jurnal jadi nian

Upload: novi-rianty

Post on 04-Apr-2018

228 views

Category:

Documents


0 download

TRANSCRIPT

  • 7/29/2019 Jurnal Jadi Nian

    1/26

    Journal Reading

    Dr. Novirianty

    Tutor :

    Dr. Puspa Zuleika, Sp.THT-KL,M.Kes

  • 7/29/2019 Jurnal Jadi Nian

    2/26

    Treatment of Postviral Olfactory Loss WithGlucocorticoids, Ginkgo biloba, and

    Mometasone Nasal Spray

    Beom Seok Seo,Hyun Jong Lee, Ji-Hun Moo,Chul Hee Lee, Chae-Seo

    Rhee,Jeong-Whun Kim

  • 7/29/2019 Jurnal Jadi Nian

    3/26

    Background

    Olfactory disorder mechanism is not

    clearly understoodWhich viruses cause postviral olfactory

    loss is unknown

    The role of the olfactory neural system inpostviral olfactory loss is unknown

  • 7/29/2019 Jurnal Jadi Nian

    4/26

    Questions

    Does treatment using prednisolone

    plus ginkgo biloba significanly

    improved for postviral olfactory loss?

  • 7/29/2019 Jurnal Jadi Nian

    5/26

    The Purpose

    To analyze the efficacy of treating postviral

    olfactory loss with glucocorticoid, Ginkgo

    biloba and mometasone nasal spary

  • 7/29/2019 Jurnal Jadi Nian

    6/26

    There is significant difference

    between the ginkgo biloba and non

    ginkgo biloba group of treatingpostviral olfactory loss.

    Hypotesis

  • 7/29/2019 Jurnal Jadi Nian

    7/26

    Material and method

    RCT ( Randomized Controlled TrialDesign

    Chemosensory Outpatient Clinic of

    Seoul National University Bundang

    Hospital, Seongmnam, KoreaPlace

    July 1,2007 through June 30,2008Time

  • 7/29/2019 Jurnal Jadi Nian

    8/26

    Inclusion criteria

    History of upper

    respiratory tract infection

    immediately before post

    viral olfactory loss

    Sudden onset of

    postviral olfactory loss

    Exclusion criteria

    History of olfactory loss

    History of head trauma

    History of oral or nasal

    corticosteroid use

    Concurrent memory loss

  • 7/29/2019 Jurnal Jadi Nian

    9/26

    Inclusion criteria

    A visit within 12 month

    after onset of postviral

    olfactory loss

    No evidence of sinus

    Inflammation on

    computed tomographic

    osteomeatal or

    paranasal sinus view

    exclusion criteria

    Presence of nasal

    discharge

    Allergic rhinitis

    Chronis rhinosinusitis

  • 7/29/2019 Jurnal Jadi Nian

    10/26

    71 patient

    monotherapy

    Male 10

    Female 18

    Combinationtherapy

    Male 10

    Female 33

    Procedure

  • 7/29/2019 Jurnal Jadi Nian

    11/26

    monotherapyCombination

    therapy

    Oral prednisolon

    for 2 weeks

    Oral prednisolon 2 weeks

    and G biloba 4 weeks

    Monometasone furoat nasal spray2 puff pernostril twice daily for 4

    weeks

  • 7/29/2019 Jurnal Jadi Nian

    12/26

    Result

    After treatment

    ( score change)

    Monotherapy Combination

    therapy

    BTT 2.2 2.9 (P=.22)

    CCSIT 1.7 2.7 (P=.11)

  • 7/29/2019 Jurnal Jadi Nian

    13/26

    Result

    After Therapy ( the

    threatment respon)

    Monotherapy Modification

    Therapy

    BTT Therpy 32% (9 from 28) 37% ( 16 fom 43) (

    P=0,66)

    CCSIT 14% ( 4 from 28) 33% ( 14 from 43)

    (P= 0,08)

    Odds ratio: 2,89( 95% Confidence interval 0,84-9,97)

  • 7/29/2019 Jurnal Jadi Nian

    14/26

  • 7/29/2019 Jurnal Jadi Nian

    15/26

  • 7/29/2019 Jurnal Jadi Nian

    16/26

  • 7/29/2019 Jurnal Jadi Nian

    17/26

  • 7/29/2019 Jurnal Jadi Nian

    18/26

  • 7/29/2019 Jurnal Jadi Nian

    19/26

    Discussion

    This study to analyze the efficacy of treating

    postviral olfactory loss with glucocorticoids, Ginkgo

    biloba and mometasone furoate nasal spray

    All patient underwent olfactory function test such

    BTT, CCSIT

    Postviral olfactory loss were treated with oral

    prednisolon,Ginkgo biloba and mometasone furoate

    nasal spray

  • 7/29/2019 Jurnal Jadi Nian

    20/26

    Critical apraisal

    1. Is an estimate of the treatment effect given ?

    yes

    2. Is it of clinical importance ?

    yes

    3. Is the estimate of threatment effect

    sufficiently precise ?

    yes

  • 7/29/2019 Jurnal Jadi Nian

    21/26

    4. Was the spectrum of patients well defined?

    yes

    5. Was the diagnosis of the disease well defined?no

    6. Were eligibility criteria suitably narrow ?yes

  • 7/29/2019 Jurnal Jadi Nian

    22/26

    7. Was assignment to treatments stated to be

    random? yes

    8. Was the method of randomized explained?no

    9 Were all patient accounted for after

    randomization? no

  • 7/29/2019 Jurnal Jadi Nian

    23/26

    10. Were loses to follow-up low ?

    yes

    11. Were the treatment groups similar inimportant factor's at the start of the trial?

    yes

    12. Were all patients otherwise treatedalike?

    yes

  • 7/29/2019 Jurnal Jadi Nian

    24/26

    13. Were patients, health care workers andinvestigator 'blind' to treatment?no

    14.Was assessment of outcome 'blind'?no

    15. Was the main analysis on 'intention to

    treat'? Yes

    16. Were appropriate statistical methods used?

    Yes

  • 7/29/2019 Jurnal Jadi Nian

    25/26

    Conclusion

    The study is valid and

    can be applied in clinicalpractice

  • 7/29/2019 Jurnal Jadi Nian

    26/26

    Thank you