<?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">OJAnes</journal-id><journal-title-group><journal-title>Open Journal of Anesthesiology</journal-title></journal-title-group><issn pub-type="epub">2164-5531</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojanes.2021.116018</article-id><article-id pub-id-type="publisher-id">OJAnes-109964</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>
 
 
  Assessment of Haemostasis in Anaesthesia for Surgery at the Sylvanus Olympio University Hospital Center in Lom&#233;
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Essohanam</surname><given-names>T. Mouzou</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>Sarakawabalo</surname><given-names>Assénouwè</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>Abd</surname><given-names>El Kader Moumouni</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>Pikabalo</surname><given-names>Tchètikè</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Akala-Yoma</surname><given-names>Gnimdou</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Anesthesiology Department, Sylvanus Olympio Teaching Hospital, Lome, Togo</addr-line></aff><aff id="aff1"><addr-line>Anesthesilogy Department, University Teaching Hospital of Kara, Kara, Togo</addr-line></aff><aff id="aff2"><addr-line>Neurosurgery Department, University Teaching Hospital of Kara, Kara, Togo</addr-line></aff><pub-date pub-type="epub"><day>18</day><month>06</month><year>2021</year></pub-date><volume>11</volume><issue>06</issue><fpage>184</fpage><lpage>193</lpage><history><date date-type="received"><day>10,</day>	<month>April</month>	<year>2021</year></date><date date-type="rev-recd"><day>18,</day>	<month>June</month>	<year>2021</year>	</date><date date-type="accepted"><day>21,</day>	<month>June</month>	<year>2021</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>
 
 
  <b>Title:</b> Assessment of haemostasis in anaesthesia for surgery at the Sylvanus Olympio University Hospital Center in Lom&#233;. 
  <b>Objectives:</b> Evaluate the prescription of the preoperative haemostasis assessment. 
  <b>Methodology:</b> This was a prospective descriptive and observational study which had taken place in the central operating room and in the operating room of the ENT department at UHC SO of Lom&#233; from January 1 to June 31, 2016. It had concerned all patients who had anaesthesia for scheduled surgery after pre-anesthetic consultation and the haemostasis assessment carried out according to the anaesthesia technique and the type of surgery. 
  <b>Results:</b> Two hundred and sixty (260) patients underwent anaesthesia during the study period. The male sex predominated (60%), the age group 18 - 40 years predominated (50.4%). GA was more practiced (62.7%) followed by spinal anaesthesia (30.3%). Minor ENT surgery was more performed (28%). ASA1 patients predominated (48.5%). The pre-anesthetic haemostasis assessment including platelet count, prothrombin rate, activated partial thromboplastin time and bleeding time was almost always done. The platelet count was achieved in all patients followed by the activated partial thromboplastin time (94%). No haemorrhagic complication related to a haemostasis disorder was observed in the perioperative period in anaesthesia than in surgery. 
  <b>Conclusion:</b> The prescription of the pre-anesthetic haemostasis assessment should not be systematic. It must take into account the clinical history, the patient’s bleeding history during the anaesthesia consultation, the type of anaesthesia, the surgery planned and the age.
 
</p></abstract><kwd-group><kwd>Haemostasis Assessment</kwd><kwd> Anaesthesia</kwd><kwd> Surgery</kwd><kwd> UHC</kwd><kwd> Lom&#233;</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Before the practice of anaesthesia of general (GA) or locoregional (LRA), several clinical and paraclinical examinations are carried out. Thus a routine preoperative haemostasis assessment (PHA) to detect any haemostasis abnormalities is likely to increase the risk of bleeding [<xref ref-type="bibr" rid="scirp.109964-ref1">1</xref>].</p><p>In Europe, particularly in France, PHA to screen for a haemostasis disorder before anaesthesia is no longer systematic [<xref ref-type="bibr" rid="scirp.109964-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref3">3</xref>].</p><p>In French-speaking black Africa, the selective prescription of a PHA remains topical [<xref ref-type="bibr" rid="scirp.109964-ref4">4</xref>].</p><p>No study was done in Togo on PHA to determine a selective prescription strategy. The aim was to assess the prescription of PHA in anaesthesia at the UHC-Sylvanus Olympio (SO).</p></sec><sec id="s2"><title>2. Methodology</title><p>Our study was carried out in the central operating rooms and in otorhinolaryngology (ENT) and maxillofacial surgery (MFS) of the UHC SO in Lom&#233;.</p><p>This prospective descriptive and observational study was carried out over a period of 6 months from January 1 to June 31, 2016. It began after authorization from the UHC SO ethics and patient protection committee and informed consent of patients to the consultation of anesthesia.</p><p>It concerned all patients who had anaesthesia for scheduled surgery after a preanaesthetic consultation. All patients operated without a preanaesthetic consultation with anaesthesia-resuscitation doctor (ARD) were excluded from the study. Anaesthesia consultation records, anaesthesia monitoring records for postoperative and anaesthesia were the means used for data collection. The parameters studied were: socio-demographic parameters; haemorrhagic history; haemorrhagic clinical aspects; anaesthetic and surgical aspects; biological abnormalities of PHA; abnormal per and postoperative bleeding; the conduct in front of haemostasis anomalies.</p><p>A count was manual. The processing was carried out by the Word 2007 computer software.</p></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Epidemiological Aspects</title><p>During the study period, 270 patients were operated on for scheduled surgery, of which 260 were included in the study, a frequency of 0.96. 57.7% of the patients were operated on in the central block and 42.3% in the ENT block.</p><p>The age of the patients is presented in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>The average age of our patients was 40 years with extremes of 8 months and 87 years. 60% of patients were male.</p><p>No preoperative patient had clinical signs of a haemostasis disorder or a history of bleeding related to a haemostasis disorder.</p><p>The PHA performed was composed: bleeding time (BT) 72.7%; activated partial thromboplastin time (APTT) 95%; prothrombin rate (PR) 95.4%; platelet count (100%) with 7.7% high platelet rate and 0.4% low platelet rate; 11.3% low PR; 6.5% of elongated APTT and 5.8% of elongated BT.</p><p>The preoperative treatments for haemostasis abnormalities were as follows: 11.3% PR of which 6.4% had received vitamin K1 + 0.8% a transfusion of fresh frozen plasma. 0.4% of severe thrombocytopenia had received platelet concentrate and had undergone a specialist haematology consultation or no haemostasis abnormality had been found. For patients with BT, prolonged APTT and high platelet count, no treatment was performed.</p><p>The PHA according to the age of the patients was as follows:</p><p>8 months to 3 years (14.6%): BT (10.3%), PR (13.4%); APTT (14.6%); platelets (14.6%); from 4 to 55 years old (64.6%): BT (47.3%); PR (58.4%); APTT (56.9%); platelets (64.6%);</p><p>56 to 87 years old (20.8%): BT (15%); PR (19%); APTT (20%); platelets (20.7%).</p><p>ASA classification is presented in <xref ref-type="table" rid="table2">Table 2</xref>.</p><p>PHA performed according to ASA1: platelets (48.5%); APTT (44.6%); PR (43%); BT (35.4%); for ASA2: platelets (40%); APTT (38%); PR (37.6%); BT (34.6%); for ASA3: platelets (11.5%); APTT (11.1%): PR (11.1%); BT (6.5%).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of patients by age</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Year</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >[0 - 18]</td><td align="center" valign="middle" >46</td><td align="center" valign="middle" >17.7</td></tr><tr><td align="center" valign="middle" >[18 - 41]</td><td align="center" valign="middle" >131</td><td align="center" valign="middle" >50.4</td></tr><tr><td align="center" valign="middle" >[41 - 61]</td><td align="center" valign="middle" >62</td><td align="center" valign="middle" >23.8</td></tr><tr><td align="center" valign="middle" >[61 - 87]</td><td align="center" valign="middle" >21</td><td align="center" valign="middle" >8.1</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >260</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Distribution of patients according to class ASA*</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >ASA1</td><td align="center" valign="middle" >126</td><td align="center" valign="middle" >48.5</td></tr><tr><td align="center" valign="middle" >ASA2</td><td align="center" valign="middle" >104</td><td align="center" valign="middle" >40</td></tr><tr><td align="center" valign="middle" >ASA3</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >11.5</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >260</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>*American society of anaesthesiologists.</p></sec><sec id="s3_2"><title>3.2. Intraoperative Stage</title><p>Types of anaesthesia are presented in <xref ref-type="table" rid="table3">Table 3</xref>.</p><p>During the intraoperative period, no incident occurred during anaesthesia related to haemostasis disorder. The same observation was made postoperatively.</p><p>Surgical aspects are presented in <xref ref-type="table" rid="table4">Table 4</xref>.</p><p>Major surgery is presented in <xref ref-type="table" rid="table5">Table 5</xref>.</p><p>Minor surgery is presented in <xref ref-type="table" rid="table6">Table 6</xref>.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Distribution of patients according to the type of anaesthesia</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >GA</td><td align="center" valign="middle" >163</td><td align="center" valign="middle" >62.7</td></tr><tr><td align="center" valign="middle" >Spinal anesthesia</td><td align="center" valign="middle" >79</td><td align="center" valign="middle" >30.3</td></tr><tr><td align="center" valign="middle" >Axillary block</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >3.1</td></tr><tr><td align="center" valign="middle" >Caudal block</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >2.7</td></tr><tr><td align="center" valign="middle" >Epidural</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >1.2</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >260</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Distribution of patients by type of surgery</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >(1) Minor ENT surgery</td><td align="center" valign="middle" >73</td><td align="center" valign="middle" >28</td></tr><tr><td align="center" valign="middle" >(2) Minor abdominal surgery</td><td align="center" valign="middle" >54</td><td align="center" valign="middle" >20.8</td></tr><tr><td align="center" valign="middle" >(3) Major orthopedic surgery</td><td align="center" valign="middle" >34</td><td align="center" valign="middle" >13</td></tr><tr><td align="center" valign="middle" >(4) Major abdominal surgery</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >11.5</td></tr><tr><td align="center" valign="middle" >(5) Major ENT surgery</td><td align="center" valign="middle" >29</td><td align="center" valign="middle" >11</td></tr><tr><td align="center" valign="middle" >(6) Minor orthopedic surgery</td><td align="center" valign="middle" >24</td><td align="center" valign="middle" >9.2</td></tr><tr><td align="center" valign="middle" >(7) Other major surgeries</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >4.2</td></tr><tr><td align="center" valign="middle" >(8) Other minor surgeries</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >260</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>(1) adenoidectomy, tonsillectomy, adeno-tonsillectomy. (2) Hernial cure, hydrocele cure, fistulectomy. (3) Osteosynthesis of the femur, hip. (4) Gastrectomy, abdominal lumpectomy. (5) Laryngectomy, thyroidectomy, ENT sphere lumpectomy. (6) Removal of osteosynthesis materials, external fixators, osteosynthesis of the legs and upper limbs. (7) Neurosurgery. (8) Skin graft, varicectomy, arterovenous fistula.</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Haemostasis assessment following major surgery</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >Platelets</td><td align="center" valign="middle" >104</td><td align="center" valign="middle" >40</td></tr><tr><td align="center" valign="middle" >APTT</td><td align="center" valign="middle" >96</td><td align="center" valign="middle" >37</td></tr><tr><td align="center" valign="middle" >PR</td><td align="center" valign="middle" >93</td><td align="center" valign="middle" >35.7</td></tr><tr><td align="center" valign="middle" >BT</td><td align="center" valign="middle" >68</td><td align="center" valign="middle" >26</td></tr></tbody></table></table-wrap><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Haemostasis balance according to minor surgery</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Effectif</th><th align="center" valign="middle" >Pourcentage</th></tr></thead><tr><td align="center" valign="middle" >Platelets</td><td align="center" valign="middle" >156</td><td align="center" valign="middle" >60</td></tr><tr><td align="center" valign="middle" >APTT</td><td align="center" valign="middle" >151</td><td align="center" valign="middle" >58</td></tr><tr><td align="center" valign="middle" >PR</td><td align="center" valign="middle" >146</td><td align="center" valign="middle" >56</td></tr><tr><td align="center" valign="middle" >BT</td><td align="center" valign="middle" >121</td><td align="center" valign="middle" >46.5</td></tr></tbody></table></table-wrap></sec></sec><sec id="s4"><title>4. Discussion</title><sec id="s4_1"><title>4.1. Epidemiological Aspects</title><p>Two hundred and sixty patients were involved in the study: 57.7% in the central block and 42.3% in the ENT block. The number of patients was reduced due to the reduction of surgical operations at the central block during the development work during the study period. The 18 to 40 age group was the most represented with 50.4%. The average age of the patients was 40 years. Our results are close to that of Sorol [<xref ref-type="bibr" rid="scirp.109964-ref6">6</xref>] with 59% for the same age group. Anaesthesia was more practiced in young adults at UHC-SO. The male sex predominated (60%). This result can be superimposed on those of Sorol and B&#233;y&#233; [<xref ref-type="bibr" rid="scirp.109964-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref6">6</xref>] with 63% and 57.4% respectively.</p></sec><sec id="s4_2"><title>4.2. Anaesthesiological Care</title><p>All of the patients had undergone anaesthesia consultation prior to the practice of anaesthesia.</p><p>The PHA was systematic. The platelet count was achieved in all patients. This result is identical to that of Koumare [<xref ref-type="bibr" rid="scirp.109964-ref7">7</xref>] with 99.6% platelet count achieved preoperatively. The prothrombin (PR) level was performed at 95.3% with an abnormal PR of 11.7%. This abnormal PR was slightly higher than that of Koumare [<xref ref-type="bibr" rid="scirp.109964-ref7">7</xref>] with 7.14%. APTT was 95% performed with 6.5% abnormal APTT. The BT was 72.7% achieved with 5.8% abnormal BT. These abnormal results in our context are partly false positives by laboratory errors. Blery [<xref ref-type="bibr" rid="scirp.109964-ref8">8</xref>] recommends in this case the abandonment of a systematic prescription and favour a selective prescription.</p><p>Several authors Samama CM [<xref ref-type="bibr" rid="scirp.109964-ref2">2</xref>], Haberer [<xref ref-type="bibr" rid="scirp.109964-ref9">9</xref>] have questioned the importance of BT in PHA. For Dominique [<xref ref-type="bibr" rid="scirp.109964-ref10">10</xref>], the preoperative BT does not have a good predictive value for the risk of haemorrhage per and postoperatively, whatever the type of anaesthesia in the absence of haemorrhagic manifestation of primary haemostasis. The only discordant argument is that of the Study Group on Haemostasis and Thrombosis (SGHT) [<xref ref-type="bibr" rid="scirp.109964-ref11">11</xref>] of the French society of haematology, which defends a minimal PHA including a level of platelets, a PR, a APTT in all preoperative patients. In our context, the prescription of PHA did not take account of the interrogation or clinical examination but was systematically prescribed most often by the surgeons who received the patients first and the paramedical anaesthesiologists who did not have the same skills than the ARD in this area. The prescription of PHA should not be systematic and the bleeding time should not be part of PHA [<xref ref-type="bibr" rid="scirp.109964-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref13">13</xref>].</p><p>The preoperative treatment of the haemostasis anomalies observed was carried out for 6.4% of low PR with vitamin K1 and 0.8% with fresh frozen plasma. A patient with severe thrombocytopenia was transfused with platelet concentrate and had no haemostasis pathology after haematological consultation. For Tetchi [<xref ref-type="bibr" rid="scirp.109964-ref14">14</xref>], the frequency of pathologies revealed by a systematic PHA in patients in whom the examination and clinical examination are normal is low. No treatment was performed for the other haemostasis abnormalities found. The various abnormalities of haemostasis come from other pathologies interfering with haemostasis, false positives, taking certain drugs interfering with haemostasis, non-compliance with the conditions of sampling for good haemostasis and not pathologies of haemostasis.</p><p>The children 8 months to 3 years old had all benefited from a sample for a platelet count and a APTT at 14.6%; 13.4% PR and 10.3% BT. Our results are different from those of Molliex [<xref ref-type="bibr" rid="scirp.109964-ref12">12</xref>] and the recommendations of the National Agency for Accreditation and Health Assessment (NAAHA) [<xref ref-type="bibr" rid="scirp.109964-ref15">15</xref>], which recommend carrying out PR, APTT and platelet count to diagnose a haemorrhagic syndrome preoperatively even in the absence of a haemorrhagic history before walking age in children. The patients aged 45 to 55 all had a platelet count (64.6%); 58.4% PR; 56.9% APTT and 47.3% BT. According to Molliex and NAAHA [<xref ref-type="bibr" rid="scirp.109964-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref15">15</xref>], PHA is not necessary in this age group if the examination for haemorrhagic syndrome is negative. Our results in this age group contradict this argument and did not take age into account. For those over 55, the NAAHA [<xref ref-type="bibr" rid="scirp.109964-ref15">15</xref>] recommends the prescription of PR, APTT and platelet count even if the examination is negative. The NAAHA recommendations [<xref ref-type="bibr" rid="scirp.109964-ref15">15</xref>] differ from our results in this age group where all the patients had a platelet count (20.7%); PR (20%), APTT (19%) and BT (15%). These results in our context were related to the fact that the majority of PHAs were not requested by the MARs at the consultation but rather by the surgeons and by the paramedical anaesthetists.</p><p>ASA1 patients were more represented (48.5%) followed by ASA2 (40%) and ASA3 patients (11.5%). Our results are close to those of Tomta [<xref ref-type="bibr" rid="scirp.109964-ref16">16</xref>] who found 53.2% of ASA1. On the other hand, these results are lower than those of Sorol [<xref ref-type="bibr" rid="scirp.109964-ref5">5</xref>] with 60% of ASA1. Indeed Molliex, Bonhomme and Haberer [<xref ref-type="bibr" rid="scirp.109964-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref17">17</xref>] had questioned the systematic nature of this prescription for ASA1 patients. Asymptomatic haemostasis disorders are exceptional in ASA1 subjects and the systematic practise of PHA in the ASA1 population generates very many false positive results according to Blery and Haberer [<xref ref-type="bibr" rid="scirp.109964-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref17">17</xref>] so it is necessary to take into account the history in favour of a haemostasis disorder. In ASA2 and ASA3 patients, PHA was performed systematically. The ASA classification did not directly influence the achievement of PHA.</p></sec><sec id="s4_3"><title>4.3. Intraoperative Stage</title><p>General anaethesia (GA) was the most common technique (62.7%). This result can be explained by the fact that all ENT and neurosurgery patients were operated on GA where other techniques were not possible.</p><p>According to anaesthesia techniques, the platelet count was achieved in all patients (<xref ref-type="table" rid="table3">Table 3</xref>). These results are contrary to the recommendations of David, ASA and NICE [<xref ref-type="bibr" rid="scirp.109964-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref20">20</xref>], according to which only the clinical examination and the interrogation should be carried out in first intention to diagnose a pathology of the coagulation before the practise of a anaesthesia whether general or locoregional. This systematic practise of PHA in our context was the work of the same previous actors (surgeons, paramedical anaesthesiologists). These systematic reviews were carried out in the haunt of optimal security for the prevention of haemorrhagic complications related to spinal anaesthesia.</p><p>No peranaesthetic incident related to a haemostasis disorder was recorded during our work; therefore, peranaesthetic incidents related to a haemostasis disorder were rare and a systematic PHA had been of no use.</p><p>No post-anaesthetic complications related to a haemostasis disorder were recorded. The occurrence of a post-anaesthetic complication linked to a haemostasis disorder, in particular compression marrow haematoma in the case of locoregional anaesthesia (LRA), was evaluated in a variable manner according to Nathan [<xref ref-type="bibr" rid="scirp.109964-ref21">21</xref>]. The haemorrhagic risk in case of peripheral LRA is considered to be less than that of central LRA due to the superficial nature of the puncture which makes compression available externally and the occurrence of even a small haematoma is directly visible.</p><p>The results of Nathan [<xref ref-type="bibr" rid="scirp.109964-ref21">21</xref>], can be superimposed on ours or no postoperative complication linked to a haemostasis disorder was recorded. For Nathan [<xref ref-type="bibr" rid="scirp.109964-ref21">21</xref>], the occurrence of a perimedullary haematoma is often linked to other favorable factors such as technical difficulties and the repetition of punctures, age but rarely to a haemostasis disorder. Although rare, post-anaesthetic complications related to a haemostasis disorder are a reality and should be taken into account whenever an anaesthesia, especially locoregional, is indicated.</p><p>Types of surgery: minor ENT surgery was the most represented (28%) followed by minor abdominal surgery (20.7%).</p><p>PHA performed for minor surgery: all patients who had minor surgery (60%) performed a minimal haemostasis assessment including a platelet count (60%), a APTT (58%), a PR (56%), a BT (46%). These results are contrary to Tetchi’s arguments [<xref ref-type="bibr" rid="scirp.109964-ref14">14</xref>] according to which if the patient has no haemorrhagic history subject to reliable questioning, if there is no pathology which could interfere with haemostasis and the estimated haemorrhagic risk of the operating procedure is low or even zero, so this PHA is unnecessary. The same arguments are shared by Samama [<xref ref-type="bibr" rid="scirp.109964-ref2">2</xref>] and Haberer [<xref ref-type="bibr" rid="scirp.109964-ref17">17</xref>]. On the other hand, the GEHT [<xref ref-type="bibr" rid="scirp.109964-ref11">11</xref>] recommends performing a simple PHA comprising a platelet count, a PR and a APTT in all preoperative patients. PHA is not necessary in case of minor surgery in the absence of elements in favour of a haemostasis disorder [<xref ref-type="bibr" rid="scirp.109964-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref20">20</xref>].</p><p>PHA performed for major surgery: almost all patients operated for major surgery (40%) had a platelet count (40%), a APTT (37%), a PR (35.7%) and a BT (26%).</p><p>Our results respond to the arguments of several authors [<xref ref-type="bibr" rid="scirp.109964-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.109964-ref19">19</xref>] who recommend the prescription of the level of platelets, APTT, and PR in the event of major surgery in all patients even in the absence of clinical sign and history in favour of a hemostasis disorder.</p><p>Intraoperative incidents and accidents: no intraoperative complications related to a haemostasis disorder were recorded after the correction of biological haemostasis disorders. According to Blery [<xref ref-type="bibr" rid="scirp.109964-ref22">22</xref>], bleeding problems are much more linked to surgical problems than to a biological disorder of haemostasis. It is very unlikely to have a severe bleeding intraoperatively related to an unknown haemostasis abnormality in asymptomatic subjects. On the other hand, the occurrence of bleeding during surgery depends not only on the abnormality of physiological haemostasis but also on the type of surgery, the quality of surgical haemostasis and the taking of certain drugs that interfere with haemostasis. Numerous studies have shown that there is no close relationship between the abnormality of haemostasis and surgical bleeding [<xref ref-type="bibr" rid="scirp.109964-ref23">23</xref>].</p><p>Postoperatively there was no abnormal postoperative bleeding from operative wounds.</p></sec></sec><sec id="s5"><title>5. Conclusion</title><p>The risk of bleeding and peri-anesthetic complications due to an abnormality of haemostasis is an individual and not a statistical risk. The simple haemostasis assessment was systematic. No complications related to a haemostasis disorder were recorded during the perioperative period. The systematic prescription of the preoperative haemostasis assessment was hardly justified. Selectively prescribe the haemostasis balance according to the patient’s age, clinical condition, field, surgical condition. For minor surgery, refrain from the haemostasis check-up; in case of major surgery, ask for a platelet count, a PR and an APTT.</p></sec><sec id="s6"><title>Acknowledgements</title><p>Thanks to Isabelle Mouzou for the secretariat and Afi H&#233;gbor for the English translation. The work is done in a more or less solitary setting.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors declare that they have no conflict of interest.</p></sec><sec id="s8"><title>Declaration</title><p>The manuscript has been read and approved by all the authors and the conditions of authorship have been fulfilled.</p></sec><sec id="s9"><title>Cite this paper</title><p>Mouzou, E.T., Ass&#233;nouw&#232;, S., Moumouni, A.E.K., Tch&#232;tik&#232;, P. and Gnimdou, A.-Y. (2021) Assessment of Haemostasis in Anaesthesia for Surgery at the Sylvanus Olympio University Hospital Center in Lom&#233;. Open Journal of Anesthesiology, 11, 184-193. https://doi.org/10.4236/ojanes.2021.116018</p></sec></body><back><ref-list><title>References</title><ref id="scirp.109964-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Blery, C. (1990) Should a Coagulation Assessment be Carried out before Locoregional Anesthesia in an ASA1 Subject? 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