<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJST</journal-id><journal-title-group><journal-title>Open Journal of Stomatology</journal-title></journal-title-group><issn pub-type="epub">2160-8709</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojst.2013.31006</article-id><article-id pub-id-type="publisher-id">OJST-28735</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Patients with dental hemorrhagic complicationsundergoing warfarin therapy exhibit excessiveinternational normalized ratio prolongation: A report of 2 cases
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>suyoshi</surname><given-names>Sato</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yasuaki</surname><given-names>Sakata</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Norimichi</surname><given-names>Nakamoto</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yousuke</surname><given-names>Fukushima</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aya</surname><given-names>Nakamoto</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yuichiro</surname><given-names>Enoki</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yoshie</surname><given-names>Sano</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Shoichiro</surname><given-names>Kokabu</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tetsuya</surname><given-names>Yoda</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Oral and Maxillofacial Surgery, Saitama Medical University, Moroyama-machi, Japan</addr-line></aff><aff id="aff2"><addr-line>Developmental Biology, Harvard School of Dental Medicine, Boston, USA</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>tsato@saitama-med.ac.jp(SS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>18</day><month>03</month><year>2013</year></pub-date><volume>03</volume><issue>01</issue><fpage>28</fpage><lpage>31</lpage><history><date date-type="received"><day>16</day>	<month>January</month>	<year>2013</year></date><date date-type="rev-recd"><day>23</day>	<month>February</month>	<year>2013</year>	</date><date date-type="accepted"><day>1</day>	<month>March</month>	<year>2013</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   Dental hemorrhagic complications, including postoperative bleeding and traumatic hemorrhage as emergency cases, often occur in patients undergoing oral anticoagulant therapy such as warfarin therapy. Recent research recommends that warfarin dosage should be assessed every 12 weeks. Therefore, most physicians generally accept international normalized ratio (INR) monitoring at longer intervals. However, cases are encountered in which the INR prolongation is observed despite of invariable dosage of warfarin. In this report, we present 2 cases of patients with dental hemorrhagic complications undergoing oral anticoagulant therapy who exhibited excessive INR prolongation. These patients exhibited decreased appetite and hypoalbuminemia. We speculate that long-term appetite loss resulted in the increase in the serum concentration of free warfarin and vitamin K deficiency. Our study indicates that we should notice malnourishment when we treat patients who have undergone warfarin therapy with dental surgical procedures. It is recommended that measurement of INR just before a dental surgical treatment. 
 
</p></abstract><kwd-group><kwd>Warfarin Therapy; International Normalized Ratio; Hypoalbuminemia; Vitamin K Deficiency</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. INTRODUCTION</title><p>Dental hemorrhagic complications, including postoperative bleeding and traumatic hemorrhage as emergency cases, often occur in patients undergoing oral anticoagulant therapy. Warfarin deters clot formation by inhibiting vitamin K-dependent synthesis of clotting factors and is commonly used in anticoagulant therapy to prevent thromboembolism such as venous thromboembolism and ischemic stroke in patients with atrial fibrillation (AF) [1,2]. Warfarin acts by inhibiting the synthesis of vitamin K-dependent clotting factors, which include Factors II, VII, IX, and X, and the anticoagulant proteins C and S. Warfarin is thought to interfere with clotting factor synthesis by inhibition of the C1 subunit of vitamin K epoxide reductase enzyme complex, thereby reducing the regeneration of vitamin K1 epoxide. Therapeutic levels of warfarin are measured using the international normalized ratio (INR). To check INR prolongation is useful for the diagnosis of oral anticoagulant therapy. American Heart Association/American College of Cardiology and European Society of Cardiology recommend an INR range of 2.0 - 3.0 to prevent thromboembolism in patients with AF [<xref ref-type="bibr" rid="scirp.28735-ref3">3</xref>]. However, the Japanese guidelines recommend that target INR levels for patients with nonvalvular AF range from 1.6 - 2.6 [<xref ref-type="bibr" rid="scirp.28735-ref4">4</xref>]. Because approximately 1% patients for whom the warfarin therapy was withdrawn for dental surgical treatment or endoscopy experienced severe thrombosis, became disabled, or died [5,6], continuous administration of a maintenance dose of warfarin is recommended during dental surgical treatment [7-9].</p><p>Although the American College of Chest Physician guidelines recommend that INR monitoring should be performed at a maximum interval of 4 weeks [<xref ref-type="bibr" rid="scirp.28735-ref10">10</xref>], recent research recommends that warfarin dosage should be assessed every 12 weeks. Therefore, most physicians generally accept INR monitoring at longer intervals. However, cases are encountered in which the INR prolongation is observed despite of invariable dosage of warfarin. Here, we present 2 cases of patients with dental hemorrhagic complications undergoing oral anticoagulant therapy who exhibited excessive INR prolongation associated with hypoalbuminemia and vitamin K deficiency.</p></sec><sec id="s2"><title>2. CASE REPORTS</title><p>The 2 cases reported in this study are of patients who were diagnosed between 2007 and 2011 at the Department of Oral and Maxillofacial Surgery, Saitama Medical University Hospital.</p><sec id="s2_1"><title>2.1. Case 1</title><p>An 83-year-old female patient with hemorrhage after teeth-extraction (teeth 35, 36, and 37) was transported to our hospital by an ambulance in 2011 (<xref ref-type="table" rid="table1">Table 1</xref>). Four days before the transfer to the hospital, her teeth were extracted a primary visiting dentist at her residence. Both 250 mg cefaclor (Kefral<sup>&#174;</sup>) 3 times daily were prescribed for 2 days and 400 mg acetaminophen (Calonal<sup>&#174;</sup>) at 1 time were prescribed. She took cefaclor for 2 days and acetaminophen twice. Persistent minor hemorrhage occurred after tooth extraction, and the dentist advised her and her family to compress the wound surface with a surgical gauze. Her medical history revealed paradoxical cerebral embolism, which may have been caused by patent foramen ovale, as diagnosed at our hospital in 2006 that was subsequently followed up by a primary care physician. For the last month, she experienced a decreased appetite because of dental trouble, and ate only 1 meal per day. She was treated with the following medication for each disease: 2.5 mg warfarin potassium (Warfarin<sup>&#174;</sup>) per day for cerebral embolism, 25 mg fluvoxamine (Luvox<sup>&#174;</sup>) and 400 mg sodium valproate (Depakene<sup>&#174;</sup>) per day for a major depressive disorder, and 20 mg fu-</p><p><xref ref-type="table" rid="table1">Table 1</xref>. Background of the 2 patients.</p><p><img src="6-1460215\69f199e8-76d8-433d-ac67-fcc118ded095.jpg" /></p><p>rosemide (Lasix<sup>&#174;</sup>) per day for hypertension. INR monitoring was conducted every 2 months through follow-up. The most recent INR value was 1.83, taken almost 1 month before presentation. Laboratory data on the day of hospital visit showed that both serum albumin and the ratio of albumin to globulins (A/G ratio) were low (2.9 g/dL and 0.7 g/dL, respectively), suggesting that the patient was malnourished (<xref ref-type="table" rid="table2">Table 2</xref>). Although aspartate aminotransferase (AST) was slightly high (53 IU/L), alanine aminotransferase (ALT) was within normal limits (25 IU/L), indicating that the liver function was normal. INR value was 6.64. She was diagnosed as having secondary hemorrhage after tooth extraction. Hemostasis was achieved using Surgicel<sup>&#174;</sup> and suture. Menatetrenone (15 mg/day) was prescribed orally, and the patient was treated with heparin under hospital care. Her INR value decreased to 1.49 after 4 days.</p></sec><sec id="s2_2"><title>2.2. Case 2</title><p>An 82-year-old female patient with hemorrhage after injury was transported to our hospital by an ambulance in 2007 (<xref ref-type="table" rid="table1">Table 1</xref>). She had tripped and fallen on her face in the house and was experienced a hard blow to the mandible. Her medical history revealed that she had been treated for breast cancer and had cardiogenic embolism that was diagnosed at our hospital in 2006 and that was followed up by a primary care physician. She reported a decreased appetite and consumed 1 or 2 meals per day for the last 3 months. She was treated with the following medication for each of the disease: 3.0 mg warfarin potassium (Warfarin<sup>&#174;</sup>) and 5 mg nitroglycerin (Nitroderm TTS<sup>&#174;</sup>) per day for cardiogenic embolism, 2.5 mg glibenclamide (Euglucon<sup>&#174;</sup>) per day for diabetes mellitus, 6 g sodium chloride (Sodium chloride<sup>&#174;</sup>) per day for hyponatremia, 0.25 mg brotizolam (Lendormin<sup>&#174;</sup>) per day for insomnia, and 15 mg lansoprazole (Takepron OD<sup>&#174;</sup>) per day for gastric ulcer. She was followed up by INR monitoring every 6 months, with her most recently recorded</p><p><xref ref-type="table" rid="table2">Table 2</xref>. Laboratory data for 2 cases.</p><p><img src="6-1460215\23134ebc-4f3c-44a4-9f14-1f0387866813.jpg" /></p><p>A/G: albumin to globulins; AST: aspartate aminotransferase; ALT: alanine aminotransferase; Cr: creatinine. BUN: blood urea nitrogen.</p><p>INR value being 2.02. Laboratory data on the day of her first visit showed that both serum albumin (3.5 g/dL) and A/G ratio (1.0) were low, suggesting that she was malnourished (<xref ref-type="table" rid="table2">Table 2</xref>). Her INR value was 9.05. She was diagnosed as having alveolar bone fracture of the mandibular bilateral central incisor and gingival laceration. We extracted her teeth (31 and 41) and inserted Avitene<sup>&#174;</sup> sheet in the extraction socket with a suture. She was administered menatetrenone (10 mg/day) intravenously under hospital care. Her INR value decreased to 1.65 after 2 days.</p></sec></sec><sec id="s3"><title>3. DISCUSSION</title><p>In this report, we presented 2 cases of INR prolongation. We adopted “above 4.50” as the standard of INR prolongation as reported previously [<xref ref-type="bibr" rid="scirp.28735-ref11">11</xref>]. The risk of overanticoagulation is increased by the following factors: poor drug compliance, hyperthyroidism, hypertension, renal failure, long-term administration of antibiotics and analgesics, hepatic dysfunction, loss of vitamin K and hypoalbuminemia [11-13].</p><p>The cognitive ability in both patients was normal despite being elderly, suggesting that their drug compliance was good. As mentioned previously, hepatic function was normal in both the cases. Moreover, both the patients did not have hyperthyroidism. Although the patient in Case 1 had hypertension, the disease progression was stable. The patient in Case 2 had diabetes mellitus, but renal failure was not complicated. Renal function in both the patients was normal. Antibiotics and analgesics were prescribed in Case 1. Recent studies demonstrated that the consumption of antibiotics or analgesics for a long time (i.e., for more than 7 days) may elevate INR values [14-16]. However, the duration of administration in the present case was so short that the probability of INR prolongation was very low.</p><p>In the elderly, poor oral intakes of dietary vitamin K is the most likely explanation for the marked prolongation of INR despite a stable dose of warfarin [<xref ref-type="bibr" rid="scirp.28735-ref17">17</xref>]. We could not exclude the possibility that both cases were insufficient for taking vitamin K. On the other hand, hypoalbuminemia due to appetite loss exhibits a marked prolongation of INR [<xref ref-type="bibr" rid="scirp.28735-ref18">18</xref>]. Since warfarin strongly binds to serum albumin [<xref ref-type="bibr" rid="scirp.28735-ref19">19</xref>], low levels of serum albumin increase the risk of INR prolongation [20,21]. A slight decline in albumin can also increase the INR value [<xref ref-type="bibr" rid="scirp.28735-ref18">18</xref>]. In our cases, serum albumin as well as A/G ratio was low, suggesting that hypoalbuminemia increased INR value. We speculate that long-term appetite loss resulted in the increase in the serum concentration of free warfarin and vitamin K deficiency. This case report indicates that we should attend to long-term appetite loss in elderly people undergoing oral anticoagulant therapy. Our study indicates that we should notice malnourishment when we treat patients who have been taking oral anticoagulant therapy with dental surgical procedures. It is recommended that measurement of INR just before a dental surgical treatment.</p></sec><sec id="s4"><title>REFERENCES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.28735-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Owens, C.D. and Belkin, M. (2005) Thrombosis and coagulation: Operative management of the anticoagulated patient. 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