Necrotiserende otitis externa – osteomyelitis schedelbasis

Initiatief: NVKNO Aantal modules: 10

Diagnostic imaging for primary diagnosis

Uitgangsvraag

Which imaging techniques are relevant in the primary diagnosis of necrotizing otitis externa?

Aanbeveling

Diagnosing necrotizing otitis externa (NOE) is often a result of a combination of clinical symptoms, laboratory findings and imaging.

 

Use imaging when suspecting NEO. Several imaging modalities are optional:

  • CT scan (most commonly used first modality and widely available). It allows evaluation of cortical bone erosions and trabecular bone destruction. Add soft tissue kernel to evaluate soft tissue abnormalities which aid in the diagnosis.
  • Contrast enhanced MRI. It will allow better evaluation of soft tissue abnormalities but also allows evaluation of vascular or intracranial complications.
  • In complex cases of NEO, FDG-PET CT (or MRI) could also be used as a baseline scan for treatment monitoring and also for possible biopsy guiding.

Overwegingen

Balance between desired and undesired effects

Different modalities

A systematic search was performed to determine the diagnostic accuracy in NEO of FDG- PET/CT or MRI, versus  CT. Only one study by Kulkarni (2020) was included, which used clinical outcome measures as a referral. It used FDG-PET/CT as index test, with a comparison to MRI. Although the diagnostic accuracy for FDG-PET/CT can be considered high, the evidence shows a high level of uncertainty comparing with MRI. In addition, no comparison with CT was made. The level of evidence was graded as very low.

 

A large meta-analysis was done by Kim (2023), in which the diagnostic accuracy for diagnosing necrotizing otitis externa of [67Ga]-citrate, [99mTc}-labelled diphosphonates for bone scintigraphy, MRI and CT was measured. The sensitivities were 0.94 (0.77–0.99), 0.97 (0.88–0.99), 0.94 (0.70–0.99) and 0.96 (0.90–0.98), respectively. Thus, showing comparative results in sensitivity when using only CT or MRI.

 

Quality of the evidence

The overall quality of evidence is very low. This means we are very uncertain about the estimated effect of the crucial outcomes found.

There is downgrading due to very serious:

  • Risk of bias: patient selection; index test.
  • Imprecision: inaccuracy, due to a very small number of events in a small sample size.

Clinical application and specific characteristics per modality

Based on the literature, there is no available evidence that shows that FDG-PET/CT or MRI leads to significantly higher accuracy compared to CT in diagnosing NOE. Diagnosing NOE can be challenging due to nonspecific symptoms, the potentially prolonged clinical course, and its clinical presentation. The diagnosis is typically made through a combination of clinical symptoms, laboratory findings (microbiology), and imaging results (Chawdhary, 2017). Various imaging modalities can be used not only to diagnose NOE but also to assess the extent of the disease and evaluate potential complications.

 

The imaging techniques used to diagnose NOE include non-contrast (most used) and contrast-enhanced CT, contrast-enhanced MRI, and nuclear medicine imaging (FDG-PET/CT) (Curtin, 1982; Tsuno, 2022; Shavit, 2018). In patients where limited disease is expected (external ear with surrounding soft tissues), an unenhanced CT is the best option for evaluating bone erosion and demineralization. With CT, opacification of the middle and/or mastoid cells can also be assessed. Adding a soft tissue kernel allows for the evaluation of soft tissue abnormalities. Post-contrast CT helps in evaluating vascular complications (such as venous sinus thrombosis or pseudoaneurysm formation) or abscess formation. CT scan is the initial imaging modality of choice for a suspected case of NOE (Hodgson, 2023).

 

Contrast-enhanced MRI is useful for evaluating the anatomic location of the NOE and can also be used to assess the extent of the infection in the adjacent soft tissues or bone marrow. Involvement of the skull base foramina and temporomandibular joint can also be visualized. MRI is superior in detecting abscess formation, intracranial extension of the infection (such as dural enhancement or empyema), or ischemic infarcts.

 

Both CT and MRI provide anatomical information and details on potential complications of NEO; however, they lack functional information. Various nuclear medicine techniques with different radiopharmaceuticals have been used, but fluorine-18 fluorodeoxyglucose ([18F]-FDG) is widely available and is the most commonly used tracer nowadays. This scan provides metabolic information and is taken up in areas of malignancy, infection, and inflammation. As a consequence, this test is highly sensitive but lacks specificity, as it cannot differentiate between infection/inflammation and malignancy. Another limitation is the physiological uptake of FDG in the brain, which makes it difficult to recognize intracranial extension of the infection.

 

Several neoplastic and inflammatory diseases may mimic the imaging findings of NEO. The most common neoplastic mimickers include nasopharyngeal carcinoma, carcinoma of the external auditory canal, metastases, and lymphoma. The most common inflammatory disease mimickers are IgG4-related disease and granulomatous diseases. Also osteoradionecrosis and medication-related ear canal osteonecrosis (MRECO) may mimic NEO. The combination of imaging modalities may help in narrowing the differential diagnosis.

 

Values and preferences of patients (and possibly their relatives/caregivers)

Imaging techniques are used to provide an accurate diagnosis without delaying the diagnostic process. In general, for younger children, an MRI scan can be challenging due to the long acquisition time, noise, or lack of cooperation. However, clinicians should be cautious about using contrast-enhanced CT scans in the diagnostic process due to radiation exposure. This limitation also applies to FDG-PET/CT, as it also involves radiation. For older patients with NEO, an MRI can also be challenging due to motion artifacts, claustrophobia, or contraindications (such as cardiac devices, for example).

 

Cost considerations

In patients suspected of NEO, an unenhanced CT scan is most frequently used because it is easily available, it has very limited contraindications and results in a first impression of disease extent. There is no evidence that MRI or FDG-PET/CT has higher accuracy than CT for the initial diagnosis of NEO. Replacing CT with MRI or FDG-PET/CT could result in higher costs. However, MRI or FDG-PET/CT may better depict potential complications of NEO, which could influence treatment decisions.

 

Acceptability, feasibility, and implementation.

Regarding acceptability, feasibility, and implementation, no significant problems are expected because CT, MRI, and FDG-PET/CT are widely available. In cases where there is limited capacity for one or two of the imaging modalities, the remaining third modality serves as a good alternative. If there is a lack of experience in image interpretation, referral to a specialized center is an option.

 

Rationale of the recommendation: weighing arguments for and against the interventions

NOE clinical symptoms are non-specific and overlap with symptoms of acute external otitis, chronic mastoiditis, and several malignancies. To date, no uniform diagnostic criteria for NOE are available. Imaging has a high sensitivity for NOE and can be suggestive but is sometimes non-specific. The diagnosis of NOE is based on a combination of clinical symptoms, clinical findings, and imaging findings.

 

Currently, there is no evidence that one imaging modality is superior to another in diagnosing NOE. Depending on the clinical presentation (or clinical suspicion), patient age, comorbidities, possible contraindications, and the patient’s own preference, a choice between the different imaging modalities can be made.

 

In daily practice, an unenhanced CT is the first imaging modality used because it is widely available and does not require intravascular contrast. A CT scan may show bony erosions or demineralization in cases of osteomyelitis. A soft-tissue kernel helps evaluate possible infiltration of fat planes, which can be suggestive of NOE.

 

When the CT scan is inconclusive or more extensive disease is expected, an additional contrast-enhanced MRI can be performed. MRI is superior in evaluating the extent of soft tissue involvement, skull base foramina, intracranial involvement, and ruling out vascular complications. If an MRI is contraindicated, a contrast-enhanced CT can be considered.

 

In case of complex (/severe) NEO (see module Definition and limiting doctor’s delay in diagnosing necrotizing otitis externa) FDG-PET/CT(or MRI) imaging provides functional imaging which may be helpful for biopsy guiding and/or in therapy evaluation.

Onderbouwing

Currently, the most commonly used imaging modality for the initial diagnosis of necrotizing otitis externa (NOE) is a CT scan. A CT scan can detect bony erosions, which are characteristic of the disease. However, due to the disease's tendency to spread through soft tissue, some clinicians also use MRI scans in addition to CT. In recent years, [18F]-FDG-PET/CT (FDG-PET/CT) has become available and can be used to demonstrate disease activity in the suspected area. The aim of this module is to evaluate the added value of MRI or FDG-PET/CT compared to CT scans in the primary diagnosis of skull base osteomyelitis.

Diagnostic accuracy FDG PET-CT

Very low GRADE

The evidence is  very uncertain about the difference in the number of false positives, true negatives, true positives, specificity and positive prediction value using of FDG-PET/CT in patients with suspected NOE.

 

Source: Kulkarni, 2020

Diagnostic accuracy MRI

-

GRADE

No evidence was found regarding whether the use of a MRI results in differences in false positive, true negatives, true positives, specificity and positive prediction value when compared to clinical/imaging follow-up in patients with suspected skull base osteomyelitis.

 

Sources: -

Description of studies

One study was included in the analysis of the literature. The assessment of the risk of bias is summarized in the risk of bias tables (under the tab ‘Evidence tabellen’).

 

Kulkarni (2020) conducted a retrospective study to evaluate the diagnostic performance of regional fluorine-18 fluorodeoxyglucose ([18F]-FDG) positron emission tomography-computed tomography (PET/CT) in patients with skull base osteomyelitis (SBO). In addition, they evaluated the agreement of the findings between FDG-PET/CT and MRI whenever available.

 

Patients clinically suspected of SBO were included. Patients with missing data, who were lost to follow-up or with known malignancy were excluded. In total, 77 patients with SBO (male : female = 56:21; mean age 66.4 ± 9.4 years; range 45 – 92 years) who were treated accordingly and with follow up available were included for analyses. All 77 included patients underwent a FDG-PET/CT. In 56 patients (72.7%), MRI scans were also available for agreement analysis for the assessment of disease extent (with a maximum of 10 days interval between FDG-PET/CT and MRI studies). The final diagnosis of the disease was based on the presence of one or more of the following criteria: presence of infective granulation tissue or necrosis on histopathological samples; culture positivity; clinical improvement (reduction in the symptoms or reduction in inflammatory markers) with antimicrobial treatment; response on imaging findings. The prevalence of SBO in the total study population was 61/77.

 

Results

Diagnostic accuracy [18F]-FDG-PET/CT (critical)

The results for [18F]-FDG-PET/CT are summarized in Table 2 (95% confidence interval not reported).

 

Table 2. Diagnostic accuracy [18F]-FDG-PET/CT (N=77) (crucial)

FN

(% N)

TP 

(% N)

FP 

(% N)

TN

(% N)

Sensitivity %

Specificity %

PPV %

NPV %

2

(3.3%)

59 (96.7%)

1

(6.2%)

15 (93.7%)

96.7%

93.3%

98.3%

87.5%

The diagnostic performance in establishing the SBO was not reported. However, agreement analysis between FDG-PET/CT and MRI for the assessment of soft tissue disease extent showed a κ value of 0.82. Bony involvement was present in 37 patients (66%). The agreement analysis between these two modalities for assessing bony involvement

showed a κ value of 0.81, suggesting good agreement.

 

Level of evidence of the literature

Diagnostic accuracy (critical)

The level of evidence regarding the outcome diagnostic accuracy originates from diagnostic accuracy studies and therefore initially started high. However, the level of evidence for the outcome measure was downgraded by three levels due to multiple study limitations. These limitations included issues with selection and patient flow (risk of bias, -2), applicability (bias due to indirectness, -1), and the number of included patients (imprecision, -1). As a result, the level of evidence was graded as very low.

A systematic review of the literature was performed to answer the following question:

What is the added value of MRI or FDG-PET/CT to the normally used CT scan in the primary diagnosis of skull base osteomyelitis?

Patients Patients clinically suspected for NOE
Intervention MRI and/or FDG-PET/CT
Control CT scan
Referral Clinical follow-up and/or histopathology/culture reports
Outcomes Diagnostic accuracy (sensitivity, specificity, positive predictive value, negative predictive value, area under the ROC curve)
Timing and setting In cases of suspected NOE, with or without symptoms suggesting involvement of tissues underlying the ear canal, evaluation should be performed in a hospital setting

Relevant outcome measures

The guideline panel considered diagnostic accuracy; sensitivity, specificity, positive predictive value and negative predictive value as a critical outcome measure for decision making (table 1).

 

Table 1. Consequences of diagnostic test characteristics

Outcome

Consequences

Relevance

True positives (TP), high sensitivity, high positive prediction value

Patients are justifiably diagnosed with NOE; surgery or giving treatment is justified

Critical

True negatives (TN), high specificity, high negative prediction value

Patients are justifiably not diagnosed with NOE; not giving (surgical) treatment is justified

Critical

False positives (FP), low specificity, low positive prediction value

Patients are unjustifiably diagnosed with NOE; surgery or giving treatment is unjustified

Critical

False negatives (FN), low sensitivity, low negative prediction value

Patients are unjustifiably not diagnosed with NOE; not giving (surgical) treatment is unjustified

Critical

A priori, the working group did not define the outcome measures listed above but used the definitions used in the studies.

 

The working group defined a difference of 5% in sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) and a difference of 50 per 1000 patients in TP, TN, FP and FN as a minimal clinically (patient) important difference.

 

Search and select (Methods)

The databases Medline (via OVID) and Embase (via Embase.com) were searched with relevant search terms until May 16, 2023. The detailed search strategy is listed under the tab ‘Literature search strategy’. The search resulted in 492 unique hits. Studies were selected based on the following criteria:

  • Systematic reviews, randomized controlled trials, and observational studies on diagnostic imaging modalities in the PICO.
  • At least one diagnostic accuracy outcome was reported.

Seven studies were initially selected based on title and abstract screening. After reading the full text, 5 studies were excluded (see the exclusion table under the tab ‘Evidence tables’), and 2 studies were included. However, both articles (from 2018 and 2020) were derived from the same population, with the same outcome measures. Therefore, only the latter (Kulkarni, 2020), was included.

  1. Chawdhary G, Pankhania M, Douglas S, Bottrill I. Current management of necrotising otitis externa in the UK: survey of 221 UK otolaryngologists. Acta Otolaryngol. 2017 Aug;137(8):818-822. doi: 10.1080/00016489.2017.1295468. Epub 2017 Mar 16. PMID: 28301961.
  2. Curtin HD, Wolfe P, May M. Malignant external otitis: CT evaluation. Radiology. 1982 Nov;145(2):383-8. doi: 10.1148/radiology.145.2.7134442. PMID: 7134442.
  3. Hodgson SH, Khan MM, Patrick-Smith M, Martinez-Devesa P, Stapleton E, Williams OM, Pretorius P, McNally M, Andersson MI; UK NOE Collaborative. UK consensus definitions for necrotising otitis externa: a Delphi study. BMJ Open. 2023 Feb 20;13(2):e061349. doi: 10.1136/bmjopen-2022-061349. PMID: 36806133; PMCID: PMC9945308.
  4. Kulkarni SC, Padma S, Shanmuga Sundaram P. In the evaluation of patients with skull base osteomyelitis, does 18F-FDG PET CT have a role? Nucl Med Commun. 2020 Jun;41(6):550-559. doi: 10.1097/MNM.0000000000001187. PMID: 32282638.
  5. Kim DH, Kim SW, Hwang SH. Predictive value of radiologic studies for malignant otitis externa: a systematic review and meta-analysis. Braz J Otorhinolaryngol. 2023 Jan-Feb;89(1):66-72. doi: 10.1016/j.bjorl.2021.08.011. Epub 2021 Oct 26. PMID: 34799270; PMCID: PMC9874358.
  6. Stern Shavit S, Bernstine H, Sopov V, Nageris B, Hilly O. FDG-PET/CT for diagnosis and follow-up of necrotizing (malignant) external otitis. Laryngoscope. 2019 Apr;129(4):961-966. doi: 10.1002/lary.27526. Epub 2018 Dec 14. PMID: 30549258.
  7. Tsuno NSG, Tsuno MY, Coelho Neto CAF, Noujaim SE, Decnop M, Pacheco FT, Souza SA, Fonseca APA, Garcia MRT. Imaging the External Ear: Practical Approach to Normal and Pathologic Conditions. Radiographics. 2022 Mar-Apr;42(2):522-540. doi: 10.1148/rg.210148. Epub 2022 Feb 4. PMID: 35119966.

Risk of Bias table

Risk of bias assessment diagnostic accuracy studies (QUADAS II, 2011)

Study reference

 

(first author, publication year)

Patient selection

 

Index test

Reference standard

Flow and timing

 

Comments with respect to applicability

Kulkarni, 2020

Was a consecutive or random sample of patients enrolled?

Yes,  due to single-center tertiary centre study a selection bias occured

 

Was a case-control design avoided?

yes

 

Did the study avoid inappropriate exclusions?

 yes

Were the index test results interpreted without knowledge of the results of the reference standard?

yes

 

If a threshold was used, was it pre-specified?

No threshold was used

Is the reference standard likely to correctly classify the target condition?

Probably

 

Were the reference standard results interpreted without knowledge of the results of the index test?

no

Was there an appropriate interval between index test(s) and reference standard?

yes

 

Did all patients receive a reference standard?

Because of the reference standard being multifactorial all patient recieved one or multiple factors

 

Did patients receive the same reference standard?

no

Were all patients included in the analysis?

yes

Are there concerns that the included patients do not match the review question?

no

 

Are there concerns that the index test, its conduct, or interpretation differ from the review question?

no

 

Are there concerns that the target condition as defined by the reference standard does not match the review question?

no

Randomization: generation of allocation sequences have to be unpredictable, for example computer generated random-numbers or drawing lots or envelopes. Examples of inadequate procedures are generation of allocation sequences by alternation, according to case record number, date of birth or date of admission.

Allocation concealment: refers to the protection (blinding) of the randomization process. Concealment of allocation sequences is adequate if patients and enrolling investigators cannot foresee assignment, for example central randomization (performed at a site remote from trial location). Inadequate procedures are all procedures based on inadequate randomization procedures or open allocation schedules.

Blinding: neither the patient nor the care provider (attending physician) knows which patient is getting the special treatment. Blinding is sometimes impossible, for example when comparing surgical with non-surgical treatments, but this should not affect the risk of bias judgement. Blinding of those assessing and collecting outcomes prevents that the knowledge of patient assignment influences the process of outcome assessment or data collection (detection or information bias). If a study has hard (objective) outcome measures, like death,  blinding of outcome assessment is usually not necessary. If a study has “soft” (subjective) outcome measures, like the assessment of an X-ray, blinding of outcome assessment is necessary. Finally, data analysts should be blinded to patient assignment to prevents that knowledge of patient assignment influences data analysis.

Lost to follow-up: If the percentage of patients lost to follow-up or the percentage of missing outcome data is large, or differs between treatment groups, or the reasons for loss to follow-up or missing outcome data differ between treatment groups, bias is likely unless the proportion of missing outcomes compared with observed event risk is not enough to have an important impact on the intervention effect estimate or appropriate imputation methods have been used.

Selective outcome reporting: Results of all predefined outcome measures should be reported; if the protocol is available (in publication or trial registry), then outcomes in the protocol and published report can be compared; if not, outcomes listed in the methods section of an article can be compared with those whose results are reported.

Other biases: Problems may include: a potential source of bias related to the specific study design used (e.g., lead-time bias or survivor bias); trial stopped early due to some data-dependent process (including formal stopping rules); relevant baseline imbalance between intervention groups; claims of fraudulent behavior; deviations from intention-to-treat (ITT) analysis; (the role of the) funding body (see also downgrading due to industry funding https://kennisinstituut.viadesk.com/do/document?id=1607796-646f63756d656e74). Note: The principles of an ITT analysis implies that (a) participants are kept in the intervention groups to which they were randomized, regardless of the intervention they actually received, (b) outcome data are measured on all participants, and (c) all randomized participants are included in the analysis.

Overall judgement of risk of bias per study and per outcome measure, including predicted direction of bias (e.g., favors experimental, or favors comparator). Note: the decision to downgrade the certainty of the evidence for a particular outcome measure is taken based on the body of evidence, i.e., considering potential bias and its impact on the certainty of the evidence in all included studies reporting on the outcome.  

 

Table of excluded studies

Reference

Reason for exclusion

Al-Noury K, Lotfy A. Computed tomography and magnetic resonance imaging findings before and after treatment of patients with malignant external otitis. Eur Arch Otorhinolaryngol. 2011 Dec;268(12):1727-34. doi: 10.1007/s00405-011-1552-8. Epub 2011 Mar 15. PMID: 21400256.

No comparison made

van der Meer WL, Waterval JJ, Kunst HPM, Mitea C, Pegge SAH, Postma AA. Diagnosing necrotizing external otitis on CT and MRI: assessment of pattern of extension. Eur Arch Otorhinolaryngol. 2022 Mar;279(3):1323-1328. doi: 10.1007/s00405-021-06809-2. Epub 2021 Apr 25. PMID: 33895893; PMCID: PMC8897339.

Wrong outcomes

Balakrishnan R, Dalakoti P, Nayak DR, Pujary K, Singh R, Kumar R. Efficacy of HRCT Imaging vs SPECT/CT Scans in the Staging of Malignant External Otitis. Otolaryngol Head Neck Surg. 2019 Aug;161(2):336-342. doi: 10.1177/0194599819838834. Epub 2019 Apr 16. PMID: 30987522.

Wrong outcome

Auinger AB, Dahm V, Stanisz I, Schwarz-Nemec U, Arnoldner C. The challenging diagnosis and follow-up of skull base osteomyelitis in clinical practice. Eur Arch Otorhinolaryngol. 2021 Dec;278(12):4681-4688. doi: 10.1007/s00405-020-06576-6. Epub 2021 Jan 28. PMID: 33511482; PMCID: PMC8553694.

Wrong outcome

Chapman PR, Choudhary G, Singhal A. Skull Base Osteomyelitis: A Comprehensive Imaging Review. AJNR Am J Neuroradiol. 2021 Mar;42(3):404-413. doi: 10.3174/ajnr.A7015. Epub 2021 Jan 21. PMID: 33478944; PMCID: PMC7959418.

Review of literature

Maramattom BV, Ram SA, Viswam V, Nair S. Central Skull Base Osteomyelitis: Multimodality Imaging and Clinical Findings from a Large Indian Cohort. Neurol India. 2022 Sep-Oct;70(5):1911-1919. doi: 10.4103/0028-3886.359218. PMID: 36352587.

No comparison made

Beoordelingsdatum en geldigheid

Laatst beoordeeld  : 25-09-2025

Initiatief en autorisatie

Initiatief:
  • Nederlandse Vereniging voor Keel-Neus-Oorheelkunde en Heelkunde van het Hoofd-Halsgebied
Geautoriseerd door:
  • Nederlandse Internisten Vereniging
  • Nederlandse Vereniging voor Keel-Neus-Oorheelkunde en Heelkunde van het Hoofd-Halsgebied
  • Nederlandse Vereniging voor Medische Microbiologie
  • Nederlandse Vereniging voor Nucleaire geneeskunde
  • Nederlandse Vereniging voor Radiologie
  • Nederlandse Vereniging van Ziekenhuisapothekers
  • Hoormij / Nederlandse Vereniging voor Slechthorenden

Algemene gegevens

For more details on the guideline methodology used, we refer you to the Werkwijze. Relevant information for the development of this guideline is presented below.

 

The revision of this guideline module was supported by the Knowledge Institute of the Federation of Medical Specialists (www.demedischspecialist.nl/kennisinstituut) and was funded by the Quality Funds for Medical Specialists (SKMS).

Samenstelling werkgroep

For the development of the guideline, a multidisciplinary guideline development group was established in 2022, consisting of representatives from all relevant specialties (see Composition of the working group) involved in the care of patients with necrotizing otitis externa.

 

Werkgroep

  • Dr. J.J. (Jérôme) Waterval (chairman), Nederlandse Vereniging voor Keel-Neus-Oorheelkunde en Heelkunde van het Hoofd-Halsgebied, otorhinolaryngologist, Maastricht University Medical Center, Maastricht; Academic Alliance Skull Base Pathology Maaastricht University Medical Center – Radboud University Medical Center
  • Dr. M.J. (Mark) van Tilburg, Nederlandse Vereniging voor Keel-Neus-Oorheelkunde en Heelkunde van het Hoofd-Halsgebied, otorhinolaryngologist, Elistabeth-TweeSteden Ziekenhuis, Tilburg
  • Drs. S.A.H. (Sjoert) Pegge, Nederlandse Vereniging voor Radiologie, radiologist, Radboud University Medical Center, Nijmegen; Academic Alliance Skull Base Pathology Maaastricht University Medical Center – Radboud University Medical Center
  • Prof. Dr. A.W.J.M. (Andor) Glaudemans, Nederlandse Vereniging voor Nucleaire Geneeskunde, nuclear physicist UMCG, Groningen
  • Dr. M. (Moniek) Heusinkveld, Nederlandse Vereniging voor Medische Microbiologie, medical microbiologist, Gelderse Vallei Hospital, Ede
  • Dr. E.J.G. (Edgar) Peters, Nederlandse Internisten Vereniging, infectious disease specialist, Amsterdam University Medical Center (tot oktober 2022)
  • Dr. J.J. (Jonne) Sikkens, Nederlandse Internisten Vereniging, infectious disease specialist, Amsterdam University Medical Center (vanaf october 2022)
  • Dr. I.R. (Raluca) Mihailescu, Nederlandse Internisten Vereniging, infectious disease specialist, Onze Lieve Vrouwe Gasthuis, Amsterdam (vanaf juli 2024)
  • Dr. S.H. (Selwyn) Lowe, Nederlandse Internisten Vereniging, infectious disease specialist, Maastricht University Medical Center, Maastricht (vanaf juli 2024)

 Klankbordgroep

  • Dr. N.G.L. (Nynke) Jager, NVZA, hospital pharmacist Radboud University Medical Center, Nijmegen
  • Drs. F.S. (Fleur) Sinkeler, NVZA, hospital pharmacist Radboudumc Nijmegen

Ondersteuning

  • Drs. J.M.H. (Jasper) Janssen, NVKNO, otorhinolaryngologist in training, Maastricht University Medical Center, Maastricht
  • Dr. A. (Anja) van der Hout, advisor Knowledge Institute of the Dutch Association of Medical Specialists

Belangenverklaringen

An overview of the conflicts of interests of the guideline development group members and the assessment of how potential conflicts of interest were addressed can be found in the table below. The signed declarations of interest are available upon request from the Secretariat of the Knowledge Institute of the Dutch Federation of Medical Specialists at secretariaat@kennisinstituut.nl.

Werkgroeplid

Functie

Nevenfuncties

Gemelde belangen

Ondernomen actie

Waterval (voorzitter)

KNO-arts MUMC

Accreditatiecommissie Stichting Audiciensregister

Geen

Geen

Glaudemans

Nucleair geneeskundige UMCG

 

Voorzitter NVNG (onbetaald)

We hebben als ziekenhuis en afdeling een samenwerking met Siemens (UMCG-Siemens PUSH collaboration/Partnership of UMCG-Siemens for building the future of Health). Hieruit vloeit uit voort dat de nieuwste camera’s bij ons komen (bv UMCG neemt nieuwe Whole-Body PET/CT-scanner in gebruik) en dat er gezamenlijk onderzoek gedaan wordt. Hierbij heb ik een aantal promovendi die door Siemens betaald worden (niet op het gebied van osteomyelitis schedelbasis)

Geen restricties. Extern gefinancierd onderzoek valt buiten bestek richtlijn

 

Heusinkveld

Arts-microbioloog in ziekenhuis Gelders Vallei

Richtlijn otitis externa

 

Bestuur SKML sectie infectieserologie (onbetaald)

Geen

Geen

Peters (tot oktober 2022)

Internist-infectioloog-acute geneeskundige, Amsterdam UMC

richtlijnontwikkeling: Covid-19 FMS, diabetische voet NIV, diabetische voet IWGDF, alle onbetaald
Organisatie internationaal congres diabetische voet. Onbetaald

 

afdeling krijgt geld van Roche voor biomarker onderzoek bij diabetische voet osteomyelitis
Voorzitter gewrichtsprothese geassocieerde infectie richtlijn.

Diabetische voet onderzoek (extern gefinancierd)

 

Geen restricties. Extern gefinancierd onderzoek valt buiten bestek richtlijn

 

Pegge

Radioloog (Neuro/Hoofdhals)

Radboud UMC Nijmegen

Geen

Geen

Geen

Van Tilburg

KNO-arts ETZ

 

Geen

Geen

Geen

Sikkens

Internist acute geneeskunde & infectioloog, Amsterdam UMC

post-doc onderzoeker Amsterdam UMC, onbetaald

 

Ja, via ZonMw (onderzoek naar COVID bij een medewerkerscohort, onderwerp infectiepreventie en vaccin-immunologie)

 

Geen restricties. Extern gefinancierd onderzoek valt buiten bestek richtlijn

 

Lowe

 

Internist-infectioloog. Afdeling Medische Microbiologie, Infectieziekten en Infectiepreventie (MMI), Maastricht UMC+

 

Geen

Geen

Geen

Mihailescu

 

Internist-infectioloog

OLVG

Amsterdam

Geen

Geen

Geen

Jasper Janssen

 

KNO-arts in opleiding bij het MUMC+ (0,8 FTE), promovendus (0,2 FTE).

Geen

Geen

Geen

Sinkeler

 

Ziekenhuisapotheker AmsterdamUMC

 

Geen

Geen

Geen

Jager

Ziekenhuisapotheker

 

Geen

Geen

Geen

Inbreng patiëntenperspectief

Attention was paid to the patient perspective by inviting Stichting Hoormij and Patiëntenfederatie Nederland for the invitational conference, and close contact with Stichting Hoormij during the development of the guideline. The report of this [see related products] was discussed in the guideline development group. The input obtained was taken into account when formulating the key questions, selecting the outcome measures, and drafting the considerations. The draft guideline was also submitted for comments to Stichting Hoormij and Patiëntenfederatie Nederland, and any comments received were reviewed and processed.

 

Kwalitatieve raming van mogelijke financiële gevolgen in het kader van de Wkkgz

Bij de richtlijnmodule voerde de werkgroep conform de Wet kwaliteit, klachten en geschillen zorg (Wkkgz) een kwalitatieve raming uit om te beoordelen of de aanbevelingen mogelijk leiden tot substantiële financiële gevolgen. Bij het uitvoeren van deze beoordeling is de richtlijnmodule op verschillende domeinen getoetst (zie het stroomschema bij Werkwijze).

Module

Uitkomst raming

Toelichting

Diagnostic imaging for primary diagnosis

geen financiële gevolgen

Uit de toetsing volgt dat de aanbeveling(en) niet breed toepasbaar zijn (<5.000 patiënten) en daarom naar verwachting geen substantiële financiële gevolgen zal hebben voor de collectieve uitgaven.

Zoekverantwoording

Algemene informatie

Cluster/richtlijn: Osteomyelitis schedelbasis – Maligne otitis externa

Uitgangsvraag/modules: Welke beeldvormende diagnostiek is relevant voor het stellen van de diagnose maligne otitis externa (diagnostische vraag)

Database(s): Ovid/Medline, Embase.com

Datum: 16 mei 2023

Periode: 2000 - heden

Talen: Engels, Nederlands

Literatuurspecialist: Miriam van der Maten

BMI-zoekblokken: voor verschillende opdrachten wordt (deels) gebruik gemaakt van de zoekblokken van BMI-Online https://blocks.bmi-online.nl/ Bij gebruikmaking van een volledig zoekblok zal naar de betreffende link op de website worden verwezen.

Toelichting:

Voor deze vraag is gezocht op de elementen:

  • Maligne otitis externa/osteomyelitis schedelbasis
  • Diagnostische modaliteiten CT of MRI of PET
  • Diagnostisch filter; termen 'diagnostic imaging' en diagnostics (in titel) toegevoegd.

De sleutelartikelen worden gevonden met de zoekopdracht.

Te gebruiken voor richtlijnen tekst:

Nederlands

In de databases Embase.com en Ovid/Medline is op 16 mei 2023 systematisch gezocht naar studies over relevante beeldvormende diagnostiek voor het stellen van de diagnose maligne otitis externa. De literatuurzoekactie leverde 492 unieke treffers op.

 

Engels

On the 16th of May 2023, we performed a systematic search in the databases Embase.com and Ovid/Medline to find literature about relevant imaging modalities for diagnosing malignant otitis externa. The search resulted in 492 unique hits.

Zoekopbrengst

 

EMBASE

OVID/MEDLINE

Ontdubbeld

Totaal

308

281

492

Zoekstrategie

Embase.com

No.

Query

Results

#6

#1 AND (#2 OR #3 OR #4) AND #5 AND ([english]/lim OR [dutch]/lim) AND [2000-2023]/py NOT (('animal experiment'/exp OR 'animal model'/exp OR 'nonhuman'/exp) NOT 'human'/exp)

308

#5

'diagnostic procedure'/mj OR 'diagnostic imaging'/exp OR 'sensitivity and specificity'/de OR sensitiv*:ab,ti OR specific*:ab,ti OR predict*:ab,ti OR 'roc curve':ab,ti OR 'receiver operator':ab,ti OR 'receiver operators':ab,ti OR likelihood:ab,ti OR 'diagnostic error'/exp OR 'diagnostic accuracy'/exp OR 'diagnostic test accuracy study'/exp OR 'inter observer':ab,ti OR 'intra observer':ab,ti OR interobserver:ab,ti OR intraobserver:ab,ti OR validity:ab,ti OR kappa:ab,ti OR reliability:ab,ti OR reproducibility:ab,ti OR ((test NEAR/2 're-test'):ab,ti) OR ((test NEAR/2 'retest'):ab,ti) OR 'reproducibility'/exp OR accuracy:ab,ti OR 'differential diagnosis'/exp OR 'validation study'/de OR 'measurement precision'/exp OR 'diagnostic value'/exp OR 'reliability'/exp OR 'predictive value'/exp OR ppv:ti,ab,kw OR npv:ti,ab,kw OR diagnos*:ti

10417931

#4

'computer assisted emission tomography'/exp OR 'gated single photon emission computed tomography'/exp OR 'single photon emission computer tomography'/exp OR petscan*:ti,ab,kw OR pet:ti,ab,kw OR ((emission NEAR/3 tomograph*):ti,ab,kw) OR radionuclid*:ti,ab,kw OR 'fluorodeoxyglucose'/exp OR 'fluorodeoxyglucose f 18'/exp OR 'fluorodeoxyglucose':ti,ab,kw OR fdg:ti,ab,kw

439885

#3

'nuclear magnetic resonance imaging'/exp OR 'mri scanner'/exp OR ('magnetic resonance':ab,ti AND (image:ab,ti OR images:ab,ti OR imaging:ab,ti)) OR mri:ab,ti OR mris:ab,ti OR nmr:ab,ti OR mra:ab,ti OR mras:ab,ti OR zeugmatograph*:ab,ti OR 'mr tomography':ab,ti OR 'mr tomographies':ab,ti OR 'mr tomographic':ab,ti OR 'proton spin':ab,ti OR ((magneti*:ab,ti OR 'chemical shift':ab,ti) AND imaging:ab,ti) OR fmri:ab,ti OR fmris:ab,ti OR ((imag* NEAR/3 modalit*):ti,ab,kw)

1554550

#2

'computer assisted tomography'/exp OR 'cat scan':ti,ab,kw OR ((compute* NEAR/3 tomograph*):ti,ab,kw) OR ct:ti,ab,kw

1670461

#1

'malignant otitis externa'/exp/mj OR (((maligna* OR necroti* OR necrosis) NEAR/3 ('otitis externa' OR 'external otitis')):ti,kw) OR ('otitis externa'/mj AND (maligna*:ti,kw OR necroti*:ti,kw OR necrosis:ti,kw)) OR (('osteomyelitis'/exp/mj OR 'osteomyelitis':ti,kw OR osteitis:ti,kw) AND ('skull'/exp/mj OR 'skull disease'/exp/mj OR skull*:ti,ab,kw OR cranial:ti,ab,kw OR cranium:ti,ab,kw))

3383

Ovid/Medline

#

Searches

Results

8

limit 7 to ((english language or dutch) and yr="2000 -Current")

281

7

6 not ((exp animals/ or exp models, animal/) not humans/)

392

6

1 and (2 or 3 or 4) and 5

398

5

exp "Sensitivity and Specificity"/ or (Sensitiv* or Specific*).ti,ab. or (predict* or ROC-curve or receiver-operator*).ti,ab. or (likelihood or LR*).ti,ab. or exp Diagnostic Errors/ or (inter-observer or intra-observer or interobserver or intraobserver or validity or kappa or reliability).ti,ab. or reproducibility.ti,ab. or (test adj2 (re-test or retest)).ti,ab. or "Reproducibility of Results"/ or accuracy.ti,ab. or *Diagnosis, Differential/ or Validation Study/ or exp diagnostic imaging/ or ppv.ti,ab,kf. or npv.ti,ab,kf. or diagnos*.ti.

9937614

4

exp *Tomography, Emission-Computed/ or "petscan*".ti,ab,kf. or "pet".ti,ab,kf. or ("emission" and "tomogra*").ti,ab,kf. or "radionuclid*".ti,ab,kf. or exp Fluorodeoxyglucose F18/ or fluorodeoxyglucose.ti,ab,kf. or FDG.ti,ab,kf.

217767

3

exp *magnetic resonance imaging/ or ("magnetic resonance" and (image or images or imaging)).ti,ab,kf. or mri.ti,ab,kf. or mris.ti,ab,kf. or nmr.ti,ab,kf. or mra.ti,ab,kf. or mras.ti,ab,kf. or zeugmatograph*.ti,ab,kf. or "mr tomography".ti,ab,kf. or "mr tomographies".ti,ab,kf. or "mr tomographic".ti,ab,kf. or "proton spin".ti,ab,kf. or ((magneti* or "chemical shift") and imaging).ti,ab,kf. or fmri.ti,ab,kf. or fmris.ti,ab,kf. or (imag* adj3 modalit*).ti,ab,kf.

825746

2

exp *Tomography, X-Ray Computed/ or computed tomograph*.ti,ab,kf. or ct.ti,ab,kf. or cts.ti,ab,kf. or cat scan*.ti,ab,kf. or computer assisted tomograph*.ti,ab,kf. or computerized tomograph*.ti,ab,kf. or computerised tomograph*.ti,ab,kf. or computed x ray tomograph*.ti,ab,kf. or computed xray tomograph*.ti,ab,kf.

668301

1

((maligna* or necroti* or necrosis) adj3 ('otitis externa' or 'external otitis')).ti,kf. or (exp *Otitis Externa/ and (maligna* or necroti* or necrosis).ti,kf.) or ((exp *Osteomyelitis/ or 'osteomyelitis'.ti,kf. or osteitis.ti,kf.) and (exp Skull/ or skull*.ti,ab,kf. or cranial.ti,ab,kf. or cranium.ti,ab,kf.))

3088

Volgende:
Microbiology and histopathology