Developing evidence-based clinical imaging guidelines of justification for radiographic examination after dental implant installation

Abstract

Background

This study aimed to develop evidence-based clinical imaging guidelines to assess the proper implant location following implant surgery and identify potential complications during follow-up.

Methods

The guideline development process employed an adaptation methodology in accordance with the Korean clinical imaging guidelines (K-CIG). Core (Ovid-Medline, Ovid-Embase, National Guideline Clearinghouse, and Guideline International Network) and domestic databases (KoreaMed, KMbase, and KoMGI) were searched used to retrieve guidelines, and two reviewers analyzed the retrieved articles. The articles were included in this review using well-established inclusion criteria.

Results

Our online search identified 66 articles, of which 3 were selected for the development of the guidelines. Consequently, based on these three guidelines, we formulated distinct recommendations regarding the appropriate imaging modalities that should be used following implant placement.

Conclusions

Conventional imaging (e.g., periapical or panoramic radiography) should be the first choice for assessing the implant following its placement and osseointegration. The metal artifacts in Cone Beam Computed Tomography (CBCT) should be considered. However, CBCT is recommended for patients with sensory abnormalities following dental implant surgery to evaluate and identify the underlying cause of implant complications and to determine the appropriate treatment.

Background

The use of dental implants has increased during the last few decades and has led to an increase in the number of related complications. Implant complications can be broadly divided as biological and technical. Biological complications include mucositis, peri-implantitis, and implant loss due to osseointegration failure, whereas technical complications involve fractures of implant prostheses, screw loosening, and loss of screw hole sealing [1]. In the event of a technical complication, the patient has the opportunity to notice the respective issue, and therefore treatment is feasible. In contrast, biological complications can be serious, including the need for removal of the implant fixture or development of severe mental damage stemming from irreversible nerve damage. Biological complications result in greater sequelae compared with technical complications.

Early diagnosis through periodic follow-up reduces the severity of complications and facilitate appropriate treatment [2]. Many of these complications are easily diagnosed on postsurgical imaging [3]. Radiological examinations for diagnosing the complications include panoramic radiography, periapical radiography, and cone-beam computed tomography (CBCT). These imaging modalities can help diagnosis of potential bone loss around the implant, osseointegration (implant-bone interface), and facilitate evaluation of the relationship between the surrounding anatomical structures and the implant [4,5,6].

Because no clear guideline on what type of modality is the first choice to assess this situation following dental implant surgery, this study aimed to develop evidence-based clinical imaging guidelines (CIGs) for this process.

Methods

The guideline development process involved collaboration between The Korean Academy of Oral and Maxillofacial Radiology (KAMOFR) and the National Evidence based Healthcare Collaborating Agency (NECA) and Korean Society of Radiology [7, 8]. To develop such guidelines a development committee, a working group and a consensus group were formed.

Committee composition

The development committee conducts a practical development process from selecting key questions to drawing final recommendations. The professional society recommends members who understand the development of clinical practice guidelines and who can actively participate in these process. A development committee is formed from these recommended members.

The working group consisted of nine oral and maxillofacial radiology experts and research methodology specialists who carried out actual tasks for development of clinical guidelines [7].

Finally, a consensus group consisted of seven nominated members from the five related societies who are expected to be end-users of clinical guidelines. They reviews key questions and participates in the expert panel survey (Delphi method) to agree on draft recommendations.

Defining the key questions

The working group generated key questions and the development group and consensus group reviewed the generated key questions. The questions formed include the elements of PICO (Population/patient, Intervention/index, Comparator/control, Outcome) and are clearly stated.

The key questions were identified as follows

• KQ1. What is the appropriate imaging modality for follow-up after the dental implant surgery?

• KQ2. What is the appropriate imaging modality in patients with sensory abnormalities following dental implant surgery?

Search for guidelines

Core databases such as Ovid-Medline, Ovid-Embase, Guideline International Network and National Guideline Clearinghouse were used to perform this guideline search. Moreover, three domestic research databases were investigated, including KoreaMed, KMbase, and KoMGI from 2000 until week one of May 2018. Extensive searches in databases used the keyword terms “Dental implant,” “Radiograph,” “guideline,” “recommendation,” and “Cone-Beam Computed Tomography.” When searching, we used operators so that there were no missing guidelines. The working group reviewed the search strategy and results and supplemented via manual search if any key guidelines were missing.

Selection of searched guidelines

According to the selection criteria outline, two individuals in the working group independently reviewed literature. To ensure objectivity, a primary screening process a secondary selection process were both conducted. The primary screening involved the reviewing of the title and abstract of a study or guideline. In the secondary selection process, the full text of the literature was reviewed. Following these two processes, the working group selected the respective literatures and in cases where certain literatures had been excluded, the reason for exclusion was noted [7, 8].

The selection criteria were as follows: 1) PICOs included that match key questions, 2) clinical guidelines published in Korean or English, 3) clinical guidelines published since 2000.

The exclusion criteria were as follows: 1) patients in key questions were not targeted, 2) imaging modalities related key questions were not included, 3) appropriate results (diagnostic accuracy, efficacy, safety, prognostic impact and patient assessment, etc.) were not reported, 4) non-clinical guidelines, 5) no recommendation is given, 6) guidelines were not generated by the evidence based method based, 7) guidelines reported in languages other than English and Korean, 8) duplicated, 9) it is impossible to acquire the original text.

If there were disagreements between reviewers in the two selection processes, the clinical practice guidelines were selected through an agreement process.

Search for recent literature

We investigated randomized controlled trials and observational studies whose literature has been reviewed since 2015.

Quality assessment

The final selected guidelines underwent quality appraisal using the Korean Appraisal of guidelines for Research & Evaluation II tools [9]. Two appraisers independently selected from the development committee assessed the selected literature. Each evaluation category was assigned a score from 1 to 7 points. To ensure reproducibility and clarity, the reason for assigning these scores was noted. Differences in scores among the appraisers greater than four, led to the re-examination of the respective the literature. Essentially, guidelines scoring 50 or above in the “Rigor of development” domain, were considered as candidates for enrollment to develop K-CIGs [7].

Grading the level of evidence and drafting the recommendation document

This process ensured that the guideline was up-to-date, acceptable, and applicable. Evidence tables which were consisted of the primary studies included in selected guidelines were made according to each key question, We extracted data from each primary studies on pre-defined format. Quality of studies was assessed by individual study level and included in evidence tables, This process was performed by two of authors independently then consensus reached. The level of evidence level in the K-CIG was merged with the evidence level in individual literature and it was categorized as high (I), moderate (II), low (III), or very low (IV) [7].

The draft recommendations consisted of recommendations for the key questions, a summary of the evidences, considerations, and references. Each recommendation includes the grade of the recommendation and the overall evidence level. The recommendation grade is composed of A, B, C, and I to indicate the direction of the recommendation, and the level of evidence indicates the strength of the recommendation [7].

Agreement of the recommendation grade

The draft version of the recommendation produced by the working group was discussed the evidence level and grade of recommendation with the development committee. Ensuring agreement between the working group and development committees, allowed for the distinct determination of the validity of the recommendation document.

Finalizing the recommendation document

The consensus group draws formal consensus through the Delphi method of anonymity. The first questionnaire is composed so that the key questions, draft recommendations, recommendation grades, and level of evidence can be viewed at a glance. The agreement level for each recommendation, the grade of each recommendation, and the evidence level were rated from strongly disagree (level 1) to strongly agree (level 9).

After the first survey, a second questionnaire is produced to reflect the degree of agreement and other opinions, and the survey is conducted. During the second survey, the distribution of all respondents and the evaluation results of each evaluator are provided by item, and the evaluator proceeds in a way that judges whether to correct or maintain the first evaluation result. Through this repetition round, consensus was reached.

Results

Pico

The PICO guideline was deduced based on key questions. Key questions were generated in the form of PICO questions by a working group. The PICO of key questions (KQ) 1 and 2 are as follows (Table 1).

Table 1 PICO of key questions

Search for guidelines

Tables 2 demonstrate the results acquired from domestic databases. No results were obtained from KGC and KoMGI. Tables 3, 4, 5 and 6 exhibit the acquired results from international databases. All searches were limited since the 2000.

Table 2 Search results from domestic databases

Table 3 Search results from international databases: Ovid-Medline

Table 4 Search results from international databases: Ovid-Embase

Table 5 Search results from international databases: GIN

Table 6 Searching result from international databases-NGC

Selection of searched guidelines

A total of 66 guidelines were retrieved from databases. Consequently, 50 guidelines were excluded following screening of their abstracts and 13 guidelines were excluded according to the selection and exclusion criteria (full-text review) Therefore, three guidelines were finally included in this review, as shown in Fig. 1.

Fig. 1

Selection process of searched guidelines

Search for recent studies

The latest studies were reviewed by 2015. Studies were selected provided that their evidence was related to the key questions were the latest or that can update the evidence table. Study designs corresponding to the top of the evidence pyramid (Meta analyses> systemic reviews> cohort studies>case-controlled studies) were primarily selected [10]. Consequently, six studies were included in this review.

Quality assessment

Table 7 demonstrates the quality assessment of the three guidelines included in this review using the AGREEII instrument [9]. All of three guidelines received > 50 scores in the “Rigor of development” domain. Furthermore, Tables 8 and 9 show the recommendation matrix of the existing guidelines and the acceptability and applicability assessment of the three guidelines.

Table 7 Results of the quality assessment of the guidelines using AGREEII instrument

Table 8 Recommendation matrix of the existing guideline

Table 9 Acceptability and applicability assessment

Grading the level of evidence and drafting the recommendation document

We compiled the individual literature related to the key question and prepared the evidence table by giving the level of evidence in our research (Table 10). Based on three guidelines, recommendations were then proposed. Each recommendation level and evidence level are as follows:

• Recommendation 1. Panoramic and periapical radiography are recommended for the evaluation of implant position, osseointegration, and for following-up the bone level around the implant.

  • (Recommendation A, evidence level II).

    • Remark1. Conventional imaging (panoramic and periapical radiography) should be the first choice to perform these processes.

    • Remark2. CBCT imaging can be used on a limited basis to follow-up an implant placement due to the generation of dental implant and prostheses artifacts.

• Recommendation 2. CBCT is recommended for patients with sensory abnormality to evaluate the position of the implant and its surrounding structures, and to determine whether the implant is removed, following dental implant surgery.

  • (Recommendation B, evidence level II).

Table 10 Evidence table

Finalizing the recommendation document

Delphi method is used, and following two rounds of assessment, the recommendation document was finalized. The average degree of agreement was 7.7 (standard deviation: 2.3) for recommendation 1 and 8.3 (standard deviation: 0.5) for recommendation 2, respectively (Table 11).

Table 11 Result of Delphi method

Discussion

A total of three guidelines were identified and which discussed the placement of implants. Literature evaluates the use of CBCT imaging in relation to implant surgery, and it is suggested that CBCT can be considered for use while reflecting the optimization of the image protocol. However, it should be used selectively as a subtest of two-dimensional image dentistry [15]. Similar to ionizing radiography, CBCT imaging should only be used in cases where the potential benefit to the patient outweighs the respective risks. The dentist should, therefore, consider this information, and hence assess whether the information obtained from the CBCT test can improve patient care, patient safety, and, ultimately, facilitates a more predictable and optimal treatment [15].

CBCT has a variety of application programs designed for the treatment of dental implants and should be used as an aid to 2-Dimentional radiographic images when clinicians believe that the benefits of this method outweigh the respective risks [12, 14].

Implants may generate artifacts that can cause significant interferences when inspecting the respective images for implant placement and performance [15].

Periapical radiography exhibited an average vertical bone gain of + 0.89 ± 0.39 mm at 36 months following implant placement, whereas bone loss averaged − 1.11 ± 0.44 mm in the first year of implant placement [17]. Three years and 1 month following implant placement, periapical radiography was performed using a film holder, and the mean radiographic marginal bone loss was 0.35 ± 0.63 mm for immediately loaded implants and 0.31 ± 0.96 mm for early loaded implants, respectively. The difference between the two groups was not statistically significant (P = 0.26) [18]. Several studies that investigated the correlation between height of implant abutment and peri-implant bone loss also used panoramic radiography and periapical radiography. And these studies showed significant results of the relationship between height of implant abutment and bone loss around the implant [20,21,22].

Conventional imaging (e.g., periapical or panoramic radiography) should the first selection criterion for the assessment and monitoring of bone levels around the implant following its placement and osseointegration. Implants and prostheses cause metal artifacts in CBCT, thus rendering this approach as difficult to perform accurate assessments with respect to implant-bone density and thickness. Therefore, CBCT should not be used for this purpose [23]. In the follow-up of implants, CBCT is often used as a means for early diagnosis of peri-implantitis. Due to metal artifact of the implant, the buccal bone of the implant is about 0.3 mm less (the diameter of the implant is 12–15% larger). Therefore, if the bone around the implant is not clearly visible due to the implant metal artifact in the cone beam CT image, the subjective judgment of the dentist is required for diagnosis [24].

Although the CBCT is useful to some extent in the structural analysis of the bony trabeculae, the CBCT is not reliable for evaluation of the bone density [25]. The Pseudo-Hounsfield value of CBCT is unreliable, so additional examination is necessary when CBCT is used in assessing quality and density of bone [26, 27]. These studies support the rationale that CBCT is not the primary examination in the follow-up after implant installation.

It is of great interest to have the capacity to increase the survivability of implants using proper occlusion adjustment and early treatment of peri-implantitis and by checking the implant location and surrounding bone mass during the follow-up period. Conventionally, radiation exposure and the significant economic burden are the limiting factors in this process, however, the radiation doses of the periapical and panoramic radiography are currently very low and the subsequent economic risk is also low compared to the alternative CT. More specifically, the radiation dose for each conventional radiography is 7.2 μSv for panoramic [23] and 1–8.3 μSv for periapical radiography, respectively [28]. In dental CBCT, the effective dose varies considerably among different apparatuses and can range from five to 1073 μSv. These variations stem from differences in the available fields of view, scanning times, and detector technologies [15].

Following implant surgery, CBCT is used to identify the location of the implant. In fact, CBCT can provide the operator with critical information of whether to remove or maintain implants in patients with paresthesia or anesthesia1 [12, 16]. A safety zone between the implant apex and the nerve canal is approximately 2 to 3 mm [29]. Direct mechanical injury to the nerve when drilling for implant placement or fixture can be very hazardous. Furthermore, if the apex of an implant is placed in the proximity of the nerve canal, it can cause compression-related injuries [30] that can facilitate the development of an altered sensation following implant placement. Consequently, this condition can be amended by immediate removal of the implant or by using pharmacologic treatments with high doses of NSAIDs to relieve the compression [30, 31].

The CBCT illustrates a three-dimensional relationship between implants and anatomical structures (inferior alveolar nerve and mental foramina) that are difficult to identify when using the panoramic image. Therefore, postoperative CBCT can be used to verify the location and distance between the implant fixture and the nerves, which is extremely useful in determining the treatment of sensory abnormalities [32].

Although this process can be harmful to the patient due to radiation exposure and economic burden involved, it is expected that it can alleviate the patients’ sensory abnormalities. Dentists performing implant surgery should then receive specific training to comprehend the optimal use of CBCT [19].

This guideline was created using systematic review and through end-user reviews and consensus. It will be very helpful when clinicians decide to use imaging to diagnose recall checks or neurological abnormalities after implant placement.

Conclusion

This study developed evidence-based CIGs following implant placement.

The applicability and monitoring of these recommended guidelines need to be continuously assessed in the future to achieve optimal patient outcomes in clinical settings.