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patient_id_23380575.json
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{
"patient_id": "23380575",
"tool_results": [
{
"tool_id": "402",
"tool_name": "Intracerebral Hemorrhage (ICH) Score",
"params": {
"Glasgow Coma Score": "13-15",
"Age >=80": "No",
"ICH volume >=30mL": "No",
"Intraventricular hemorrhage": "No",
"Infratentorial origin of hemorrhage": "Yes"
},
"tool_summary": "ICH Score: [1, 13% mortality]"
},
{
"tool_id": "801",
"tool_name": "CHA₂DS₂-VASc Score for Atrial Fibrillation Stroke Risk",
"params": {
"Age": "<65",
"Sex": "Male",
"CHF history": "No",
"Hypertension history": "Yes",
"Stroke/TIA/thromboembolism history": "Yes",
"Vascular disease history (prior MI, peripheral artery disease, or aortic plaque)": "No",
"Diabetes history": "No"
},
"tool_summary": "CHA2DS2-VASc Score: [3, moderate stroke risk]"
},
{
"tool_id": "807",
"tool_name": "HAS-BLED Score for Major Bleeding Risk",
"params": {
"Hypertension": "Yes",
"Renal disease": "No",
"Liver disease": "No",
"Stroke history": "No",
"Prior major bleeding or predisposition to bleeding": "Yes",
"Labile INR": "No",
"Age >65": "No",
"Medication usage predisposing to bleeding": "Yes",
"Alcohol use": "No"
},
"tool_summary": "HAS-BLED Score: [3, high risk of major bleeding]"
},
{
"tool_id": "3883",
"tool_name": "Functional Outcome in Patients With Primary Intracerebral Hemorrhage (FUNC) Score",
"params": {
"ICH volume (cm³)": "<30",
"Age": "<70",
"ICH location": "Infratentorial",
"GCS score": ">=9",
"Pre-ICH cognitive impairment": "No"
},
"tool_summary": "Mini Functional Independence Measure (Mini-FIM) Score: [9, moderate risk of dependence]"
},
{
"tool_id": "10003",
"tool_name": "Rome IV Diagnostic Criteria for Functional Constipation",
"params": {
"Straining": "No",
"Lumpy or hard stools ": "Yes",
"Sensation of incomplete evacuation": "No",
"Sensation of anorectal obstruction/blockage": "No",
"Manual maneuvers to facilitate defecation": "No",
"<3 spontaneous bowel movements per week": "Yes",
"Loose stools rarely present without use of laxatives": "Yes",
"Does NOT meet Rome IV Criteria for IBS": "Yes"
},
"tool_summary": "Functional Constipation Diagnosis Tool: [Positive, moderate risk]"
},
{
"tool_id": "10038",
"tool_name": "Braden Score for Pressure Ulcers",
"params": {
"Sensory perception": "No impairment: responds to verbal commands, able to feel and express pain/discomfort",
"Moisture": "Rarely moist: skin usually dry, linen only requires changing at routine intervals ",
"Activity": "Chairfast: ability to walk severely limited or non-existent; cannot bear own weight and/or must be assisted into chair/wheelchair",
"Mobility": "Very limited: makes occasional slight changes in body or extremity position but unable to make frequent or significant changes independently ",
"Nutrition": "Very poor: never eats complete meal; rarely eats >⅓ of any food offered; eats <=2 servings protein (meat or dairy) daily; takes fluids poorly; does not take liquid dietary supplement; or is NPO and/or maintained on clear liquids or IV for >5 days",
"Friction and shear": "Potential problem: moves feebly or requires minimum assistance; during a move, skin probably slides to some extent against sheets, chair restraints, or other devices; maintains relatively good position in chair or bed most of the time but occasionally sli"
},
"tool_summary": "Braden Score: [15, moderate risk]"
},
{
"tool_id": "10064",
"tool_name": "Wexner Score for Obstructed Defecation Syndrome (ODS)",
"params": {
"Incontinence to solid stool": "Never",
"Incontinence to liquid stool": "Never",
"Incontinence to gas": "Never",
"Wears pad": "Never",
"Lifestyle alteration": "Less than once a day but at least once a week"
},
"tool_summary": "Incontinence Scale/Score: [3, mild incontinence]"
},
{
"tool_id": "10471",
"tool_name": "Acute Renal Failure after Cardiac Surgery (Thakar Score)",
"params": {
"Gender": "Male",
"Congestive heart failure": "No",
"Left ventricular ejection fraction ": "No",
"Preoperative use of IABP": "No",
"COPD": "No",
"Insulin-requiring diabetes": "No",
"Previous cardiac surgery": "No",
"Emergency surgery": "No",
"Surgery type": "None",
"Preoperative creatinine, mg/dL": "<1.2"
},
"tool_summary": "Thakar Score: [0, 0.4% risk of ARF]"
},
{
"tool_id": "10462",
"tool_name": "American Urological Association Symptom Index (AUA-SI)/International Prostate Symptom Score (IPSS)",
"params": {
"Incomplete emptying: How often have you had the sensation of not emptying your bladder?": "Less than 1 in 5 times",
"Frequency: How often have you had to urinate less than every two hours?": "Less than 1 in 5 times",
"Intermittency: How often have you found you stopped and started again several times when you urinated?": "Less than 1 in 5 times",
"Urgency: How often have you found it difficult to postpone urination?": "Less than 1 in 5 times",
"Weak stream: How often have you had a weak urinary stream?": "Less than 1 in 5 times",
"Straining: How often have you had to strain to start urination?": "Less than 1 in 5 times",
"Nocturia: How many times do you typically get up at night to urinate?": "1 time",
"If you were to spend the rest of your life with your urinary condition just the way it is now, how would you feel about that?": "Mixed"
},
"tool_summary": "AUA-SI/IPSS Score: [7, mild BPH symptom severity]"
},
{
"tool_id": "10092",
"tool_name": "ACR/EULAR 2010 Rheumatoid Arthritis Classification Criteria",
"params": {
"Joint involvement": "1 large joint",
"Serology (need at least one serology test result to use these criteria)": "Negative rheumatoid factor and negative anti-citrullinated protein antibody",
"Acute-phase reactants (need at least one acute-phase reactant test result to use these criteria)": "Normal CRP and normal ESR",
"Duration of symptoms": "<6 weeks"
},
"tool_summary": "ACR/EULAR Criteria for Rheumatoid Arthritis: [0, Unlikely RA]"
},
{
"tool_id": "10051",
"tool_name": "HOSPITAL Score for Readmissions",
"params": {
"Hemoglobin level at discharge, g/dL": ">=12 ",
"Discharged from oncology service": "No",
"Sodium level at discharge, mEq/L": ">=135 ",
"Any ICD-9 coded procedure performed during hospital stay": "Yes",
"Index admission type": "Urgent or emergent",
"Number of hospital admissions during the previous year": "0-1",
"Length of stay": ">=5 days"
},
"tool_summary": "HOSPITAL Score: [4 points, Low risk of potentially avoidable 30-day readmission (5.8%)]"
},
{
"tool_id": "3912",
"tool_name": "Barthel Index for Activities of Daily Living (ADL)",
"params": {
"Feeding": "Independent",
"Bathing": "Independent",
"Grooming": "Independent",
"Dressing": "Needs help",
"Bowel control": "Continent",
"Bladder control": "Continent",
"Toilet use": "Needs help",
"Transfers (bed to chair and back)": "Needs minor help (verbal or physical)",
"Mobility on level surfaces": "Wheelchair independent, including corners, >50 yards",
"Stairs": "Needs help (verbal, physical, carrying aid)"
},
"tool_summary": "Barthel Index: [70, minimally dependent]"
},
{
"tool_id": "10140",
"tool_name": "GCS-Pupils Score",
"params": {
"Eye response": " Eyes open spontaneously",
"Verbal response": "Oriented",
" Motor response": "Obeys commands",
" Pupil response": "Both pupils reactive to light (normal)"
},
"tool_summary": "GCS-Pupils Score: [15, 2.54% mortality at 6 months post-injury; 11.75% risk of unfavorable outcome (vegetative state or severe disability) at 6 months post-injury]"
},
{
"tool_id": "1739",
"tool_name": "Revised Cardiac Risk Index for Pre-Operative Risk",
"params": {
"Elevated-risk surgery": "No",
"History of ischemic heart disease": "No",
"History of congestive heart failure": "No",
"History of cerebrovascular disease": "No",
"Pre-operative treatment with insulin": "No",
"Pre-operative creatinine >2 mg/dL / 176.8 µmol/L": "No"
},
"tool_summary": "Revised Cardiac Risk Index (RCRI): [0, 3.9% risk of major cardiac event]"
},
{
"tool_id": "10161",
"tool_name": "COPD Assessment Test (CAT)",
"params": {
"Cough": "0 (“I never cough”)",
"Phlegm": "0 (“I have no phlegm in my chest at all”)",
"Chest tightness": "0 (“My chest does not feel tight at all”)",
"Breathlessness": "2",
"Activities": "3",
"Confidence": "0 (“I am confident leaving my home despite my lung condition”)",
"Sleep": "1",
"Energy": "2"
},
"tool_summary": "COPD Assessment Test (CAT): [8, low health impact]"
},
{
"tool_id": "10410",
"tool_name": "Utah COVID-19 Risk Score",
"params": {
"Age, years": "61-70",
"Diabetes mellitus": "No",
"Obesity (BMI >30 kg/m2)": "No",
"Active cancer": "No",
"Other immunosuppressive therapies and conditions": "No",
"Hypertension": "Yes",
"Coronary artery disease": "No",
"Cardiac arrhythmia": "Yes",
"Congestive heart failure": "No",
"Chronic kidney disease": "No",
"Chronic pulmonary disease": "No",
"Chronic liver disease": "No",
"Cerebrovascular disease": "Yes",
"Chronic neurologic disease": "No",
"New shortness of breath": "No"
},
"tool_summary": "Utah COVID-19 Risk Score: [6.5, moderate risk]"
},
{
"tool_id": "10016",
"tool_name": "Dual Antiplatelet Therapy (DAPT) Score",
"params": {
"Age, years": "<65",
"Cigarette smoking": "No",
"Diabetes mellitus": "No",
"MI at presentation": "No",
"Prior PCI or prior MI": "No",
"Paclitaxel-eluting stent": "No",
"Stent diameter <3 mm": "No",
"CHF or LVEF <30%": "No",
"Vein graft stent": "No"
},
"tool_summary": "DAPT Score: [0, Low risk]"
},
{
"tool_id": "10552",
"tool_name": "PECARN Cervical Spine Injury Prediction Rule",
"params": {
"Glasgow Coma Score": "15",
"AVPU": "Alert and conscious",
"Abnormal airway, breathing, or circulation": "No",
"Focal neurologic deficits": "Yes",
"Other signs of altered mental status": "No",
"Self-reported neck pain or neck tenderness on examination": "No",
"Substantial head or torso injury": "Yes"
},
"tool_summary": "PECARN c-spine score: [12.1%, moderate risk of c-spine injury]"
}
]
}