<?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">OJBD</journal-id><journal-title-group><journal-title>Open Journal of Blood Diseases</journal-title></journal-title-group><issn pub-type="epub">2164-3180</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojbd.2023.132011</article-id><article-id pub-id-type="publisher-id">OJBD-125907</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>
 
 
  Factors Associated with Haemolytic Anaemia in the Internal Medicine Department of the Douala General Hospital in Cameroon
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Eveline</surname><given-names>Ngouadjeu Dongho</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>Brice</surname><given-names>Utrich Afana</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>Clémence</surname><given-names>Olemba</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>Jean</surname><given-names>Pierre Nda Mefo’o</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>Cécile</surname><given-names>Ebongue Okalla</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>Abdou</surname><given-names>Temfomo</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>Jules</surname><given-names>Clement Nguedia Assob</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Henry</surname><given-names>Namme Luma</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Internal Medicine, Douala General Hospital, Douala, Cameroon</addr-line></aff><aff id="aff2"><addr-line>Department of Biological Sciences, Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon</addr-line></aff><pub-date pub-type="epub"><day>17</day><month>05</month><year>2023</year></pub-date><volume>13</volume><issue>02</issue><fpage>83</fpage><lpage>91</lpage><history><date date-type="received"><day>2,</day>	<month>March</month>	<year>2023</year></date><date date-type="rev-recd"><day>26,</day>	<month>June</month>	<year>2023</year>	</date><date date-type="accepted"><day>29,</day>	<month>June</month>	<year>2023</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>
 
 
  Introduction: 
  Haemolytic anaemia (HA) is defined as a decrease in haemoglobin (Hb) levels below baseline due to excessive and premature destruction of red blood cells (RBCs) in the periphery resulting in a shortened life span of less than 120 days. Haemolysis can be corpuscular or extra-corpuscular. The aim of our study was to investigate the factors associated with it for optimal management of patients hospitalised in internal medicine at the Douala General Hospital (DGH).
   
  <b>Methodology: </b>
  We conducted an analytical cross-sectional
   study, including all patients admitted to the internal medicine department of the DGH from 11 February to 20 May 2022, and excluding patients with non-compliant samples. The search for haemolytic anaemia was carried out by means of blood count, reticulocyte count, blood smear, unconjugated bilirubin, lactate dehydrogenase and direct Coombs test. Sociodemographic, clinical and biological parameters were collected and analysed. Correlation was defined for a p value 
  &lt;
   0.05. 
  <b>Results: </b>
  This study included 147 patients, 50.34% of whom were men, for a sex ratio of 1.01. The mean age was 52 &#177; 17.9 years. The most represented age group was 56 - 70 years (n = 49; 33%) with extremes from 15 to 90 years. We counted 29.3% cases of haemolytic anaemia (HA) and 13.9% cases of autoimmune haemolytic anaemia (AIHA). Haemolytic anaemia (HA) was present in 54.14% of men for a sex ratio of 1.38; the most represented age group was 40 - 55 years, 37.2%. HA was associated with jaundice (OR: 3.74, CI: [1.70 - 8.22], p = 0.001), HIV - AIDS (OR: 2.72, CI: [0.98 - 7.53], p = 0.05), thrombocytopaenia (OR: 3.53, CI: [1.58 - 7.89], p = 0.02). LDH was elevated (OR: 2.86, CI: [1.30 - 6.26], p = 0.00) as well as elevated reticulocyte count (OR: 3.84, CI: [1.75
   
  -
   
  8.44], p = 0.01). Unconjugated bilirubin was elevated in all these patients. In multivariate analysis, factors associated with HA were a history of HIV/AIDS, jaundice, thrombocytopaenia and elevated reticulocyte count.
   
  <b>Conclusion:</b>
   Hemolytic anaemia is common in internal medicine and 
  is 
  significantly associated with thrombocytopenia, HIV/AIDS infection and jaundice.
 
</p></abstract><kwd-group><kwd>Haemolytic Anaemia</kwd><kwd> Internal Medicine</kwd><kwd> DGH</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Anaemia is an abnormal decrease in the amount of functional haemoglobin below reference values. These values in adults vary according to gender and physiological status [<xref ref-type="bibr" rid="scirp.125907-ref1">1</xref>] . According to the World Health Organisation (WHO) these values are between 12 and 15 g/dl in women and between 13 and 16 g/dl in men [<xref ref-type="bibr" rid="scirp.125907-ref2">2</xref>] . Anaemia is classified as one of the ten most serious diseases of the modern world, with a very high prevalence, and affects mostly women of childbearing age, pre-school children and elderly people [<xref ref-type="bibr" rid="scirp.125907-ref3">3</xref>] . anaemia in the latter increases morbidity and mortality [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] . Two billion people worldwide are affected, mainly those in developing countries, with prevalence rates of 39.8% in pregnant women, 22.4% in children under 12 months, 64.4% in those aged 12 - 56 months, 13.5% in those over five years and 43.2% in the elderly [<xref ref-type="bibr" rid="scirp.125907-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.125907-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.125907-ref7">7</xref>] . There are several types of anaemia with different and varied aetiology, the most common being martial deficiency anaemia and the least common being haemolytic anaemia (HA) [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] .</p><p>Haemolytic anaemia is defined as a decrease in haemoglobin levels due to excessive and premature destruction of red blood cells resulting in a reduction in the lifespan of red blood cells to less than 120 days. Classically, a distinction is made between corpuscular haemolysis, which is mostly constitutional, and extra-corpuscular haemolysis, which is acquired [<xref ref-type="bibr" rid="scirp.125907-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.125907-ref9">9</xref>] . Although most haemolytic anaemias are hereditary, their occurrence is not exceptional in adults [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] . Their aetiological diagnosis requires a hierarchical approach that allows the identification of the haemolytic mechanism [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] .</p><p>Haemolytic anaemia is a relatively rare condition as epidemiological studies have found an incidence of approximately 3 cases/100,000 population per year in the Western world [<xref ref-type="bibr" rid="scirp.125907-ref5">5</xref>] . This figure does not reflect reality, as it does not take into account the forms associated with other pathologies that are sometimes in the forefront [<xref ref-type="bibr" rid="scirp.125907-ref10">10</xref>] . In 2021, Garrigue et al. found a prevalence of 65.7% in France [<xref ref-type="bibr" rid="scirp.125907-ref11">11</xref>] . In Morocco in 2017 the prevalence of haemolytic anaemia was 7.33% [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] . In Mali, Seydou et al. noted a prevalence of autoimmune haemolytic anaemia of 4.7% in the Nephrology and Haemodialysis Department of the Point G University Hospital [<xref ref-type="bibr" rid="scirp.125907-ref10">10</xref>] .</p><p>In view of the almost systematic use of iron-rich drugs and foods in the suspicion of anaemia by the population, and the possibility of optimal management of HA at the GHD, we thought it appropriate to investigate the frequency and associated factors in patients hospitalised at the internal medicine Department.</p></sec><sec id="s2"><title>2. Methodology</title><p>This is an analytical cross-sectional study, covering a period from 11 February to 20 May 2022. The recruitment was done in the Internal Medicine Department and the analysis of the samples in the clinical biology laboratory of the Douala General Hospital. We had consenting patients of both sexes, aged 15 years and over, during our study period. Patients with difficult specimens were excluded. Age, sex, reason for hospitalisation, functional signs, medical and transfusion history, haemogram, reticulocyte count, blood smear, free bilirubin, lactate dehydrogenase and direct Coombs test were performed for each patient. The search for anaemia was carried out by means of blood count tests on the Urit 3000 plus machine (Serial No. 3000PE05587). Stigmata of haemolysis were investigated by free bilirubin and lactate dehydrogenase tests on the BT 1500 (Serial No. 47184504). The blood smear was performed with the optical microscope and the reticulocyte count test was also performed. The direct Coombs test allowed us to determine the proportion of autoimmune haemolytic anaemia (AHAI). The study was conducted after approval from the institutional ethics committee of the University of Douala and the research committee of the Douala General Hospital. The definition of anaemia and severity was based on the haemoglobin level according to WHO [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] . The mean corpuscular volume was considered normal between 80 and 100 fl and the mean corpuscular haemoglobin concentration was normal between 32 - 36 g/dl. The anaemia was regenerative when the reticulocyte count was above 120 G/L. The stigmata of haemolysis was observed when the free bilirubin level was greater than 3 mg/l and the lactate dehydrogenase activity was elevated, i.e. greater than 480 IU/I. The haemolytic anaemia was autoimmune when the direct Coombs test was positive.</p><p>● Statistical analysis</p><p>The data were processed with Microsoft Excel 2007 and analysed using StataMP 13, IBM SPSS Statistics 20. Qualitative and quantitative variables were grouped into classes, means &#177; standard deviations (SD). To check the association between the variables, we used the chi-square test, univariate and multivariate binary logistic. Differences were considered significant for p &lt; 0.05.</p></sec><sec id="s3"><title>3. Results</title><p>A total of 43 patients with haemolytic anaemia were identified out of 147 patients recruited, a prevalence of 29.3%. Six patients had autoimmune haemolytic anaemia (13.9%). <xref ref-type="table" rid="table1">Table 1</xref> shows the distribution of patients by age group and there was a predominance of haemolytic anaemia in the 40 - 45 year age group. Males were the most affected by haemolytic anaemia, with a sex ratio of 1.38. The mean age was 52.3 &#177; 18.3 years with extremes of 17 and 88 years.</p><p>Altered general condition was the main reason for hospitalisation with a proportion of 30.2%. Mucocutaneous pallor, asthenia, fever and jaundice were the clinical signs found in most of the patients with the respective proportions of 88.3%, 86%, 16.3% and 34.9%. Arterial hypertension and HIV infection were the most frequent antecedents as shown in <xref ref-type="table" rid="table2">Table 2</xref>.</p><p>The mean haemoglobin level in patients with haemolytic anaemia was 9.1 &#177; 1.8 g/dl. The haemolytic anaemia was generally moderate, but severe in 11.4% of cases (<xref ref-type="table" rid="table3">Table 3</xref>).</p><p>Normochromic normocytic anaemia accounted for 93% and normochromic macrocytic anaemia for 7% of cases. An elevated reticulocyte count was found in 67% of cases. Abnormalities of structures, including acanthocytes, schizocytes and sickle cells were found in 27.9% of patients (<xref ref-type="table" rid="table4">Table 4</xref>). Free bilirubin was elevated in 100% of patients and elevated lactate dehydrogenase in 49% of patients (<xref ref-type="table" rid="table4">Table 4</xref>).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of patients by age group</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Age groups (Year)</th><th align="center" valign="middle" >Total population N = 147 (%)</th><th align="center" valign="middle" >Patients with no anaemia n = 24 (%)</th><th align="center" valign="middle" >Patients without haemolytic anaemia n = 80 (%)</th><th align="center" valign="middle" >Patients with haemolytic anaemia n = 43 (%)</th></tr></thead><tr><td align="center" valign="middle" >&lt;30</td><td align="center" valign="middle" >22 (15)</td><td align="center" valign="middle" >6 (25)</td><td align="center" valign="middle" >14 (17.5)</td><td align="center" valign="middle" >2 (4.7)</td></tr><tr><td align="center" valign="middle" >[30 - 39]</td><td align="center" valign="middle" >17 (11.6)</td><td align="center" valign="middle" >1 (4.2)</td><td align="center" valign="middle" >10 (12.5)</td><td align="center" valign="middle" >6 (13.9)</td></tr><tr><td align="center" valign="middle" >[40 - 55]</td><td align="center" valign="middle" >39 (26.5)</td><td align="center" valign="middle" >6 (25)</td><td align="center" valign="middle" >17 (21.3)</td><td align="center" valign="middle" >16 (37.2)</td></tr><tr><td align="center" valign="middle" >[56 - 70]</td><td align="center" valign="middle" >49 (33.3)</td><td align="center" valign="middle" >9 (37.5)</td><td align="center" valign="middle" >26 (32.5)</td><td align="center" valign="middle" >14 (32.6)</td></tr><tr><td align="center" valign="middle" >&gt;70</td><td align="center" valign="middle" >20 (13.6)</td><td align="center" valign="middle" >2(8.3)</td><td align="center" valign="middle" >13 (16.2)</td><td align="center" valign="middle" >5 (11.6)</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >147</td><td align="center" valign="middle" >24</td><td align="center" valign="middle" >80</td><td align="center" valign="middle" >23</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 by medical history</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Background Medical</th><th align="center" valign="middle" >Total population N = 147 (%)</th><th align="center" valign="middle" >Patients with no anaemia n = 24 (%)</th><th align="center" valign="middle" >Patients without haemolytic anaemia n = 80 (%)</th><th align="center" valign="middle" >Patients with haemolytic anaemia n = 43 (%)</th></tr></thead><tr><td align="center" valign="middle" >Diabetes</td><td align="center" valign="middle" >24 (16.3)</td><td align="center" valign="middle" >4 (16.6)</td><td align="center" valign="middle" >14 (17.5)</td><td align="center" valign="middle" >5 (11.6)</td></tr><tr><td align="center" valign="middle" >BPH</td><td align="center" valign="middle" >53 (36.1)</td><td align="center" valign="middle" >7 (29.2)</td><td align="center" valign="middle" >31 (38.7)</td><td align="center" valign="middle" >15 (34.9)</td></tr><tr><td align="center" valign="middle" >HIV/AIDS</td><td align="center" valign="middle" >20 (13.6)</td><td align="center" valign="middle" >2 (8.3)</td><td align="center" valign="middle" >8 (10)</td><td align="center" valign="middle" >10 (23.25)</td></tr><tr><td align="center" valign="middle" >Hepatitis</td><td align="center" valign="middle" >5 (3.4)</td><td align="center" valign="middle" >1 (4.2)</td><td align="center" valign="middle" >1 (1.3)</td><td align="center" valign="middle" >3 (6.9)</td></tr><tr><td align="center" valign="middle" >Respiratory disease</td><td align="center" valign="middle" >14 (9.5)</td><td align="center" valign="middle" >1 (4.2)</td><td align="center" valign="middle" >11 (13.7)</td><td align="center" valign="middle" >2 (4.6)</td></tr><tr><td align="center" valign="middle" >CKD</td><td align="center" valign="middle" >22 (14.96)</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >14 (17.5)</td><td align="center" valign="middle" >8 (18.6)</td></tr><tr><td align="center" valign="middle" >Stroke</td><td align="center" valign="middle" >9 (6.1)</td><td align="center" valign="middle" >1 (4.2)</td><td align="center" valign="middle" >7 (8.7)</td><td align="center" valign="middle" >1 (2.3)</td></tr><tr><td align="center" valign="middle" >Cancers</td><td align="center" valign="middle" >20 (13.6)</td><td align="center" valign="middle" >2 (8.3)</td><td align="center" valign="middle" >13 (16.3)</td><td align="center" valign="middle" >5 (11.6)</td></tr><tr><td align="center" valign="middle" >Inflammatory disease</td><td align="center" valign="middle" >9 (6.1)</td><td align="center" valign="middle" >3 (12.5)</td><td align="center" valign="middle" >5 (6.25)</td><td align="center" valign="middle" >3 (6.9)</td></tr></tbody></table></table-wrap><p>VIH/AIDS: People Living with AIDS; HBP: High Blood Pressure; CKD: Chronic Kidney Disease.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Distribution of patients by biological data</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Patients without haemolytic anaemia n (%)</th><th align="center" valign="middle" >Patients with haemolytic anaemia n (%)</th><th align="center" valign="middle" >OR [95% CI]</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Reticulocytes Icterus PLWHIV Thrombocytopenia</td><td align="center" valign="middle" >28 (35) 28 (35) 8 (10) 17 (21.3)</td><td align="center" valign="middle" >29 (67.5) 15 (34.9) 10 (23.25) 21(48.8)</td><td align="center" valign="middle" >1.41 [0.49 - 2.33] 1.07 [0.11 - 2.04] 1.58 [0.19 - 2.97] 1.12 [0.18 - 2.06]</td><td align="center" valign="middle" >0.002 0.029 0.026 0.006</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Associated factors in bivariate analysis</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="2"  >Variables</th><th align="center" valign="middle" >Total population N = 147 (%)</th><th align="center" valign="middle" >Patients with no anaemia n = 24 (%)</th><th align="center" valign="middle" >Patients without haemolytic anaemia n = 80 (%)</th><th align="center" valign="middle" >Patients with haemolytic anaemia n = 43 (%)</th></tr></thead><tr><td align="center" valign="middle" >Hb</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >10.2 &#177; 2.48</td><td align="center" valign="middle" >14.0 &#177; 1.21</td><td align="center" valign="middle" >9.6 &#177; 1.76</td><td align="center" valign="middle" >9.1 &#177; 1.89</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >3.7 - 16.7</td><td align="center" valign="middle" >12.1 - 16.7</td><td align="center" valign="middle" >5.2 - 12.5</td><td align="center" valign="middle" >3.7 - 12.5</td></tr><tr><td align="center" valign="middle" >MCV</td><td align="center" valign="middle" >Average</td><td align="center" valign="middle" >88.4 &#177; 7.14</td><td align="center" valign="middle" >90.3 &#177; 4.88</td><td align="center" valign="middle" >86.6 &#177; 8.04</td><td align="center" valign="middle" >90.6 &#177; 7.45</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >70 - 123</td><td align="center" valign="middle" >77 - 99.2</td><td align="center" valign="middle" >70 - 105</td><td align="center" valign="middle" >80.1 - 123</td></tr><tr><td align="center" valign="middle" >MCHC</td><td align="center" valign="middle" >Average</td><td align="center" valign="middle" >32.9 &#177;1.3</td><td align="center" valign="middle" >42.1 &#177; 4.33</td><td align="center" valign="middle" >32.6 &#177; 1.22</td><td align="center" valign="middle" >33.34 &#177; 1.29</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >29.5 - 38.1</td><td align="center" valign="middle" >34.8 - 52.2</td><td align="center" valign="middle" >29.5 - 36</td><td align="center" valign="middle" >32 - 38.1</td></tr><tr><td align="center" valign="middle" >White blood cells</td><td align="center" valign="middle" >Average</td><td align="center" valign="middle" >8.6 &#177; 5.8</td><td align="center" valign="middle" >7.33 &#177; 3.22</td><td align="center" valign="middle" >9.0 &#177; 6.5</td><td align="center" valign="middle" >8.7 &#177; 6.2</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >1 - 39.2</td><td align="center" valign="middle" >2.3 - 14.4</td><td align="center" valign="middle" >1 - 39.2</td><td align="center" valign="middle" >2.6 - 22.8</td></tr><tr><td align="center" valign="middle" >Trays</td><td align="center" valign="middle" >Average</td><td align="center" valign="middle" >8.6 &#177; 5.8</td><td align="center" valign="middle" >224.1 &#177; 78.5</td><td align="center" valign="middle" >261 &#177; 157.4</td><td align="center" valign="middle" >163.9 &#177; 147.5</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >16 - 780</td><td align="center" valign="middle" >68 - 364</td><td align="center" valign="middle" >23 - 780</td><td align="center" valign="middle" >16 - 409</td></tr><tr><td align="center" valign="middle" >Free bilirubin (mg/l) ≤ 03</td><td align="center" valign="middle" >Average</td><td align="center" valign="middle" >2.11</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.11</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >0.22 - 3</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.22 - 3</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >Free bilirubin (mg/l) &gt; 03</td><td align="center" valign="middle" >Average</td><td align="center" valign="middle" >14.3</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >6.96</td><td align="center" valign="middle" >18.41</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >3.12 - 186.58</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >3.12 - 35.98</td><td align="center" valign="middle" >3.28 - 186.58</td></tr><tr><td align="center" valign="middle" >LDH (IU/l) ≤ 480</td><td align="center" valign="middle" >Average</td><td align="center" valign="middle" >262.3</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >264.19</td><td align="center" valign="middle" >257.1</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >100.66 - 478.52</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >100.66 - 478.52</td><td align="center" valign="middle" >156.38 - 438.5</td></tr><tr><td align="center" valign="middle" >LDH (IU/l) &gt; 480</td><td align="center" valign="middle" >Average</td><td align="center" valign="middle" >1033.64</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >909</td><td align="center" valign="middle" >1157.32</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Extremes</td><td align="center" valign="middle" >483.23 - 471.81</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >483.23 - 3442.42</td><td align="center" valign="middle" >486.12 - 4471.81</td></tr></tbody></table></table-wrap><p>Age [40 - 50] years and single status were factors associated with the occurrence of haemolytic anaemia (p = 0.02; OR = 6.5 and p = 0.02; OR = 6.6) as shown in <xref ref-type="table" rid="table5">Table 5</xref>. Jaundice was significantly associated with haemolytic anaemia (p = 0.001; OR = 3.74). <xref ref-type="table" rid="table6">Table 6</xref> shows that HIV/AIDS, jaundice, reticulocytosis and thrombocytopenia were associated with haemolytic anaemia in the multivariate factors analysis.</p></sec><sec id="s4"><title>4. Discussion</title><p>Our study was conducted from January to June 2022, with as general objective to</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Multivariate factors associated with haemolytic anaemia</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Socio-demographic factors</th><th align="center" valign="middle" >Patients without haemolytic anaemia n = 80 (%)</th><th align="center" valign="middle" >Patients with haemolytic anaemia n = 43 (%)</th><th align="center" valign="middle" >OR [95% CI]</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Age group [40 - 55] Marital status Single Functional sign Icterus Medical history PLWHA Respiratory disease Thrombocytopenia Reticulocytes &gt; 120 g/L LDH &gt; 480 IU/l</td><td align="center" valign="middle" >17 (21.3) 18 (22.5) 28 (35) 8 (10) 11 (13.7) 17 (21.3) 28 (35) 20 (25)</td><td align="center" valign="middle" >16 (37.2) 14 (32.6) 15 (34.9) 10 (23.25) 2 (4.6) 21 (48.8) 29 (67.5) 21 (48.8)</td><td align="center" valign="middle" >6.5 [1.29 - 33.67] 6.6 [1.29 - 34.48] 3.74 [1.70 - 8.22] 2.72 [0.98 - 7.53] 0.30 [0.13 - 1.44] 3.53 [1.58 - 7.89] 3.84 [1.75 - 8.44] 2.86 [1.30 - 6.26]</td><td align="center" valign="middle" >0.02 0.02 0.001 0.05 0.04 0.02 0.01 0.00</td></tr></tbody></table></table-wrap><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Distribution of anaemic patients according to degree of severity</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Type of anaemia n = 123</th><th align="center" valign="middle" >Total n (%)</th><th align="center" valign="middle" >Slight anaemia n (%)</th><th align="center" valign="middle" >Moderate anaemia n (%)</th><th align="center" valign="middle" >Severe anaemia n (%)</th></tr></thead><tr><td align="center" valign="middle" >haemolytic anaemia</td><td align="center" valign="middle" >43 (100)</td><td align="center" valign="middle" >14 (41.5)</td><td align="center" valign="middle" >22 (47.1)</td><td align="center" valign="middle" >7 (11.4)</td></tr><tr><td align="center" valign="middle" >Without haemolytic anaemia</td><td align="center" valign="middle" >80 (100)</td><td align="center" valign="middle" >37 (46.25)</td><td align="center" valign="middle" >36 (45.0)</td><td align="center" valign="middle" >7 (8.75)</td></tr></tbody></table></table-wrap><p>determine the factors associated with haemolytic anaemia at the Internal Medicine Department of HGD. We identified 43 patients with HA out of 147 patients recruited, giving a prevalence of 29.3%. This prevalence was lower than that of Garrigues et al. who found a prevalence of 65.7% in 2021 during their work on the profile of haemolytic anaemias encountered in an internal medicine department in France on 108 files [<xref ref-type="bibr" rid="scirp.125907-ref11">11</xref>] . This was higher than the prevalence found by Zinebi et al. (7.33%) in Morocco on a population of 150 patients [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] . The prevalence of autoimmune haemolytic anaemia was 13.9% in our series, which was lower than that noted by Garrigues et al. (34.2%) and higher than the 4.7% noted by Seydou et al. in 2021 in the Nephrology and Haemodialysis Department of the Point G University Hospital [<xref ref-type="bibr" rid="scirp.125907-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.125907-ref11">11</xref>] . The 40 - 55 age group was predominantly represented with a proportion of 37.2%, i.e. an average of 52.3 &#177; 18.3 years and extremes of 17 and 88 years. Our result was similar to that of Hachini et al. who in 2016 in Tunisia observed a mean age of 52 years and extremes ranging from 19 to 87 years [<xref ref-type="bibr" rid="scirp.125907-ref12">12</xref>] . The sex ratio was 1.38 with a male predominance, i.e. a proportion of 58.14%. Pouchelon et al. in a French multicentre observational study found a male predominance similar to ours, i.e. 58% [<xref ref-type="bibr" rid="scirp.125907-ref13">13</xref>] . In a population of patients with AHAI, Zulfiqar et al. in 2016 observed a female predominance with 71.4% of cases [<xref ref-type="bibr" rid="scirp.125907-ref14">14</xref>] .</p><p>We found that impairment of general condition was the main reason for hospitalization with a proportion of 30.2%. This result was different from that of Seydou et al. who noted renal failure in 85.2% of cases [<xref ref-type="bibr" rid="scirp.125907-ref10">10</xref>] . Pallor and asthenia were the most common clinical signs with prevalences of 88.3% and 86% respectively. Anouun et al. found in 2022 that the elderly had a lower prevalence of pallor than ours, i.e. 82.6% [<xref ref-type="bibr" rid="scirp.125907-ref15">15</xref>] . Similarly, Zinebi et al. found lower values for pallor and asthenia, respectively 16% and 41% [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] .</p><p>The mean value of the haemoglobin level in our study was 9.1 g/dl, higher than 6 g/dl in Pouchelon et al., 8 g/dl in Zinebi et al. [<xref ref-type="bibr" rid="scirp.125907-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.125907-ref14">14</xref>] . The anaemia was normocytic normochromic in 93% higher than that of Oubelkacem et al. who noted in his series 11% [<xref ref-type="bibr" rid="scirp.125907-ref16">16</xref>] . Indeed, these authors looked for haemolytic anaemia in a group of patients with chronic myeloid leukaemia. Hachini observed a lower proportion than ours (41.1%). But Hachini in his series found 44.4% normochromic macrocytic anaemia, whereas we had only 7% [<xref ref-type="bibr" rid="scirp.125907-ref12">12</xref>] . Haemolytic anaemia was regenerative in 29 patients, i.e. a proportion of 67.5% higher than that of Oubelkacem et al. which was 11% [<xref ref-type="bibr" rid="scirp.125907-ref16">16</xref>] . The consequences of haemolysis in our study were elevated free bilirubin and LDH with values of 100% and 49% respectively. Hachini et al., in a series of 90 cases, found 44% and 67% respectively [<xref ref-type="bibr" rid="scirp.125907-ref12">12</xref>] . HA was associated with the age group 40-55 years (p = 0.02; OR: 6.5). Jaundice was significantly associated with HA (p = 0.00; OR: 3.74) as also noted by Anoun et al. [<xref ref-type="bibr" rid="scirp.125907-ref15">15</xref>] . Pallor and fever were also factors associated with HA (OR = 1.63) as fever may be related to malaria. Our study showed that HIV/AIDS was a predisposing factor for HA (p = 0.05; OR: 2.72) as found in the study of Coulibaly in 2020 and Gourguechon et al. [<xref ref-type="bibr" rid="scirp.125907-ref17">17</xref>] . This could be due to increased destruction of red blood cells by a direct effect of the virus and the adverse effects of ARV drugs. Patients with cancer had a risk of developing haemolytic anaemia, a value of 11.6%. Garrigues et al. noted a proportion of 24.3% HA associated with cancer [<xref ref-type="bibr" rid="scirp.125907-ref11">11</xref>] , in contrast, Mama et al. observed 8.9% [<xref ref-type="bibr" rid="scirp.125907-ref18">18</xref>] . This could be due to the cytotoxic action of anticancer drugs. In our study, thrombocytopenia as well as increased free bilirubin and reticulocyte count were factors associated with haemolytic anaemia (p = 0.02; 0.00 and 0.0). Our results are consistent with those found in the literature [<xref ref-type="bibr" rid="scirp.125907-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.125907-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.125907-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.125907-ref17">17</xref>] .</p></sec><sec id="s5"><title>5. Conclusion</title><p>Male patients and patients aged 40 - 55 years are mostly affected by haemolytic anaemia. One in three patients had HA, which was usually moderate in one- third of cases and most often normochromic normocytic. Factors associated with HA were HIV/AIDS, jaundice, high reticulocyte count, thrombocytopenia. This HA correlated with elevated free bilirubin, LDH, reticulocyte count and thrombocytopenia.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflict of interest.</p></sec><sec id="s7"><title>Authors’ Contributions</title><p>Ngouadjeu Dongho Eveline, Afana Brice and Olemba Cl&#233;mence designed and wrote the protocol, Afana Brice, Nda Mefo’o Jean Pierre and Okalla Ebongue C&#233;cile contributed to data collection and analyses of biological data. Temfomo Abdou and Assob Cl&#233;ment contributed to the manuscript drafting; Luma Namme Henry supervised write up of the manuscript.</p></sec><sec id="s8"><title>Cite this paper</title><p>Ngouadjeu Dongho, E., Afana, B.U., Olemba, C., Nda Mefo’o, J.P., Okalla, C.E., Temfomo, A., Assob, J.C.N. and Luma, H.N. (2023) Factors Associated with Haemolytic Anaemia in the Internal Medicine Department of the Douala General Hospital in Cameroon. 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