Implant Tribune Middle East & Africa Edition | 06/2023 C3 IMPLANT TRIBUNE Extra-shor t and u ltra-shor t im plants in tran screstal sinu s lift with autologou s bone obtained from dr illin g as graftin g m ater ial Retrospective study By Dr Eduardo Anitua, Spain Introduction Sinus elevation, both through the lateral approach and the transcr- estal approach, is one of the most widely used techniques for the reha- bilitation of the posterior maxillary area with dental implants when this area is atrophic in height.1-3 Both techniques have a long history with multiple publications in the interna- tional literature that endorse their use, with success rates for implants placed by both methods of 96.9% success when placed directly (at the same time as the elevation proce- dure) and 97% when placed after the height recovery process (in the case of lateral sinus elevation exclusively).4 In most of the articles that analyze the indications for each of the two surgical procedures—transcrestal or lateral elevation—they recommend the use of the conventional lateral window when there is less than 5 mm of residual bone height or the exist- ing bone volume presents low den- sity with diffi culty in stabilizing the dental implant. In the rest of the sit- uations, transcrestal elevation would be indicated, there being therefore a range of clinical cases where both techniques would be indicated.1-8 If both techniques are indicated, it is usual to select the one that presents the least morbidity for the patient, which is why the transcrestal eleva- tion technique is gaining importance nowadays. In order to make its use increasingly safe and predictable, the neoalveolar genesis protocols have been modifi ed (diff erent drill- ing protocols and drills) as well as the morphology of the implants and their surface, allowing better primary stability in more extreme situations and faster integration for more com- plex cases.9-12 Our study group has described a variation of the conventional transcr- estal elevation technique described by Summers in 199413 in which a bio- logical drilling procedure (at low rev- olutions) is used to create the alveo- lus where the implant will be placed, and the fi nal portion of the sinus fl oor is removed using a front cutting drill.10,12,14-16 This drill is atraumatic and allows gradual wear of the sinus cortex with a low risk of perforation of Schneider's membrane. Further- more, both procedures, when per- formed at low revolutions without ir- rigation (normal and cortical drilling), allow us to harvest all the bone dis- lodged from the crest to subse- quently form a particulate bone graft, which can sometimes even be the only graft material to be placed in the elevation, embedded in PRGF-Endoret14 from the time of har- vesting. With this procedure based on the density of the receptor bed, the morphology of the implant, and a meticulous analysis of each clinical situation, the placement of ex- tra-short implants has been achieved by means of transcrestal elevation in residual bone height of less than 5 mm, which is the limit recom- mended by most studies for using this procedure, without renouncing the predictability of treat- ment.10,12,15,16 In the following retrospective study, the survival of extra-short (5.5 and 6.5 mm) and ultra-short (4.5 mm) implants inserted using the previously described transcrestal el- evation technique, with autologous bone obtained from drilling as the only grafting material, was assessed as the main variable. As secondary variables, mesial and distal crestal bone loss after loading and the maintenance of bone volume achieved at the implant apex after loading were assessed. the Material and methods We reviewed retrospectively the clinical histories of patients undergo- ing transcrestal sinus lift with the in- sertion of extra-short and ultra-short implants with autologous bone ob- tained from the drill itself as grafting material in the period between No- vember 2019 and November 2021. The data were collected in a data col- lection notebook for subsequent statistical analysis, the main variable of the study being the survival of the implants placed using this technique, and the secondary variables being the measurement of crestal bone loss (mesial and distal), bone gain at the apex of the implant, and its main- tenance after functional loading of the implant. Diagnostic and surgical proto- col All patients were studied prior to implant insertion by means of diag- nostic models, intraoral exploration, and a dental CT scan (Cone-beam) subsequently analyzed using specifi c software (BTI-Scan III). Prior to im- plant insertion, antibiotic pre-medi- cation consisted of amoxicillin 2g orally one hour before surgery and paracetamol 1g orally (as an analge- sic). Subsequently, patients were treated with amoxicillin 500-750 mg orally every 8 hours (according to weight) for 5 days. The implants were placed by the same surgeon, using the biological drilling technique, at low revolutions, without irrigation, collecting all the bone and keeping it in PRGF-Endoret (fraction 2 without activation) until it was used as a particulate graft for transcrestal elevation.10 The fi nal milling of the sinus cortex is carried out with the frontal cutting drill (de- signed for this technique, as de- scribed above), which allows us to re- move the fl oor of the maxillary sinus by progressive wear without damag- ing Schneider's membrane. Once the membrane is accessible through the crestal perforation, it is carefully re- moved with a blunt instrument that allows the graft and the implant to be placed without generating exces- sive pressure on it. Once this maneuver has been carried out, the implant is inserted with the surgical motor set at 25 Ncm and 25 rpm, fi nalizing the insertion of the implant with the torque spanner. The drilling is adapted to achieve correct primary stability, considering the density of the area and the resid- ual bone volume. The implant slowly lifts the membrane as it is inserted into the neo-alveolus and contains between the apex and the mem- brane the bone graft which will be the volume to be increased added to the total length of the implant. Follow-up visits Patients are subsequently seen for intraoral radiographs with a con- trol parallelizer, and the necessary measurements are taken on these radiographs to check the stability and crestal bone loss of the implants. Once the radiograph was obtained in digital format, it was calibrated using specifi c software (Digora for Win- dows, SOREDEX Digital Imaging sys- tems) through a known length in the radiograph such as the dental im- plant. Data collection was carried out by two independent examiners. Statistical analysis Medical records were reviewed to obtain demographic, social, pres- ence of parafunctions, and medical data of interest. The implant was the unit of analysis for descriptive statis- tics in terms of location, implant di- mensions, and radiographic mea- surements. The patient was the unit of measurement for the analysis of age, sex, and medical history. A Shapiro-Wilk test was per- formed on the data obtained to ver- ify the normal distribution of the sample. Qualitative variables were described by frequency analysis. 1 Fig. 1: Implants included in the study according to diameter and length. The po- sitions of the inserted implants varied from second premolar to third premolar. 2 Fig. 2: Positions of the implants included in the study, where we observe that the right and left fi rst molars and the right second molar are the most frequent. 3 Fig. 3: Bone type and different lengths of residual ridge with a similar distribution in both groups. Quantitative variables were de- scribed by mean and standard devi- ation. Implant survival was calculated using the Kaplan-Meier method. The diff erence between the apical bone volume at the time of surgery (sum of implant and bone graft over the apex) and the fi nal bone volume after loading was compared using a Student's t-test. Data were analyzed with SPSS v15.0 for Windows (SPSS). Statistically signifi cant diff erences were considered to exist when p<0.05. Results Seventeen patients were re- cruited, and 25 implants were in- serted that fulfi lled the above-men- tioned inclusion criteria. Forty-eight percent of the patients were female, and the mean age of the study group was 56 +/- 13.35 years. The length of the implants included in the study the most was 6.5 mm in 12% of cases, 5.5 mm in 12% of cases, and 4.5 mm in 76% of cases. The diameter ranged from 2.5 mm to 6 mm maximum diameter, with frequent being 4.75 mm in 36% of cases, followed by 4.25 mm in 24% of cases. All the diam- eters of the implants analyzed ac- cording to their length (Fig. 1). The most commonly rehabilitated posi- tions were 16, 17, and 26, each ac- counting for 28% of the cases. The re- maining positions with their fre- quency (Fig. 2). The mean bone height of the re- sidual ridge was 4.34 mm (+/- 0.78), with a range between 3.18 and 6.37 mm in the sample. The bone type was III in 52% of the cases and IV in the remaining 48%. The height distribu- tion between the two bone types was ▶ Page C4