n CHECKSUM ERROR: 10\n <ENQ>: 10\nDELAYS:\n LAST MASTER: DEFAULT 10 SET HIGHER\n 4--|\n INTER-RECORD: DEFAULT 10 SET HIGHER\n INTERMESSAGE: DEFAULT 10 SET HIGHER\nEND OF RECORD FORMATS\n STX: ENABLED ETX: DISABLED\n RS: DISABLED GS: DISABLED\nTOTAL NUMBER OF FAILED MESSAGED ALLOWED: 3\nFIELD TERMINATION CHARACTER(S): |\nSTART UP MESSAGE: DISABLED\n \nIn some instances the VITEK will not recieve our acknowledge back in the\n 5--|\n10 second time limit of VITEK and will retransmit the record a second time.\nIf this is occuring from the console of the VITEK enter /ETC/HOSTCTS OFF\nThis command will in most cases clear up double sending of records.\n \nThe VITEK has one caution that must be remembered. If during transmission\nthe VITEK does not receive acknowledgement from the CPU that the records\nhad been received within 3 tries it will turn the interface off. When \nthis occurs several things must be remembered.\n1. The VITEK will not transmit again until the operator turns the\ninterface back on.\n \n2. Once the interface has been turned back on the operator can retransmit\nrecords ONLY if the cards have NOT been removed from the machine. If they\nhave been removed the entire test must be rerun.\n \nThis node of the Auto Instrument file is configured to support revision\nAI of the VITEK software. Sometime around release of Revision L there was\na change in the reporting of values out of the VITEK. Then with the release\nof Revisions W and above to Revision AI they have periodically changed\nvalues being reported. The entries in this file have been set up for\nRevision AI and therefore NOTE that we will support only revision AI or\n 6--|\nlater.\n \nThe VITEK has several tables which need to be built before the\ninstrument can be run. These tables have an entry and then a\nabbrreviation. These tables are set up to match your DHCP tables.\n \nNow we are ready to start setting up the VITEK entry which has several\nsteps that must be followed in sequence in order to set the entry up\nproperly.\n \n 8--|---------------------20\nSTEP 1.\nThe VITEK uses a large number of drugs when doing its reporting.\nYou MUST have all drugs entered into the Antimicrobial Sensitivity file\n(62.06) and the Lab Data File (63) before setting up the Autoinstrument\nfile (62.4). See the Lab installation guide for particulars for \nadding new drugs to the system.\n \nSTEP 2.\nAlso since the VITEK can report over 100 different organisms make sure that\nall the organisms are entered into the Etiology file (61.2) before setting\n\n
\nParam 2 may be used to divide value. Param 1 must be set up.\nUse format option 4.\n\n
\nThe program, LABMD87P, is used with the report format from the\nprinter port.\nThe test name is entered in Param 3.\nInstrument interface requires bidirectional communication.\n\n
\nThis is the entry to be used as the system line from the LSI to the CPU.\n \nRESTART: K ^LA(*),^LA("Q")\n \nFor all LSI's except for #1 the RESTART field should only be:\nRESTART: K ^LA(*)\n \nRemember to replace * with the appropriate number in the examples.\n \nFor sites running multiple LSI's for automated instruments, the\nfollowing information is needed to set the fields NEW DATA and RESTART\nin the auto instrument file. Let * equla 1, 11, 21, 31, etc.\n(corresponding to the internal entry number in the auto instrument file\nfor the LSI).\n \nNEW DATA: S T=* D SET\n\n\nRA2X thru port expander 1200 BAUD, 1 STOP, NO PARITY\nThe internal number of the CHEM TEST entry in this file must match\nthe test code transmitted with the test name and value.\n\n
\nProgram, LAACA4, may be used with DuPont ACA4, ACA5, DIMENSION. Format\nfrom the DIMENSION should be similar to ACA. Param 3 should contain the\ntest code.\n\n
\nThe keyboard urinanalysis is divided into 3 screens MAIN, CAST's, CRYSTAL's\nThe MAIN screen is numbers 1-27\nThe CAST screen is numbers 31-57\nThe CRYSTAL screen is numbers 61-87\nTo enter the value for a given test press the key assoiated with PARAM 3.\nThis part is the same a the second part of the keyboard diff.\n\n
\nInternal entry for Chem Test should match Test I.D. #. Param 2 is the\nnumber of decimal places for the result.\n\n
\nThe internal number for each test is the test code transmitted by the \nGLU 04 5\nBUN 05 6\nCREATININE 06 7\nTP or CA 07 8\ninstrument + 1.\n \nTEST CODE FROM IL 508 CHEM TESTS NUMBER\n--------------------------------------------------------------\nNA 00 1\nK 01 2\nTCO2 02 3\nCL 03 4\n\n
\nCross link by ID or CUP. Must use load list with instrument. Param 3\nshould have the name of the test as transmitted. example NA, K, LI.\n\n
\nUsed with the patient result printout from the printer.\nParam 3 contains the name of the test as it appears on the printout\nwith the exception that no spaces should be included. Example: if\nthe printout is Urea N, then param 3 should contain UreaN.\n\n
\nTest id # should match the internal entry for test in auto instrument file.\nParam 2 will determine # of decimal places for result.\n\n
\nUses Param 3 to identify test which must match the test name that\nis transmited.\n\n
\nTest id # should match the internal entry for test in auto instrument file.\nParam 2 will determine # of decimal places for result.\n\n
\nLAEKT7B is used to process output taken from the instrument interface.\nwill be in the 3rd piece.\nWhen the EKTACHEM 700 is setup to run in the BI-directional mode, and\nthe site has the new LSI rom. The best setings to use are 7 or 8 bits\nwith ODD parity and 1 stop bit. This routine can't be used in the\nUni-directional mode. The routine calls LAKERM3 as part of the\nIN subroutine to unpack the raw kermit data from ^LA(tsk,"O",n)\n to ^LA(tsk,"C",n), then parses the tests into \nTY(testcode)=data^codes. If the error flag has a value other than\n0,1,2,7 then the value will be <null> and the tranmited value\n\n
\nThis instrument setup will work for both unidirectional and bi directional\nwith the routine LAH717U. To run bidirectional you have to fill in the\nfields: HANDSHAKE RESPONSE with "D ^LAH717H" (miss the quotes)\n FILE BUILD ROUTINE: with LAH717D\n \n****NOTE**** to run bidirectional the serial interface board must have\nswitch block 5 dip switch in position 2 (bit 1) turned on to shut off\nsending the BCC. If this is not done the instrument handshake routine\nwill not work.\n\n
\nSetup of the MicroScan: There is a special version of the interface\nThere is only one MICRO card type and it's internal number must be\n1. The 'ORGANISM' subfile is used to look up the organism number\nby the 'Card Code For Organism field'. The 'DRUG' subfile is used to\nlookup the Drug abbreviation by the 'Card Code' field.\nAt the time the PARAM1 mumps code is executed the variable V\nis set to the MIC value "^" the NCCLS code. All the "M" record fields\nare in Y(field number). There is a subroutine DGT that will load the\nMicroScan Dosage Guide Text into the COMMENT field preceded by the Drug\nname.\n \ncode in the MicroScan to work with the VA LSI.\nX-ref to build in the MicroScan:\n The specimen information is downloaded from the VA to the MicroScan\nusing the abbreviation from the TOPOGRAPHY file.\nThe provider is sent down using the initals from the PROVIDER file.\nThe location is sent as found in the ACCESSION file, and service\nis sent if found in the ACCESSION file.\n \nUse the LAMILL routine to add accessions to the load list and enter the\npanel TEST number to be done (these numbers are provided in the MicroScan\ndocumentation), and the ISOLATE number if known. If the ISOLATE number is in\nSet the following paramaters on the MicroScan:\nquestion leave the isolate blank and the MicroScan will assign.\nThis allows the TECH to only load the MicroScan with accession\nthat are prepared for the MicroScan.\n \nNOTE: The MicroScan must have one of its console's active in the\ninterface routine before starting any downloads.\nIf a download is started and the MicroScan isn't in the right\nmode, Then on the VA side the MicroScan instrument will have to\nbe restarted to clear the LA global and then the download\nstarted again. This procedure can easily by done by using the 'Restart\nTimeout >20 sec, String delimiter to zero (No delimiter),\nProcessing of Instrument data' option [LRJOB] located in the Lab Interface\nMenu.\n \nTo use the MicroScan in a upload only mode clear the HANDSHAKE\nfield from the auto instrument file and set the MicroScan protocall\nto XON only.\n \nCommunication parameters and formats menu selection definitions\n(refer to pgs 2-4 through 2-7 of Vol 1)\n \nField delimiter to | (ascii 124), Protocall to NO ACK/NAK.\n2.5.1 Baud Rate 3 for 1200\n2.5.2 word lenght 8 for 8\n2.5.3 # of stop bits 1 for 1\n2.5.4 parity 0 for none\n2.5.5 protocol 1 for XON/XOFF\n2.5.6 serial port # 2 for comm2\n2.5.7 timeout delay 20 seconds\n2.5.8 checksum type 2 for sum-ascii\n2.5.9 null field OK yes\n2.5.10 hospital/lb ID none\nYou may want to use the Single Therapy reporting.\n2.5.11 delimiter value\n field delimiter | (ascii 124)\n string delimiter 0\n2.5.12 edit suppression list K\n2.5.13 custom format # 2\n \nCustom data fild formats and conversion menu selection definitions\n(refer tp pgs 2-8 through 2-18 fo Vol 1)\n \n2.6.1 specimen number normal\n \n2.6.2 date/time format YYMMDD|HHMMSS\n2.6.3 organism name format abbreviation\n2.6.4 single therapy reporting? NO\n2.6.5 sort transmissiont select by specimen number\n2.6.6 -\n2.6.7 -\n2.6.8 cross reference tables 1) words\n 2) source mnemonics\n2.6.9 customize protocol character\n definitions change #5 <1f> to 13\nIn the Auto Instrument file: To setup for Bi-directional operation\n2.6.10 not used for Autoscan 4\n \nNOTE *** Regarding customization of the system (microscan) mnemonics\nmake sure the urine entry in the source file has the urine flag set to\nYES.\nset the HANDSHAKE field to D ^LAMSP to handle the ack handshaking.\n\n
\n Re Direct Connect (bypassing interface) :\n CRT : Y\n Login Allowed : Y\n Output Margin : 255\n Tie Rtn : 1 (optional)\n Auto Baud : N\n ZUSE : Y\n \n RS 232 : same as terminal; Pins 2, 3, and 7 with Pin 4 connected to \n Pin 5 and Pin 6 connected to Pin 20. \n ( Latter 2 connects short modem contrl )\n \n \n EPX : Serial Out @ 1200 baud, 8 Data, 1 Stop, No Parity.\n \nRe Setting files for operation:\n AUTO INSTRUMENT FILE:\n When entering tests into the CHEM TESTS field be sure the PARAM 3\n subfields have no spaces in the test names entered here.\n LOAD/WORKLIST FILE:\n In order to display the tests for verification using EA in the\n same order as they come off on the EPX printouts you must:\n MUX settings:\n 1) Create a test in the LAB TEST FILE (e.g. EPX PROFILE) with\n the tests in LAB TESTS INCLUDED IN PANEL entered in the order\n they display from your EPX printout. TYPE is OUTPUT.\n 2) Enter this test into the LOAD/WORKLIST Profile you have\n given for the EPX. This test should be BUILD NAME ONLY: NO.\n All the other tests should be set to BUILD NAME ONLY: YES.\n 3) LOAD TRANSFORM should be set to UNIVERSAL. INITIAL SETUP\n needs to be set to INITIAL SET.\nFrom ABBOTT\n In regard to smooth operation of the Downloading routine:\n Speed (RCVR & XMT) : 1200\n 1) Must reindex the disk at least weekly, if not more frequently.\n 2) Use a separate carousel (e.g. 99) for running controls,\n calibrators, and water. If system prompts for these\n parameters should appear during a run on your test\n carousel they will interfere with the download.\n 3) You may use the same carousel until it is full. The routines\n will progress to the next carousel. Do not use a carousel\n that has previously been employed without first doing the\n reindex (see #1 above).\n 4) Auto send- ON\n Modem Cntrl : NONE\n 5) The rationale for the reindexing is that current EPX software\n will not consistently delete the PID which is assigned during\n the download. This causes problems when trying subsequent\n downloads to the same carousel. Hence, reindex or use\n a different carousel.\n 6) Everytime there is a glitch with the host computer the\n EPX stops talking to the host and must be rebooted.\n Stall Count : 0\n Output Only : N\n Tab Cntrl : Y\n Lowcase Cntrl : Y\n\n
\nUses Param 3 to identify test which must match the test name that\nis transmited.\n\n
\nSample LA format:\n^LA(5,"I",5) = R|853|63 |003|1|1| 28.2|0| |0| |000|0| |0|0| |\n \nPARAM 3: should have the test identifier entered for all tests except \nthe INR. The identifier number can be found in the Test ID section of \nthe MLA documentation. The most common ones are: PT=1, APTT=3, \nFibrinogen=4, TT=5. The documentation will list tehm as 001 or 012 but you \nshould just enter the number without the preceding zeros.\nPARAM 1 is used to hold the extract code for the INR, it should be: \nS V=+Y(2) D NUM\nWiring requirements are:\n^LA(5,"ENV") = VAH^ROU^50000VA0\nBAUD RATE=1200, PARITY=none, STOP BITS=1, CHARACTER BITS=8 (standard\nunmodified LSI port). Set instrument to SEND DURING RUN=ON, \nDATA FORMAT=E1000C. Pins 2 and 3 will need to be reversed.\n^LA(5,"I") = 6\n^LA(5,"I",O) = 6\n^LA(5,"I",1) = R|848|61 |001|1|1| 13.9|0| |0| |000|0| |0|0|1.2|\n^LA(5,"I",2) = R|849|61 |003|1|1| 42.5|0| |0| |000|0| |0|0| |\n^LA(5,"I",3) = R|850|62 |001|1|1| 12.3|0| |0| |000|0| |0|0|0.9|\n^LA(5,"I",4) = R|851|62 |003|1|1| 27.7|0| |0| |000|0| |0|0| |\n^LA(5,"I",5) = R|852|63 |001|1|1| 12.0|0| |0| |000|0| |0|0| |\n\n
\n Released in patch LR*5.1*99, 8/20/93\n DOWNLOAD CODE: \n Select TEST: GLUCOSE \n ARE YOU ADDING 'GLUCOSE' AS A NEW CHEM TEST (THE 2ND FOR THIS AUTO \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 2// \n PARAM 1: \n PARAM 2: \n PARAM 3: 2 \n DOWNLOAD CODE: \n Select TEST: UREA NITROGEN \n\n ARE YOU ADDING 'UREA NITROGEN' AS A NEW CHEM TESTS (THE 3RD FOR THIS AUTO \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 3// \n PARAM 1: \n PARAM 2: \n PARAM 3: 3 \n DOWNLOAD CODE: \n Select TEST: (continue entering all tests that this instrument will run \n using PARAM 3 to hold the instrument identifier # that you \n have set up on the instrument) \n Select TEST: CO2 \n\n\n Sample LA format: \n ^LA(XX,"ENV") = VAH^ROU^5000VA0 \n ^LA(XX,"I") = 6 \n ^LA(XX,"I",0) = 0 \n ^LA(XX,"I",1) = ~B \n ^LA(XX,"I",2) = 1AA 33 161 1624 1 25@ 2 160@ 3 11@ 4 1.6 \n @5 125@ 6 5.3@ 7 4.3@ 8 7.6@ 9 9.6@10 611 188@12 2.0@13 12 \n @14 24@15 0.8@16 0.2@17 238@18 177@19 93@20 19@21 100 \n ARE YOU ADDING 'CO2' AS A NEW CHEM TEST (THE 1ST FOR THIS AUTO \n @24 198@25 1.6@47 142@~C \n ^LA(XX,"I",3) = 37 \n ^LA(XX,"I",4) = \n ^LA(XX,"I",5) = :AA 33 161 161048 4.9@49 107@53 7@54 3.3 @ \n 55 136@56 1@57 1@58 10@59 1@60 233@19 107@20 30@ \n 21 4@24 1 72@25 1.4@47 134@~C \n ^LA(XX,"I",6) = 3A \n ^LA(XX,"U",7) = ~B \n \n PARAM 3: should have the test identifier entered for all tests \n INSTRUMENT)? Y (YES) \n that will be run on this instrument. The identifier number is that \n number your site has assigned to a test on the instrument. \n\n The instrument should be set to RESULTS ONLY MODE. \n\n CHEM TESTS NUMBER: 1// \n PARAM 1: \n PARAM 2: \n PARAM 3: 1 \n\n
\n Released in Patch LR*5.1*113, 8/26/93\n PARAM 3: \n\n Sample LA format: \n ^LA(XX,"ENV") = VAH^ROU^5000VA0 \n ^LA(XX,"I") = 17 \n ^LA(XX,"I",0) = 0 \n ^LA(XX,"I",1) = ~B \n ^LA(XX,"I",2) = \n ^LA(XX,"I",3) = #1-271 06-15-93 \n ^LA(XX,"I",4) = ID=89 \n ^LA(XX,"I",5) = Color: YELLOW \n DOWNLOAD CODE: \n ^LA(XX,"I",6) = Clarity: CLEAR \n ^LA(XX,"I",7) = GLU NEGATIVE \n ^LA(XX,"I",8) = BIL NEGATIVE \n ^LA(XX,"I",9) = KET NEGATIVE \n ^LA(XX,"I",10) = SG >=1.030 \n ^LA(XX,"I",11) = BLO TRACE \n ^LA(XX,"I",12) = pH 5.0 \n ^LA(XX,"I",13) = PRO NEGATIVE \n ^LA(XX,"I",14) = URO 0.2 E.U./dL \n ^LA(XX,"I",15) = NIT NEGATIVE \n Select TEST: URINE PH \n ^LA(XX,"I",16) = LEU NEGATIVE \n ^LA(XX,"I",17) = ~C \n \n PARAM 1: this parameter is used to extract the result from the data- \n stream and can also be used to convert your results if you wish. \n The >= or <= may be removed from "V" by the following code: \n S V="" I Y(9)[TC(I,4) S V=$S(V[">=":$P(V,">=",2),V["<=":V=$P(V,"<=",2), \n 1:V) \n Basically, any executable MUMPS code can be entered here including \n a call to a local routine for more complicated conversions of the \n ARE YOU ADDING 'URINE PH' AS A NEW CHEM TESTS (THE 2ND FOR THIS AUTO \n results. \n\n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 2// \n PARAM 1: S V="" I Y(9)[TC(I,4) S V=$E(Y(9),6,50) D NUM \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n\n Select TEST: URINE PROTEIN \n ARE YOU ADDING 'URINE PROTEIN' AS A NEW CHEM TESTS (THE 3RD FOR THIS \n AUTO INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 3// \n PARAM 1: S V="" I Y(10)[TC(I,4) S V=$E(Y(10),6,50) D NUM,FIX \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n Select TEST: URINE GLUCOSE \n ARE YOU ADDING 'URINE GLUCOSE' AS A NEW CHEM TESTS (THE 4TH FOR THIS \n\n AUTO INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 4// \n PARAM 1: S V="" I Y(4)[TC(I,4) S V=$E(Y(4),6,50) D NUM,FIX \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n Select TEST: URINE KETONES \n ARE YOU ADDING 'URINE KETONES' AS A NEW CHEM TESTS (THE 5TH FOR THIS \n AUTO INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 5// \n Select TEST: SPECIFIC GRAVITY \n PARAM 1: S V="" I Y(6)[TC(I,4) S V=$E(Y(6),6,50) D NUM,FIX \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n Select TEST: URINE BILI \n ARE YOU ADDING 'URINE BILI' AS A NEW CHEM TESTS (THE 6TH FOR THIS AUTO \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 6// \n PARAM 1: S V="" I Y(5)[TC(I,4) S V=$E(Y(5),6,50) D NUM,FIX \n PARAM 2: \n ARE YOU ADDING 'SPECIFIC GRAVITY' AS A NEW CHEM TESTS (THE 1ST FOR \n PARAM 3: \n DOWNLOAD CODE: \n Select TEST: URINE BLOOD \n ARE YOU ADDING 'URINE BLOOD' AS A NEW CHEM TESTS (THE 7TH FOR THIS AUTO \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 7// \n PARAM 1: S V="" I Y(8)[TC(I,4) S V=$E(Y(8),6,50) D NUM,FIX \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n THIS AUTO INSTRUMENT)? Y (YES) \n Select TEST: URINE NITRITE \n ARE YOU ADDING 'URINE NITRITE' AS A NEW CHEM TESTS (THE 8TH FOR THIS \n AUTO INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 8// \n PARAM 1: S V="" I Y(12)[TC(I,4) S V=$E(Y(12),6,50) D NUM,FIX \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n Select TEST: UROBILINOGEN \n ARE YOU ADDING 'UROBILINOGEN' AS A NEW CHEM TESTS (THE 9TH FOR THIS AUTO \n CHEM TESTS NUMBER: 1// \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 9// \n PARAM 1: S V="" I Y(11)[TC(I,4) S V=$E(Y(11),6,50) D NUM \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n Select TEST: UR LEU ESTERASE \n ARE YOU ADDING 'UR LEU ESTERASE' AS A NEW CHEM TESTS (THE 10TH FOR \n THIS AUTO INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 10// \n PARAM 1: S V="" I Y(7)[TC(I,4) S V=$E(Y(7),6,50) D NUM \n PARAM 1: S V="" I Y(13)[TC(I,4) S V=$E(Y(13),6,50) D NUM,FIX \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n Select TEST: URINE COLOR \n ARE YOU ADDING 'URINE COLOR' AS A NEW CHEM TESTS (THE 11TH FOR THIS AUTO \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 11// \n PARAM 1: S V="" I Y(2)[TC(I,4) S V=$E(Y(2),8,50) D NUM \n PARAM 2: \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n Select TEST: UR APPEARANCE \n ARE YOU ADDING 'UR APPEARANCE' AS A NEW CHEM TESTS (THE 12TH FOR THIS \n AUTO INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 12// \n PARAM 1: S V="" I Y(3)[TC(I,4) S V=$E(Y(3),10,50) D NUM \n PARAM 2: \n PARAM 3: \n DOWNLOAD CODE: \n\n
\nReleased in patch LR*5.1*117, 1/5/94\n DOWNLOAD CODE: \n Select TEST: COHB% \n ARE YOU ADDING 'COHB%' AS A NEW CHEM TESTS (THE 2ND FOR THIS AUTO \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 2// \n PARAM 1: \n PARAM 2: \n PARAM 3: COHb% \n DOWNLOAD CODE: \n Select TEST: (continue entering all tests that this instrument will run \n\n using PARAM 3 to hold the identifier as transmitted by the \n ABL500.) \n\n Sample LA datastream: \n ^LA(209,0) = ABL 500 DATASTREAM \n ^LA(209,"ENV") = VAH^ROU^5000V1 \n ^LA(209,"I") = 50 \n ^LA(209,"I",0) = 0 \n ^LA(209,"I",1) = 5H|\\^&||ABL500^||||1|19930518135924| \n ^LA(209,"I",2) = P|1||16||^||U|||0^years|0^cm|0^kg||||\n Select TEST: FIO2 \n ^LA(209,"I",3) = O|1||Sample #^2766|||||||Blood^Arterial| \n ^LA(209,"I",4) = R|1|^^^FIO2^D|21.0|%||F|3952|19930518135825| \n ^LA(209,"I",5) = R|2|^^^RQ^D|0.86|||F \n ^LA(209,"I",6) = R|3|^^^T^D|37.0|Cel||F \n ^LA(209,"I",7) = R|4|^^^Qt^I|.....|L/min||X \n ^LA(209,"I",8) = R|5|^^^VO2^I|.....|mL/min||X \n ^LA(209,"I",9) = R|6|^^^AaDpO2^E|32.5|mmHg||F \n ^LA(209,"I",10) = R|7|^^^AaDpO2,T^E|32.5|mmHg||F \n ^LA(209,"I",11) = R|8|^^^ABE^C|-0.6|mmol/L||F \n ^LA(209,"I",12) = R|9|^^^a/ApO2^E|65.5|%||F \n ARE YOU ADDING 'FIO2' AS A NEW CHEM TESTS (THE 1ST FOR THIS AUTO \n ^LA(209,"I",13) = R|10|^^^a/ApO2,T^E|65.5|%||F \n ^LA(209,"I",14) = R|11|^^^COHb^M|1.9|%||F|||OSM| \n ^LA(209,"I",15) = R|12|^^^cx^C|2.6|Vol %||F \n ^LA(209,"I",16) = R|13|^^^DO2|.....|mL/min||X \n ^LA(209,"I",17) = R|14|^^^HbF|0.0|%||F|||OSM| \n ^LA(209,"I",18) = R|15|^^^HCO3-^C|24.3|mmol/L||F \n ^LA(209,"I",19) = R|16|^^^Hct^C|27.6|%||F \n ^LA(209,"I",20) = R|17|^^^MetHb^M|0.7|%||F|||OSM| \n ^LA(209,"I",21) = R|18|^^^O2CAP^C|12.1|Vol %||F \n ^LA(209,"I",22) = R|19|^^^O2Hb^M|87.9|%||F|||OSM| \n INSTRUMENT)? Y (YES) \n ^LA(209,"I",23) = R|20|^^^pCO2^M|44.5|mmHg||F \n ^LA(209,"I",24) = R|21|^^^pCO2(T)^M|44.5|mmHg||F \n ^LA(209,"I",25) = R|22|^^^pH^M|7.358|||F \n ^LA(209,"I",26) = R|23|^^^pH(st)^C|7.390|||F \n ^LA(209,"I",27) = R|24|^^^pH(T)^M|7.358|||F \n ^LA(209,"I",28) = R|25|^^^pO2^M|61.7|mmHg||F \n ^LA(209,"I",29) = R|26|^^^pO2(A)^E|94.2|mmHg||F \n ^LA(209,"I",30) = R|27|^^^pO2(A),T^E|94.2|mmHg||F \n ^LA(209,"I",31) = R|28|^^^pO2(T)^M|61.7|mmHg||F \n ^LA(209,"I",32) = R|29|^^^px^C|27.2|mmHg||F \n CHEM TESTS NUMBER: 1// \n ^LA(209,"I",33) = R|30|^^^p50(act)^C|27.91|mmHg||F \n ^LA(209,"I",34) = R|31|^^^p50(act),T^C|27.91|mmHg||F \n ^LA(209,"I",35) = R|32|^^^p50(st)^C|27.40|mmHg||F \n ^LA(209,"I",36) = R|33|^^^Qx^C|2.0|||F \n ^LA(209,"I",37) = R|34|^^^RHb^C|9.5|%||F \n ^LA(209,"I",38) = R|35|^^^RI^E|53|%||F \n ^LA(209,"I",39) = R|36|^^^RI,T^E|53|%||F \n ^LA(209,"I",40) = R|37|^^^SBC^C|23.8|mmol/L||F \n ^LA(209,"I",41) = R|38|^^^SBE^C|-0.4|mmol/L||F \n ^LA(209,"I",42) = R|39|^^^Shunt^E|14.8|%||F \n PARAM 1: \n ^LA(209,"I",43) = R|40|^^^Shunt,T^E|14.8|%||F \n ^LA(209,"I",44) = R|41|^^^sO2^M|90.2|%||F|||OSM| \n ^LA(209,"I",45) = R|42|^^^tCO2(B)^C|23.2|mmol/L||F \n ^LA(209,"I",46) = R|43|^^^tCO2(P)^C|25.7|mmol/L||F \n ^LA(209,"I",47) = R|44|^^^tHb^M|8.9|g/dL||F|||OSM| \n ^LA(209,"I",48) = R|45|^^^tO2^C|11.1|Vol %||F \n ^LA(209,"I",49) = L|1|N \n ^LA(209,"I",50) = ~CLA(309,"I",448) Global ^ \n PARAM 2: \n PARAM 3: FIO2 \n\n
\n To enable the interface, press SYSTEM, then FILES, enter 1.18, then press\n crossed so that it will transmit as a DTE interface.\n ^LA(19,"I",26) = --------------------------------\n ^LA(19,"I",27) = A 0. 6.2\n ^LA(19,"I",28) = B 2. 71.4\n ^LA(19,"I",29) = C 10. 294.6\n ^LA(19,"I",30) = D 30. 720.2\n ^LA(19,"I",31) = E 60. 1157.2\n ^LA(19,"I",32) = F 100. 1539.7\n ^LA(19,"I",33) =\n ^LA(19,"I",34) = LOC ID ng/mL RATE NOTE\n ^LA(19,"I",35) = ----------------------------------------\n \n ^LA(19,"I",36) = 2 CONTROL L 3.88 128.0\n ^LA(19,"I",37) = 3 CONTROL M 14.17 396.3\n ^LA(19,"I",38) = 4 CONTROL H 42.42 923.2\n ^LA(19,"I",39) = 5 000000400 0.68 29.5 LOW\n ^LA(19,"I",40) = 6 000000191 1.24 47.5 LOW\n ^LA(19,"I",41) = 7 000000301 2.54 88.0\n ^LA(19,"I",42) =\n ^LA(19,"I",43) =\n ^LA(19,"I",44) = HIGH > 100.000 ng/mL\n ^LA(19,"I",45) = LOW < 2.000 ng/mL\n The LAIMX routine is written to process data that is transmitted in\n ^LA(19,"I",46) =\n ^LA(19,"I",47) =\n ^LA(19,"I",48) = TESTS USED TO DATE : 61\n ^LA(19,"I",49) =\n ^LA(19,"I",50) =\n ^LA(19,"I",51) =\n ^LA(19,"I",52) =\n ^LA(19,"I",53) = ]\n ^LA(19,"I",54) = C\n ^LA(19,"I",55) = !!\n the MEIA Quantitative layout as defined in the IMX unidirectional RS232\n Interface Guide, pages 7-10.\n \n Param 2 holds the number of decimal places for the result.\n Param 3 holds the number of the test as identified by the instrument.\n\n This interface will transmit in a multiple of different formats depending\n DISPLAY. Enter the password 2215 and press STORE. Set the\n on the tests being run. This version as of 8/13/93 will handle the data\n streams for the ASSAY NUMBER, %GHb and %A1C tests, as well as linearity\n checking.\n **The %A1C test will require the following code to be placed into Param\n 1: S LATFLG=1. All other tests should not have this variable set. The\n linearity functionality can be controlled by entering the following code\n in Param 1: S LRLN(III)="X.X" where the X.X represents the linearity value\n for this test. If no linearity checking is to be enabled, Param 1 should\n be set LRLN(III)="0.0".\n\n communication defaults for the COM2 port, turn the IMX system\n Select TEST: PSA \n ARE YOU ADDING 'PSA' AS A NEW CHEM TESTS (THE 1ST FOR THIS AUTO \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 1// \n PARAM 1: S LRLN(III)="0.1" \n PARAM 2: 1 \n PARAM 3: 53 \n DOWNLOAD CODE: \n Select TEST: CEA \n ARE YOU ADDING 'CEA' AS A NEW CHEM TESTS (THE 2ND FOR THIS AUTO \n off, wait 10 seconds, then turn it back on. This initializes the\n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 2// \n PARAM 1: S LRLN(III)="1.0" \n PARAM 2: 1 \n PARAM 3: 76 \n DOWNLOAD CODE: \n Select TEST: FERRITIN \n ARE YOU ADDING 'FERRITIN' AS A NEW CHEM TESTS (THE 3RD FOR THIS AUTO \n INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 3// \n parameters in memory.\n PARAM 1: S LRLN(III)="1.0" \n PARAM 2: 0 \n PARAM 3: 27 \n DOWNLOAD CODE: \n Select TEST: HEMOGLOBIN A1C \n ARE YOU ADDING '"HEMOGLOBIN A1C' AS A NEW CHEM TESTS (THE 4TH FOR THIS \n AUTO INSTRUMENT)? Y (YES) \n CHEM TESTS NUMBER: 4// \n PARAM 1: S LRLN(III)="0.0" \n PARAM 2: 1 \n\n PARAM 3: 79 \n DOWNLOAD CODE: \n Select TEST: (continue entering all tests that this instrument will run \n using PARAM 3 to hold the ASSAY # assigned by Abbott.) \n\n \n ******************************************************************\n SAMPLE DATASTREAM\n FYI: This instrument produces several different data streams not all of\n which are currently supported.\n The interface may be tested by reprinting the results from the last run.\n ******************************************************************\n \n ^LA(19,"ENV") = VAH^ROU^583VA0^ROU583VA0\n ^LA(19,"I") = 55\n ^LA(19,"I",0) = 55\n ^LA(19,"I",1) = [\n ^LA(19,"I",2) =\n ^LA(19,"I",3) =\n ^LA(19,"I",4) = DATE: 4/27/93\n ^LA(19,"I",5) = TIME: 13:45:30\n \n ^LA(19,"I",6) =\n ^LA(19,"I",7) = TECH ID : _________\n ^LA(19,"I",8) = RGNT LOT: _________\n ^LA(19,"I",9) = SERIAL #: 22642\n ^LA(19,"I",10) = CRSL ID : 2\n ^LA(19,"I",11) = CURVE : 1\n ^LA(19,"I",12) = CAL DATE: 4/02/93\n ^LA(19,"I",13) = CAL TIME: 10:37:52\n ^LA(19,"I",14) =\n ^LA(19,"I",15) = ASSAY 53 PSA 2245 Revision 1\n ***The instrument uses a DCE configuration. Lines 2 and 3 must be\n ^LA(19,"I",16) =\n ^LA(19,"I",17) = MODE 1 CALIBRATOR\n ^LA(19,"I",18) =\n ^LA(19,"I",19) = LOC ng/mL RATE FACTOR\n ^LA(19,"I",20) = ----------------------------\n ^LA(19,"I",21) = 1 10. 294.6 0.926\n ^LA(19,"I",22) =\n ^LA(19,"I",23) = MODE 1 CALIBRATION CURVE\n ^LA(19,"I",24) =\n ^LA(19,"I",25) = CALIB ng/mL AVGR\n\n