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Review Article
Orthodontic care of medically
compromised patients
Sandhya Maheshwari, Sanjeev Kumar Verma, Juhi Ansar, KC Prabhat
Department of Orthodontics and Dental Anatomy, Aligarh Muslim University, Aligarh, India
ABSTRACT
Key words: Guidelines, interdisciplinary management, life expectancy, medically compromised patient,
orthodontic considerations, orthodontic treatment
Orthodontic considerations • A
traumatic extraction procedures are reported to
• O rthodontic treatment is not contraindicated in patients reduce the risk for ORN.
with bleeding disorders.[10]
• D uration of treatment should be given careful Thalassemia
consideration. Lengthier the treatment duration may
increase potential complications.[11] Thalassemia is an inherited disorder of hemoglobin
• C hronic irritation from orthodontic appliances synthesis. It can be can be classified as α‑thalassemia,
should be avoided. Fixed appliances are preferable to β‑thalassemia, γ‑thalassemia and δ‑thalassemia indicating
removable appliances as the latter can cause gingival which blood hemoglobin chains are affected.[18] Based on
irritation.[7] their clinical and genetic orders they are classified into
• S elf‑ligating brackets are preferable to conventional major (homozygous) and minor (heterozygous) types.[19]
brackets. If conventional brackets are used, archwires β‑Thalassemia major (Cooleys anemia) is the most severe
should be secured with elastomeric modules instead of form of congenital hemolytic anemia. The most common
wire ligatures. oral and facial manifestation is enlargement of the maxilla,
• I f extractions or surgery is to be performed increase bossing of the skull and prominent malar eminences
factor VIII production with 1-desamino-8-darginine due to the intense compensatory hyperplasia of the
vasopressin (DDAVP). Parentaral DDAVP can be used maxilla. This lead to expansion of the marrow cavity and
to raise factor VIII levels 2‑3‑fold to prevent surgical a facial appearance known as “chipmunk” face.[20,21] the
hemorrhage.[12] overdevelopment of the maxilla frequently result in an
increased overjet and spacing of maxilla teeth and other
Hematological Malignancies degree of malocclusion.[22]
needs and do not treat the lower jaw.[15] The lower jaw admission for blood transfusion, i.e. when hemoglobin
is at risk of osteoradionecrosis (ORN) because of its level is at its highest, with the administration of
limited blood supply. A group of 104 patients who antibiotics.[23]
developed ORN of the jaws were reviewed and treated • Thalassemic patients are at an increased risk of viral
between 1972 and 1992. The most common affected hepatitis and AIDS due to repeated blood transfusion
site was the mandible (99 cases, 95.2%), followed by and therefore screening test for the same should be
the maxilla (5 cases, 4.8%). Among all cases, 93 (89.4%) carried out at regular intervals.
were trauma induced‑ORN.[16]
• O rthodontic treatment may start or resume after Bronchial Asthma
completion of all medical therapy and after at least
2‑year event free survival when risk of relapse has Asthma is a chronic disease that affects the lower airways.
been decreased. In adults receiving head and neck It is characterized by recurrent and reversible airflow
radiotherapy the incidence of ORN is 8.2%.[17] limitation due to an underlying inflammatory process.[25] Signs
hepatitis is surely of importance to the orthodontist. syndrome in 1866, although he did not know the cause
HBV, hepatitis C virus, and hepatitis D virus are blood of the syndrome. He was then termed the “father” of the
borne and can be transmitted via contaminated sharps syndrome.[65]
and droplet infection.
• A erosols generated by dental hand pieces could infect The primary skeletal abnormality affecting the orofacial
skin, oral mucous membrane, eyes or respiratory structures in Down syndrome is an underdevelopment
passages of dental personnel. The main orthodontic of the midfacial region. The bridge of the nose, bones
procedures to result in aerosol generation are removal of the midface and maxilla are relatively smaller in
of enamel during interproximal stripping, removal of size.[66] In many instances this causes a prognathic class III
residual cement after debonding, and prophylaxis.[56] occlusal relationship, which contributes to an open bite.[66]
• I nfection control protocol should be followed Individuals with Down syndrome have delayed eruption
according to the guideline laid down by occupational pattern. There is usually some sort of enamel defect
safety and health administration.[57] All members of affecting the teeth. There is usually congenitally missing
the team should be immunized against HBV. Barrier teeth and they can have unusually shaped teeth.
technique such as gloves, eye glasses, and mouth mask
should be used. Orthodontic considerations
• H BV can survive on innate subjects for 7 days. • C ongenital heart defects are present in 40‑60% of
Impressions can be one of the links in transmitting infants with Down syndrome. Children with heart
the HBV to orthodontics. The impressions must defects who are undergoing dental procedures should
be disinfected by dipping them in glutaldehyde or be given antibiotic prophylaxis against subacute
by spraying sodium hypochlorite and leaving it for bacterial endocarditis.[67]
10 min.[58] • R educed muscle tone causes less efficient chewing
• P ost-exposure prophylaxis for HBV infection should and natural cleansing of the teeth. More food may
be given to those who are exposed percutaneously or remain on the teeth after eating due to this inefficient
through mucus membrane to blood or body fluids of chewing.[66] hence oral hygiene instruction should be
known or suspected. If the source individual is Hepatitis given in every visit.
B surface antigen (HBsAg) positive and the exposed • I t is ensure that patient is vaccinated for hepatitis before
person is unvaccinated or antibody level is less than starting dental treatment. This is necessary because
10 mIU/ml, hepatitis B immunoglobulin (0.6 ml/kg) should persons with Down syndrome are at increased risk of
be administered (preferably within 24 h) along with the developing the carrier state if they are infected with
vaccine series given at a different site.[59] HBV.[68]
• L iver disease can result in depressed plasma levels of • S eizures occur in 5‑10% of children with Down
coagulation factors. If extraction is required, special syndrome.[69] Generalized tonic clonic seizures are the
attention should be paid as the risk of bleeding most common. Seizures are diagnosed and treated
increases; an infusion of fresh frozen plasma may be similarly in children with and children without Down
indicated. Advanced oral surgical procedures or any syndrome.
dental procedures with the potential to cause bleeding • Impressions using quick‑set materials with fun flavors
performed on a patient with multiple or a severe single should be used as these may reduce the tendency for
coagulopathy may need to be provided in a hospital activation of the more sensitive gag reflex frequently
setting.[60,61] experienced with Down syndrome patients.
• C are should be taken when prescribing any medication • H igh‑memory wires allow a longer activation interval
for patients with liver disease. Hepatic impairment between appointments.
can lead to failure of metabolism of some drugs • S elf‑ligating brackets allow a more patient‑friendly
and result in toxicity.[62] Caution should be used in activation appointment.
prescribing medications metabolized in the liver, such
as acetaminophen, nonsteroidal anti‑inflammatory Autism
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Source of Support: Nil, Conflict of Interest: None declared
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