immediate rehabilitation of the edentulous jaws with full fixed prostheses supported by four...

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Immediate rehabilitation of the edentulous jaws with full fixed prostheses supported by four implants: interim results of a single cohort prospective study Enrico Agliardi Stefano Panigatti Matteo Clerico ` Cristina Villa Paulo Malo ` Authors’ affiliations: Enrico Agliardi, Private Practice, Bollate, Milano, Italy Stefano Panigatti, Private practice, Milano, Italy Matteo Clerico `, Private practice, Arese (MI), Italy Cristina Villa, Private practice, Monza, Italy Paulo Malo `, MaloClinic, Lisbon, Portugal Correspondence to: Enrico Agliardi via Roma 15 20021 Bollate Milano, Italy e-mail: [email protected] Key words: dental implants, edentulous mandible, edentulous maxilla, immediate loading, tilted implants Abstract Objectives: The purpose of this study was to prospectively evaluate the clinical and radiographic outcomes of immediately loaded full-arch fixed prostheses supported by a combination of axially and non-axially positioned implants in a large cohort of patients with completely edentulous jaws, up to 5 years of function. Materials and methods: One hundred and seventy-three edentulous patients (80 males and 93 females) were enrolled according to specific selection criteria. Each patient received a full-arch fixed prosthesis supported by two distal tilted implants and two anterior axially placed implants. The provisional functional acrylic prosthesis was delivered the same day as surgery in all cases. All cases were finalized 4–6 months later. The patients were scheduled for follow-up at 6 and 12 months of function, and annually up to 5 years. At each follow-up plaque and bleeding score was assessed and radiographic evaluation of marginal bone level was performed. Results: The overall follow-up range was 4–59 months. A total of 154 immediately loaded prostheses (61 in the maxilla and 93 in the mandible) were in function for at least 1 year and were considered for the analysis. Four axially placed implants failed in the maxilla and one tilted implant in the mandible, all within 6 months of loading. No further implant failure occurred to date. Implant survival at 1 year was 98.36% and 99.73% for the maxilla and the mandible, respectively. Marginal bone loss at 1 year averaged 0.9 0.7 mm in the maxilla (204 implants) and 1.2 0.9 mm in the mandible (292 implants). No difference was found in marginal bone loss between axial and tilted implants. Plaque and bleeding scores progressively improved from 6 to 12 months. Fracture of the acrylic prosthesis occurred in 14% of total cases. Conclusions: The present preliminary results from a relatively large sample size suggest that the present technique can be considered a viable treatment option for the immediate rehabilitation of both mandible and maxilla. In the recent years, the immediate loading procedure for the rehabilitation of edentu- lous jaws using osseointegrated implants has gained popularity among clinicians. This was due to both the excellent success rates for several types of immediately loaded pros- thetic reconstructions, and the technical advantages and simplification introduced by such procedure as widely reported in previous reviews (Attard & Zarb 2005; Ioannidou & Doufexi 2005; Del Fabbro et al. 2006; Nkenke & Fenner 2006; Avila et al. 2007; Esposito et al. 2007; Jokstad & Carr 2007; Sennerby & Gottlow 2008). However, the rehabilitation of edentu- lous jaws is often complicated by poor bone Date: Accepted 5 September 2009 To cite this article: Agliardi E, Panigatti S, Clerico ` M, Villa C, Malo ` P. Immediate rehabilitation of the edentulous jaws with full fixed prostheses supported by four implants: interim results of a single cohort prospective study. Clin. Oral Impl. Res. 21, 2010; 459–465. doi: 10.1111/j.1600-0501.2009.01852.x c 2010 John Wiley & Sons A/S 459

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  • Immediate rehabilitation of theedentulous jaws with full fixedprostheses supported by four implants:interim results of a single cohortprospective study

    Enrico AgliardiStefano PanigattiMatteo Clerico`Cristina VillaPaulo Malo`

    Authors affiliations:Enrico Agliardi, Private Practice, Bollate, Milano,ItalyStefano Panigatti, Private practice, Milano, ItalyMatteo Clerico`, Private practice, Arese (MI), ItalyCristina Villa, Private practice, Monza, ItalyPaulo Malo`, MaloClinic, Lisbon, Portugal

    Correspondence to:Enrico Agliardivia Roma 1520021 BollateMilano, Italye-mail: [email protected]

    Key words: dental implants, edentulous mandible, edentulous maxilla, immediate loading,

    tilted implants

    Abstract

    Objectives: The purpose of this study was to prospectively evaluate the clinical and

    radiographic outcomes of immediately loaded full-arch fixed prostheses supported by a

    combination of axially and non-axially positioned implants in a large cohort of patients

    with completely edentulous jaws, up to 5 years of function.

    Materials and methods: One hundred and seventy-three edentulous patients (80 males and

    93 females) were enrolled according to specific selection criteria. Each patient received a

    full-arch fixed prosthesis supported by two distal tilted implants and two anterior axially

    placed implants. The provisional functional acrylic prosthesis was delivered the same day as

    surgery in all cases. All cases were finalized 46 months later. The patients were scheduled

    for follow-up at 6 and 12 months of function, and annually up to 5 years. At each follow-up

    plaque and bleeding score was assessed and radiographic evaluation of marginal bone level

    was performed.

    Results: The overall follow-up range was 459 months. A total of 154 immediately loaded

    prostheses (61 in the maxilla and 93 in the mandible) were in function for at least 1 year and

    were considered for the analysis. Four axially placed implants failed in the maxilla and one

    tilted implant in the mandible, all within 6 months of loading. No further implant failure

    occurred to date. Implant survival at 1 year was 98.36% and 99.73% for the maxilla and the

    mandible, respectively. Marginal bone loss at 1 year averaged 0.9 0.7mm in the maxilla

    (204 implants) and 1.2 0.9mm in the mandible (292 implants). No difference was found

    in marginal bone loss between axial and tilted implants. Plaque and bleeding scores

    progressively improved from 6 to 12 months. Fracture of the acrylic prosthesis occurred in

    14% of total cases.

    Conclusions: The present preliminary results from a relatively large sample size suggest

    that the present technique can be considered a viable treatment option for the immediate

    rehabilitation of both mandible and maxilla.

    In the recent years, the immediate loading

    procedure for the rehabilitation of edentu-

    lous jaws using osseointegrated implants has

    gained popularity among clinicians. This

    was due to both the excellent success rates

    for several types of immediately loaded pros-

    thetic reconstructions, and the technical

    advantages and simplification introduced

    by such procedure as widely reported in

    previous reviews (Attard & Zarb 2005;

    Ioannidou & Doufexi 2005; Del Fabbro

    et al. 2006; Nkenke & Fenner 2006; Avila

    et al. 2007; Esposito et al. 2007; Jokstad

    & Carr 2007; Sennerby & Gottlow 2008).

    However, the rehabilitation of edentu-

    lous jaws is often complicated by poor bone

    Date:Accepted 5 September 2009

    To cite this article:Agliardi E, Panigatti S, Clerico` M, Villa C, Malo` P.Immediate rehabilitation of the edentulous jaws withfull fixed prostheses supported by four implants: interimresults of a single cohort prospective study.Clin. Oral Impl. Res. 21, 2010; 459465.doi: 10.1111/j.1600-0501.2009.01852.x

    c 2010 John Wiley & Sons A/S 459

  • quality, especially in the posterior region,

    and reduced bone volume due to long-term

    edentulism. Bone grafting procedures to

    increase the bone volume available for

    implant placement may be a viable treat-

    ment option but they often imply demand-

    ing surgical procedures and can be

    associated to complications, morbidity

    and high costs. Therefore their acceptance

    by patients is often poor.

    In order to overcome such limitations,

    different therapeutic alternatives have been

    proposed, such as long distal cantilever

    (Shackleton et al. 1994), short implants

    (Goene et al. 2005; Renouard & Nisand

    2005; Malo et al. 2007) or implants placed

    in specific anatomical areas like, for the

    maxilla, the pterygoid region, the tuber or

    the zygoma (Bahat 1992; Khayat & Nader

    1994; Venturelli 1996; Balshi et al. 1999;

    Branemark et al. 2004; Galan Gil et al.

    2007; Aparicio et al. 2008; Malo et al.

    2008). Any of these procedures requires

    considerable surgical expertise and has its

    own advantages, limits, surgical risks and

    complications involving biological and fi-

    nancial costs.

    In the last years, several clinical studies

    have reported that tilting of the implants

    may represent another feasible treatment

    option (Krekmanov 2000; Krekmanov et

    al. 2000; Aparicio et al. 2001; Fortin et al.

    2002; Malo et al. 2003, 2005; Calandriello

    & Tomatis 2005; Capelli et al. 2007;

    Agliardi et al. 2008, 2009). Such technique

    is related to several surgical and prosthetic

    advantages, like the possibility of placing

    long implants with improvement of bone

    anchorage, the reduction of the need for

    bone grafting, the avoidance of long canti-

    levers and the possibility of increasing the

    distance between anterior and posterior

    abutments, with improvement of the load

    distribution.

    Furthermore, no difference in the mar-

    ginal bone loss between tilted and axially

    placed implants, placed in either jaw has

    been reported, suggesting that tilting of the

    implants causes no detrimental effect on

    the osseointegration process (Krekmanov

    2000; Aparicio et al. 2001; Capelli et al.

    2007; Koutouzis & Wennstrom 2007;

    Agliardi et al. 2009). A high degree of

    patient satisfaction was also reported as

    related to this clinical procedure (Capelli

    et al. 2007; Testori et al. 2008; Agliardi

    et al. 2009).

    The aim of this prospective study was to

    assess the clinical and radiographic out-

    come of immediately loaded full-arch fixed

    prostheses supported by a combination of

    axially and non-axially placed implants in a

    large cohort of patients with edentulous

    jaws, up to 5 years of function. This article

    reports preliminary data on implants survi-

    val and peri-implant bone loss.

    Materials and methods

    Study protocol

    Thiswas an open, single cohort prospective

    study in which patients with severely re-

    sorbed mandible or maxilla were consecu-

    tively enrolled and treated.

    The investigation was conducted accord-

    ing to the principles embodied in the

    Helsinki Declaration of 1975 for biomedi-

    cal research involving human subjects, as

    revised in 2004. At the preliminary visit all

    patients were duly informed on the nature

    of the study and on any possible alternative

    treatment. Before enrolment a written in-

    formed consent was obtained.

    Selection criteria

    Patients of any race and gender were in-

    cluded in the study if they were at least 18

    years old and in good general health condi-

    tion, physically and psychologically able to

    undergo conventional implant surgery and

    restorative procedures (ASA-1, ASA-2).

    Further inclusion criteria were: presence

    of atrophic fully edentulous mandible or

    maxilla, in need for bone augmentation

    procedures, or presence of teeth with an

    unfavourable long-term prognosis; rehabi-

    litation with oral implants was the elective

    treatment; patients manifested their prefer-

    ence for a fixed solution but were reluctant

    to undergo grafting procedures.

    Exclusion criteria were: presence of ac-

    tive infection or inflammation at the sites

    intended for implantation; presence of sys-

    temic diseases (i.e. haematologic disease,

    uncontrolled diabetes, serious coagulopa-

    thies and diseases of the immune system);

    irradiation to the head or neck region

    within 12 months before surgery; presence

    of unresorbed allograft at the implant site;

    severe bruxism or clenching habits; preg-

    nancy; poor oral hygiene; poor motivation

    to return for scheduled follow-up visits.

    Preliminary radiographic screening was

    performed using panoramic orthopantomo-

    graphs and computed tomography (CT)

    scans. A careful clinical examination of

    the patients was performed assessing jaw

    size and relations, bone volume and occlu-

    sal relations. Figs 1 and 2 show examples of

    a panoramic radiograph and a CT scan,

    respectively, for a patient included in the

    study.

    The included patients were treated in a

    dental clinic by a single surgeon (E.A.) with

    considerable clinical expertise in immedi-

    ate loading procedures.

    According to the above criteria from

    April 2004 to January 2009 a total of 173

    patients have been rehabilitated with an

    immediately loaded implant supported

    fixed full prosthesis supported by four im-

    plants in the mandible or in the maxilla. A

    total of 692 implants was inserted (404 in

    the mandible and 288 in the maxilla).

    Pharmacological treatment associated withsurgical procedure

    Antibiotic prophylaxis was prescribed 1h

    before surgery, consisting of 2 g of amox-

    icillin and clavulanic acid (Augmentins

    ,

    Roche S.p.A., Milan, Italy).

    Starting 3 days before surgery and then

    daily for 7 days following surgery, chlor-

    hexidine digluconate 0.2% mouthwash

    (Curasepts

    , Curaden HealthCare s.r.l.,

    Saronno, Italy) was prescribed. A sedative

    presurgery medication with 5mg i.v.

    Fig. 1. Pre-operative OPG.

    Agliardi et al Immediate loading in fully edentulous jaws

    460 | Clin. Oral Impl. Res. 21, 2010 / 459465 c 2010 John Wiley & Sons A/S

  • diazepam (Valiums

    , Roche S.p.A.) was

    administered.

    Implant surgery was performed using lo-

    cal anaesthesia with articaine chlorhydrate

    4% and epinephrin 1 : 100,000 (Alfacaina

    N, Weimer Pharma, Rastat, Germany).

    Corticosteroids (dexamethasone 4mg,

    Soldesams

    , Laboratorio Farmacologico

    Milanese S.r.L., Milano, Italy), anti-in-

    flammatory drugs (ketorolac trometha-

    mine 30mg, Lixidols

    , Roche S.p.A.)

    and anti-acidity drugs (ranitidine, Zantacs

    50mg, Glaxo Wellcome S.p.A., Verona,

    Italy) were given during the surgery.

    Surgical procedure for the mandible

    A crestal incision was made from the first

    molar region to the contralateral side. The

    incision started on the lingual side of the

    crest, and was as smaller as possible in

    order to preserve vascularization as much

    as possible and reduce the patient discom-

    fort. A full-thickness buccal flapwas raised

    exposing the vestibulary bony wall.

    After flap reflection and detection of the

    mental foramina, the length of the mental

    nerve loop and the shape of the bone were

    assessed, using an atraumatic instrument,

    in order to determine the ideal angulation

    of the posterior implants.

    Soon before implants placement all com-

    promised teeth were extracted, when pre-

    sent, and sockets were carefully debrided.

    All patients received four intraforaminal

    implants (Branemark Systems

    MKIV or

    NobelSpeedyt Groovys

    , Nobel Biocare

    AB, Goteborg, Sweden). At first the two

    distal tilted fixtures were placed. The

    drill was inserted crestally in correspon-

    dence with the alveolar nerve foramen

    and tilted by about 301 relative to theocclusal plane. Thereafter, the two mesial

    fixtures were inserted at the level of the

    lateral incisors.

    Bone density was assessed by the clin-

    ician during the early phase of drilling and

    scored according to the Lekholm and Zarb

    classification (Lekholm& Zarb 1985). The

    implant site was usually under prepared by

    avoiding countersink, so as to maximize

    implant stability.

    A torque controller (Osseocares

    , Nobel

    Biocare AB) with a torque limit of 50Ncm

    was used during implant placement. A

    manual wrench was also used in case of

    incomplete seating of the fixture.

    Multi-unit abutments (MUAs

    , Nobel

    Biocare AB) were connected to the im-

    plants. On the distal fixtures abutments

    with an inclination of 301 relative to thefixture axis were placed (n 202), to allowfor an optimal prosthetic screw access,

    while standard abutments were placed

    over themesial fixtures (n 202). A torquecontroller (Osseocare

    s

    , Nobel Biocare AB)

    with a torque limit of 50Ncm was used to

    tight abutment screws at 25Ncm.

    Surgical procedure for the maxilla

    A crestal incision was performed starting

    from the pterygomaxillary region and a

    mucoperiosteal buccal flap was raised ex-

    posing the vestibular bony wall so as to

    identify the anterior wall of the maxillary

    sinus.

    The most distal implants were firstly

    placed, engaging the anterior wall of the

    maxillary sinus. They were inserted with

    an angulation of about 30451 relative tothe occlusal plane. In order to control if the

    implant site was entirely bordered by bone

    and to assess the proper axis of the drill, a

    direction pin was positioned into the im-

    plant site before fixture insertion and a

    radiograph taken. In case of risk of perfora-

    tion of the sinus membrane, the drilling

    axis was corrected. The two axial implants

    were then inserted in the lateral incisors

    position. All the implant sites were under-

    prepared avoiding countersinking so as en-

    gage as much cortical bone as possible.

    Multi-unit abutments (MUAs

    , Nobel

    Biocare AB) were connected to the im-

    plants. On the distal fixtures, abutments

    with an inclination of 301 relative to thefixture axis were placed (n 144), whilestandard (n 127) or 171 (n 20) abut-ments were placed over the mesial fixtures

    (n 202). The same torque controller usedfor mandible was used to tight abutment

    screws at 25Ncm.

    Delivery of the provisional prosthesis

    After positioning the coping, the soft tis-

    sues were sutured with a 5-0 resorbable

    suture (monocryl or vicryl, Johnson

    & Johnson Intl., St Stevens, Woluwe,

    Belgium) and an impression was taken by

    means of a silicon putty (Elite Implant

    Impression Material, Zhermack S.p.A.,

    Badia Polesine, Italy) directly on the cop-

    ing. Healing capswere then positioned over

    the multi-unit abutments.

    Fig. 2. Pre-operative CT-Scan.

    Agliardi et al Immediate loading in fully edentulous jaws

    c 2010 John Wiley & Sons A/S 461 | Clin. Oral Impl. Res. 21, 2010 / 459465

  • No later than 3h of surgery an acrylic

    provisional prosthesis with 10 teeth was

    delivered. Again a torque controller was

    used to tight prosthetic screws at 15Ncm.

    Centric and lateral contacts were limited

    to the intercanine zone. An orthopantomo-

    graph was made to check implant position

    and the coupling between prosthetic com-

    ponents (Fig. 3).

    Post-surgical phase

    After surgery patients were instructed to

    avoid brushing and any trauma to the

    surgical site. Cold food was suggested for

    the first day and a soft diet for the first

    week. Pain killers (sodium naproxene,

    Synflex Fortes

    , Recordati, Milano, Italy)

    were prescribed in case of pain.

    After 46 months of function, in the

    absence of pain and inflammation, the

    patients underwent the final prosthetic

    protocol. The final prosthesis was fabri-

    cated using the CAD-CAM Proceras

    Sys-

    tem (Nobel Biocare, Stockholm, Sweden)

    (Fig. 4).

    Variables assessed

    The following outcome measures were

    evaluated in this study:

    (a) Implant survival: Implant functional

    and stable (the stability of individual

    implantswas tested using two opposing

    instruments pressure after unscrewing

    the prosthesis), no peri-implant radiolu-

    cency on radiographs, no suppuration

    or pain at the implant site, no signs of

    peri-implantitis, no neuropathies or

    persistent paraesthesia.

    (b) Marginal bone level: All radiographs

    were scanned at 600 dpi with a scan-

    ner and the marginal bone level (the

    most coronal bone-to-implant con-

    tact) was assessed onmesial and distal

    aspects using an image analysis soft-

    ware. The implant neck was the re-

    ference for each measurement. Mesial

    and distal values were averaged so as

    to have a single value for each im-

    plant.

    (c) Plaque index and bleeding index:

    Every implant was inspected on four

    sites. The sites in which plaque or

    bleeding could be detected were re-

    corded as positive or negative, as de-

    scribed previously (Francetti et al.

    2008).

    (d) Prosthesis success (i.e. prosthesis

    functional and stable): A prosthesis

    was considered failed if the function

    was compromised for any reason.

    All biological complications such as peri-

    implantitis, periimplant mucositis, bleed-

    ing on probing, suppuration, fistulas,

    abscesses numbness of the lower lip or

    chin, as well as mechanical or prosthetic

    complications, like fracture of the implant

    or of any prosthetic component, were re-

    corded.

    Follow-up

    During the first month after surgery the

    patients were seen once a week for control

    visits, in which tissue healing and prosthe-

    sis function were evaluated. Further visits

    were scheduled at 6 and 12 months and

    yearly thereafter up to 5 years.

    During the first year plaque index and

    bleeding index were assessed every 6

    months. Orthopantomographs and, when

    possible, periapical radiographs were taken

    at any scheduled control visit to assess the

    marginal bone loss and the overall bone

    level throughout the study. Fig. 5 shows

    OPT follow-up.

    At the 1-year control visit stability of the

    implants and prosthesis as well as proper

    occlusion were also checked.

    Data analysis

    Cumulative implant survival rate was as-

    sessed using the KaplanMeier statistics

    Fig. 3. Post-surgical OPG.

    Fig. 4. Final prosthesis.

    Fig. 5. OPG with final prosthesis.

    Agliardi et al Immediate loading in fully edentulous jaws

    462 | Clin. Oral Impl. Res. 21, 2010 / 459465 c 2010 John Wiley & Sons A/S

  • (life table analysis). Marginal bone loss

    around axially placed and tilted implants

    was compared using paired Students t-test.

    For the analysis of the plaque and bleeding

    index the Pearson w2-test was used.P 0.05 was considered as the significancelevel.

    Results

    A total of 692 implants (92 Branemark

    System MKIV and 600 Nobel Speedy

    Groovy, all with TiUnite surface) were

    placed in 173 patients [80 males and 93

    females, mean age at surgery 57.3 8.5(SD) years, range 4274 years]. Forty-eight

    of the included patients (27.8%) were smo-

    kers. Seventy-two maxillary and 101 man-

    dibular prostheses were delivered. All

    prostheses were supported by four im-

    plants. All implants could be seated with

    an insertion torque of at least 30Ncm. All

    provisional prostheses could be delivered

    the same day of surgery as planned.

    Implant distribution according to im-

    plant type and implant length is detailed

    in Tables 1 and 2, respectively.

    The outcome analysis is based on those

    154 patients (89% of total patients treated)

    that have had their prosthesis in function

    for at least 1 year at the time of the present

    clinical report.

    Ninety-three prostheses (372 implants)

    were immediately loaded in the mandible.

    The follow-up range was 1255 months

    (mean value 26.9 12.5m). Patients haddifferent types of opposing dentition: remo-

    vable prostheses (50 cases), natural teeth

    (15 cases), natural teeth and fixed pros-

    theses on natural teeth (12 cases), fixed

    prostheses on natural teeth (three cases),

    implant-supported bridges (nine cases),

    natural teeth and two implant-supported

    bridges (four cases).

    Sixty-one prostheses (244 implants)

    were immediately loaded in the maxilla.

    The follow-up range was 1259 months

    (mean value 31.3 14m). The opposingdentitions were implant-supported fixed

    prostheses (25 cases), removable prostheses

    (22 cases), natural teeth (nine cases) and

    fixed prostheses on teeth (five cases).

    No complications occurred during the

    surgical phase. None of the patients reported

    any post-surgical biological complication.

    Four axially placed implants in the max-

    illa (in four female patients) and one tilted

    implant in the mandible (in one male

    patient) failedwithin 6 months of function,

    due to mobility. In all cases implant failure

    did not compromise prosthesis function.

    All implants could be successfully re-

    placed. No late failures have been recorded

    to date. No relation was found between

    implant failure and the opposing dentition.

    The overall cumulative implant survival

    after 1 year was 99.19% (98.36% and

    99.73% for implants placed in the maxilla

    and mandible, respectively, as shown in

    the two life table analyses of Tables 3 and 4

    that include only cases with more than 1-

    year follow-up).

    The only prosthetic complication in this

    study was the fracture of the acrylic pros-

    thesis that occurred in 24 cases (15.6%), of

    which 14 in the mandible (15%) and 10 in

    the maxilla (16.4%).

    The average marginal bone loss after 1

    year from implant placement was

    0.9 0.7mm in the maxilla (204 im-plants in 51 patients) and 1.2 0.9mmin the mandible (292 implants in 73 pa-

    tients). Such differencewas not statistically

    significant. No significant differences in

    bone loss were found between axially

    placed and tilted implants.

    A progressive decrease in plaque and

    bleeding scores was observed in the first

    year.

    Plaque index averaged 29.1% at 6

    months (from 153 patients) and 20.7% at

    12 months (from 124 patients); bleeding on

    probing averaged 7.4% at 6 months and

    2.6% at 12 months. The improvement at

    12 months was statistically significant for

    both indexes.

    Discussion

    This prospective study aimed at evaluating

    the clinical and radiographic outcomes of a

    technique for the immediate rehabilitation

    of patients with edentulous jaws. The pre-

    liminary results indicate that such techni-

    que may lead to excellent prognosis, at

    least in the short term. To our knowledge,

    this is the largest prospective study on

    patients treated using a combination of

    axially placed and tilted implants in either

    jaw.

    The excellent results of the present study

    are well comparable with previous retro-

    spective (Malo` et al. 2003, 2005) and pro-

    spective single cohort studies (Capelli et al.

    2007; Agliardi et al. 2008, 2009; Testori et

    al. 2008) that adopted similar techniques.

    Indeed, in some of these prospective reports

    (Capelli et al. 2007; Agliardi et al. 2008,

    2009; Testori et al. 2008), six implants

    instead of four were used for the immediate

    maxillary rehabilitation. Furthermore, a

    different implant system was adopted in

    two of these studies (Capelli et al. 2007;

    Testori et al. 2008), with a different type

    and angulation of the implantabutment

    connection for the tilted implants, and also

    a different technique for the fabrication of

    the final prosthesis.

    The incidence of fracture of the acrylic

    prostheses in the present study (15.6% of

    the total cases) was lower as compared

    with that reported by Malo et al. (2003)

    (27%), and similar to that previously re-

    ported by Francetti et al. (2008) and

    Agliardi et al. (2008) (11%). This compli-

    cation was observed mainly in men with a

    short face morphotype, usually between 3

    and 6 months of function. It could be

    hypothesized that a possible cause for

    such trouble was the progressive modifica-

    tion of the diet, from a diet consisting of

    Table1. Implant distribution according tothe implant type

    Maxilla Mandible Total

    MKIV 44 48 92Speedy groovy 244 356 600Total 288 404 692

    Table2. Implant distribution according to the implant length

    18mm 15mm 13mm 11.5mm 10mm 8.5mm Total

    Number of implants (% maxilla) 18 (6.25) 164 (56.94) 49 (17.01) 40 (13.88) 17 (5.91) 0 288 (100)Number of implants (% mandible) 0 210 (51.98) 101 (25) 53 (13.11) 28 (6.93) 12 (2.98) 404 (100)Number of implants (% total) 18 (2.6) 374 (54.05) 150 (21.68) 93 (13.44) 45 (6.5) 12 (1.73) 692 (100)

    Agliardi et al Immediate loading in fully edentulous jaws

    c 2010 John Wiley & Sons A/S 463 | Clin. Oral Impl. Res. 21, 2010 / 459465

  • soft food to a one including hard food.

    Another factor in the genesis of provisional

    prosthesis fracture could be the progressive

    wear of the resin due to repeated degluti-

    tion and mastication cycles. It was noted

    thatmost of the fractures took place next to

    one of the anterior temporary abutments,

    which is a weak point of the prosthetic

    reconstruction. All the fractures had been

    promptly repaired by the clinician without

    sending the prostheses back to the labora-

    tory, thereby avoiding further discomfort to

    the patient. No correlation between these

    fractures and the type of opposing dentition

    could be found.

    For the rehabilitation of the edentulous

    mandible and maxilla, especially in those

    cases of extremely reduced posterior ridges,

    the ideal approach should endeavour at the

    following: minimization of the total num-

    ber of implants to decrease surgical mor-

    bidity, reduction of the distal cantilever

    without compromising the functional sup-

    port, avoidance of demanding bone grafting

    procedures and decrease of total treatment

    time and costs. The latter item may be

    achieved by adopting an immediate loading

    protocol. Another predictable and cost-

    effective solution for the immediate reha-

    bilitation of the fully edentulous mandible

    can be represented by implant-supported

    overdentures (Bryant et al. 2007). How-

    ever, due to their partial mucosal support

    in the posterior regions, patients with ex-

    tremely reduced posterior mandible might

    experience pain due to compression of the

    retroforaminal zones during mastication.

    With the present protocol the level of

    patients satisfaction was very good, post-

    surgical discomfort was limited and an

    immediate recovery of mastication and

    aesthetic function could be provided. In

    general, the treatment acceptance by pa-

    tients was extremely favourable.

    The progressive reduction of plaque and

    bleeding scores reflected a good compliance

    of the patients to the oral hygiene instruc-

    tions. In this instance, the role of the dental

    hygienist could be of utmost importance,

    not only for the professional cleaning but

    also for its active role in patients education

    and motivation.

    Concluding remarks

    The results of the present prospective study

    show that a combination of axially placed

    and tilted implant for the immediate reha-

    bilitation of edentulous jaws leads to ex-

    cellent clinical outcomes. The advantages

    of the immediate loading procedure, the

    reduced morbidity, the high patients

    satisfaction and the relatively low costs of

    this surgical technique should be taken

    into account when a decision among the

    alternative therapeutic options has to be

    made.

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