Secondary Logo

Journal Logo

Clinical Science and Techniques

Medical Contraindications to Implant Therapy: Part I: Absolute Contraindications

Hwang, Debby DMD*; Wang, Hom-Lay DDS, MSD

Author Information
doi: 10.1097/01.id.0000247855.75691.03
  • Free

Abstract

In order to ensure implant success, it is necessary to select patients who do not have local or systemic contraindications to therapy. Failure may arise from 3 major etiologies: impaired host healing, disruption of a weak bone-to-implant interface after abutment connection, and infection.1 The intrinsic ability of a patient to retain an implant relies on his or her health status. Jolly2 described dental care modification with respect to medical risk assessment as defined by the American Society of Anesthesiologists; a summary appears in Table 1.

Table 1
Table 1:
ASA Status and Dental Care Alterations2

A retrospective analysis of Veterans Administration registry data demonstrated that surgical and healing complications, as well as patient medical status (i.e., medical history, American Society of Anesthesiologists’ level, medication history), correlated with implant failure.3 Smith et al,4 on the other hand, detected no statistically significant association between compromised medical status with perioperative morbidity or failure of implants in 104 patients. These studies differ in the type of medical conditions and degree of disease control included in analysis. It is obvious that incongruous reports exist in the dental literature as to the extent of systemic factor influence on clinical implant failure; the fact that medical status may influence success is not in dispute.

Despite the functional and emotional toll edentulism wreaks on a person, implant therapy remains elective treatment. For any noncompulsory surgery, there exist certain minimal thresholds that cannot be crossed. Absolute contraindications will, if ignored, jeopardize the overall health of a patient. Those with uncontrolled or unknown but suspected metabolic illnesses necessitate an immediate medical consultation prior to dental care. Some of these problems, however, are self-limiting or treatable, so elective oral procedures may be possible in the future. This manuscript reviews medical conditions that categorically preclude implantation and, in some cases, threaten life if unaddressed.

Recent Myocardial Infarction or Cerebrovascular Accident

Given an adequate amount of time, ischemia to the heart or the brain generates necrosis and functional deficits. With intervention and a healing period of roughly 6–12 months after preliminary care, patient stability occurs. In the interim period and for 3–6 months after initial stability, it is necessary to avoid any stress, including surgical, that could trigger post-ischemia complications. About 75% of patients who had a myocardial infarction experience further complications, often within hours or days after the incident, that range from cardiogenic shock or “pump failure,” arrhythmias (e.g., sinus bradycardia, premature ventricular contractions, ventricular tachycardia, ventricular fibrillation, asystole), myocardial rupture, pericarditis, or chronic ischemic heart disease, which is progressive heart failure.5 In regard to a cerebrovascular accident, or ischemic stroke, 15% of patients die within the first 3 months.6 Functional recovery occurs within the first month but may continue up to a year following the incident. During that time, complications arise, including recurrent stroke, rebleeding in the case of aneurysm, cerebral vasospasm, seizures, hydrocephalus, and hyponatremia.6

Due to the high risk of complications following a myocardial infarction or cerebrovascular accident, the dental provider must wait until preliminary stabilization. The patient may pursue elective dental care only if at least 6 months have passed since the ischemic incident and he or she obtains medical clearance. The health care professional must be aware of any anticoagulant or thrombolytic therapy administered and understand that the desire for oral implants does not necessarily justify interruption of a therapeutic international normalized ratio (INR).

Valvular Prosthesis Placement

Repair of cardiac or vascular defects with autografts or particular materials often become completely encased in endocardium or endothelium within the first month, rendering them relatively impervious to bacterial seeding. Not all materials consistently become fully covered (e.g., polyethylene terephthalate [Dacron®; INVISTA, Wichita, KS]), depending on morphology, location, or inherent constitution, and possible risks from exposure include endocarditis or endarteritis. Especially prone to microbial infection, prosthetic valves restore function to those with progressive congestive heart failure, systemic emboli, or endocarditis.7 Three forms of prosthetic valve exist: bioprostheses, mechanical valves, and homografts or autografts. All but the autograft fall subject to endocarditis, as well as regurgitation, stenosis, and degeneration. The prevalence of prosthetic valve endocarditis hovers around 1% to 3%, and the greatest risk occurs within the first 3 months.8 By 6 months, the prosthetic valve endocarditis rate drops to 0.4%. Early seeding arises because as soon as implantation takes place, fibrin and platelet thrombi aggregate at the surgical site (sewing ring and annulus), attracting microbes from intraoperative contamination. With time, endothelialization progresses, sealing the prosthesis off from infective organisms, and, thus, lowering risk. Staphylococcus epidermidis, other coagulase-negative staphylococci, Staphylococcus aureus, and fungi cause early onset prosthetic valve endocarditis; bacteria responsible for native-valve endocarditis, Staphylococcus viridans and its α-hemolytic streptococci brethren, lead to late-onset prosthetic valve endocarditis.

With prosthetic valve replacement, stability occurs at least 6 months to 1 year after cardiac surgery.7,8 Avoidance of invasive periodontal procedures is mandatory in order to prevent bacteremia and possible subsequent valve loss. Depending on the type of valve used (mechanical or bioprosthesis [porcine]), the patient requires different drug regimens (anticoagulants or plasma volume elevators, respectively).7 Any dental treatment must take such medications into consideration.

Bleeding

If proper hemostasis cannot occur, elective surgery must not take place. A loss of 500 mL of blood requires volume replacement.9 Uncontrolled hemorrhage stems from a multitude of conditions, including platelet and clotting factor disorders, but often originates from drug therapy. Patients taking oral anticoagulants (e.g., aspirin, warfarin, clopidogrel, among others) for cardiovascular maladies must receive careful supervision of bleeding time and INR. Little risk of significant bleeding following dental surgical procedures in patients with a prothrombin time of 1.5–2 times is normal.10 Fazio and Fang11 suggested an INR of 2.2 or lower for surgical procedures. The medical literature, however, proposes that a patient with an INR of 3 or less tolerates invasive oral therapies, including extractions; tranexamic acid or epsilon amino caproic acid may be used to treat residual hemorrhage.12 If for some reason, the INR must be kept higher, elective implant treatment is inappropriate.

A lack of platelets due to infection, idiopathic thrombocytopenia purpura, radiation therapy, myelosuppression, and leukemia may lead to bleeding issues during or after surgery as well. The normal platelet count has a wide range, between 100,000 and 500,000/mm3. Mild thrombocytopenia, or 50,000–100,000/mm3, may produce abnormal postoperative bleeding. Levels below 50,000/mm3 lead to major postsurgical bleeding; spontaneous bleeding of mucous membranes occurs below 20,000 cells/mm3.13 Such patients often require transfusion before surgery.

For most dental patients, the hematocrit is crucial to outpatient care only when values drop to roughly 60% of low normal range. Patients who are to undergo sedation or general anesthesia require hemoglobin and hematocrit values within about 75% to 80% of normal.14

Immunosuppression

The ability to rally an adequate immune response is crucial to wound healing. Oral surgery is typically contraindicated when the total white blood count falls below 1500–3000 cells/mm3, as the patient becomes susceptible to infection and compromised repair or regeneration.15 Despite a total white blood count within normal range (5000–10,000 cells/mm3), a grossly abnormal absolute neutrophil count, which includes polymorphonuclear neutrophils and bands, renders the patient unable to combat an immediate antigenic challenge. A normal absolute neutrophil count level lies between 3500 and 7000 cells/mm3. A person with levels between 1000 and 2000 cells/mm3 requires broad-spectrum antibiotic coverage.14 Those with less than 1000 cells/mm3 require immediate medical consultation and cannot receive dental implantation.

In order to sustain health and homeostasis, the normal CD4+ T-cell count measures above 600 cells/mm3; values below 500 cells/mm3 are considered immunosuppressed.14 At present, there is not a definitive lower limit of CD4+ lymphocytes that precludes surgery, but the clinician must realize that less than 400 cells/mm3 increases infection risk, especially from Candida. In these cases, broad-spectrum antibiotic coverage is suggested. In addition, the lower the CD4+:CD8 ratio, which normally approximates 2.0, the more immunocompromised the patient.14

Active Cancer Therapy

While needed to destroy rapidly dividing malignant cells, both ionizing radiation and chemotherapy disrupt host defense mechanisms and hematopoiesis. Because the patient on such regimens cannot mount an appropriate response to wounding from surgery, implantation is prohibited. The total dose of ionizing radiation for cancer treatment ranges from 50 to 80 Gy. This is given in fractions of 1–10 Gy per week in order to maximize death of neoplastic cells and minimize injury to host cells. Four stages of biological interactions occur with radiation.16 Ultimately, cell death occurs from necrosis and apoptosis, both p53-mediated and otherwise. Bone loses osteocytes and undergoes osteoclastic and non-osteoclastic resorption.17 In addition, cell injury fails to regress after termination of radiotherapy; in fact, it compounds. Past the first 6 months post-radiation (in which bone-healing capacity may rebound somewhat), less net vascularity exists and more fibrosis occurs; a hypovascular, hypoxic, and hypocellular state predominates.16 In 3% to 35% of patients who undergo head and neck radiation, spontaneous and traumatic osteoradionecrosis ensues.16

Overall, the tissues and systems of the periodontium have intermediate radiosensitivity compared to those with more rapid turnover (marrow, skin, gastrointestinal cells). Typical head and neck radiation, however, makes the periodontal apparatus prone to injury. Osteocytes of outer lamellar and haversian bone in the direct path of ionizing radiation die, and blood vessels of the haversian canals may be obliterated. Mucositis and xerostomia resulting from radiation damage to mucosa and salivary glands, respectively, contribute also to a poor oral environment. Patency and hemopoietic potential of bone decrease. The posterior mandible in particular experiences osteoradionecrosis simply because it often lies adjacent to the radiation source. Additionally, it is less vascular, and contains less and larger trabeculae. Most studies that involve implant placement in irradiated bone reflect this.18

Cytotoxic anticancer drugs induce rapid granulocytopenia, followed by thrombocytopenia. Myelosuppression occurs often from a multiple drug regimen. In addition to bone marrow toxicity and immunosuppression, anticancer agents cause gastrointestinal toxicity and skin reactions. This leads to infection, hemorrhage, mucositis, and pain. Thus, active use of such medications may contraindicate implant rehabilitation. A very limited number of investigations have been conducted on chemotherapeutic effects on implant survival. Case reports on subjects with dental implants who then undergo cancer chemotherapy show conflicting, though mostly adverse, results.19–21

Psychiatric Disorders

In a patient unable to comprehend and anticipate dental treatment logically, it is best not to place implants. Often, mental illnesses are undiagnosed or unreported. Blomberg22 identified several conditions as incongruous with implant placement. These include psychotic disorders (e.g., schizophrenia), severe character disorders (hysteroid and borderline personalities), dysmorphophobia, cerebral lesions, and presenile dementia, as well as alcohol and drug abuse. There exist no biological reasons for patients with most of the above disorders to lose implants (at least none that have been determined), but various case reports blame removal of osseointegrated fixtures on psychiatric factors.23,24 Addictions to alcohol and other drugs, however, lower resistance to disease, increase possibility of infection, retard healing aggravated by malnutrition, cause incoherence, and result in poor oral hygiene.25 Alcohol abuse in particular induces hepatic disease and subsequent platelet disorders, hypertension, distress infarction, aneurysm, and insidious hemorrhage. A patient who abuses alcohol or drugs may suffer from an inability not only to recognize or accept realistic treatment outcomes but also to heal.

Intravenous Bisphosphonate Treatment

Recently, a number of clinicians published links between intravenous (IV) bisphosphonate use to osteonecrosis of the jaws. Bisphosphonates inhibit bone resorption, and, thus, treat osteoporosis, hypercalcemia of malignancy, and Paget’s disease. They tend to dwell in the bone for long periods of time. There exist both oral and IV routes of administration for bisphosphonates (Table 2). The mechanism of action is unclear, though it is proposed to work in the manner shown in Fig. 1. Bisphosphonates also may inhibit osteoclast precursors and cholesterol synthesis, as well as promote osteoclast apoptosis and osteoblast proliferation.

Table 2
Table 2:
Types of Bisphosphonates
Fig. 1.
Fig. 1.:
Bisphosphonate mechanism of action.

A rash of recent case reports suggest a link between IV bisphosphonate use (i.e., pamidronate and zoledronic acid) to osteonecrosis of the jaw. In 2003, Marx26 found 36 cases of osteonecrosis of the jaw in cancer patients receiving such a treatment regimen. Twenty-five percent of the cases occurred spontaneously, the rest post-extraction. Eighty-one percent had mandibular involvement. That same year, Migliorati27 as well as Wang et al28 described 3 and 5 mostly mandibular osteonecrosis of the jaw cases, respectively, in IV bisphosphonate users. The only drug used by all patients was a bisphosphonate; both authors stated that it directly caused osteonecrosis. The largest case report described 63 cases of osteonecrosis of the jaw in cancer and osteoporosis patients on pamidronate, zoledronic acid, or both.29 Again, most patients experienced mandibular necrosis (62%) and had recent dentoalveolar procedures performed on them (86%). In 2005, Bagan et al30 published 10 cases of osteonecrosis of the jaw in the mandible or in both jaws.

The medical establishment responded to this information, and the International Myeloma Foundation conducted a survey in 2004. Ten percent of 211 patients on zoledronic acid and 4% of 413 patients on pamidronate developed osteonecrosis of the jaw within 36 months of therapy initiation.31 Like the previous case reports, the majority of victims had a history of dental infection or extraction. Due to this and other literature, Novartis (Basel, Switzerland),32 the manufacturer of pamidronate (Aredia®) and zoledronic acid (Zometa®), published an addendum to drug guidelines warning of a potential risk of osteonecrosis of the jaw beginning September 2004. The corporation suggested to dentists to follow this protocol: (1) examine cancer patients prior to IV bisphosphonate initiation, (2) avoid “invasive” dental procedures during the period the patient is on such treatment, and (3) report any serious adverse effects to Novartis or the Food and Drug Administration.

The American Dental Association and the American Academy of Periodontology reiterated those positions.33,34 Only initial data exist, however, and there are no studies on osteonecrosis of the jaw risk after drug discontinuation. Nevertheless, a patient considering IV bisphosphonate therapy requires a thorough oral examination, and must attain dental and periodontal stability before drug instigation. Elimination of any active infection, whether it is periodontitis, gingival abscess, or caries, is a prerequisite. If any issue warrants oral surgery, healing must be complete prior to bisphosphonate use.35 The patient already taking pamidronate or zoledronic acid should be monitored judiciously and, unless necessary, nonsurgically.

With respect to oral bisphosphonate use, 1 case report links it to osteonecrosis of the jaw, and the American Dental Association does not suggest modification of treatment plans for most people on such drugs.36 If other risk factors (i.e., prolonged use, concomitant estrogen or glucocorticoid therapy, older age) exist, however, and the patient requires dental surgery that involves the periosteum or bone, he or she should be informed of potential complications.37 Surgery is not contraindicated with use of oral bisphosphonate, but the dental provider must exercise caution. In the case of IV bisphosphonates, on the other hand, elective surgery is not allowed.

Conclusions

Patient selection is the critical factor for implant survival. In most cases, an appropriate healing response allows for, if not ensures, success. Not all of those who desire implant rehabilitation, however, are candidates for surgery. Absolute medical contraindications exist and must be adhered to, lest the clinician contend with infection, implant failure, or even patient death. There are conditions that, if stabilized, do not seem to interfere perceptibly with repair; a subsequent paper concerns these relative contraindications to elective oral surgery. The careful practitioner understands the nature of a number of diseases evaluates evidence regarding implant therapy in such patients and picks his or her cases based on this knowledge. It is an informed choice that we make, and if we choose properly, predictability results.

Disclosure

The authors claim to have no financial interest in any company or any of the products mentioned in this article.

Acknowledgments

The University of Michigan, Periodontal Graduate Student Research Fund partially supported this study.

References

1. Esposito M, Thomsen P, Ericson LE, et al. Histopathologic observations on early oral implant failures. Int J Oral Maxillofac Implants. 1999;14:798–810.
2. Jolly DE. Evaluation of the medical history. Anesth Prog. 1995;42:84–89.
3. Weyant RJ. Characteristics associated with the loss and peri-implant tissue health of endosseous dental implants. Int J Oral Maxillofac Implants. 1994;9:95–102.
4. Smith RA, Berger R, Dodson TB. Risk factors associated with dental implants in healthy and medically compromised patients. Int J Oral Maxillofac Implants. 1992;7:367–372.
5. Schoen F. The heart. In: Kumar V, ed. Robbins and Cotran: Pathologic Basis of Disease. 7th ed. St. Louis, MO: Saunders; 2005:584–586.
6. Zivan J. Approach to cerebrovascular diseases. In: Goldman L, ed. Cecil Textbook of Medicine. 22nd ed. St. Louis, MO: Saunders; 2004:2280–2287.
7. Carabello B. Valvular heart disease. In: Goldman L, ed. Cecil Textbook of Medicine. 22nd ed. St. Louis, MO: Saunders; 2004:439–442.
8. Chambers H. Infective endocarditis. In: Goldman L, ed. Cecil Textbook of Medicine. 22nd ed. St. Louis, MO: Saunders; 2004:1795–1796.
9. Baab DA, Ammons WF Jr, Selipsky H. Blood loss during periodontal flap surgery. J Periodontol. 1977;48:693–698.
10. Benoliel R, Leviner E, Katz J, et al. Dental treatment for the patient on anticoagulant therapy: Prothrombin time value-What difference does it make? Oral Surg Oral Med Oral Pathol. 1986;62:149–151.
11. Fazio RC, Fang LST. Bleeding disorders. In: Sonis ST, Fazio RC, Fang LST, eds. Oral Medicine Secrets. 1st ed. Philadelphia, PA: Hanley & Belfus, Inc.; 2003:113.
12. Proceedings of the Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy: Evidence-based guidelines. Chest. 2004;126:172S–696S.
13. Drews RE. Critical issues in hematology: Anemia, thrombocytopenia, coagulopathy, and blood product transfusions in critically ill patients. Clin Chest Med. 2003;24:607–622.
14. Jolly DE. Interpreting the clinical laboratory. J Calif Dent Assoc. 1995;23:32–40.
15. Mealey BL. Periodontal implications: Medically compromised patients. Ann Periodontol. 1996;1:256–321.
16. Marx RE, Johnson RP. Studies in the radiobiology of osteoradionecrosis and their clinical significance. Oral Surg Oral Med Oral Pathol. 1987;64:379–390.
17. Brogniez V, Nyssen-Behets C, Gregoire V, et al. Implant osseointegration in the irradiated mandible. A comparative study in dogs with a microradiographic and histologic assessment. Clin Oral Implants Res. 2002;13:234–242.
18. Nishimura RD, Roumanas E, Beumer J III, et al. Restoration of irradiated patients using osseointegrated implants: Current perspectives. J Prosthet Dent. 1998;79:641–647.
19. Karr RA, Kramer DC, Toth BB. Dental implants and chemotherapy complications. J Prosthet Dent. 1992;67:683–687.
20. Steiner M, Windchy A, Gould AR, et al. Effects of chemotherapy in patients with dental implants. J Oral Implantol. 1995;21:142–147.
21. Fugazzotto PA. Success and failure rates of osseointegrated implants in function in regenerated bone for 6 to 51 months: A preliminary report. Int J Oral Maxillofac Implants. 1997;12:17–24.
22. Blomberg S. Psychological response. In: Brånemark PI, Zarb GA, Albrektsson T, eds. Tissue-Integrated Prostheses: Osseointegration in Clinical Dentistry. 1st ed. Chicago, IL: Quintessence; 1985:58.
23. de Lange G, Tadjoedin E. Fate of the HA coating of loaded implants in the augmented sinus floor: A human case study of retrieved implants. Int J Periodontics Restorative Dent. 2002;22:287–296.
24. Piattelli A, Scarano A, Vaia E, et al. Histological evaluation of the peri-implant bone around plasma-sprayed non-submerged titanium implants retrieved from man: A report of two cases. Biomaterials. 1996;17:2219–2224.
25. Kennedy J. Alcohol use disorders. In: Jacobson J, ed. Psychiatric Secrets. 2nd ed. Philadelphia, PA: Hanley & Belfus; 2001:103.
26. Marx RE. Pamidronate (Aredia) and zoledronate (Zometa) induced avascular necrosis of the jaws: A growing epidemic. J Oral Maxillofac Surg. 2003;61:1115–1117.
27. Migliorati CA. Bisphosphonates and oral cavity avascular bone necrosis. J Clin Oncol. 2003;21:4253–4254.
28. Wang J, Goodger NM, Pogrel MA. Osteonecrosis of the jaws associated with cancer chemotherapy. J Oral Maxillofac Surg. 2003;61:1104–1107.
29. Ruggiero SL, Mehrotra B, Rosenberg TJ, et al. Osteonecrosis of the jaws associated with the use of bisphosphonates: A review of 63 cases. J Oral Maxillofac Surg. 2004;62:527–534.
30. Bagan JV, Murillo J, Jimenez Y, et al. Avascular jaw osteonecrosis in association with cancer chemotherapy: Series of 10 cases. J Oral Pathol Med. 2005;34:120–123.
31. Durie BG, Katz M, Crowley J. Osteonecrosis of the jaw and bisphosphonates. N Engl J Med. 2005;353:99–102.
32. Novartis Important Safety Information. September 20, 2005. Available at: http://www.novartis.com, http://www.us.zometa.com/info/patientsafetyinfo.jsp. Accessed August 27, 2006.
33. American Academy of Periodontology Statement on Bisphosphonates. August 26, 2005. Available at: http://www.perio.org/resources-products/bisphosphonates.htm. Accessed August 27, 2006.
34. American Dental Association. Osteonecrosis of the jaw. July 12, 2006. Available at: http://www.ada.org/prof/resources/topics/osteonecrosis.asp. Accessed August 27, 2006.
35. Ruggiero S, Gralow J, Marx RE, et al. Practical guidelines for the prevention, diagnosis, and treatment of osteonecrosis of the jaw in patients with cancer. J Oncol Prac. 2006;2:7–14.
36. Nase JB, Suzuki JB. Osteonecrosis of the jaw and oral bisphosphonate treatment. J Am Dent Assoc. 2006;137:1115–1119.
37. American Dental Association Council on Scientific Affairs. Dental management of patients receiving oral bisphosphonate therapy: Expert panel recommendations. J Am Dent Assoc. 2006;137:1144–1150.

Abstract Translations

GERMAN / DEUTSCH

AUTOR(EN): Debby Hwang, DMD*, Hom-Lay Wang, DDS, MSD**. *Ehemalige Assistenzärztin, Abteilung für Orthodontie und Oralmedizin, zahnmedizinische Fakultät, Universität von Michigan, Ann Arbor, MI, USA. Zur Zeit privat praktizierende Árztin, niedergelassen in Fairfield, CT, USA. **Professor und Leiter des Graduiertenkollegs für Orthodontie. Abteilung für Orthodontie und Oralmedizin, zahnmedizinische Fakultät, Universität von Michigan, Ann Arbor, MI, USA. Schriftverkehr: Dr. Hom-Lay Wang, Professor und Leiter des Graduiertenkollegs für Orthodontie (Professor and Director of Graduate Periodontics), Abteilung für Orthodontie und Oralmedizin (Department of Periodontics and Oral Medicine), zahnmedizinische Fakultät der Universität von Michigan (University of Michigan School of Dentistry). 1011 North University Avenue, Ann Arbor, Michigan 48109-1078, USA. Telefon: (734) 763-3383, Fax: (734) 936-0374. eMail: [email protected]

Implantierungsbehandlungen und ihre medizinischen Gegenanzeigen: Teil I: Absolute Kontraindikationen

ABSTRACT: Um den Erfolg einer Implantierungsbehandlung zu garantieren, müssen die Patienten sorgfältig auf das Bestehen eventueller lokaler oder systemischer Gegenanzeigen zur bevorzugten Therapiemethode hin ausgewählt werden. Daher zielt die vorliegende Arbeit darauf ab, diejenigen medizinischen Krankheiten auszuloten, die nachgewiesenermaßen eine konventionelle Zahnimplantierung ausschließen. Zu den absoluten Kontraindikationen einer Wiederherstellungsbehandlung durch Implantierung gehören vorangegangener Herzmuskelinfarkt sowie zerebrovaskuläre Unpässlichkeit, chirurgischer Einsatz einer neuen Herzklappe, Immunsuppression, Blutungsprobleme, aktive Malignitätsbehandlung, Drogenmissbrauch, psychische Erkrankungen und die Einnahme von IV-Bisphosphonaten. Jede der oben genannten Gegenanzeigen stellt einen Hinderungsgrund für eine elektive Operation im Mundraum dar und bedarf der genauen Überwachung durch sowohl den behandelnden Arzt als auch den Zahntechniker. Wird das vorgeschlagene Protokoll nicht befolgt, kann dies im schlimmsten Fall sogar zum Tod des Patienten führen.

SCHLÜSSELWÖRTER: Medizinische Kontraindikationen, Zahnimplantate, Versagen eines Implantats, Rauchen, Osteoporose

SPANISH / ESPAÑOL

AUTOR(ES): Debby Hwang, DMD*, Hom-Lay Wang, DDS, MSD**. *Antiguo Residente, Departamento de Periodóntica y Medicina Oral, Facultad de Odontología, Universidad de Michigan, Ann Arbor, MI, EE.UU. Actualmente en práctica privada, Fairfield, CT, EE.UU. **Profesor y Director de Periodóntica para Graduados. Departamento de Periodóntica y Medicina Oral, Facultad de Odontología, Universidad de Michigan, Ann Arbor, MI, EE.UU. Correspondencia a: Dr. Hom-Lay Wang, Professor and Director of Graduate Periodontics, Department of Periodontics and Oral Medicine, University of Michigan School of Dentistry, 1011 North University Avenue, Ann Arbor, Michigan 48109-1078, USA. Teléfono: (734) 763-3383, Fax: (734) 936-0374. Correoelectrónico:[email protected]

Contraindicaciones médicas a la terapia de implantes: Parte I: Contraindicaciones absolutas

ABSTRACTO: Para poder asegurar el éxito del implante, es esencial seleccionar pacientes que no posean contraindicaciones locales o sistémicas a la terapia. Por lo tanto, el propósito de este trabajo es evaluar las enfermedades que se saben impiden el tratamiento convencional con implantes dentales. Las contraindicaciones absolutas a la rehabilitación con implantes incluyen un infarto reciente del miocardio y accidente cerebrovasccular, cirugía para colocar una prótesis valvular, inmunosupresión, cuestiones de sangramiento, tratamiento activo de malignidad, abuso de drogas, enfermedades psiquiátricas así como el uso de bisfosfanato por vía intravenosa. Cualquiera de estas condiciones, excepto cirugía oral elegida y requiere una monitorización sensata del médico así como el dentista. El incumplimiento del protocolo sugerido podría, en el peor caso posible, resultar en la mortalidad del paciente.

PALABRAS CLAVES:Contraindicaciones médicas, implantes dentales, falla de un implante, fumar, osteoporosis

PORTUGUESE / PORTUGUÊS

AUTOR(ES): Debby Hwang, Doutor em Medicina*, Hom-Lay Wang, Cirurgião-Dentista, Mestre em Odontologia**. *Ex-residente, Departamento de Periodontia e Medicina Oral, Faculdade de Odontologia, Universidade de Michigan, Ann Arbor, MI, USA. Atualmente em clínica particular, Fairfield, CT, Estados Unidos. **Professor e Diretor de Periodontia Graduada. Departamento de Periodontia e Medicina Oral, Faculdade de Odontologia, Universidade de Michigan, Ann Arbor, MI, USA. Correspondência para: Dr. Hom-Lay Wang, Professor and Director of Graduate Periodontics, Department of Periodontics and Oral Medicine, University of Michigan School of Dentistry. 1011 North University Avenue, Ann Arbor, Michigan 48109-1078, USA. Telefone: (734) 763-3383, Fax: (734) 936-0374. e-mail: [email protected].

Contra-indicações Médicas à Terapia de Implante: Parte I: Contra-indicações absolutas

RESUMO: A fim de assegurar o sucesso do implante é essencial selecionar pacientes que não possuam contra-indicações locais ou sistêmicas à terapia. Daí, é objetivo deste artigo revisar as doenças médicas que notadamente impede o tratamento convencional de implante dentário. Contra-indicações absolutas à reabilitação de implante incluem infarto do miocárdio recente e acidente cerebrovascular, cirurgia de prótese valvular, imunossupressão, questões de sangramento, tratamento ativo de malignidade, abuso de drogas, doença psiquiátrica, bem como uso de bisfosfonato IV. Qualquer dessas condições impedem a cirurgia oral eletiva e exige monitoramento criterioso pelo médico, bem como pelo fornecedor dentário. O não-cumprimento do protocolo sugerido pode, no pior caso possível, resultar em mortalidade do paciente.

PALAVRAS-CHAVE: Contra-indicações médicas, implantes dentários, falha de implante, tabagismo, osteoporose

JAPANESE / SYMBOL

Symbol
Symbol
Figure
Figure

CHINESE / SYMBOL

Symbol
Symbol
Figure
Figure
Keywords:

medical contraindications; dental implants; implant failure; smoking; osteoporosis

© 2006 Lippincott Williams & Wilkins, Inc.