Background <p>Evaluation of neurosensory disturbances (ND) and the success rate of dental implants related to inferior alveolar nerve lateralization (IANL) and immediate dental implant placement in the posterior atrophic mandible.</p> Methods <p>A prospective clinical case series was conducted among five edentulous patients with posterior mandibular atrophy. The study included 9 IANL sites. Nerve function and implant success rate were assessed during follow-up. Differences between pre- and post-operative outcomes were analyzed.</p> Results <p>The study included patients aged 24–72 years, with a mean age of 56.22 ± 16.49 years and a male predominance (77.7%). Surgical procedures were performed on the right side in 55.56% of cases and on the left side in 44.44%. By one month, 44.4% reported full recovery, 33.3% reported moderate hypoesthesia, and 22.3% had mild hypoesthesia. At three months, 33.3% had full recovery, 55.6% experienced mild hypoesthesia, and 11.1% (1 patient) reported anesthesia. At six months, 88.9% had recovered, with only one patient (11.1%) still reporting anesthesia. A statistically significant difference in ND was observed across follow-ups at day one, week one, month one, month three, and month six (χ² = 30.3, <i>p</i> &lt; 0.001). Pairwise comparisons revealed significant improvements from day one to month one (<i>p</i> = 0.03), day one to month three (<i>p</i> = 0.008), and day one to month six (<i>p</i> = 0.005), while the difference between day one and week one was not significant (<i>p</i> = 1.00). No significant correlations were found between ND recovery and patient age or membrane type at any follow-up interval (<i>p</i> &gt; 0.05).</p> Conclusion <p>The study showed that IANL with immediate implant placement is an effective technique for rehabilitating atrophic posterior mandibles.</p> Trial registration <p>The study protocol has been registered in ClinicalTrials.gov (Identifier NCT07104994, 5/8/2025), and the date of registration was retrospectively determined.</p>

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Inferior alveolar nerve relocation and immediate dental implant placement in severely resorbed mandibles: a prospective clinical case series

  • Hisham Suliman Hwaiti,
  • Yasser Ahmed Al-Rubidi,
  • Ahmed Al-Ashwal,
  • Yahya Al-Hadi,
  • Taghreed Al-Kibsi,
  • Mohammed Ali Al-Wesabi

摘要

Background

Evaluation of neurosensory disturbances (ND) and the success rate of dental implants related to inferior alveolar nerve lateralization (IANL) and immediate dental implant placement in the posterior atrophic mandible.

Methods

A prospective clinical case series was conducted among five edentulous patients with posterior mandibular atrophy. The study included 9 IANL sites. Nerve function and implant success rate were assessed during follow-up. Differences between pre- and post-operative outcomes were analyzed.

Results

The study included patients aged 24–72 years, with a mean age of 56.22 ± 16.49 years and a male predominance (77.7%). Surgical procedures were performed on the right side in 55.56% of cases and on the left side in 44.44%. By one month, 44.4% reported full recovery, 33.3% reported moderate hypoesthesia, and 22.3% had mild hypoesthesia. At three months, 33.3% had full recovery, 55.6% experienced mild hypoesthesia, and 11.1% (1 patient) reported anesthesia. At six months, 88.9% had recovered, with only one patient (11.1%) still reporting anesthesia. A statistically significant difference in ND was observed across follow-ups at day one, week one, month one, month three, and month six (χ² = 30.3, p < 0.001). Pairwise comparisons revealed significant improvements from day one to month one (p = 0.03), day one to month three (p = 0.008), and day one to month six (p = 0.005), while the difference between day one and week one was not significant (p = 1.00). No significant correlations were found between ND recovery and patient age or membrane type at any follow-up interval (p > 0.05).

Conclusion

The study showed that IANL with immediate implant placement is an effective technique for rehabilitating atrophic posterior mandibles.

Trial registration

The study protocol has been registered in ClinicalTrials.gov (Identifier NCT07104994, 5/8/2025), and the date of registration was retrospectively determined.