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5147a805-329c-4900-8c29-758eb2a19610
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{"name": "scanned_report_SKMC250i26020 {"name": "scanned_report_SKMC250i260203100800034.jpg", "content_type": "image/jpeg", "size": 859023, "data": {"additionalProp1": {}}}...
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1771619708
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{"status": "pending"}
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{"name": "labs-1759511987-pexels-ladyh {"name": "labs-1759511987-pexels-ladyhelga-23731967.jpg", "content_type": "application/octet-stream", "size": 738835, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "error {"status": "failed", "error": "Timeout reached while detecting encoding for /home/sid/xevyo/open-webui-dev/backend/data/uploads/c19a8f0c-b443-4109-9679-3e97a9467607_labs-1759511987-pexels-ladyhelga-23731967.jpg"}...
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{"name": "labs-1759511764-pexels-ladyh {"name": "labs-1759511764-pexels-ladyhelga-23731967.jpg", "content_type": "application/octet-stream", "size": 738835, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "error {"status": "failed", "error": "Timeout reached while detecting encoding for /home/sid/xevyo/open-webui-dev/backend/data/uploads/c0faa05a-8e55-4255-bad4-684f17878aff_labs-1759511764-pexels-ladyhelga-23731967.jpg"}...
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labs-1763577386-6a85a9a3-70cd-42c4-acf9-b274286533 labs-1763577386-6a85a9a3-70cd-42c4-acf9-b27428653399.png...
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{"name": "labs-1763577386-6a85a9a3-70c {"name": "labs-1763577386-6a85a9a3-70cd-42c4-acf9-b27428653399.png", "content_type": "application/octet-stream", "size": 1071208, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "error {"status": "failed", "error": "Timeout reached while detecting encoding for /home/sid/xevyo/open-webui-dev/backend/data/uploads/a57c0c8a-69d7-4445-b183-4f054edba32f_labs-1763577386-6a85a9a3-70cd-42c4-acf9-b27428653399.png"}...
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labs-33c238b6-c04b-4e78-8652-cbb09d8b6379.pdf
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{"name": "labs-33c238b6-c04b-4e78-8652 {"name": "labs-33c238b6-c04b-4e78-8652-cbb09d8b6379.pdf", "content_type": "application/octet-stream", "size": 9, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "error {"status": "failed", "error": "Stream has ended unexpectedly"}...
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/home/sid/xevyo/open-webui-dev/backend/data/upload /home/sid/xevyo/open-webui-dev/backend/data/uploads/5262f107-1ef1-40f0-b951-aa233f8604d2_labs-33c238b6-c04b-4e78-8652-cbb09d8b6379.pdf...
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labs-56c78c4b-0e5e-445f-9cb3-442b3ef0ddbc.pdf
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{"name": "labs-56c78c4b-0e5e-445f-9cb3 {"name": "labs-56c78c4b-0e5e-445f-9cb3-442b3ef0ddbc.pdf", "content_type": "application/octet-stream", "size": 9, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "error {"status": "failed", "error": "Stream has ended unexpectedly"}...
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labs-1c3627e1-f03b-495d-98d7-3c28a207c085.pdf
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{"name": "labs-1c3627e1-f03b-495d-98d7 {"name": "labs-1c3627e1-f03b-495d-98d7-3c28a207c085.pdf", "content_type": "application/octet-stream", "size": 9, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "error {"status": "failed", "error": "Stream has ended unexpectedly"}...
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/home/sid/xevyo/open-webui-dev/backend/data/upload /home/sid/xevyo/open-webui-dev/backend/data/uploads/30a96926-7506-4876-b7b3-e18ff1ec0995_labs-1c3627e1-f03b-495d-98d7-3c28a207c085.pdf...
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labs-e53ea416-415e-457e-a879-3dc2c8a78bf6.pdf
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{"name": "labs-e53ea416-415e-457e-a879 {"name": "labs-e53ea416-415e-457e-a879-3dc2c8a78bf6.pdf", "content_type": "application/octet-stream", "size": 9, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "error {"status": "failed", "error": "Stream has ended unexpectedly"}...
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{"name": "labs-RKMC224e251030163840.ti {"name": "labs-RKMC224e251030163840.tif", "content_type": "application/octet-stream", "size": 379252, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "error {"status": "failed", "error": "Could not detect encoding for /home/sid/xevyo/open-webui-dev/backend/data/uploads/ed8dee18-beb3-4dff-b667-93312a553525_labs-RKMC224e251030163840.tif"}...
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{"name": "labs-1743545111-skm-c450i250 {"name": "labs-1743545111-skm-c450i25040114280-0013.jpg", "content_type": "application/octet-stream", "size": 827984, "data": {"patient_id": "3e448bf0-0f45-11f0-8be5-73d44ea410c5"}}...
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{"status": "failed", "error {"status": "failed", "error": "Could not detect encoding for /home/sid/xevyo/open-webui-dev/backend/data/uploads/ea54cb81-13d6-4279-812f-b204b570e1ec_labs-1743545111-skm-c450i25040114280-0013.jpg"}...
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scanned_report_SKMC250i26012304120(1).pdf
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{"name": "scanned_report_SKMC250i26012 {"name": "scanned_report_SKMC250i26012304120(1).pdf", "content_type": "application/pdf", "size": 210300, "data": {"patient_id": "01"}}...
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e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca4 e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca495991b7852b855...
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{"status": "failed", "content& {"status": "failed", "content": "", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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scanned_report_SKMC250i26012304120(1).pdf
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{"name": "scanned_report_SKMC250i26012 {"name": "scanned_report_SKMC250i26012304120(1).pdf", "content_type": "application/pdf", "size": 210300, "data": {"patient_id": "01"}}...
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{"status": "failed", "content& {"status": "failed", "content": "", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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scanned_report_SKMC250i26012304120(1).pdf
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{"name": "scanned_report_SKMC250i26012 {"name": "scanned_report_SKMC250i26012304120(1).pdf", "content_type": "application/pdf", "size": 210300, "data": {"patient_id": "01"}}...
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{"status": "failed", "content& {"status": "failed", "content": "", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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labs-1763065604-scan-2.pdf
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{"name": "labs-1763065604-scan-2.pdf&# {"name": "labs-1763065604-scan-2.pdf", "content_type": "application/octet-stream", "size": 310721, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca4 e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca495991b7852b855...
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{"status": "failed", "content& {"status": "failed", "content": "", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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labs-SKMC250i25110604180.pdf
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{"name": "labs-SKMC250i25110604180.pdf {"name": "labs-SKMC250i25110604180.pdf", "content_type": "application/octet-stream", "size": 190475, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "content& {"status": "failed", "content": "", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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labs-20251027092409-9387-1_1_1559460818.pdf
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{"name": "labs-20251027092409-9387-1_1 {"name": "labs-20251027092409-9387-1_1_1559460818.pdf", "content_type": "application/octet-stream", "size": 80175, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca4 e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca495991b7852b855...
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{"status": "failed", "content& {"status": "failed", "content": "", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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labs-test(17).pdf
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{"name": "labs-test(17).pdf", " {"name": "labs-test(17).pdf", "content_type": "application/octet-stream", "size": 85095, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca4 e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca495991b7852b855...
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{"status": "failed", "content& {"status": "failed", "content": "", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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labs-SKMC450i25040711080.pdf
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{"name": "labs-SKMC450i25040711080.pdf {"name": "labs-SKMC450i25040711080.pdf", "content_type": "application/octet-stream", "size": 58742, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca4 e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca495991b7852b855...
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labs-1758829048-scan-1.pdf
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{"name": "labs-1758829048-scan-1.pdf&# {"name": "labs-1758829048-scan-1.pdf", "content_type": "application/octet-stream", "size": 310721, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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{"status": "failed", "content& {"status": "failed", "content": "", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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labs-20251118060210-2886-1_2_1571792887.pdf
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{"name": "labs-20251118060210-2886-1_2 {"name": "labs-20251118060210-2886-1_2_1571792887.pdf", "content_type": "application/octet-stream", "size": 47428, "data": {"patient_id": "b3e7cc30-1ba8-11f0-b706-c183bb9a9165"}}...
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36a9e7f1c95b82ffb99743e0c5c4ce95d83c9a430aac59f84e 36a9e7f1c95b82ffb99743e0c5c4ce95d83c9a430aac59f84ef3cbfab6145068...
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{"status": "failed", "content& {"status": "failed", "content": " ", "error": "The content provided is empty. Please ensure that there is text or data present before proceeding."}...
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{"status": "completed", "conte {"status": "completed", "content": "{\"support_email\":null,\"address\":\"#201-3151 27st\nNE\",\"city\":\"Calgary\",\"state\":\"Alberta\",\"postal_code\":\"T1YOB4\",\"full_phone\":\"+14032354109\",\"fax\":\"403-235-4147\"}\nFax\nTo: {{REFDOCNAME}} From: Patient Care Coordinator\nFax: {{REFDOCFAX}} Pages: including cover page\nPhone: {{REFDOCPHONE}} Date: {{TODAYSDATE}}\nRe: {{PATIENTNAME}} - {{PATIENTPHN}} CC:\n \nDear: {{REFDOCNAME}} \n \nThank you for your referral.\n \nWe have been unable to contact the patient after several attempts to do so. We have checked the patient contact information on\nNetcare with no success.\n \nTel No Tried:__________\n \nKindly send us an updated contact number so as we can book the patient for their appointments.\nIf you have any questions please don't hesitate to contact me, and thank you for your referral.\n \nRegards\nPatient Care Coordinator\n \n \nInformation contained in this communication may be confidential and is intended only for the use of the recipient(s). If the reader of\nthis message is not the intended recipient, you are hereby notified that any dissemination, distribution, or copying of this\ncommunication or any of its contents is strictly prohibited. If you received this communication in error, Please return it to the sender\nand contact Advanced Cardiology 403-235-4109.\nThank you for your referral..."}...
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{"status": "completed", "conte {"status": "completed", "content": "{\"support_email\":null,\"address\":\"#201-3151 27st\nNE\",\"city\":\"Calgary\",\"state\":\"Alberta\",\"postal_code\":\"T1YOB4\",\"full_phone\":\"+14032354109\",\"fax\":\"403-235-4147\"}\nFax\nTo: {{REFDOCNAME}} From: Patient Care Coordinator\nFax: {{REFDOCFAX}} Pages: including cover page\nPhone: {{REFDOCPHONE}} Date: {{TODAYSDATE}}\nRe: {{PATIENTNAME}} - {{PATIENTPHN}} CC:\n \nDear: {{REFDOCNAME}} \n \nThank you for your referral.\n \nWe have been unable to contact the patient after several attempts to do so. We have checked the patient contact information on\nNetcare with no success.\n \nTel No Tried:__________\n \nKindly send us an updated contact number so as we can book the patient for their appointments.\nIf you have any questions please don't hesitate to contact me, and thank you for your referral.\n \nRegards\nPatient Care Coordinator\n \n \nInformation contained in this communication may be confidential and is intended only for the use of the recipient(s). If the reader of\nthis message is not the intended recipient, you are hereby notified that any dissemination, distribution, or copying of this\ncommunication or any of its contents is strictly prohibited. If you received this communication in error, Please return it to the sender\nand contact Advanced Cardiology 403-235-4109.\nThank you for your referral..."}...
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{"status": "completed", "conte {"status": "completed", "content": "XXXX 27 Aug, 1979 Page 1 of 16 XXXX 27 Aug, 1979 Page 2 of 16 \n \nPatient Information: \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \nCopyright Protection \nThis report, inclusive of its design and content, is copyright-protected and remains the sole property of BioAro Inc. globally. Unauthorized \nreproduction, distribution, copying of design elements, or dissemination of any content from this report, in whole or in part, is strictly \nprohibited. Any individual or entity found infringing upon this copyright without obtaining prior written consent from BioAro Inc. may be \nsubjected to severe legal penalties, including but not limited to financial damages, injunctiv e relief, and other remedies available under \napplicable laws. We urge all parties to respect our intellectual property rights and adhere to the terms set forth herein. \n \nName XXXX Sample Type BLOOD \nGender Female Collection Date 3 March, 2024 \nDate of Birth 27 Aug, 1979 Report Date 23 March, 2024 \nID P3626 Patient's Address 159, Birch Road XXXX 27 Aug, 1979 Page 3 of 16 \n \n \n \nVariations in multiple genes have been identified in this individual. The report has examined variants that have been flagged \nas 'Pathogenic or Likely Pathogenic', as well as some of the VUS variants. Many of these variants have been implicated, by \nmultiple peer -reviewed clinical studies and Genomic databases in different hereditary and acquired diseases. A clinical \ncorrelation of these variants with any symptoms or family history of the patient, by a physician is advised. \n \nAMPD1, TSFM, MAGI3, PSRC1, MYO15A, LPR2, COL3A1, CACNA1D, FLG, MASP1, DST, COL9A1, TBXAS1, \nCPT1A, INPPL1, KRT3, KRT4, KRT8, HPD, TNFSF11, NKX2-1, COQ9, GAMT, IFIH1, ITGB2, FOXQ1, ABCG8, \nPCSK9, MSX2. \n \n \n \nWGS has identified multiple variants in the individual. As per ACMG guidelines, \"Pathogenic' and \"Likely Pathogenic\" variants \nare treated as Pathogenic. These variants are likely to alter the normal functioning of a gene, cause disease, and affect the \nhealth of an individual. However, an analysis of some variants of unknown significance (VUS), is also included for this patient. \nSummary of genes associated with specific disease. \nSummary of genetic variants associated with cancer-associated genes. \n \n \n \n \n \n \n \nSummary \nOverall Summary of the Genomic test XXXX 27 Aug, 1979 Page 4 of 16 \n \n \nSummary of genetic variants associated with cardiovascular diseases. XXXX 27 Aug, 1979 Page 5 of 16 \n \nSummary of genetic variants associated with longevity. \n \n \nBelow is a summary of the variant genes identified in this individual. This section has been segregated into two categories: \nNote: The presence of these variants does not imply the individual shall necessarily manifest the disease or its symptoms XXXX 27 Aug, 1979 Page 6 of 16 \n \nSummary of Pathogenic/Likely Pathogenic Genetic Variants from the Screen XXXX 27 Aug, 1979 Page 7 of 16 \n \n \nSummary of VUS / Uncertain significance mutations found in the client include: \nThese variant genes include those for which firm clinical evidence may not yet be available (VUS or conflicting). These \nvariations need correlation with clinical symptoms or family history to determine risk assessment. Further investigations and \nmonitoring may be prescribed by the physician or geneticist. XXXX 27 Aug, 1979 Page 8 of 16 XXXX 27 Aug, 1979 Page 9 of 16 XXXX 27 Aug, 1979 Page 10 of 16 XXXX 27 Aug, 1979 Page 11 of 16 XXXX 27 Aug, 1979 Page 12 of 16 XXXX 27 Aug, 1979 Page 13 of 16 XXXX 27 Aug, 1979 Page 14 of 16 \n \n \n \n \n \n \nAs per the criteria laid out by the American College of Medical Genetics and Genomics (ACMG), this report has separated \ngenes with alterations, into those which are either \"pathogenic\" or \"likely pathogenic\". \nPathogenic alterations in a gene imply that the specific alteration is 100% associated with the disease observed in the \npopulation. While likely pathogenic implies that there is a 90% certainty of the variant gene being responsible for the disease \nin the population. \nThese genetic alterations can compromise the functioning of the listed genes and affect the health of the individual. \nThe presence of these variants does not imply the individual shall necessarily manifest the disease or its symptoms. A clinical \ncorrelation of these variants with any symptoms or family history of the patient is required to be performed by a physician or \ngeneticist (and interpretation made by a genetic counselor for the patient). \nMultiple variant genes have been found, which are pathogenic/likely pathogenic or VUS. Many of these are heterozygous \nrecessive (unlikely to produce a disease). However, a clinical correlation with any symptoms or family history is strongly \nadvised to support further investigations or risk assessment. \nA few key variants are summarized below: \n \nAMPD1, TSFM, MAGI3, PSRC1, MYO15A, LPR2, COL3A1, CACNA1D, FLG, MASP1, DST, COL9A1, TBXAS1, \nCPT1A, INPPL1, KRT3, KRT4, KRT8, HPD, TNFSF11, NKX2-1, COQ9, GAMT, IFIH1, ITGB2, FOXQ1, ABCG8, \nPCSK9, MSX2. \n \n \n \n \nWhat this result means to you? XXXX 27 Aug, 1979 Page 15 of 16 \n \n \n \nVariations in multiple genes have been identified in this individual. The report has examined variants that have been flagged \nas 'Pathogenic or Likely Pathogenic', as well as some of the VUS variants. Many of these variants have been implicated, by \nmultiple peer-reviewed clinical studies and Genomic databases, in different diseases. \nIn the case of an autosomal dominant variant, a single copy of the variant gene is sufficient to produce the symptoms/disease \nin the individual (or modify the response to drugs). Additionally, where both copies of a variant gene are affected \n(homozygous), the offspring/children have a 50% chance of getting the disease (and a 100% probability of getting the disease \nif a similar variant gene is inherited from the other parent). \nThe gene alterations identified in this client can lead to the development of associated diseases, however, not all individuals \ndevelop actual symptoms. Several studies have shown that positive modifications to diet, gut microbiome, and other \nenvironmental factors (e.g. smoking) can ameliorate the effect of genetic variations. \nThe individual is strongly advised to have a genetic analysis completed for all their siblings/children/grandchildren to help \nidentify variant genes that may have been transmitted to the children (or grandchildren). This would allow appropriate \ncounseling and management of children to help prevent (or reduce the severity) of any inflammatory disease in them (or \ntheir children). The individual is advised to discuss a TRIO analysis. \n \n \n \n \nWhole genome sequencing (WGS) was carried out on a blood sample obtained from the patient. WGS examines the entire \nset of known genes present in humans (over 22,000 genes) and compares it with a reference human genome (GRCh37). The \ntest and subsequent analysis of the data, helps identify which genes show alterations or variations, as compared to the \nreference genome. \nFurther analysis (tertiary analysis and clinical correlation) of the data, help to distinguish, which of these gene variants may \nbe responsible for: \n1. Any diseases (or clinical symptoms) the patient has today. \n2. Can be harmful (pathogenic) to the patient, and put her/him at high risk of getting a disease in the future. \n3. Which genetic variants and/or associated disease/s could have been inherited from parents? \n4. If there is a Proband in the family, how does the individual correlate to the proband clinically and genetically? \n5. Adverse effects/correlation with any medication the patient is taking today (Pharmacogenomic Analysis/on \ndemand). \nBioAro uses the DNBSEQ G400 for WGS. All collected data is analyzed in -house and stored locally, without \ncompromising the security or privacy of the data. \nAs per ACMG guidelines (American College of Medical Genetics and Genomics): \nRecommendation / Next step \nSummary of Genomic test performed XXXX 27 Aug, 1979 Page 16 of 16 \n \n1. Alterations in genes are often referred to as 'variations'; altered genes are often called 'variant genes' or simply \n'variants'. \n2. Pathogenic and likely pathogenic variants, carry >90% certainty of being responsible for a disease and hence are \naccorded the same level of association. \n3. Variants of unknown significance (VUS) are variations/changes in a person's DNA sequence, which \nhave a yet unknown effect on an individual's health or correlation to the disease/symptoms. \n4. Autosomal dominant* implies that the variant gene is located on a numbered non-sex chromosome and a single copy \nof the gene is enough to cause a disease in the individual. A child of a person having an autosomal dominant variant \nhas a 50% chance of being affected by the same disorder. However, in some cases, it is not possible to determine if the \nvariant gene is dominant or recessive. In such instances, further testing is advised to determine the risk to an offspring. \n5. BioAro offers a Genetic monitoring program (GMP) that monitors published, peer-reviewed scientific literature and \nclinical studies for new information that may correlate VUS with known diseases or symptoms. \n \n \n \n \nGenetic testing using the methods applied by BioAro is expected to be accurate but reflex to analysis testing may be sought \nfor confirmation. No diagnostic claims are being made or implied. An absence of definitive pathogenic findings does not rule \nout the diagnosis of a genetic disorder because there are abnormalities that cannot be detected by this test, and pathogenic \nclassifications are subject to change. It is also possible that a disease -causing variant is located in a region not covered by \nthe analys is. The chance of a false positive or false negative due to laboratory error cannot be completely excluded. \nConsultation with a genetics professional is recommended for interpretation of results. This test was performed and \ndeveloped according to the characteristics of BioAro Inc. following the recommended standards and QC measures by the test \nmanufacturers and industry. \n \n \nAll gene references are hyperlinked for convenience. \nInformation has been confirmed from Clinvar, ACMG guidelines and https://www.genecards.org/ \n \n \n \nLiterature references \nDisclaimer"}...
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{"status": "completed", "conte {"status": "completed", "content": "Ultrasound Request\nPreferred Facility Inpatient Location\nPatient Phone Number (Cell # preferred) Patient Address\nCity Postal Code WCB Claim Number\nOrdering Provider Name Provider ID Department ID\nProvider Fax Provider Phone Contact Number for Critical Test Results\nProvider Address/Location City Postal Code\nLocum \uf06f No \uf06f Yes \u25ba Primary Provider Name and Provider ID _______________________________________\nSignature Date (dd-Mon-yyyy) Copy to Provider (last,first and middle) Copy to Fax\nRequested Procedure\nReason for Exam \nClinical question to be answered\nRelevant Previous Imaging Studies (Mandatory)\nModality Location Date (dd-Mon-yyyy) Attached copy \uf06f No \uf06f Yes\nn ALL fields must be completed in order to process request\nn Fax to Diagnostic Imaging; fax numbers listed at\nhttp://www\n.albertahealthservices.ca/diagnosticimaging\nn Urgent/Emergent requests must be discussed by direct consultation with\na radiologist\nFollow Up\nStat report requested\n\uf06f No \uf06f Yes (phone/pager):\nPatient follow up \uf06f n/a\n\uf06f In ER \uf06f With GP \uf06f Other (specify):\nCurrent Patient Condition Weight \uf06f kg \uf06f lbs Height \uf06f cm \uf06f in\nCondition No Yes If Yes: \nPatient Pregnant \uf06f n/a \uf06f \uf06f Date of LMP:\nContraceptive Use \uf06f \uf06f Specify:\nIsolation Precautions \uf06f \uf06f Specify:\nAllergies \uf06f \uf06f Specify:\nMedications \uf06f \uf06f Specify:\nMechanical lift/ transfer required \uf06f \uf06f Specify:\nResearch Study \uf06f \uf06f Study Name: Study #:\nObstetrical History (if applicable)\nDescribe: G T P\nL A\nLMP (dd-Mon-yyyy)\nDepartment Use Only\nAppointment Priority \uf06f 24 hr \uf06f 1 week \uf06f Next Avail. \uf06f Other (specify):\nDate Received (dd-Mon-yyyy) Time Received (hh:mm) Date of Appointment (dd-Mon-yyyy) Time of Appointment (hh:mm)\nLast Name (Legal) First Name (Legal)\nPreferred Name /box1 Last /box1 FirstDOB(dd-Mon-yyyy)\nPHN ULI /box1 Same as PHNMRN\nAdministrative Gender /box1 Male /box1Female\n/box1\nNon-binary/Prefer not to disclose (X) /box1 Unknown\n09922 (Rev2022-08) \nKash\nDiv\n1998-12-11\n578788878\n4032354147\nCalgary\n52 Castlefall Way NE\nCaglary\nT3J1M7"}...
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{"status": "completed", "conte {"status": "completed", "content": "To cancel or rebook your appointment, please call Central Booking: Mon-Fri: 8AM-7PM, Sat: 9AM-4PM, Sun: Closed\nBreast Procedure Requisition\nCentral Booking\n780-669-2222\nToll Free\n1-866-771-9446\nName: Appointment Details:\nAddress: Date:\nInsurance: W.C.B. ( ) Other: Location:\nToll Free Fax\n1-855-930-1593\nFax\n780-930-1593\nPhone: FemaleMale Non-Binary Time:\nPhysician's Stamp\n& Practice ID\nURGENT FAX REPORT (until 4 pm, M-F)\nReferring Physician's Information\nAddress:\nName:\nDate:\nSignature:\nPhone: Fax: \nCopy To:\nPhone:\nFax:\nName:\nPregnant? Yes No LMP:\nRelevant History, Physical Findings, and Provisional Diagnosis\nDiagnostic Mammo\nL R Bilat\nBreast Ultrasound\nL R Bilat\nAxilla Ultrasound\nL R Bilat\nAxilla Biopsy: L R\nWire Localization (please specify if bracketing is requested)\nSite 1: L R\nSite 2: L R\nSite 3: L R\nFine Needle Aspiration CytopathologySend for: Microbiology\nSite 1: L R\nSite 2: L R\nSite 3: L R\nSentinel Node Injection: L R\nBreast Biopsy\nVAB\nVAB (Vacuum Assisted Biopsy) - Lendrum only\nVAB\nVAB\nSite 1: L R\nSite 2: L R\nSite 3: L R\n(Meadowlark and Sherwood Park only)\nIncomplete requisitions \nwill be returned\nPLEASE\nNOTE:\nDOB: \nMM/DD/YYYY\nREV 01/2022\n1998-12-11\n4036481926\n4036481926\n1\n1 ** ALL EXAMINATIONS ** \nFREE PARKING AT ALL SITES\nRemember to bring the Imaging Requisition plus your Health Care Card and photo ID. \nIf you are unable to keep your appointment, and need to reschedule, please phone the clinic directly. (There is no facility to look after small \nchildren). The following examinations are by appointment only. When making an appointment, please notify if patient is diabetic or pregnant.\nPlease phone 780-669-2222 to\nschedule your appointment\nFREE PARKING AT ALL SITES\nLendrum Women's Imaging\n10381 - 51 Avenue T6H 0K4 \nPh: 780-434-9171 | F: 780-436-5211\nMeadowlark\n200 Meadowlark Shopping Centre\n156 Street - 89 Avenue T5R 5W9 \nPh: 780-489-8430 | F: 780-481-6630\nSherwood Park\n136 Athabascan Avenue T8A 4E3 \nPh: 780-464-1515 | F: 780-464-1216\nLOCATIONS & SERVICES\nMammography\n- It is suggested that you wear a two-piece outfit so you may change into your robe more easily.\n- Do not use deodorant, talcum (body powder), or lotion/oil the day of your exam.\n- If you have significant premenstrual breast tenderness, you may reschedule your appointment.\n- We recommend avoiding caffeine intake for 2 days prior to your mammogram to decrease discomfort during your exam.\nBreast Biopsy\n- It is suggested that you wear a two-piece outfit so you may change into your robe more easily.\n- Do not use deodorant, talcum (body powder), or lotion/oil the day of your procedure.\n- We recommended that you eat breakfast or lunch before coming for your procedure.\n- Expect to be at our clinic for approximately 60-90 minutes.\n- Notify the clinic of any drug or latex allergies before your procedure.\n- No heavy lifting or strenuous activity for 48 hours after your procedure.\n- Vacuum assisted biopsy only: If you are on blood thinners, we recommend that you check with your family\nphysician about discontinuing your blood thinners prior to your procedure.\nServices\n\u2022 Breast wire localizations\n\u2022 Breast and axilla ultrasound guided biopsies\n\u2022 Fine needle breast and axilla aspirations\n\u2022 Sentinel node injections\nServices\nServices\n\u2022 Sentinel node injections\nPATIENT PREPARATION INSTRUCTIONS:\nGateway Blvd.\n99 St\nCalgary Trail NW\n106 St\n51 Ave NW\nWhitemud Dr NWWhitemud Dr NW\nBroadmoor Blvd.Broadmoor Blvd.\nChippewa Rd.\nAnthony Henday Dr.\nBaseline Road\nMain Blvd.Blackfoot Rd.\n\u2022 Breast wire localizations\n\u2022 Breast and axilla ultrasound guided biopsies\n\u2022 Stereotactic guided biopsies\n\u2022 Vacuum assisted biopsies\n\u2022 Fine needle breast and axilla aspirations"}...
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{"name": "Synthetic_Cardiology_Patient {"name": "Synthetic_Cardiology_Patient_Record.pdf", "content_type": "application/pdf", "size": 5724, "data": {"patient_id": "dip_patient_123"}, "collection_name": "patient-dip_patient_123"}...
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{"status": "completed", "conte {"status": "completed", "content": "Synthetic Cardiology Patient Record (For RAG\nTesting)\nPatient Demographics\nName:\nArindam Sen (Synthetic Data)\nAge:\n62 years\nGender:\nMale\nDOB:\n14 March 1963\nBlood Group:\nB+\nMRN:\nCARD-2026-001-SYN\nPrimary Physician:\nDr. R. Mukherjee, MD (Cardiology)\nChief Complaint\nProgressive shortness of breath for 3 months, orthopnea, and intermittent chest discomfort on\nexertion.\nPast Medical History\n\nType 2 Diabetes Mellitus (15 years)\n\nHypertension (18 years)\n\nChronic Kidney Disease - Stage 2\n\nIschemic Heart Disease\n\nAnterior Wall Myocardial Infarction (2019)\n\nChronic Heart Failure with Reduced Ejection Fraction (HFrEF)\nCurrent Medications\n\nAspirin 75 mg OD\n\nClopidogrel 75 mg OD\n\nAtorvastatin 40 mg HS\n\nMetoprolol Succinate 50 mg OD\n\nRamipril 5 mg OD\n\nSpironolactone 25 mg OD\n\nFurosemide 40 mg OD\n\nMetformin 500 mg BD\n\nInsulin Glargine 14 units HS\nAllergies No known drug allergies (NKDA).\nLaboratory Reports (Last 3 Visits)\nTest\nJan 2026\nFeb 2026\nMar 2026\nHbA1c\n8.4%\n8.1%\n7.9%\nSerum Creatinine\n1.5 mg/dL\n1.6 mg/dL\n1.7 mg/dL\nBNP\n480 pg/mL\n510 pg/mL\n620 pg/mL\nLDL\n112 mg/dL\n98 mg/dL\n92 mg/dL\nPotassium\n4.6 mmol/L\n5.1 mmol/L\n5.4 mmol/L\nEchocardiography Report (March 2026)\nLeft ventricular ejection fraction (LVEF): 32%. Global hypokinesia present. Mild mitral regurgitation.\nLeft atrial enlargement. No pericardial effusion.\nECG Report\nSinus rhythm. Q waves in V1-V4 suggestive of old anterior wall MI. Left ventricular hypertrophy\npattern noted.\nAdmission Note (SOAP Format)\nS (Subjective): Patient reports worsening dyspnea (NYHA Class III), mild pedal edema,\nand reduced exercise tolerance. No syncope.\nO (Objective): BP 150/92 mmHg, HR 88 bpm, RR 20/min. Bilateral basal crepitations.\nPitting edema grade 2+. BNP elevated. LVEF 32%.\nA (Assessment): Acute on chronic systolic heart failure exacerbation.\nPoor glycemic control. Rising creatinine levels.\nP (Plan): Increase Furosemide dose temporarily to 80 mg/day. Add SGLT2 inhibitor.\nStrict salt restriction (<2g/day). Fluid restriction (1.5L/day).\nCardiology follow-up in 2 weeks. Repeat renal function test in 7 days.\nDischarge Summary\nPatient stabilized after IV diuretics. Symptoms improved. Discharged with optimized heart failure\nregimen. Advised cardiac rehabilitation and lifestyle modification. NOTE: This is entirely synthetic patient data generated for AI/RAG system testing. No real patient\ninformation is included."}...
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