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Evaluation of pharmaceutically compounded oral caffeine on the impact of medication adherence and risk of readmission among preterm neonates: A single-center quasi-experimental study
Caffeine is available in an ampoule, used via parenteral and enteral routes in preterm neonates to treat apnea of prematurity (AOP) in neonates of gestational age [greater than or equal to] 35-40 weeks. A longer duration of therapy has a higher risk of medication non-adherence due to higher costs an...
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Published in: | PloS one 2022-11, Vol.17 (11), p.e0275655-e0275655 |
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description | Caffeine is available in an ampoule, used via parenteral and enteral routes in preterm neonates to treat apnea of prematurity (AOP) in neonates of gestational age [greater than or equal to] 35-40 weeks. A longer duration of therapy has a higher risk of medication non-adherence due to higher costs and inappropriate dosage forms. Pharmaceutically compounded oral caffeine (PCC) could be an appropriate alternate dosage form. The researchers aimed to determine the impact of PCC on medication-related factors influencing medication adherence (MA) and the frequency of hospital readmission with apnea (HRA) in preterm neonates. We conducted a single-center quasi-experimental study for this quality improvement project using PCC among the preterm neonates admitted in a tertiary care level-III NICU at the Aga Khan University Hospital Karachi, Pakistan, received caffeine therapy, and survived at discharge. The researchers compared pre-PCC data (April-December 2017) with post-PCC data (April-Dec 2018) each for nine months, with three months intervals (January-March 2018) of PCC formulation and implementation phase. The study was conducted according to the SQUIRE2.0 guidelines. The Data were collated on factors influencing MA, including the cost of therapy, medication refill rates, and parental complaints as primary outcome measures. The Risk factors of HRA were included as secondary outcomes. After PCC implementation cost of therapy was reduced significantly from Rs. 97000.0 (729.0 USD) to Rs. 24500.0 (185.0 USD) (p |
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A longer duration of therapy has a higher risk of medication non-adherence due to higher costs and inappropriate dosage forms. Pharmaceutically compounded oral caffeine (PCC) could be an appropriate alternate dosage form. The researchers aimed to determine the impact of PCC on medication-related factors influencing medication adherence (MA) and the frequency of hospital readmission with apnea (HRA) in preterm neonates. We conducted a single-center quasi-experimental study for this quality improvement project using PCC among the preterm neonates admitted in a tertiary care level-III NICU at the Aga Khan University Hospital Karachi, Pakistan, received caffeine therapy, and survived at discharge. The researchers compared pre-PCC data (April-December 2017) with post-PCC data (April-Dec 2018) each for nine months, with three months intervals (January-March 2018) of PCC formulation and implementation phase. The study was conducted according to the SQUIRE2.0 guidelines. The Data were collated on factors influencing MA, including the cost of therapy, medication refill rates, and parental complaints as primary outcome measures. The Risk factors of HRA were included as secondary outcomes. After PCC implementation cost of therapy was reduced significantly from Rs. 97000.0 (729.0 USD) to Rs. 24500.0 (185.0 USD) (p<0.001), significantly higher (p<0.001) number of patients completed remaining refills (77.6% pre-phase vs 97.5% post-phase). The number of parental complaints about cost, ampoule usage, medication drawing issue, wastage, inappropriate dosage form, and longer duration of therapy reduced significantly in post-phase. HRA reduced from 25% to 6.6% (p<0.001). Post-implementation of PCC (RR 0.14; 95% CI: 0.07-0.27) was a significant independent risk factor for reducing HRA using a multivariate analysis model. Longer duration of caffeine therapy after discharge (RR 1.05; 95% CI: 1.04-1.04), those who were born in multiple births (RR 1.15; 95% CI: 1.15-1.15), and those who had higher number of siblings were other significant independent risk factors for HRA. PCC dispensation in the appropriate dosage form at discharge effectively reduced cost, non-adherence to therapy, and risk of hospital readmissions. This neonatal clinical and compounding pharmacist-led model can be replicated in other resource-limiting setting.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0275655</identifier><identifier>PMID: 36350877</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Apnea ; Apnea neonatorum ; Biology and Life Sciences ; Caffeine ; Care and treatment ; Diagnosis ; Dosage ; Drug dosages ; Drugs ; Evaluation ; Extubation ; Gestational age ; Health aspects ; Health risks ; Infants (Premature) ; Medication adherence ; Medicine and Health Sciences ; Multiple births ; Multivariate analysis ; Neonates ; Newborn babies ; Patient compliance ; Pediatrics ; People and Places ; Pharmacists ; Physical Sciences ; Quality control ; Quasi-experimental methods ; Risk analysis ; Risk factors ; Services ; Socioeconomic factors ; Tertiary ; Therapy ; Ventilators</subject><ispartof>PloS one, 2022-11, Vol.17 (11), p.e0275655-e0275655</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Ambreen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 Ambreen et al 2022 Ambreen et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c603t-da80ea8dd760c79d752a4530ce1218388f575ec0b8366efb5a90325d7ce402d53</citedby><cites>FETCH-LOGICAL-c603t-da80ea8dd760c79d752a4530ce1218388f575ec0b8366efb5a90325d7ce402d53</cites><orcidid>0000-0003-2728-6726 ; 0000-0002-6287-6898</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2734593548/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2734593548?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids></links><search><contributor>Baratta, Francesca</contributor><creatorcontrib>Ambreen, Gul</creatorcontrib><creatorcontrib>Kumar, Manoj</creatorcontrib><creatorcontrib>Ali, Amin</creatorcontrib><creatorcontrib>Shah, Syed Akbar Ali</creatorcontrib><creatorcontrib>Saleem, Syed Muzafar</creatorcontrib><creatorcontrib>Tahir, Ayesha</creatorcontrib><creatorcontrib>Salat, Muhammad Sohail</creatorcontrib><creatorcontrib>Aslam, Muhammad Shahzad</creatorcontrib><creatorcontrib>Hussain, Kashif</creatorcontrib><title>Evaluation of pharmaceutically compounded oral caffeine on the impact of medication adherence and risk of readmission among preterm neonates: A single-center quasi-experimental study</title><title>PloS one</title><description>Caffeine is available in an ampoule, used via parenteral and enteral routes in preterm neonates to treat apnea of prematurity (AOP) in neonates of gestational age [greater than or equal to] 35-40 weeks. A longer duration of therapy has a higher risk of medication non-adherence due to higher costs and inappropriate dosage forms. Pharmaceutically compounded oral caffeine (PCC) could be an appropriate alternate dosage form. The researchers aimed to determine the impact of PCC on medication-related factors influencing medication adherence (MA) and the frequency of hospital readmission with apnea (HRA) in preterm neonates. We conducted a single-center quasi-experimental study for this quality improvement project using PCC among the preterm neonates admitted in a tertiary care level-III NICU at the Aga Khan University Hospital Karachi, Pakistan, received caffeine therapy, and survived at discharge. The researchers compared pre-PCC data (April-December 2017) with post-PCC data (April-Dec 2018) each for nine months, with three months intervals (January-March 2018) of PCC formulation and implementation phase. The study was conducted according to the SQUIRE2.0 guidelines. The Data were collated on factors influencing MA, including the cost of therapy, medication refill rates, and parental complaints as primary outcome measures. The Risk factors of HRA were included as secondary outcomes. After PCC implementation cost of therapy was reduced significantly from Rs. 97000.0 (729.0 USD) to Rs. 24500.0 (185.0 USD) (p<0.001), significantly higher (p<0.001) number of patients completed remaining refills (77.6% pre-phase vs 97.5% post-phase). The number of parental complaints about cost, ampoule usage, medication drawing issue, wastage, inappropriate dosage form, and longer duration of therapy reduced significantly in post-phase. HRA reduced from 25% to 6.6% (p<0.001). Post-implementation of PCC (RR 0.14; 95% CI: 0.07-0.27) was a significant independent risk factor for reducing HRA using a multivariate analysis model. Longer duration of caffeine therapy after discharge (RR 1.05; 95% CI: 1.04-1.04), those who were born in multiple births (RR 1.15; 95% CI: 1.15-1.15), and those who had higher number of siblings were other significant independent risk factors for HRA. PCC dispensation in the appropriate dosage form at discharge effectively reduced cost, non-adherence to therapy, and risk of hospital readmissions. This neonatal clinical and compounding pharmacist-led model can be replicated in other resource-limiting setting.</description><subject>Apnea</subject><subject>Apnea neonatorum</subject><subject>Biology and Life Sciences</subject><subject>Caffeine</subject><subject>Care and treatment</subject><subject>Diagnosis</subject><subject>Dosage</subject><subject>Drug dosages</subject><subject>Drugs</subject><subject>Evaluation</subject><subject>Extubation</subject><subject>Gestational age</subject><subject>Health aspects</subject><subject>Health risks</subject><subject>Infants (Premature)</subject><subject>Medication adherence</subject><subject>Medicine and Health Sciences</subject><subject>Multiple births</subject><subject>Multivariate analysis</subject><subject>Neonates</subject><subject>Newborn babies</subject><subject>Patient compliance</subject><subject>Pediatrics</subject><subject>People and Places</subject><subject>Pharmacists</subject><subject>Physical Sciences</subject><subject>Quality 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of pharmaceutically compounded oral caffeine on the impact of medication adherence and risk of readmission among preterm neonates: A single-center quasi-experimental study</title><author>Ambreen, Gul ; Kumar, Manoj ; Ali, Amin ; Shah, Syed Akbar Ali ; Saleem, Syed Muzafar ; Tahir, Ayesha ; Salat, Muhammad Sohail ; Aslam, Muhammad Shahzad ; Hussain, Kashif</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c603t-da80ea8dd760c79d752a4530ce1218388f575ec0b8366efb5a90325d7ce402d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Apnea</topic><topic>Apnea neonatorum</topic><topic>Biology and Life Sciences</topic><topic>Caffeine</topic><topic>Care and treatment</topic><topic>Diagnosis</topic><topic>Dosage</topic><topic>Drug dosages</topic><topic>Drugs</topic><topic>Evaluation</topic><topic>Extubation</topic><topic>Gestational age</topic><topic>Health aspects</topic><topic>Health 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Kashif</au><au>Baratta, Francesca</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of pharmaceutically compounded oral caffeine on the impact of medication adherence and risk of readmission among preterm neonates: A single-center quasi-experimental study</atitle><jtitle>PloS one</jtitle><date>2022-11-09</date><risdate>2022</risdate><volume>17</volume><issue>11</issue><spage>e0275655</spage><epage>e0275655</epage><pages>e0275655-e0275655</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Caffeine is available in an ampoule, used via parenteral and enteral routes in preterm neonates to treat apnea of prematurity (AOP) in neonates of gestational age [greater than or equal to] 35-40 weeks. A longer duration of therapy has a higher risk of medication non-adherence due to higher costs and inappropriate dosage forms. Pharmaceutically compounded oral caffeine (PCC) could be an appropriate alternate dosage form. The researchers aimed to determine the impact of PCC on medication-related factors influencing medication adherence (MA) and the frequency of hospital readmission with apnea (HRA) in preterm neonates. We conducted a single-center quasi-experimental study for this quality improvement project using PCC among the preterm neonates admitted in a tertiary care level-III NICU at the Aga Khan University Hospital Karachi, Pakistan, received caffeine therapy, and survived at discharge. The researchers compared pre-PCC data (April-December 2017) with post-PCC data (April-Dec 2018) each for nine months, with three months intervals (January-March 2018) of PCC formulation and implementation phase. The study was conducted according to the SQUIRE2.0 guidelines. The Data were collated on factors influencing MA, including the cost of therapy, medication refill rates, and parental complaints as primary outcome measures. The Risk factors of HRA were included as secondary outcomes. After PCC implementation cost of therapy was reduced significantly from Rs. 97000.0 (729.0 USD) to Rs. 24500.0 (185.0 USD) (p<0.001), significantly higher (p<0.001) number of patients completed remaining refills (77.6% pre-phase vs 97.5% post-phase). The number of parental complaints about cost, ampoule usage, medication drawing issue, wastage, inappropriate dosage form, and longer duration of therapy reduced significantly in post-phase. HRA reduced from 25% to 6.6% (p<0.001). Post-implementation of PCC (RR 0.14; 95% CI: 0.07-0.27) was a significant independent risk factor for reducing HRA using a multivariate analysis model. Longer duration of caffeine therapy after discharge (RR 1.05; 95% CI: 1.04-1.04), those who were born in multiple births (RR 1.15; 95% CI: 1.15-1.15), and those who had higher number of siblings were other significant independent risk factors for HRA. PCC dispensation in the appropriate dosage form at discharge effectively reduced cost, non-adherence to therapy, and risk of hospital readmissions. This neonatal clinical and compounding pharmacist-led model can be replicated in other resource-limiting setting.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>36350877</pmid><doi>10.1371/journal.pone.0275655</doi><tpages>e0275655</tpages><orcidid>https://orcid.org/0000-0003-2728-6726</orcidid><orcidid>https://orcid.org/0000-0002-6287-6898</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_2734593548 |
source | PMC (PubMed Central); Publicly Available Content (ProQuest) |
subjects | Apnea Apnea neonatorum Biology and Life Sciences Caffeine Care and treatment Diagnosis Dosage Drug dosages Drugs Evaluation Extubation Gestational age Health aspects Health risks Infants (Premature) Medication adherence Medicine and Health Sciences Multiple births Multivariate analysis Neonates Newborn babies Patient compliance Pediatrics People and Places Pharmacists Physical Sciences Quality control Quasi-experimental methods Risk analysis Risk factors Services Socioeconomic factors Tertiary Therapy Ventilators |
title | Evaluation of pharmaceutically compounded oral caffeine on the impact of medication adherence and risk of readmission among preterm neonates: A single-center quasi-experimental study |
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