Evaluation of A Single-Tooth Implant
Evaluation of A Single-Tooth Implant
Evaluation of A Single-Tooth Implant
Fifty-nine commercially pure titanium implants in 59 subjects were compared with internal con-
trol teeth for 3 years. Nineteen coated implants of identical design were placed in 17 of the sub-
jects and compared with the titanium implants. Demographic data, microbial DNA, aspartate
aminotransferase levels, Plaque Index, width of adjacent keratinized tissue, probing depths,
bleeding on probing, relative attachment levels, mobility, and radiographic bone height were
studied. The only statistically significant changes over time were improved plaque scores in the
subjects and slight bone loss around the implants. There were no differences between the 2
types of implants. Mobility was less and probing depth and bleeding on probing were greater in
the implant sites than in the control sites. (INT J ORAL MAXILLOFAC IMPLANTS 2000;15:396–404)
Key words: dental implants, dental radiography, oral diagnosis, patient satisfaction,
surface properties
times: at baseline and at 3, 6, 12, 18, 24, 30, and 36 Oral hygiene instructions were given to all sub-
months after final restoration. The patients’ age, jects during the first 2 visits (baseline and 3 months)
gender, medical conditions, history of smoking, and and then reinforced if needed throughout the 3
reason for tooth loss were noted. The time between years. Each patient received an ultrasoft manual
tooth loss and placement of the implant, placement toothbrush. Subjects with anterior implants were
of the implant and second-stage surgery, and sec- given Super Floss (Oral-B Laboratories, Belmont,
ond-stage surgery and final crown cementation were CA) for interproximal cleaning to protect the
recorded, as were the length and diameter of each height of the papillae. Individuals with posterior
implant. Implant placement sites were grouped into implants were instructed in the use of an interprox-
maxillary anterior, maxillary posterior, mandibular imal brush and sometimes Super Floss. On one
anterior, and mandibular posterior regions. The occasion in each of 2 patients, a universal scaler for
type of bone was classified as dense or porous by the dental implants (Steri-Oss, Yorba Linda, CA) was
surgeon. Complications encountered at the time of used to clean around the implant. With these 2
the 2 surgeries, during the postoperative healing exceptions, the implants and control teeth were not
period, at crown placement, and at any of the 8 data cleaned professionally during the 3 years of the
collection visits were noted, along with any correc- investigation. Polishing agents were never
tive intervention. A natural tooth (usually in the employed.
contralateral position to the implant) was selected to
serve as an internal control. Statistical Analyses
At each visit over the 3 years, the subjects were Descriptive statistics were used to analyze the study
asked about any change in health status and medica- material. Differences in change over time between
tions. They rated their satisfaction with the appear- each implant and its control tooth were studied
ance, the function, and the overall process of receiv- using paired t test and Chi-square analyses.
ing their implant(s) and crown(s) on a scale of 0 to Changes over time were studied for implants and
2, where 0 = not pleased, 1 = moderately pleased, teeth separately using 1-way analysis of variance
and 2 = very pleased. Possible altered sensation at (ANOVA) and Kruskal-Wallis non-parametric
the implant site was reported as none (0), mild (1), ANOVA. SPSS software version 8.0 (Chicago, IL)
moderate (2), or severe (3). Two sets of gingival was used for data analyses.
crevicular fluid samples were collected from each
implant and control tooth to determine aspartate
aminotransferase (AST) levels40 and DNA detection RESULTS
of Bacteroides forsythus, Porphyromonas gingivalis, and
Prevotella intermedia.41 One hundred ninety-two individuals were screened,
The following clinical data were recorded on the from whom 59 subjects were accepted for the
implants and control teeth. Probing depth (PD) and placement of a non-coated, commercially pure
relative attachment level (RAL) were measured on the grade 2 Ti implant. Nineteen HA-coated implants
mesiobuccal (MB), buccal (B), distobuccal (DB), and were placed in 17 of the same subjects. The
lingual/palatal (L) using an automated probe and an implants were placed in the following sites: 58%
automated attachment level probe (Florida Probe mandibular posterior, 26% maxillary anterior, 15%
Corp, Gainesville, FL), respectively, each calibrated maxillary posterior, and 1% mandibular anterior.
to 0.1 mm and a standardized pressure of 0.2 N. Six surgical sites exhibited a bony dehiscence or
Bleeding on probing (BOP), Plaque Index (PI),42 narrow alveolar housing that required regenerative
width in mm of B and L keratinized tissue, and procedures or splitting and expansion of the ridge.
mobility using the Periotest (Siemens, Bioresearch, Forty-eight of the implants had a diameter of 4.75
Milwaukee, WI) were also recorded. Baseline and mm; the other 30 were 3.75 mm in diameter. Rela-
annual periapical radiographs were taken of the tive to length, 42% were 10 mm, 37% were 13 mm,
implants and control teeth. Linear measurements and 21% were 16 mm long. An average of 7.3
were made on digitized images of the radiographs.43 months (8.2 months for the maxillary sites and 6.5
At baseline and years 1, 2, and 3, the amount of mesial months for mandibular sites) elapsed prior to surgi-
and distal radiographic bone change in mm was calcu- cal uncovering and attachment of the restorative
lated by comparing the distance from the apical mar- post and core. Temporary crowns were immediately
gin of the crown to the bone crest at implant sites. In placed on anterior implants; definitive crowns were
the case of control teeth, the measurements were cemented a mean of 8.5 weeks after second-stage
made between the bone crest and either the cemen- surgery.
toenamel junction or a crown margin.
For the tooth, the mean was 3.7 mm (SD 1.3) on control teeth ranged from –4 to +16. Most of the
the facial and 3.9 mm (SD 1.5) on the lingual. Sta- scores (92.4%) were in the –4 to +9 range, which,
tistical analyses (ANOVA) failed to demonstrate any when converted to Miller’s44 original classification
change in gingival width over time at either the for tooth mobility, equates with a “0” or “no distin-
implant or control sites. Statistical analyses failed to guishable movement.”45 In the remaining 7.6% of
demonstrate a relationship among gingival width, the teeth, the Periotest scores of +10 to +16 trans-
plaque scores, and BOP. late to a Miller’s class “1.” Mobility scores for the
Baseline and annual PD data for implants and implants ranged between –7 and +6. Thus, 100% of
control teeth are presented in Table 2. At baseline, the implants were within Miller’s “0” classification.
PD values were statistically significantly greater at The mean paired difference in the change in Peri-
the implant sites than at the corresponding control otest values over time between implants and teeth
tooth sites (P values varied between .001 and .05; was 1.6 units (SD 3.3; 95% confidence interval 0.5
independent t test). The mean PD difference was 0.4 to 2.6) and significantly different (t = 3.5; P < .001)
mm (t = 3.6, P < .001). At year 3, the PDs around the with a lesser degree of mobility for implants (Fig 2).
implants were statistically significantly greater than The Periotest data were analyzed to determine
around the control teeth. The mean PD difference whether there was a difference in the mobility scale
was 0.8 mm (standard error 0.1; 95% confidence among implants of different length. In the posterior
interval 0.5 to 1.0; t = 6.2; P < .001). When the regions at year 3, the 16-mm implants had a statisti-
changes over time for PD between implants and cally significantly lower Periotest reading than did
matched control teeth were compared, the mean the 10-mm implants (mean difference 4.2; P < .001,
paired difference in PD was 0.5 mm (SD 1.1; 95% one-way ANOVA, Bonferroni test), as well as the
confidence interval 0.2 to 0.8; t = 3.0; P < .01), with a 13-mm implants (mean difference 3.1; P < .01).
greater increase in PD at implant sites. The PD at Moreover, all of the 16-mm implants had a diame-
implant sites increased over time in 43 (73%) of the ter of 3.75 mm; the shorter implants were a mix of
cases. There was no statistically significant change in 3.75 mm and 4.75 mm. No differences in mobility
RAL at either the implant sites (F = 1.2; P < .3) or the were found between the 10-mm and 13-mm
tooth sites (F = 0.4; P < .9) between baseline and year implants. Relative to implant width and mobility,
3 (Fig 1). An increase in RAL ≥ 1 mm was found at 9 implants that were 13 mm long and 4.75 mm in
implant sites (15.3%) and 4 tooth sites (6.8%). diameter displayed statistically significantly lower
The Periotest has a range between –8 and +50, Periotest readings than did the implants that were
representing increasing mobility. The scores for the 13 mm long and 3.75 mm in diameter (P < .0001).
1.0 4
0.9 Control tooth Ti implant
Control tooth Ti implant 3
0.8
0.7
Mean RAL change (mm)
Fig 1 Changes in relative attachment level (RAL) in mm Fig 2 Mean Periotest scores for titanium implants and control
between baseline and years 1, 2, and 3 for titanium implants and teeth at baseline and years 1, 2, and 3. The instrument’s range is
control teeth. A positive value indicates a loss of attachment, and from –8 to +50. The lower (more negative) the score, the tighter
a negative value indicates a gain in attachment. the implant or tooth.
The lack of variation in implant length at anterior threshold value for evidence of disease activity.40
sites did not allow for similar comparison. These values were not consistently found at specific
sites and were equally distributed between the
Radiographic Bone Height implants and control teeth. The AST values failed
Radiographic bone height values for the implants to identify sites of changed RAL, PD, or radio-
and control teeth can be found in Table 2. Statistical graphic bone height.
analysis (one-way ANOVA) failed to demonstrate a Different models were used in regression analy-
difference over time for the control teeth. At Ti ses in an attempt to identify significant explanatory
implant sites, there was a statistically significant variables (eg, patient’s age or gender, reason for
change (loss) in bone height between baseline and tooth loss, time interval between tooth loss and
year 1 (mean difference at mesial sites 0.6 mm; stan- implant placement, surgical site) that were associ-
dard error 0.1; P < .01; and mean difference at distal ated with changes over time for radiographic bone
sites 0.7 mm; standard error 0.2; P < .001). There height or RAL measurements. No such variables
was no significant change between years 1 and 2, were identified.
years 1 and 3, or years 2 and 3.
Ti Versus HA Implants
Laboratory Data Nineteen Ti plasma-sprayed, HA-coated 6/4 Ti
The presence of P gingivalis, P intermedia, or B alloy implants were placed in 17 of the 59 patients
forsythus was found only once at 4 implants and 3 at the time of placement of the commercially pure
control teeth from more than 900 samples col- grade 2 Ti implants. The same clinical and labora-
lected. Mean baseline AST values were 170 µIU tory data were collected from the 19 HA-coated
(SD 145) for the implant sites and 186 µIU (SD implants over the 3 years of the investigation. The
129) for the control teeth. The corresponding val- 17 subjects were treated as a subgroup, and statisti-
ues after 3 years were 263 µIU (SD 213) and 299 cal analyses were performed to compare all of the
µIU (SD 300), respectively. The changes over time variables for the 2 types of implants. All of the
were statistically significant (F = 4.3; P < .001), coated implants were successfully integrated. Statis-
although not between implants and control teeth. tical analyses failed to demonstrate any differences
Only 2.4% of the AST samples demonstrated a in study outcomes between the 2 types of implants
value greater than 800 µIU, which is considered the for any of the parameters studied.
During the healing phase between first-stage and 35 µm of Ti plasma and 25 µm of porous HA were
second-stage surgeries, bone can re-form around the threaded, single-tooth, and the same dimensions.
collar and even cover the head of the implant. Jung et Comparisons were restricted to implants placed in
al53 have reported that regardless of implant design, the same patient. No differences were found in any
rapid alveolar bone loss will occur in the first 3 to 12 of the clinical or laboratory data. These data are
months after the placement of the second-stage abut- consistent with those of Evans et al,55 who com-
ment. This resorption continues until the apical mar- pared commercially pure Ti threaded implants and
gin of the polished neck or collar of the implant is HA-coated threaded implants of similar geometric
reached. Bone loss slows dramatically when contact is design and dimensions. They found no difference in
made with the first thread or area of surface rough- mobility, PD, percentage of osseointegration, or
ness.51,52 The design and vertical dimension of the crestal bone position.
collar therefore impacts the amount of initial bone The patients overwhelmingly responded that
loss. In the system under investigation, there is no they were “very pleased” with both the appearance
external hex. Moreover, the polished collar is the and the overall success of their restored implants.
same diameter as the outside dimension of the The only reported symptoms were “mild” altered
threads and is only 1 mm in height. Thus the sensation and were restricted to the first 3 months
omnipresent bone loss that occurs in the first year after cementation of the crown. The few subjects
should be restricted to 1 mm. The current data sup- who were “moderately pleased” with the surgical
port this. The crestal resorption, as measured radi- and restorative procedures and the function of their
ographically, was on average 0.6 mm on the mesial implants stated that the process had taken longer
surface of the implant and 0.7 mm on the distal, than they had expected or that the embrasure spaces
which is well within the 1-mm range (Table 2). between the implant and adjacent teeth were food
The radiographs of 6 patients displayed more traps. The only patients who ranked their cosmetic
bone loss on the mesial or distal of the implants satisfaction as “moderately pleased” had implants
than the norm. The person with the most loss was placed in mandibular posterior sites and received
a smoker and a recovering alcoholic and had an gold castings rather than ceramometal crowns.
allogenic bone graft and expanded polytetrafluo-
roethylene (e-PTFE) placed at the time of surgery
to cover exposed threads resulting from a thin CONCLUSIONS
alveolar housing. The only other smoker in the
study was also among the 6 subjects with greater The 3-year data of this prospective study suggest
bone loss. Two of the 6 were in orthodontic reten- that both types of implants (Ti and HA) were suc-
tion, having just completed active treatment to cre- cessful and functional, with a high degree of patient
ate space for an implant. In both, a facial dehis- acceptance. The implants were less mobile than the
cence was noted at the time of surgery, and a bone control teeth. The rest of the collected clinical data
graft and e-PTFE were placed. The fifth subject revealed some statistically significant differences (eg,
had undergone orthodontic therapy as a result of a PD and BOP) when the implants were compared to
congenitally missing mandibular second premolar. the control teeth, but none of the differences were
The surgeon described the bone as extremely soft, considered clinically significant. Radiographically,
and a pinhead-sized abscess occurred immediately slight bone loss was recorded on the mesial and dis-
postoperatively. The sixth patient’s implant, replac- tal surfaces of the implants in the first year; minimal
ing a maxillary central incisor that had been lost loss, if any, was noted over the next 2 years. The
because of facial trauma 30 years earlier, was in tested bacterial flora and AST levels of the peri-
close proximity to a large nasopalatine canal. Thus, implant tissues were consistent with healthy gingival
all 6 subjects presented with factors that potentially conditions. Among the important reasons for the
placed the implants at risk29–32 and may be useful high survival rate of the studied implants were the
considerations during treatment planning. Never- lack of a history of periodontal disease as the cause
theless, the subset of 6 implants displayed no of tooth loss and the excellent personal plaque con-
detectable mobility or other clinical signs for con- trol practiced by each subject.
cern after 3 years.
The influence of an implant’s composition and
surface texture on survival rates has been addressed
in numerous papers.36–39,54 In the current prospec-
tive investigation, both the commercially pure Ti
implants and the 6/4 Ti alloy implants coated with
ACKNOWLEDGMENTS 17. Silverstein LH, Kurtzman D, Garnick JJ, Schuster GS, Ste-
flik DE, Moskowitz ME. The microbiota of the peri-implant
The investigation was supported by the Elam M. and Georgina region in health and disease. Implant Dent 1994;3:170–174.
Hack Memorial Research Fund, Department of Periodontics, 18. Sordyl CM, Simons AM, Molinari JA. The microbial flora
University of Washington, and by the Regional Clinical Dental associated with stable endosseous implants. J Oral Implantol
Research Center, NIH/NIDR grant #P30 DE09743. The 1995;21:19–22.
authors would like to thank Dr Stan Sapkos of Genetic Implant 19. Kohavi D, Greenberg R, Raviv E, Sela MN. Subgingival and
Systems for placing the implants, Dr James W. Cherberg for supragingival microbial flora around healthy osseointegrated
fabricating the crowns, and Ms Teresa Oswald for performing implants in partially edentulous patients. Int J Oral Maxillo-
the laboratory tests. fac Implants 1994;9:673–678.
20. Meffert RM, Langer B, Fritz ME. Dental implants: A
review. J Periodontol 1992;63:859–870.
21. Thomas-Neal D, Evans GH, Meffert RM. Effects of various
REFERENCES prophylactic treatments on titanium, sapphire, and hydroxy-
apatite-coated implants: An SEM study. Int J Periodontics
1. Jaffin RA, Berman CL. The excessive loss of Brånemark fix- Restorative Dent 1989;9:301–311.
tures in Type IV bone: A 5-year analysis. J Periodontol 22. Rapley JW, Swan RH, Hallmon WW, Mills MP. The surface
1991;62:2–4. characteristics produced by various oral hygiene instruments
2. Haas R, Mensdorff-Pouilly N, Mailath G, Watzek G. Sur- and materials on titanium implant abutments. Int J Oral
vival of 1,920 IMZ implants followed for up to 100 months. Maxillofac Implants 1990;5:47–52.
Int J Oral Maxillofac Implants 1996;11:581–588. 23. Fox SC, Moriarty JD, Kusy RP. The effects of scaling a tita-
3. Listrom RD, Smith D, Symington JM. A clinical trial of a nium implant surface with metal and plastic instruments: An
new dental implant. J Can Dent Assoc 1996;62:785-208;794. in vitro study. J Periodontol 1990;61:485–490.
4. Block MS, Gardiner D, Kent JN, Misiek DJ, Finger IM, 24. Meschenmoser A, d’Hoedt B, Meyle J, Elssner G, Korn D,
Guerra L. Hydroxyapatite-coated cylindrical implants in the Hammerle H, Schulte W. Effects of various hygiene proce-
posterior mandible: 10-year observations. Int J Oral Max- dures on the surface characteristics of titanium abutments. J
illofac Implants 1996;11:626–633. Periodontol 1996;67:229–235.
5. Artzi Z, Tal H, Moses O, Kozlovsky A. Mucosal considera- 25. Dmytryk JJ, Fox SC, Moriarty JD. The effects of scaling
tions for osseointegrated implants. J Prosthet Dent 1993; titanium implant surfaces with metal and plastic instruments
70:427–432. on cell attachment. J Periodontol 1990;61:491–496.
6. Silverstein LH, Lefkove MD, Garnick JJ. The use of free 26. Kwan JY, Zablotsky MH, Meffert RM. Implant maintenance
gingival soft tissue to improve the implant/soft tissue inter- using a modified ultrasonic instrument. J Dent Hyg 1990;64:
face. J Oral Implantol 1994;20:36–40. 422–430.
7. Warrer K, Buser D, Lang NP, Karring T. Plaque-induced 27. Homiak AW, Cook PA, DeBoer J. Effect of hygiene instru-
peri-implantitis in the presence or absence of keratinized mentation on titanium abutments: A scanning electron
mucosa. An experimental study in monkeys. Clin Oral microscopy study. J Prosthet Dent 1992;67:364–369.
Implants Res 1995;6:131–138. 28. Matarasso S, Quaremba G, Coraggio F, Vaia E, Cafiero C,
8. Wennstrom JL, Bengazi F, Lekholm U. The influence of the Lang NP. Maintenance of implants: An in vitro study of tita-
masticatory mucosa on the peri-implant soft tissue condi- nium implant surface modifications subsequent to the appli-
tion. Clin Oral Implants Res 1994;5:1–8. cation of different prophylaxis procedures. Clin Oral
9. Apse P, Zarb GA, Schmitt A, Lewis DW. The longitudinal Implants Res 1996;7:64–72.
effectiveness of osseointegrated dental implants. Int J Peri- 29. Lindquist LW, Carlsson GE, Jemt T. Association between
odontics Restorative Dent 1991;11:95–111. marginal bone loss around osseointegrated mandibular
10. Mericske-Sterne R, Steinlin Schaffner T, Marti P, Gerring implants and smoking habits: A 10-year follow-up study. J
AH. Peri-implant mucosal aspects of ITI implants support- Dent Res 1997;76:1667–1674.
ing overdentures. Clin Oral Implants Res 1994;5:9–18. 30. Bain CA. Smoking and implant failure—Benefits of a smok-
11. Bauman GR, Mills M, Rapley JW, Hallmon WW. Plaque- ing cessation protocol. Int J Oral Maxillofac Implants 1996;
induced inflammation around implants. Int J Oral Maxillo- 11:756–759.
fac Implants 1992;7:330–337. 31. Gorman LM, Lambert PM, Morris HF, Ochi S, Winkler S.
12. Mombelli A, Van Oosten MAC, Schurch E, Lang NP. The The effect of smoking on implant survival at second-stage
microbiota associated with successful or failing osseointe- surgery: Dental Implant Clinical Research Group interim
grated titanium implants. Oral Microbiol Immunol 1987; report no. 5. Implant Dent 1994;3:165–168.
49:145–151. 32. De Bruyn H, Collaert B. The effect of smoking on early
13. Klinge B. Implants in relation to natural teeth. J Clin Peri- implant failure. Clin Oral Implants Res 1994;5:260–264.
odontol 1991;18:482–487. 33. Becker W, Becker B. Replacement of maxillary and
14. Mombelli A, Marxer M, Gaberthuel T, Grunder U, Lang mandibular molars with single endosseous implant restora-
NP. The microbiota of osseointegrated implants in patients tions: A retrospective study. J Prosthet Dent 1995;74:51–55.
with a history of periodontal disease. J Clin Periodontol 34. Balshi TJ, Wolfinger GJ. Two-implant-supported single
1995;22:124–130. molar replacement: Interdental space requirements and
15. Ong ES, Newman HN, Wilson M, Bulman JS. The occur- comparison to alternative options. Int J Periodontics
rence of periodontitis-related microorganisms in relation to Restorative Dent 1997;17:427–435.
titanium implants. J Periodontol 1992;63:200–205. 35. Sharifi MN, Pang LC, Chai J. Alternative restorative tech-
16. Mombelli A. Microbiology of the dental implant. Adv Dent niques of the CeraOne single-tooth abutment: A technical
Res 1993;7:202–206. note. Int J Oral Maxillofac Implants 1994;9:235–238.
36. Gher ME, Quintero G, Assad D, Monaco E, Richardson 46. Quirynen M, Listgarten M. The distribution of bacterial
AC. Bone grafting and guided bone regeneration for imme- morphotypes around natural teeth and titanium implants ad
diate dental implants in humans. J Periodontol 1994;65: modum Brånemark. Clin Oral Implants Res 1990;1:8–13.
881–891. 47. Apse P, Ellen R, Overall C, Zarb GA. Microbiota and crevic-
37. Wheeler SL. Eight-year clinical retrospective study of tita- ular fluid collagenase activity in the osseointegrated dental
nium plasma-sprayed and hydroxyapatite-coated cylinder implant sulcus: A comparison of sites in edentulous and par-
implants. Int J Oral Maxillofac Implants 1996;11:340–350. tially edentulous patients. J Periodont Res 1989;24:96–105.
38. Biesbrock AR, Edgerton M. Evaluation of the clinical pre- 48. Palmisano DA, Mayo JA, Block MS, Lancaster DM. Subgin-
dictability of hydroxyapatite-coated endosseous dental gival bacteria associated with hydroxyapatite-coated dental
implants: A review of the literature. Int J Oral Maxillofac implants: Morphotypes and trypsin-like enzyme activity. Int
Implants 1995;10:712–720. J Oral Maxillofac Implants 1991;6:313–318.
39. Quirynen M, Bollen CML, Willems G, van Steenberghe D. 49. Gatewood RR, Cobb CM, Killoy WJ. Microbial coloniza-
Comparison of surface characteristics of six commercially tion on natural tooth structure compared with smooth and
pure titanium abutments. Int J Oral Maxillofac Implants plasma-sprayed dental implant surfaces. Clin Oral Implants
1994;9:71–76. Res 1993;4:53–64.
40. Persson RG, DeRouen T, Page RC. Relationship between 50. DaSilva ID, Schnitman PA, Wöhrle PS, Wang HN. Influ-
levels of aspartate aminotransferase in gingival crevicular ence of site on implant survival: 6-year results [abstract
fluid and gingival inflammation. J Periodont Res 1990;25: 1200]. J Dent Res 1992;71:256.
17–24. 51. Adell R, Lekholm U, Rockler B, Brånemark P-I. A 15-year
41. Moncla BJ, Braham P, Persson RG, Page RC, Weinberg A. study of osseointegrated implants in the treatment of the
Direct detection of Porphyrmononas gingivalis in Macaca fasci- edentulous jaw. Int J Oral Surg 1981;6:387–416.
cularis in dental plaque samples using an oligonucleotide 52. Adell R, Lekholm U, Rockler B, Brånemark P-I, Lindhe J,
probe. J Periodontol 1994;65:398–403. Eriksson B, Sbordone L. Marginal tissue reactions at
42. Silness J, Loe H. Periodontal disease in pregnancy. II. Cor- osseointegrated fixtures. I. A three-year longitudinal
relation between oral hygiene and periodontal condition. prospective study. Int J Oral Surg 1986;15:39–52.
Acta Odontol Scand 1964;11:21–32. 53. Jung Y-C, Han C-H, Lee K-W. A 1-year radiographic evalu-
43. Jeffcoat MK. Radiographic methods for the detection of ation of marginal bone around dental implants. Int J Oral
progressive alveolar bone loss. J Periodontol 1992;63: Maxillofac Implants 1996;11:811–818.
367–372. 54. Jones JD, Saigusa M, Van Sickels JE, Tiner BD, Gardner
44. Miller SC. Textbook of Periodontia. Philadelphia: Blakiston WA. Clinical evaluation of hydroxyapatite-coated titanium
Company, 1938:91. plasma-sprayed and titanium plasma-sprayed cylinder dental
45. Schulte W, d’Hoedt B, Lukas D, Maunz M, Steppeler M. implants. A preliminary report. Oral Surg Oral Med Oral
Periotest for measuring periodontal characteristics—Corre- Pathol Oral Radiol Endod 1997;84:137–141.
lation with periodontal bone loss. J Periodont Res 1992;27: 55. Evans GH, Mandez AF, Caudill RF. Loaded and non-loaded
184–190. titanium versus hydroxyapatite-coated threaded implants in
the canine mandible. Int J Oral Maxillofac Implants 1996;
11:360–371.