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INFECTIOUS DISEASES

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suggested bone scan, colonoscopy, TEE. change ATBs to cefotaxime. repeat CT abd in 2-3 weeks ... Colonoscopy. Scheduled as an OPD procedure ... – PowerPoint PPT presentation

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Title: INFECTIOUS DISEASES


1
INFECTIOUS DISEASES CASE CONFERENCE
  • Pimpawan Boapimp, MD
  • Wake Forest Baptist Medical Center
  • August 2, 2004

2
CASE I
3
HPI
  • 49 y/o BM
  • DM, HTN, h/o ETOH abuse
  • s/p cholecystectomy in 2002
  • lost 25 lbs over 4 weeks
  • intermittent fever and night sweats
  • and intermittent Rt flank pain x 2 weeks worse
    with inhalation

4
  • saw PCP labs were normal
  • had CT abd and pelvis scheduled one week after
    that
  • CT showed small fluid collection
  • Pt was sent to ED
  • denied F/C, N/V
  • was seen by surgical team in ED and underwent CT
    guided aspiration by a radiologist

5
CT scan Abd and Pelvis
  • 4.0 x 1.7 cm low attenuation, rim enhancing
    lesion adjacent to the posterior aspect of the
    right hepatic lobe is most consistent in
    appearance with subhepatic abscess.
  • This lesion contacts both the posterior aspect of
    the right hepatic lobe and adjacent abdominal
    wall.
  • Status post cholecystectomy.
  • Colonic diverticulosis without evidence of acute
    diverticulitis.

6
  • 2 CC of purulent material and blood was obtained
    and sent for C/S
  • Was started on Clindamycin and admitted
  • Allergy- Unasyn causes rash
  • Meds - Glucotrol and Enalapril

7
Physical Examination
  • VS T 97.1 P 65 RR 20 BP 124/70
  • PO 96 RA
  • GA AO X3, NAD, afebrile
  • HEENT WNL
  • Neck supple
  • Chest CTA bilaterally
  • Heart RSR, no murmur

8
Physical Examination
  • Abd benign
  • Ext no edema
  • NS no focal deficit
  • Back Rt flank pain on palpation
  • LN no lymphadenopathy

9
Diagnostic Data
  • CBC
  • WBC 6.5 Hb 13.2 Hct 38.4 Plt 282
  • N 49 L 42 M 7
  • CMP
  • Cr 1, liver enzymes- WNL
  • TTE No vegetation

10
CULTURE
  • Abscess STREPTOCOCCI, BETA HEMOLYTIC
    GROUP B
  • SENSITIVITY MIC
  • PENICILLIN G 0.06 SUSCEPTIBLE
  • ERYTHROMYCIN 2
    RESISTANT
  • CLINDAMYCIN
  • VANCOMYCIN
  • AMOX/CLAVULANIC
  • MEROPENEM
  • CEFTRIAXONE
  • CEFUROXIME
  • GATIFLOXACIN
  • TETRACYCLINE 8
    RESISTANT
  • TMP/SMX

11
  • BC no growth (after ATBs)

12
  • ID was consulted
  • suggested bone scan, colonoscopy, TEE
  • change ATBs to cefotaxime
  • repeat CT abd in 2-3 weeks

13
TEE
  • No vegetation
  • Normal LV function

14
Bone Scan
  • Increased radiotracer noted within the right
    maxilla. Unclear if this is within the lower
    aspect of the sinus versus within the bone.
  • Clinical correlation recommended.
  • Degenerative changes noted within bilateral
    shoulders and within a mid thoracic vertebral
    body.

15
Colonoscopy
  • Scheduled as an OPD procedure
  • Was D/Cd home with Cefotaxime x 3 weeks with CT
    abd in 2-3 weeks

16
CASE II
17
  • 84 y/o WF
  • Rt hip replacement in Feb 2003
  • was admitted for back pain
  • one week PTA , pt started having back pain, both
    sides, band-like
  • worse with movement
  • sometimes pain radiated to Rt leg

18
  • N/V x one day
  • no skin rashes
  • no F/C, night sweats
  • no GU symptoms

19
  • Allergy None
  • PMH HTN, IBS, gout, OA, osteoporosis,
  • Strep Gr B bacteremia in June
  • 2003 Txd with dicloxacillin for
  • 14 days ( TTE no vegetation)
  • FHX negative
  • ROS otherwise negative

20
Physical Examination
  • VS T 100.1 P 90 RR 18 BP 110/40
  • PO 99 RA
  • GA elderly WF, well-nourished, NAD
  • HEENT WNL
  • Neck supple
  • Chest CTA bilaterally
  • Heart RSR, SEM grade I-II/VI at LSB

21
Physical Examination
  • Abd distended but not tender, BS present
  • no organomegaly
  • Ext no edema
  • Back mild tenderness at Lt lumbar
    paraspinal area
  • NS no focal deficit

22
Diagnostic Data
  • UC grew E. coli -Zosyn was started
  • BC grew strep/enterococci
  • Vancomycin was added
  • MRI showed poss. discitis at L3-L4
  • TTE, TEE no vegetation
  • Bone scan showed increased uptake at L1 and L4
    bodies most likely represent degenerative
    compression fractures

23
  • CT abd and pelvis showed ascites
  • Final BC- Streptococcus Group B
  • was D/Cd home with Rocephin X 6 weeks

24
Group B streptococcus (GBS)
  • Since the 1970s, GBS has been recognized mainly
    as a pathogen in neonates and peripartum women.
  • But the incidence of adult GBS infection rose
    steadily
  • Risk factors for invasive GBS infection
  • -DM, malignancy, HIV
  • -Liver disease

25
Clinical Syndromes
  • Bacteremia without clear source
  • Skin and soft tissue infection
  • - foot and decubitus ulcers
  • - cellulitis, abscesses
  • - necrotizing fasciitis
  • - balanitis
  • - sternal wound infections after CABG

26
Clinical Syndromes
  • UTI
  • Pneumonia
  • Bone and joint infections
  • Cardiac
  • - Endocarditis mainly occurs on native valves,
    involving valves Lt Rt
  • - often associated with large, friable
    vegetations
  • - high mortality rate
  • - myocarditis/pericarditis

27
Clinical Syndromes
  • CNS infection
  • hematogenously seeded endophthalmitis-rare
  • IV catheter infection

28
  • Duration of therapy
  • -10 days for skin and soft tissue infections
  • -2 - 3 weeks for meningitis,
  • -a minimum of four weeks for osteomyelitis or
    endocarditis
  • Significant and rising resistance to macrolides,
    tetracyclines, and clindamycin

29
  • Factors associated with worse outcome - age 65
    years
  • - CNS disease
  • - alcoholism
  • - shock
  • - renal failure
  • - impaired level of consciousness
  • - confinement to bed

30
Group B streptococcal disease in nonpregnant
adults.
  • Farley MM.
  • Emory University School of Medicine Atlanta, GA
  • Clin Infect Dis. 2001 Aug 1533(4)556-61.
  • 2-4 folds increases in incidence of invasive GBS
    infection over the last 2 decades
  • rates 4.1-7.2 case per 100,000 nonpregnant adults
  • Recurrent infection occurs in 4.3 of survivors.

31
  • Capsular serotypes Ia, III, and V account for the
    majority of disease in nonpregnant adults.
  • Meningitis and endocarditis are less common but
    associated with serious morbidity and mortality.

32
  • GBS are susceptible to penicillin but MIC are
    4-fold to 8-fold higher than for group A
    streptococci.
  • Resistance to erythromycin and clindamycin is
    increasing.

33
Relapsing invasive group B streptococcal
infection in adults.
  • Harrison LH, et al.
  • Ann Intern Med. 1995 Sep 15123(6)421-7.
  • Nov 1991- Sep 1993
  • 751 residents of Maryland 18 years of age or
    older with invasive GBS infection
  • 449 were nonpregnant

34
  • 395 patients with invasive GBS infection who
    survived the first episode
  • median duration of follow up was 23 months
  • 17 (4.3 95 CI, 2.6 to 6.9) had second
    episode.
  • 5 additional pts had first episode after
  • Sep 03
  • Several patients had endocarditis or
    osteomyelitis during the second episode.

35
  • GBS isolates from both episodes were obtained
    from 18 of 22 patients.
  • Of the 18 isolate pairs, 13 (72 CI, 46 to
    90) had identical REAC patterns.
  • Recurrent infection caused by the same strain,
    the interval between episodes was shorter (mean,
    14 weeks) than that among patients with recurrent
    infection caused by another strain (mean, 43
    weeks P 0.05).

36
  • The second episode occurred an average of 24
    weeks after the first episode (range, 2 to 95
    weeks)
  • The mean age of patients with recurrent infection
    was 60 years (range, 27 to 89 years).
  • All patients had at least one serious underlying
    medical condition including cancer, diabetes,
    cirrhosis, and renal transplantation.

37
  • All adults with a first GBS bacteremic episode
    should have a careful physical examination to
    identify deep-site infection, i.e., endocarditis
    or osteomyelitis, and further evaluation as
    indicated.
  • Patients with recurrent GBS should be routinely
    evaluated more thoroughly for deep-site
    infection echocardiography should be done during
    these routine evaluations.

38
  • Although the precise duration of therapy in
    patients with these syndromes is unknown, a
    prolonged course of parenteral therapy with
    antibiotic agents is warranted.
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