POMR Intro for DC_2007

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    The Problem Oriented

    Medical Record(POMR or POVMR)

    Master Problem Lists

    Writing SOAPs

    Master Plan

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    The purpose of a POMR

    Teaching & Learning Emphasize a systematic, analytic approach Help you learn patterns Review (learn)

    Integrateproblems & causes Maintain focus on the patient & his/her problems Student evaluatione.g. in your clinical blocks

    Communication among members of the medical team(optimize the quality of care and minimize the potential for mistakes)

    Legal Record (sign your entries!)

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    Dr. Lawrence Weed: 1968

    Medical Records that Guideand Teach

    Patient focused

    Problem oriented

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    POMR = part of an attempt to address the mostcommon problems in diagnosis & case management:

    Inadequate hypothesis generation

    Inattention or misinterpretation of findings

    history, PE, laboratory data, etc.

    Premature closure= the clinician stopsgenerating new hypotheses before the correct

    diagnosis has been added to the list of DfDxs

    The most common interpretive error= overinterpretation or misinterpretation of

    findings in light of suspected disease

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    Common diseases occur commonly. Duh !

    The Challenges:

    The uncommon presentation of the common disease The common presentation of the uncommon disease

    The disease (common or not)that you personally havenot seen before or at least not recognized before.

    Pattern recognition.

    A function of experience and

    knowledge base.

    Why are diagnosis USUALLY correct?

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    POVMR

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    Master Problem List

    A PROBLEM is anything that potentially threatens thehealth of the animal (or herd)and may require medical

    attention (at least eventually).

    MPL is always kept at the front of the

    recordfront and centerThe MPL is updated DAILY

    (or at each submission during a DC).

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    Updating & Revising MPL

    NEW problems are added(e.g. new discoveries & new developments)

    Some problems are resolved

    Problems are re-defined

    Combined with other problems

    Upgraded to another problem(defined at higher level of understanding)

    Problems can be inactivated

    Disposition of problems

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    Example:

    1. Vomiting2. Hematemesis

    3. Inappetance

    4. Lethargy5. Pale mucous membranes

    6. Tachypnea

    13 year-old intact maleGerman Shorthaired Pointer

    7. Anemianon-regenerative8. Azotemia

    9. Isosthenuria

    10. Hypoproteinemia

    Upgrade to #7

    Use slide showfunction & click to see

    updating MPL

    (next slide)

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    1. Vomiting

    2. Hematemesis

    3. Inappetance

    4. Lethargy

    5. Pale mucous membranes

    6. Tachypnea

    7. Anemianon-regenerative8. Azotemia

    9. Isosthenuria

    10. Hypoproteinemia

    11. Gastric ulceration- endoscopy

    12. Interstitial nephritis & fibrosis(end stage kidney)renal biopsy

    Upgrade to #11 and/or 12

    Upgrade to #11

    Upgrade to #12

    Upgrade to #12

    Upgrade to #11

    Upgrade to #11

    13. Chronic renal failure (final Diagnosis)

    Upgrade to #13

    Upgrade to #13

    Upgrade to #7

    Upgrade to #13

    Upgrade to #13

    resolved 9/27

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    Diagnosis

    Client Complaint

    PROBLEMS

    on MPL

    Specific Rx

    TREATMENT:

    symptomatic

    supportive

    presumptive

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    S.O.A.P.

    Subjective:

    attitude, appetite, activity, improving?,

    Unchanged? - include clients observations

    Objective:

    Summarizethe measurable clinical data(fever?, laboratory?, rads?, etc.)

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    Problem 1. Pale mucous membranes

    SO: oral mucous membranes are pale on physicalexamination

    Problem 2. Icterus

    SO: Yellow tint to oral mucous membranes and scleraare indicative of icterus (accumulation of bilirubin intissues).

    Problem 3. Tachypnea

    SO: A respiratory rate of 44 is higher than expected ofa normal, inactive dog.

    In the VTH, S.O. are often combined:

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    Problem 4. Diarrhea

    SO:Diarrhea in this animal is chronic and appears to be progressing(getting worse). The high volume & low frequency suggests thatthe diarrhea is small intestinal in origin, as does the absence of freshblood, mucus, and tenesmus, which are the cardinal signs of largebowel diarrhea in small animals. The chronic small bowel diarrheaaccompanied by weight loss is most suggestive of a small intestinalmalassimilation syndrome, possibly with protein loss into the feces.

    Problem 5. Hepatomegaly

    SO: Physical examination revealed hepatomegaly characterizedby extension of the liver beyond the ribs and by rounded edges.The hepatomegaly appears to be diffuse, but further assessment(imaging) would be required to confirm.

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    S.O.A.P. continued

    Assessment: = Analysis of the problem

    3 components for each Assessment:[A]General pathophysiologic mechanisms for the

    problem.

    [B]Pathophysiologic mechanisms likely for THIS CASE.

    [C]Differential Diagnoses (DfDx's) for THIS problem.

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    Considerations:

    First: think & write about the problem by itself Before you think about other problems

    Before you try to think about specific DfDxs

    Then, think and write about the problem in relationto other problems on the MPL and other information.

    The most common interpretive error =overinterpretation or misinterpretation offindings in light of suspected disease

    e.g. Hypoproteinemia

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    Has your understanding of the problems changed?- notably changed in light of new data

    How can you pull the case or problems together ?

    CRITICAL THINKING & INTEGRATION

    Can you localize the disease?

    (e.g. to an organ system?) Is the signalment important or useful?

    species, breed, age, sex

    Duration & Course?

    Are other animals affected? Was there previous treatment / response?

    REMEMBER: The record should capture yourTHOUGHT PROCESSES

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    DfDxs for the Problem:

    Localization

    Process (e.g. DAMNIT)

    Specific Diseases

    Premature closure = the clinician stopsgenerating new hypotheses before the correctdiagnosis has been added to the list of DfDxs

    One goal is to avoid:

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    Initial PLANto address THISproblem.

    The plan should help rule in / rule out your

    primary DfDx's, or treat the patient.

    The initial plan can include: specific diagnostic tests specific treatments

    doing nothing (wait & see) client communication plans (including questions)

    The proposed plan may be stated as a sequenceof plans or possible courses of actions

    S.O.A.P. continued

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    SOAP Example:Edema

    a) General mechanisms

    Increased hydrostatic pressure Heart failure, venous obstruction, overhydration

    Decreased plasma oncotic pressure: d/t hypoalbuminemiaalbumin production d/t liver disease

    intake (malnutrition or protein malabsorption)

    protein loss

    Renal, GI, skin (wounds & burns), body cavities

    Lymphatic obstruction or hypertension (not common) Neoplasia, surgical or traumatic injury, lymphangitis, congenital

    Vasculitis

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    b) This case: No evidence of GI disease

    No evidence of heart disease or vasculitis

    No obvious evidence of lymphatic disease

    Good appetite

    Accompanied by weight loss

    Possible polyuria & polydipsia according to owners

    c) DfDxs: Protein-losing nephropathy

    (e.g. glomeronephritis or renal amyloidosis)

    Loss in GI, but without producing other enteric signssuch as diarrhea (e.g. lymphangiectasia, chronicparasitism, intestinal neoplasia)

    Chronic Liver diseasewould have to be severe

    (>80% loss) to produce hypoalbuminemia & edema

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    RememberSOAPs are written daily

    EACH DAY (or at each submission during a DC)

    You should SOAP all NEW problems

    AND

    Re-SOAPall ACTIVE problems on your MPL

    IMPORTANT

    In particular, your SOAPs of pre-existingproblems should address your updatedanalysis/interpretation of the problem in light ofnew information and any changes in the case.

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    Also ..

    Make sure everyone in the group is sharinghis/her SOAPs and teaching the others

    what youve learned.

    Otherwise, its like everyone has a PIECE ofthe puzzle, but maybe no one has enough of

    the puzzle to pull it together in a cohesiveway.

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    Do NOT Just copy and paste your SOAP from

    one day to the next or from oneproblem to another

    unchanged from yesterday, page 12

    See Problem #9

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    P: Initial Planto address this problem

    Panel: R/O hypoalbuminemia assess renal function via BUN & creatinine access liver enzymes as evidence of liver disease

    Urinalysis:

    R/O proteinuria in conjunction with BUN-creatinine, assess renal function

    Fecal floatation: R/O intestinal parasites causing protein or blood losss

    Depending on results of minimal data base, considerfuturecardiac consultation to rule out congestive heartfailure (chest rads, ECG, echocardiography, stress testing)

    Consider bile acids in future, as most sensitive measureof liver function

    Talk to ownerabout a more appropriate diet

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    Master Plan

    Panel

    UrinalysisFecal Floatation

    CBC

    At the end of the days record, enter a:

    This is what you really want to do NOW.

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    Questions ?Look at the examples you were

    provided

    file://Shared/DiagnosticChallenge/Medical_Records_DC