12: Maintenance

CHAPTER 12
Maintenance

12.1 INTRODUCTION

The literature lays out clear criteria for success and failure for dental implants, and classifies what constitutes high success rates when measured against these. Adell et al. reported 81% success rates in the maxilla and 91% in the mandible over 5–9 years after placement [1].

Implants may have complications for a variety of reasons, but it is accepted that a key predicator for the long‐term survival of implant treatment is the condition of the surrounding mucosa and the quality of the maintenance programme.

Mucositis is a precursor to peri‐implantitis [2]. Based on the uncertain nature of success in treating peri‐implant disease, it is clear that preventing the progression from mucositis to peri‐implantitis is a key objective in ensuring the long‐term health of implants (Figure 12.1) [3] (B).

12.2 RECALL INTERVAL

The recall interval is very patient‐specific and takes into account factors such as the type of prosthesis, risk factors, oral hygiene, referral or own case, complications, complexity of case insertion torque/bone quality and the patient’s previous implant experience (B).

Two photographs comparing peri-implant mucositis and healthy tissues with inflammation, swelling, and bleeding due to poor hygiene around a cantilevered F P D and restored healthy peri-implant tissue after supportive therapy and education.

FIGURE 12.1 Comparison of peri‐implant mucositis and healthy peri‐implant tissues. (a) Presence of gingival inflammation, soft tissue swelling and tissue that bleeds easily on gentle probing. The patient was reluctant to perform basic hygiene around the cantilevered provisional fixed partial denture (FPD) UR 2–3 on the implant in the UR 3 position. (b) Restoration of a healthy peri‐implant environment on the same individual around the final cantilevered FPD UR 2–3 after non‐surgical supportive therapy and patient education. Note the lack of swelling, inflammation and bleeding.

Aspirational Basic Conditional
Maximum of 6 months to elapse between recall appointments. (ii) The recall interval is patient‐specific [4], taking into consideration factors such as the type of prosthesis, risk factors, oral hygiene, referral or own case, complications, complexity of case insertion torque/bone quality and the patient’s previous implant experience. (i).

The literature is lacking when we search for an ideal recall interval, and this reflects the individual nature of the recall. However, we need to highlight the importance of preventing the progression of mucositis to peri‐implantitis [3], and therefore a maximum recall interval of 6 months is recommended (B).

12.3 RADIOGRAPHIC REVIEW

A baseline radiograph is recommended to determine alveolar bone levels after the completion of the initial adaptive bone remodelling phase to record crestal bone levels, to assess the fit of the prosthesis and to ensure the interproximal sulcus is clear of cement [5]. The panoramic radiograph is not generally suitable to visualise peri‐implant bone levels consistently [5] (B).

Aspirational Basic Conditional
Radiographic assessment at 1 year post placement to check the stability of peri‐implant bone support. (ii) Baseline radiograph to be taken, justified and reported. (i) Radiographic assessment to be undertaken when clinical parameters indicate disease. (i)
The frequency of radiological investigations to be dictated by the individual clinical parameters and the patient’s individual risk factors [5]. (ii)
Three radiographs demonstrating crestal bone stability at baseline, one year, and six years, and two clinical images depicting soft tissue health at baseline and six years.

FIGURE 12.2

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Mar 15, 2026 | Posted by in Implantology | Comments Off on 12: Maintenance

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