<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2 20190208//EN" "http://jats.nlm.nih.gov/publishing/1.2/JATS-journalpublishing1.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" article-type="other" dtd-version="1.2" xml:lang="en">
    <front>
        <journal-meta>
            <journal-id journal-id-type="pmc">F1000Research</journal-id>
            <journal-title-group>
                <journal-title>F1000Research</journal-title>
            </journal-title-group>
            <issn pub-type="epub">2046-1402</issn>
            <publisher>
                <publisher-name>F1000 Research Limited</publisher-name>
                <publisher-loc>London, UK</publisher-loc>
            </publisher>
        </journal-meta>
        <article-meta>
            <article-id pub-id-type="doi">10.12688/f1000research.135708.1</article-id>
            <article-categories>
                <subj-group subj-group-type="heading">
                    <subject>Study Protocol</subject>
                </subj-group>
                <subj-group>
                    <subject>Articles</subject>
                </subj-group>
            </article-categories>
            <title-group>
                <article-title>Rapid, Economic, Acetic acid, Papanicolaou (REAP) staining technique analogous to the routine Papanicolaou staining (PAP) technique</article-title>
                <fn-group content-type="pub-status">
                    <fn>
                        <p>[version 1; peer review: 2 not approved]</p>
                    </fn>
                </fn-group>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author" corresp="yes">
                    <name>
                        <surname>Alone</surname>
                        <given-names>Prachi</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Conceptualization</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Original Draft Preparation</role>
                    <uri content-type="orcid">https://orcid.org/0009-0009-6275-1188</uri>
                    <xref ref-type="corresp" rid="c1">a</xref>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Vodithala</surname>
                        <given-names>Sahitya</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Conceptualization</role>
                    <role content-type="http://credit.niso.org/">Supervision</role>
                    <role content-type="http://credit.niso.org/">Validation</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Review &amp; Editing</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Vagha</surname>
                        <given-names>Sunita</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Conceptualization</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Original Draft Preparation</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <aff id="a1">
                    <label>1</label>Pathology, Jawaharlal Nehru Medical College, Datta Meghe Institute Of Higher Education and Research, Wardha, Maharashtra, 422001, India</aff>
            </contrib-group>
            <author-notes>
                <corresp id="c1">
                    <label>a</label>
                    <email xlink:href="mailto:prachialoney17@gmail.com">prachialoney17@gmail.com</email>
                </corresp>
                <fn fn-type="conflict">
                    <p>No competing interests were disclosed.</p>
                </fn>
            </author-notes>
            <pub-date pub-type="epub">
                <day>3</day>
                <month>8</month>
                <year>2023</year>
            </pub-date>
            <pub-date pub-type="collection">
                <year>2023</year>
            </pub-date>
            <volume>12</volume>
            <elocation-id>931</elocation-id>
            <history>
                <date date-type="accepted">
                    <day>27</day>
                    <month>6</month>
                    <year>2023</year>
                </date>
            </history>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2023 Alone P et al.</copyright-statement>
                <copyright-year>2023</copyright-year>
                <license xlink:href="https://creativecommons.org/licenses/by/4.0/">
                    <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
                </license>
            </permissions>
            <self-uri content-type="pdf" xlink:href="https://f1000research.com/articles/12-931/pdf"/>
            <abstract>
                <p>The current research compared classical 
                    <italic toggle="yes">Papanicolaou stain with REAP (Rapid, Economic, Acetic Acid Papanicolaou)</italic> stain to evaluate staining character, range, charge virtue, and sustaining of stain. The 
                    <italic toggle="yes">PAP Stain</italic> is the standard dye in support of shielding cell study for any cell study and is used in various research centers with several reductions. In certainty, PAP Stain has lowered squamous cell carcinoma incidence by 
                    <italic toggle="yes">70</italic>%, particularly within wealthy provinces with effectively-designed broadcasting systems. But the stain has gone through several changes, moving from the uncreative formal mechanism -&gt; gradual REAP 
                    <italic toggle="yes">PAP staining</italic> in which staining duration level is decreased, it improves the quality, it is cost-effective, easily available, and ethyl alcohol is temporarily superseded with 1% ethanoic acid in advanced nations with guarding programs with careful planning. It has been used to access FNAC (fine needle aspiration cytology). Because of its precise nuclear and nucleoli staining, PAP staining of FNAC and fluid smears is a trustworthy stain. FNAC is a straightforward, speedy, and reliable pre-operative assessment and diagnosis process that has sparked advancements in dyeing technology which utilizes minimal coloring count with a clear cell framework. Around 40 minutes are needed for the standard methodology for traditional PAP Stain. REAP Stain was developed to address this, improving quality while cutting staining time to about one minute. This study&#x2019;s objective was to evaluate the value of the Rapid-Pap stain utilizing quantifiable investigation. The effectiveness of cytoplasmic and nuclear staining, stain preservation, value, and overall course of action for the two techniques&#x2014;conventional PAP stain and REAP stain&#x2014;were collated. When compared to traditional Papanicolaou, REAP stain offers a good, quick, and affordable replacement for the screening of cells. The REAP technique also does a superb job for the maintenance of stains.</p>
            </abstract>
            <kwd-group kwd-group-type="author">
                <kwd>Conventional PAP Stain</kwd>
                <kwd>REAP Stain</kwd>
                <kwd>cervical (squamous cell) smears</kwd>
                <kwd>FNAC</kwd>
                <kwd>alcohol</kwd>
                <kwd>1% ethanoic acid</kwd>
                <kwd>Eosin Azure.</kwd>
            </kwd-group>
            <funding-group>
                <funding-statement>The author(s) declared that no grants were involved in supporting this work.</funding-statement>
            </funding-group>
        </article-meta>
    </front>
    <body>
        <sec id="sec1" sec-type="intro">
            <title>Introduction</title>
            <p>George Papanicolaou created the PAP dye, a vivid color examination of the cell tinge method, in the year 1942. Dr. Papanicolaou afterward updated his research in the years 1954 and 1960.
                <sup>
                    <xref ref-type="bibr" rid="ref1">1</xref>
                </sup> As G.N. Papanicolaou initially studied the PAP stain, he went through numerous alterations, and was later modified by him in the year 1960.
                <sup>
                    <xref ref-type="bibr" rid="ref1">1</xref>
                </sup> The Mallory aniline blue method, the Masson trichrome method, and the short methods can all be found in the history of the Papanicolaou staining method.
                <sup>
                    <xref ref-type="bibr" rid="ref2">2</xref>
                </sup> In human medicine, Pap is the gold-standard staining technique for FNAC or exfoliate cells, which are used to diagnose neoplastic disorders.
                <sup>
                    <xref ref-type="bibr" rid="ref3">3</xref>
                </sup>
            </p>
            <p>
                <italic toggle="yes">SB Dighe (2005)</italic> published the REAP method.
                <sup>
                    <xref ref-type="bibr" rid="ref4">4</xref>
                </sup> To compare the excellence of REAP blotching of spatter to conventional PAP staining using upcoming guidelines: Solar &amp; protoplasmic blotching intensity, staining time, vanished success, lengthy duration of shade maintenance.
                <sup>
                    <xref ref-type="bibr" rid="ref5">5</xref>
                </sup>
            </p>
            <p>Papanicolaou stain has been modified to increase staining quality and/or to shorten staining time.
                <sup>
                    <xref ref-type="bibr" rid="ref6">6</xref>
                </sup> PAP stains are accustomed to detecting and differentiating units from smears obtained in different physical fluids,
                <sup>
                    <xref ref-type="bibr" rid="ref7">7</xref>
                </sup> gynecological smears,
                <sup>
                    <xref ref-type="bibr" rid="ref8">8</xref>
                </sup> and FNAC
                <sup>
                    <xref ref-type="bibr" rid="ref9">9</xref>
                </sup> smears from different organs. Various types of body fluids and needle biopsies are used to stain the specimens; the samples include gynecological Papanicolaou spatter, froth, grazing, cleaning, discharge, BAL, ascitic fluidic, pericardial fluidic, CSFs,
                <sup>
                    <xref ref-type="bibr" rid="ref10">10</xref>
                </sup> malignant ascites, pleural effusion, joint effusion, semen discharge,
                <sup>
                    <xref ref-type="bibr" rid="ref11">11</xref>
                </sup> FNAC,
                <sup>
                    <xref ref-type="bibr" rid="ref8">8</xref>
                </sup> neoplasm affecting specimens, and matter containing loose cells. An application of spot-on tissue slides is connected with loose cell inspection. Papanicolaou spots are gold standard cells of the cervix covering up. It produces a metachronous, clear spotting response by distinct solar &amp; cellular characteristics.</p>
            <p>Conventional Papanicolaou Staining Procedure: Shift glass slides immediately out of the alcohol aether adhesive to 80% alcohol watery, then via 
                <italic toggle="yes">70</italic>% &amp; 
                <italic toggle="yes">50</italic>% alcohol to D/W. For 4 minutes, &#x2018;stain&#x2019; with &#x2018;
                <italic toggle="yes">Harris hematoxylin&#x2019;.</italic> Drain with D/W for a few seconds. Six times, bath through 
                <italic toggle="yes">0.25</italic>% Hydrochloric Acid in 
                <italic toggle="yes">50</italic>% eth-an-ol (20-60 sec). 6 minutes in flowing tap water Run through 50%, 70%, 80%, and 95% alcohol after rinsing with distilled water. 2 minutes staining in OG-6. Rinse in two 95% alcohol changes. For 2 minutes, stain in EA 36/EA 50. Rinse three times in 
                <italic toggle="yes">95</italic>% alcohol. Remove water from the abs. alc-oh-ol, then in similar pieces xylol and abs. alc; clear in dimethylbenzene and cover with DPx.
                <sup>
                    <xref ref-type="bibr" rid="ref12">12</xref>
                </sup>
            </p>
            <p>REAP P-A-P Staining Method: 1% ACID ACETIC ten soaks. 
                <italic toggle="yes">Harris Haematoxylin</italic> 10 dips. [Previously heat to 
                <italic toggle="yes">60&#x00b0;C</italic>] Ten soaks in running H2O. ethanoic acid 1%, 10 dips for OG-6. 1%acetic acids ten soaks. Eosin azure-50 ten dips. 1.0% acetic - acid Meth-an-ol ten 
                <italic toggle="yes">dips</italic> dissolvent ten dips perform mop up with every process. Install in DPx. In REAP, at every stage of alc-oh-ol in standard Papanicolaou was changed with 1%ethanoic acid.
                <sup>
                    <xref ref-type="bibr" rid="ref13">13</xref>
                </sup>
                <list list-type="bullet">
                    <list-item>
                        <label>&#x2022;</label>
                        <p>The spotting emulsion, which consists of 
                            <italic toggle="yes">Hematoxylin</italic> and spots the cellular nucleus. 
                            <italic toggle="yes">Harris hematoxylin</italic> was utilized by Papanicolaou within every 3 articulations for spots he proclaimed.
                            <sup>
                                <xref ref-type="bibr" rid="ref14">14</xref>
                            </sup>
                        </p>
                    </list-item>
                    <list-item>
                        <label>&#x2022;</label>
                        <p>The 2
                            <sup>nd</sup> spotting emulsion (named OrangeG-6 dye) includes 
                            <italic toggle="yes">95</italic>% ethanol and a trace of phosphor-tungstic acid. The OG-6 stands for Orange G, &amp; the 
                            <italic toggle="yes">&#x2018;6&#x2019;</italic> represents the conc. of phosphor-tungstic acid utilized; extra category encompassed OrangeG-
                            <italic toggle="yes">5</italic> and OrangeG-
                            <italic toggle="yes">8</italic>).
                            <sup>
                                <xref ref-type="bibr" rid="ref14">14</xref>
                            </sup>
                        </p>
                    </list-item>
                    <list-item>
                        <label>&#x2022;</label>
                        <p>The 3
                            <sup>rd</sup> spotting emulsion contains 3 stains 
                            <underline>
                                <bold>
                                    <italic toggle="yes">Eosin-Y, Light-Green-SF-yellowish</italic>
                                </bold>
                            </underline>, Bis-marc brown-
                            <bold>
                                <italic toggle="yes">Y</italic>
                            </bold>, within 
                            <underline>
                                <italic toggle="yes">95</italic>
                            </underline>% eth-an-ol through the trace of phos-pho-tungstic acid &amp; carbolic. Other formulations include EosinAzure-36, EosinAzure-50, and EosinAzure-65. The emulsions are labeled E. A, next to the count indicating the number 
                            <italic toggle="yes">of</italic> stains.
                            <sup>
                                <xref ref-type="bibr" rid="ref15">15</xref>
                            </sup>
                        </p>
                    </list-item>
                </list>
            </p>
            <p>Phosphotungstic acid is applied to counterstains to modify the pH and aid maximize the color potency. This Eosin Azure contrast stain comprises Bis-marck-brown and phos-pho-tungstic acid, both of which settled down away from emulsion when combined, limiting usable lifespan concerning blending.
                <sup>
                    <xref ref-type="bibr" rid="ref16">16</xref>
                </sup>
            </p>
            <p>This dye must produce very clear units, allowing often thick samples of merged units to be analyzed. Cellular nuclei should be frangible and blue-black in chroma, with well-defined histone designs. Cellular cytosol colors blue to green, while protein keratin gets &#x2013; 
                <italic toggle="yes">orange.</italic>
                <sup>
                    <xref ref-type="bibr" rid="ref17">17</xref>
                </sup>
                <list list-type="bullet">
                    <list-item>
                        <label>&#x25aa;</label>
                        <p>Cell outline &#x2013; Identifying a crisp, sharp cell outline with no darkness.</p>
                    </list-item>
                    <list-item>
                        <label>&#x25aa;</label>
                        <p>Nucleus outer view &#x2013; to Identify transparently, sharply nucleus lining &amp; chroma&#x2019;s strength</p>
                    </list-item>
                    <list-item>
                        <label>&#x25aa;</label>
                        <p>Detailed nucleus &#x2013; Detection of fragments, chroma-tin networks, &amp; &#x2018;nuclear inclusion</p>
                    </list-item>
                    <list-item>
                        <label>&#x25aa;</label>
                        <p>Distinction identifies the cell&#x2019;s color distinction</p>
                    </list-item>
                    <list-item>
                        <label>&#x25aa;</label>
                        <p>Clear recognition &#x2013; cytosol cells in the absence of particulate</p>
                    </list-item>
                    <list-item>
                        <label>&#x25aa;</label>
                        <p>Micronuclei &#x2013; The recognition of well-defined micronuclei.</p>
                    </list-item>
                </list>
            </p>
            <p>The benefits of REAP stain include: superior to normal Pap staining, good nucleus/cytosol stain improved color clarity, and low value.
                <sup>
                    <xref ref-type="bibr" rid="ref18">18</xref>
                </sup> Acetic acid substitutes expensive eth-an-ol (
                <italic toggle="yes">25</italic>% of the complete price -of normal 
                <underline>
                    <italic toggle="yes">Papanicolaou</italic>
                </underline> stain), allowing for lasting duration color retention (&gt;
                <italic toggle="yes">1</italic> FY without dwindling), The technique is rapid, and the stain-ing 
                <italic toggle="yes">of</italic> transitional cells such as 
                <italic toggle="yes">RedBloodC/WhiteBloodC/Bacteria</italic> is safely stored, the nucleus/histones/karyon features = transparent/bracing, the cyno-philia/raised eosinophils within smears
                <sup>
                    <xref ref-type="bibr" rid="ref19">19</xref>
                </sup> is equivalent to 
                <underline>
                    <italic toggle="yes">PAP stain</italic>
                </underline>, which breakdown RED blood Cells without alteration in tubular-cells shape.
                <sup>
                    <xref ref-type="bibr" rid="ref9">9</xref>
                </sup> Due to its low value, it&#x2019;s a viable option for regular 
                <underline>
                    <italic toggle="yes">PAP</italic>
                </underline> smear seen within a lump of cervix carcinoma identified in underdeveloped nations. The downside though 
                <underline>
                    <italic toggle="yes">REAP stain</italic>
                </underline> comprises discoloration observable within the smudge coat, especially observed cellular clumping, because of its low color accumulation.
                <sup>
                    <xref ref-type="bibr" rid="ref20">20</xref>
                </sup> Some scientists believe that when slides are stored for more than 6 months, REAP stain provides lower color standards regarding improper storage.
                <sup>
                    <xref ref-type="bibr" rid="ref21">21</xref>
                </sup> Also, stains &#x2013; are best employed in resource-constrained contexts in which there is a price issue, rather than in exploration/triennial settings.
                <sup>
                    <xref ref-type="bibr" rid="ref15">15</xref>
                </sup>
            </p>
            <p>Ashok Kumar Deshpande 
                <italic toggle="yes">et al.</italic>
                <sup>
                    <xref ref-type="bibr" rid="ref4">4</xref>
                </sup> conducted a study comparing 
                <underline>
                    <italic toggle="yes">Papanicolaou stain (PAP) with Rapid Economic Acetic acid Papanicolaou Stain</italic>
                </underline> [REAP] at the cellular level of the cervix.
                <sup>
                    <xref ref-type="bibr" rid="ref12">12</xref>
                </sup> This research comprised 200 samples from persons of various ages. The study found that PAP Stain is substantially more time-consuming and costly than REAP Stain- lump scanning of cervical carcinoma. When juxtapose with 
                <underline>
                    <italic toggle="yes">PAP stain,</italic>
                </underline> these smears&#x2019; scenarios 
                <underline>
                    <italic toggle="yes">stained</italic>
                </underline> with 
                <underline>
                    <italic toggle="yes">REAP</italic>
                </underline> = highly transparent and free of detritus.</p>
            <p>Abhilasha Asthana 
                <italic toggle="yes">et al.</italic> (2014) conducted research comparing the regular Papanicolaou staining procedure to the fast, economical, acetic acid, Papanicolaou (REAP) approach. This study covers a total of 100 samples from two separate sites, each with 50 sample sets. When compared to standard PAP stain, the REAP approach yields good colorful slides thus less expensive and takes less set-up considering lump scanning of mouth carcinoma.
                <sup>
                    <xref ref-type="bibr" rid="ref18">18</xref>
                </sup>
            </p>
            <p>Ranu Roy Biswas 
                <italic toggle="yes">et al.</italic> (2008) investigated 
                <underline>
                    <italic toggle="yes">Rapid Economic, Acetic Acid, Papanicolaou Stain</italic>
                </underline> {REAP} &#x2014; &#x201c;Is an acceptable substitute for traditional PAP Stain. There are 220 PAP smears from 110 participants in the research. According to the findings of the study, REAP stain, when compared to standard Papanicolaou stain, provides an appropriate, good, and speedy option for cytological screening at a low cost. Overall, absolute alcohol consumption is low. The stain preservation in the REAP process is also good. In our nation with a high prevalence of the illness, it may be regarded as a good alternative to traditional PAP stain for cell screening programs.
                <sup>
                    <xref ref-type="bibr" rid="ref13">13</xref>
                </sup>
            </p>
            <p>Kalyani Raju 
                <italic toggle="yes">et al.</italic> conducted research comparing convectional PAP stain with rapid PAP stain. The study covers 50 samples in all. According to the study, - the superiority 
                <italic toggle="yes">of</italic> 
                <underline>
                    <italic toggle="yes">REAP</italic>
                </underline> &#x2018;stain&#x2019; 
                <italic toggle="yes">is</italic> as follows: prevailing over regular &#x201c;
                <underline>
                    <bold>
                        <italic toggle="yes">Pap stain&#x201d;</italic>
                    </bold>
                </underline>, marvelous 
                <italic toggle="yes">nuclear</italic>/protoplasm coloring more advance color-magnitude/clarity, worthwhile just like ethan-oic-acid replaces costly ethanol {
                <italic toggle="yes">25</italic>% -complete cost&#x2019;s general quality 
                <underline>
                    <italic toggle="yes">Pap stain</italic>
                </underline>}, prolonged color safeguard [&gt; one annual aside from vanishing], clever concept, varnishing of 
                <italic toggle="yes">karyon/histones/nucleole</italic> characteristics &#x2013; transparent comparable to Pap stain. Because of its low cost, it is a viable substituent for regular 
                <underline>
                    <italic toggle="yes">PAP</italic>
                </underline> smears under cervix carcinoma lump scanning in developed nations.
                <sup>
                    <xref ref-type="bibr" rid="ref22">22</xref>
                </sup>
            </p>
        </sec>
        <sec id="sec2">
            <title>Rationale</title>
            <p>FNAC is a technique whereby cells are obtained from a lesion using a thin bore needle and smears are made for cytological diagnosis.</p>
            <p>The benefits of REAP stain over standard Pap stain include superior nuclear and cytoplasmic staining, improved color intensity and transparency, and lower cost. Acetic acid replaces expensive ethanol, which accounts for 25% of the cost of standard Pap stain, and provides long-term color preservation (more than a year without fading), a quick procedure, less time required, staining of non-epithelial cells like RBC/WBC/bacteria that are well preserved, nuclear/chromatin/nucleolus details that are clear/crisp, comparable cynophilia/eosinophilia of the cells.</p>
            <sec id="sec3">
                <title>Objectives</title>
                <p>
                    <list list-type="order">
                        <list-item>
                            <label>1.</label>
                            <p>To determine the REAP staining span and PAP staining span.</p>
                        </list-item>
                        <list-item>
                            <label>2.</label>
                            <p>To screen Prolonged color maintenance Intensity of nuclear &amp; cytoplasmic staining.</p>
                        </list-item>
                        <list-item>
                            <label>3.</label>
                            <p>To evaluate cost-effectiveness.</p>
                        </list-item>
                        <list-item>
                            <label>4.</label>
                            <p>To assess the superiority of staining of smears by REAP technique compared to the routine PAP technique</p>
                        </list-item>
                    </list>
                </p>
            </sec>
            <sec id="sec4">
                <title>Approach to the present study</title>
                <p>Patients participating in the study will be asked to give prior written informed consent. Clinical history will be taken, an appropriate physical examination will be done on new patients and clinical details of the previously diagnosed cases will be obtained considering the inclusion and exclusion criteria. Fluids will be extracted from clinically questionable cases and forwarded to the Department of Pathology, Jawaharlal Nehru Medical College (J.N.M.C.), Sawangi Meghe, for histopathological evaluation. The specimens accepted in the Dept. of Pathology, J.N.M.C., will be dipped in alcohol&#x2013;ether for fixation, fixed smear slides will be taken for diagnosis, and confirmed for further examination. Gross examination and diagnosis of the specimens will be done followed by the taking of appropriate fluid specimens. The smear is made from fluids and undergoes the REAP and PAP Stain.</p>
            </sec>
            <sec id="sec5">
                <title>Protocol</title>
                <p>The study is conducted among the common population of the Vidarbha district in AVBRH hospital. The study is about the Rapid, Economic, Acetic acid, Papanicolaou (REAP) staining technique analogous to the routine Papanicolaou staining (PAP) technique. The study is helpful in the awareness of cervical cancer among people. The conceptual research on cervical cancer will be done. The recruitment of the people is independently done and the awareness will be observed.</p>
            </sec>
        </sec>
        <sec id="sec6" sec-type="methods">
            <title>Methods</title>
            <p>The following study is a cross-sectional investigative study that will be conducted in the Cytopathological division of the Dept. of Pathology, Jawaharlal Nehru Medical College (JNMC), Sawangi (Meghe), Wardha, in collaboration with the Acharya Vinoba Bhave Rural Hospital (AVBRH), Sawangi (Meghe), Wardha, from 2021 to 2023. The institutional Ethical Committee approval has been obtained from Datta Meghe Institute of Medical Sciences (DMIMS (DU)/IEC/2022/1205). This investigation will take place after obtaining the patients&#x2019; written informed consent.</p>
            <sec id="sec7">
                <title>Materials</title>
                <p>
                    <list list-type="order">
                        <list-item>
                            <label>1.</label>
                            <p>Thirty (30) fluid specimens from patients accepted in the Department of General Pathology, Jawaharlal Nehru Medical College (JNMC), Sawangi (Meghe) were used in the study.</p>
                        </list-item>
                        <list-item>
                            <label>2.</label>
                            <p>Alcohol &#x2013; ether fixed, smear on slides obtained from the specimens.</p>
                        </list-item>
                        <list-item>
                            <label>3.</label>
                            <p>Alcohol &#x2013; ether fixative.</p>
                        </list-item>
                        <list-item>
                            <label>4.</label>
                            <p>FNAC instruments.</p>
                        </list-item>
                        <list-item>
                            <label>5.</label>
                            <p>PAP &amp; REAP Staining assembly.</p>
                        </list-item>
                        <list-item>
                            <label>6.</label>
                            <p>Glass slides (Blue Star
                                <sup>&#x00ae;</sup>). Dimensions: 7.5 &#x00d7; 2.5 centimeters.</p>
                        </list-item>
                        <list-item>
                            <label>7.</label>
                            <p>Binocular research microscope.</p>
                        </list-item>
                    </list>
                </p>
            </sec>
            <sec id="sec8">
                <title>Study design</title>
                <p>It is a observational cross-sectional study.</p>
            </sec>
            <sec id="sec9">
                <title>Study settings</title>
                <p>The study will be conducted in Aacharya Vinoba Bhave Rular Hospital Sawangi (Meghe), Wardha.</p>
            </sec>
            <sec id="sec10">
                <title>Inclusion criteria</title>
                <p>Subjects of both sexes, aged 18 to 50 years getting diagnostic fine needle aspiration cytology (FNACs) done at the Acharya Vinoba Bhave Rural Hospital (AVBRH), Sawangi (Meghe), Wardha, will be included.</p>
            </sec>
            <sec id="sec11">
                <title>Exclusion criteria</title>
                <p>Cases under therapy, vulnerable personnel, patients in emergency conditions, ethnic minority groups, homeless people, nomads, refugees, and minors will be excluded from the study.</p>
            </sec>
            <sec id="sec12">
                <title>Bias</title>
                <p>All necessary measures to control bias at all levels will be taken. As it is an observational study, all the samples which are routinely received in the section of cytopathology are taken into consideration for comparison between REAP staining technique analogous to the routine PAP technique. Institutional supply of dyes and chemical constituents present in dyes from different companies make minor modifications, that remain consistent, an essential part of staining protocol. Diagnostic search influences the findings of cells staining. The influence of content of result captions in response to diagnosis of samples. The purpose of study is to access the comparison between REAP staining technique analogous to the routine PAP technique for estimation of diagnostic accuracy for test samples.</p>
            </sec>
            <sec id="sec13">
                <title>Sample size</title>
                <p>Cochran formula for sample size estimation:</p>
                <p>N= Total patients of fluid cytology during the last one and half years = 3000
                    <disp-formula id="e1">
                        <mml:math display="block">
                            <mml:mtext>Sample&#x2009;size n</mml:mtext>
                            <mml:mo>=</mml:mo>
                            <mml:mfrac>
                                <mml:mrow>
                                    <mml:msup>
                                        <mml:mn>3.84</mml:mn>
                                        <mml:mo>&#x2217;</mml:mo>
                                    </mml:msup>
                                    <mml:msup>
                                        <mml:mn>300</mml:mn>
                                        <mml:mo>&#x2217;</mml:mo>
                                    </mml:msup>
                                    <mml:msup>
                                        <mml:mn>0.50</mml:mn>
                                        <mml:mo>&#x2217;</mml:mo>
                                    </mml:msup>
                                    <mml:mn>0.50</mml:mn>
                                </mml:mrow>
                                <mml:mrow>
                                    <mml:mfenced close=")" open="(">
                                        <mml:mrow>
                                            <mml:msup>
                                                <mml:mn>0.05</mml:mn>
                                                <mml:mrow>
                                                    <mml:mn>2</mml:mn>
                                                    <mml:mo>&#x2217;</mml:mo>
                                                </mml:mrow>
                                            </mml:msup>
                                            <mml:mn>2999</mml:mn>
                                        </mml:mrow>
                                    </mml:mfenced>
                                    <mml:mo>+</mml:mo>
                                    <mml:mfenced close=")" open="(">
                                        <mml:mrow>
                                            <mml:msup>
                                                <mml:mn>3.84</mml:mn>
                                                <mml:mo>&#x2217;</mml:mo>
                                            </mml:msup>
                                            <mml:msup>
                                                <mml:mn>0.5</mml:mn>
                                                <mml:mo>&#x2217;</mml:mo>
                                            </mml:msup>
                                            <mml:mn>0.5</mml:mn>
                                        </mml:mrow>
                                    </mml:mfenced>
                                </mml:mrow>
                            </mml:mfrac>
                            <mml:mo>=</mml:mo>
                            <mml:mn>340.52</mml:mn>
                            <mml:mo>=</mml:mo>
                            <mml:mn>340</mml:mn>
                            <mml:mspace width="0.30em"/>
                            <mml:mtext>patients&#x2009;needed&#x2009;in&#x2009;the&#x2009;study</mml:mtext>
                        </mml:math>
                    </disp-formula>
                </p>
                <p>The data analysis will be done using a relevant Chi-squared test for understanding the comparative difference between groups and among groups will be compared. Whereas, the results obtained during the research will be analyzed using appropriate statistical methods (SPSS) by a qualified statistician.</p>
            </sec>
            <sec id="sec14">
                <title>Dissemination</title>
                <p>The results of the study will be published in an indexed journal.</p>
            </sec>
            <sec id="sec15">
                <title>Scope</title>
                <p>This study will evaluate the significance of REAP staining over the conventional PAP staining method. The study will demonstrate a considerable decrease in turnaround time for REAP as compared to conventional pap stain. This staining technique aids in an easy understanding of the pathophysiology of smears. The technique will also help in the assessment of the quality of the smear and will aid in providing easy and rapid diagnosis to patients.</p>
                <p>The simplicity of the procedure (uniform 10 dips) also reduced the risk of human errors during staining will help researchers reduce the period of the staining procedure. The modifications that will apply to conventional pap stains have been described will suitable alternatives for REAP stains.</p>
            </sec>
            <sec id="sec16">
                <title>Study status</title>
                <p>The study is yet to start.</p>
            </sec>
        </sec>
        <sec id="sec17" sec-type="results">
            <title>Results</title>
            <p>The present study explores whether the qualitative and quantitative analysis of stained smears by REAP Stain is much better than conventional PAP Stain for nucleus and cytoplasm staining.</p>
        </sec>
        <sec id="sec18" sec-type="discussion">
            <title>Discussion</title>
            <p>Cervical cancer develops progressively over a certain amount of time.
                <sup>
                    <xref ref-type="bibr" rid="ref23">23</xref>
                </sup> Most accidents take place in less developed countries where there are no reliable testing campaigns available. Some of the risk factors include acquired immunodeficiency syndrome, smoking, and human papillomavirus exposure. Treatment-related extended morbidity is common, however, most women with early-stage tumors can be cured. According to the outcomes of randomized clinical research, chemotherapy,
                <sup>
                    <xref ref-type="bibr" rid="ref24">24</xref>
                </sup> and radiation therapy is considered a standard of care for cancer-developed patients and especially for women with locally advanced cancer, whereas its applicability to women in less developed nations is largely not tested.
                <sup>
                    <xref ref-type="bibr" rid="ref25">25</xref>
                </sup>
            </p>
            <p>In 2006, Dighe SB 
                <italic toggle="yes">et al.</italic>, conducted research on the development of PAP stain and compared traditional PAP stain to REAP stain. The study evaluated the nuclear and cytoplasmic characteristics of both stains. The study concludes that REAP stain&#x2019;s cytoplasm differentiation and transparency were ideal, and the nuclear features and chromatin pattern were visible.
                <sup>
                    <xref ref-type="bibr" rid="ref15">15</xref>
                </sup>
            </p>
            <p>In 2008, Ranu Roy Biswas 
                <italic toggle="yes">et al.</italic>, the question of whether Rapid Economic, Acetic Acid, Papanicolaou Stain (REAP), a suitable substitute for traditional PAP Stain, has been examined. 110 participants provided 220 PAP smears for the study. According to the study&#x2019;s findings, REAP stain offers an appropriate, excellent, quick, and affordable alternative to traditional Papanicolaou for cytological screening.
                <sup>
                    <xref ref-type="bibr" rid="ref26">26</xref>
                </sup> Overall, very little alcohol is consumed. The REAP technique also does a superb job of stain preservation. In our nation, where the disease is quite prevalent, it might be thought of as a good substitute for the traditional PAP stain for cells screening program.
                <sup>
                    <xref ref-type="bibr" rid="ref13">13</xref>
                </sup>
            </p>
            <p>In 2014, Abhilasha Asthana 
                <italic toggle="yes">et al</italic>., compared the conventional Papanicolaou staining method with the quick, inexpensive acetic acid, Papanicolaou (REAP) method in a study. This study uses a total of 100 samples from two different sites, with 50 sets of samples per site. The study concluded that REAP method, as opposed to traditional PAP Stain, generates superior stained smears that are cost-effective and require less time for mass screening of oral cancer.
                <sup>
                    <xref ref-type="bibr" rid="ref18">18</xref>
                </sup>
            </p>
            <p>In 2014, Shabnam Izhar 
                <italic toggle="yes">et al.</italic> studied the effectiveness of a quick, affordable, acetic acid Papanicolaou stain as an alternative to traditional Papanicolaou stain in cervical smears. There are 737 smears in the study. According to the study&#x2019;s findings, traditional PAP stain does a better job of color retention than REAP PAP stain, reduces turnaround time, and provides unmistakable cell shape due to superior staining quality.
                <sup>
                    <xref ref-type="bibr" rid="ref15">15</xref>
                </sup>
            </p>
            <p>In 2015, Ashok Kumar Deshpande 
                <italic toggle="yes">et al</italic>., Papanicolaou stain (PAP) and Rapid Economic Acetic acid Papanicolaou Stain (REAP) were compared in a study on cervical cytology. In total, 200 samples from persons of various ages were used in this investigation. The study found that PAP Stain required more time and money than REAP Stain for routine cervical cancer screening. When compared to PAP stain, the background of smears stained by REAP was incredibly clean and debris-free.
                <sup>
                    <xref ref-type="bibr" rid="ref27">27</xref>
                </sup>
            </p>
            <p>In 2016, Bhagat P. 
                <italic toggle="yes">et al.</italic> undertook research on the effectiveness of a modified, quick, affordable, acetic acid-based Papanicolaou stain. 102 liquid base cytology samples are included in Ref. 
                <xref ref-type="bibr" rid="ref28">28</xref>. The investigation concludes that standard PAP staining produced good cytoplasmic staining. The study endorsed the adoption of the REAP approach as a practical substitute.
                <sup>
                    <xref ref-type="bibr" rid="ref29">29</xref>
                </sup>
            </p>
            <p>In 2016, Kalyani Raju 
                <italic toggle="yes">et al</italic>. studied the differences between the conventional PAP stain and the rapid PAP stain. The study uses 50 samples in total.
                <sup>
                    <xref ref-type="bibr" rid="ref30">30</xref>
                </sup> The study came to the conclusion that REAP stain has several advantages over standard Pap stain, including superior nuclear/cytoplasmic staining with better color intensity/transparency, cost-effectiveness due to the substitution of acetic acid for expensive ethanol (which accounts for 25% of the cost of standard Pap stain), long-term color preservation (more than a year without fading), a quick procedure, and staining of nuclear/chromatin/nucleolus details that are clear and comparable It is a good substitute for the traditional pap smear in developing nations&#x2019; widespread cervical cancer screening programs due to its low cost.
                <sup>
                    <xref ref-type="bibr" rid="ref31">31</xref>
                </sup>
            </p>
            <p>In 2018, Suresh Amin 
                <italic toggle="yes">et al</italic>., conducted research on PAP Stain for mass screening of micronuclei in buccal smears. Identification and counting of micronuclei are made possible by the stained smear backdrop.
                <sup>
                    <xref ref-type="bibr" rid="ref32">32</xref>
                </sup>
            </p>
            <p>In 2020, Garima Goel 
                <italic toggle="yes">et al</italic>. completed research on Papanicolaou Stain, a cheap, quick, and suitable alternative to traditional PAP Stain for cervical smear staining. 100 smears from 50 female patients
                <sup>
                    <xref ref-type="bibr" rid="ref33">33</xref>
                </sup> are included in the study. In comparison to traditional PAP stain, the study finds that REAP is a quick, affordable, and good approach for both cytoplasmic and nuclear staining with minimal alcohol use.
                <sup>
                    <xref ref-type="bibr" rid="ref34">34</xref>
                </sup>
            </p>
            <p>In 2022, Karthika Panneerselvam 
                <italic toggle="yes">et al</italic>. performed research on Papanicolaou, Acetic acid, and Rapid Staining techniques versus traditional staining techniques in the healthy oral mucosa. Eight patients and 160 slides were used in the investigation. The study&#x2019;s findings show that even though the REAP staining technique had shorter staining times and costs, conventional staining methods were still preferred over them.
                <sup>
                    <xref ref-type="bibr" rid="ref29">29</xref>
                </sup>
            </p>
            <sec id="sec19">
                <title>Limitations</title>
                <p>
                    <list list-type="order">
                        <list-item>
                            <label>1.</label>
                            <p>Inter-observer and Intra-observer flexibility.</p>
                        </list-item>
                        <list-item>
                            <label>2.</label>
                            <p>Practical errors during the process can affect the interpretation of staining.</p>
                        </list-item>
                        <list-item>
                            <label>3.</label>
                            <p>Loss of follow-up patients.</p>
                        </list-item>
                    </list>
                </p>
            </sec>
            <sec id="sec20">
                <title>Ethical consideration</title>
                <p>Approved by the Institutional Ethics Committee of Datta Meghe Institute of Higher Education and Research Sawangi (M) Wardha (ref. no. DMIMS (DU)/IEC/2022/1205).</p>
            </sec>
        </sec>
    </body>
    <back>
        <sec id="sec23" sec-type="data-availability">
            <title>Data availability</title>
            <p>No data are associated with this article.</p>
        </sec>
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    <sub-article article-type="reviewer-report" id="report205008">
        <front-stub>
            <article-id pub-id-type="doi">10.5256/f1000research.148839.r205008</article-id>
            <title-group>
                <article-title>Reviewer response for version 1</article-title>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author">
                    <name>
                        <surname>Okodo</surname>
                        <given-names>Mitsuaki</given-names>
                    </name>
                    <xref ref-type="aff" rid="r205008a1">1</xref>
                    <role>Referee</role>
                </contrib>
                <aff id="r205008a1">
                    <label>1</label>Kyorin University, Tokyo, Japan</aff>
            </contrib-group>
            <author-notes>
                <fn fn-type="conflict">
                    <p>
                        <bold>Competing interests: </bold>No competing interests were disclosed.</p>
                </fn>
            </author-notes>
            <pub-date pub-type="epub">
                <day>29</day>
                <month>9</month>
                <year>2023</year>
            </pub-date>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2023 Okodo M</copyright-statement>
                <copyright-year>2023</copyright-year>
                <license xlink:href="https://creativecommons.org/licenses/by/4.0/">
                    <license-p>This is an open access peer review report distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
                </license>
            </permissions>
            <related-article ext-link-type="doi" id="relatedArticleReport205008" related-article-type="peer-reviewed-article" xlink:href="10.12688/f1000research.135708.1"/>
            <custom-meta-group>
                <custom-meta>
                    <meta-name>recommendation</meta-name>
                    <meta-value>reject</meta-value>
                </custom-meta>
            </custom-meta-group>
        </front-stub>
        <body>
            <p>
                <bold>General comments:</bold>
            </p>
            <p> I do not agree with this study protocol. If this study is to be conducted, I believe it needs to be substantially revised.</p>
            <p> </p>
            <p> 
                <bold>Specific comments:</bold> 
                <list list-type="order">
                    <list-item>
                        <p>The abstract should explain why this protocol is interesting. However, most of the abstract is dominated by previous studies that are not interesting. Please specify the samples and methods used to evaluate the value of Rapid-Pap Stain.</p>
                    </list-item>
                    <list-item>
                        <p>The study protocol is not clearly described. Please describe it in detail to allow replication by others.</p>
                    </list-item>
                    <list-item>
                        <p>REAP Stain is not a staining method known to everyone. Please provide the staining procedure. Since this is a research protocol and you are publishing it, there must be a difference between the existing REAP stain and the authors' staining method. Please clarify the difference.</p>
                    </list-item>
                    <list-item>
                        <p>It is not clear what evaluation criteria will be used to compare REAP stain and Pap stain samples. Please provide a detailed scoring methodology.</p>
                    </list-item>
                </list>
            </p>
            <p>Is the study design appropriate for the research question?</p>
            <p>Partly</p>
            <p>Is the rationale for, and objectives of, the study clearly described?</p>
            <p>Partly</p>
            <p>Are sufficient details of the methods provided to allow replication by others?</p>
            <p>Partly</p>
            <p>Are the datasets clearly presented in a useable and accessible format?</p>
            <p>No</p>
            <p>Reviewer Expertise:</p>
            <p>Oncopathology, Cervical cytology, Virology, Molecular Biology</p>
            <p>I confirm that I have read this submission and believe that I have an appropriate level of expertise to state that I do not consider it to be of an acceptable scientific standard, for reasons outlined above.</p>
        </body>
    </sub-article>
    <sub-article article-type="reviewer-report" id="report204995">
        <front-stub>
            <article-id pub-id-type="doi">10.5256/f1000research.148839.r204995</article-id>
            <title-group>
                <article-title>Reviewer response for version 1</article-title>
            </title-group>
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                <contrib contrib-type="author">
                    <name>
                        <surname>Raghavan</surname>
                        <given-names>Vijayashree</given-names>
                    </name>
                    <xref ref-type="aff" rid="r204995a1">1</xref>
                    <role>Referee</role>
                </contrib>
                <aff id="r204995a1">
                    <label>1</label>Chettinad Hospital &amp; Research Institute, Kelambakkam, Tamil Nadu, India</aff>
            </contrib-group>
            <author-notes>
                <fn fn-type="conflict">
                    <p>
                        <bold>Competing interests: </bold>No competing interests were disclosed.</p>
                </fn>
            </author-notes>
            <pub-date pub-type="epub">
                <day>26</day>
                <month>9</month>
                <year>2023</year>
            </pub-date>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2023 Raghavan V</copyright-statement>
                <copyright-year>2023</copyright-year>
                <license xlink:href="https://creativecommons.org/licenses/by/4.0/">
                    <license-p>This is an open access peer review report distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
                </license>
            </permissions>
            <related-article ext-link-type="doi" id="relatedArticleReport204995" related-article-type="peer-reviewed-article" xlink:href="10.12688/f1000research.135708.1"/>
            <custom-meta-group>
                <custom-meta>
                    <meta-name>recommendation</meta-name>
                    <meta-value>reject</meta-value>
                </custom-meta>
            </custom-meta-group>
        </front-stub>
        <body>
            <p>
                <list list-type="bullet">
                    <list-item>
                        <p>The study objectives, design, protocol and material/samples are not clearly mentioned. There are many contradicting statements. The language used does not clearly state if the study has been done or yet to be carried out.</p>
                    </list-item>
                    <list-item>
                        <p>At one point it mentions a cross-sectional study, but the inclusion/exclusion criteria do not correlate and the study also compares the new REAP technique with Routine PAP technique - not comprehensible.</p>
                    </list-item>
                    <list-item>
                        <p>The study design/method must be appropriate (if it is a comparative study/case-control/experimental).</p>
                    </list-item>
                    <list-item>
                        <p>Samples inclusion has to be very clear if all types of cytology specimen are to be included or restricted only to FNAC/Exfoliative smears.</p>
                    </list-item>
                    <list-item>
                        <p>Language is poor with too much grammatical inappropriateness.</p>
                    </list-item>
                    <list-item>
                        <p>This study cannot be approved in the present format/protocol. It needs a major revision if the study must be done.</p>
                    </list-item>
                    <list-item>
                        <p>Modifications of PAP staining has been done long ago and many laboratories are routinely using REAP/Ultrafast PAP techniques. So, no new information is expected from this study.</p>
                    </list-item>
                </list>
            </p>
            <p>Is the study design appropriate for the research question?</p>
            <p>No</p>
            <p>Is the rationale for, and objectives of, the study clearly described?</p>
            <p>Partly</p>
            <p>Are sufficient details of the methods provided to allow replication by others?</p>
            <p>No</p>
            <p>Are the datasets clearly presented in a useable and accessible format?</p>
            <p>No</p>
            <p>Reviewer Expertise:</p>
            <p>Dermatopathology, Oncopathology, Histomorphology, Cytology, Hemato-immunology and molecular biology</p>
            <p>I confirm that I have read this submission and believe that I have an appropriate level of expertise to state that I do not consider it to be of an acceptable scientific standard, for reasons outlined above.</p>
        </body>
    </sub-article>
</article>
