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Home > Clinical Assessment of Pediatric Pharmacotherapy and its Predictors at Tertiary Care Hospitals of Peshawar, Pakistan

Clinical Assessment of Pediatric Pharmacotherapy and its Predictors at Tertiary Care Hospitals of Peshawar, Pakistan

Thesis Info

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External Link

Author

Muhammad Aamir

Program

PhD

Institute

University of Peshawar

City

Peshawar

Province

KPK

Country

Pakistan

Thesis Completing Year

2018

Thesis Completion Status

Completed

Subject

Pharmacy

Language

English

Link

http://prr.hec.gov.pk/jspui/bitstream/123456789/10374/1/Muhammad_Aamir_Pharmacy_2018_UoPsw_PRR.pdf

Added

2021-02-17 19:49:13

Modified

2024-03-24 20:25:49

ARI ID

1676725732131

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Pediatric pharmacotherapy aims to ensure safe and effective use of drugs in various population of children. However, due to varied pediatric pharmacokinetic drug profile and lack of pediatric drug data as compared to adults, it is difficult to achieve the optimal drug therapy in pediatrics. Studies regarding dosage errors, drug interactions, unlicensed and off label drug use in pediatric population will help the health care professionals in identification and management of drug interactions as well as unlicensed and off label drug use. Patient drug profiles of 4240 patients were evaluated using Micromedex Drug-Dex and Drug-Reax at pediatric department in four tertiary care hospitals of Pakistan (3 public and 1 private). The association between studied risk factors was analyzed using logistic regression to calculate the odds ratio (OR) and 95% confidence interval (CI). In pediatric surgical units, total of 895 patients drug profiles were analyzed which described mean number of drug was 3.51 ± 1.50. Of all the patients, 351 (39.21%) had sub-therapeutic doses and 67 (7.48%) had overdoses, while 148 (16.54%) patients were exposed to DDIs. A total of 11 drug combinations were observed that led to 160 DDIs. Overall, 3168 drugs were prescribed of which 1931 (64.89%) were unlicensed and 1542 (48.67%) were off labeled. Indication (38.71%) and dose (34.82%) were the most frequent off label categories in all the therapeutics classes. Chi square value revealed that unlicensed drug use was significantly associated with the type of hospital (p<0.0001). A significant association was also found between unlicensed (p<0.0001) and off label (p<0.031) drug prescribing with age groups. Multivariate binary logistic regression analysis revealed that infants (OR 4.092, 95%CI 2.272-7.370) and children (OR 2.691, 95%CL 1.581-4.581) age groups were 4 times and 2.6 times respectively more likely to receive unlicensed medicines, while they were significantly less likely, Abstract v (OR 0.270, 95%CI 0.109-0.667) and (OR 0.320, 95%CL 0.133-0.769), to receive off label medicines than adolescent group. Pediatric patients receiving less than 5 medications were significantly less likely to receive unlicensed drug (OR 0.105, 95%CL 0.051-0.213) and off-label drugs (OR 0.117, 95%CL 0.42-0.323) as compared to pediatric patients that received 5 or more medications. Male patients were 2.1 times more likely to receive unlicensed medicines (OR 2.103, 95%CL 1.507-2.937), while they received substantially less amount of off-label medicines (OR 0.685, 95%CL 0.458-1.024) as compared to females. Hospital stay of less than 5 days (OR 0.397, 95%CL 0.228-0.629) carried significantly less risk of off label prescription as compared to patients staying at hospital for more than 5 days. In the pediatric medical wards of all the hospitals 1375 patients were analyzed. The mean number of prescribed drugs per patient was 3.93 ± 1.85. Analysis of 1375 cases revealed sub-therapeutic doses in 571 (41.2%) cases while overdoses was observed in 136 (9.89%) cases. In 1375 medical ward patients, 239 (17.38%) had at least one DDI regardless of type of severity. A total of 101 interacting drug pairs were identified causing 417 drug-drug interactions, while 100 drugs were prescribed 5708 times, of which 65.66% prescriptions were unlicensed by FDA. The percentage of off label prescriptions were 52.99%. Evaluating off label drug categories showed that dose (35.7%) and age (19.4%) were the highest reason observed for off label prescriptions. Significant association was found between unlicensed drug use with type of hospitals (p<0.001). A significant association was also found between unlicensed (p<0.002) and off label (p<0.0001) use of drugs with age groups. Multivariate binary logistic regression revealed that pediatric patients receiving drugs 5 or less drugs were significantly less likely to receive unlicensed prescriptions (OR 0.112, CL95% 0.027- Abstract vi 0.461) and off label drugs (OR 0.180, CL95% 0.073-447) as compared to patients who received 5 or more drugs. Analysis of 250 patients in the cardiology ward of HMC revealed the mean number of prescribed drugs to be 4.67±2.07. Of all the patients, 59.69% had sub-therapeutic doses and 5.52% had overdoses while132 (52.8%) had at least one DDI regardless of type of severity. Out of total drug prescriptions (1231), 43.05% were unlicensed and 44.59% were off labeled. In multivariate analysis, occurrence of unlicensed prescriptions were significantly more likely associated with infants (OR 10.288, CL 1.839-57.547) and children (OR 12.822, CL 2.004-62.025) age group as compared to adolescent group, while infant (OR 5.850, CL 1.131-30.246) age group was significantly 5.8 times more likely to receive off label prescription as compared to adolescent group. Among 1300 neonatal patients, 192 (14.76%) were premature in all nurseries of four tertiary care hospitals. Mean number of prescribed drugs were 2.85±1.35, while 358 (27.5%) had sub-therapeutic doses and 50 (3.8%) had overdoses. At least one DDI was present in 7.38% patients and a total of 21 drug combinations attributed to 112 DDIs. A total of 52 drugs were prescribed 3448 times, of which 1150 (33.35%) were unlicensed and 1798 (52.14%) were off labeled. Dose (61.29%) and indication (13.68%) were the most frequent off label categories in all the therapeutics classes. Chi square value determine that unlicensed drug use was significantly associated with the type of hospital (p<0.0001) and age groups (p<0.0001). Off label drug prescribing was also significantly associated with age groups (p<0.001). Multivariate binary logistic regression analysis showed that neonatal patients of age 0 to 7 days (OR 1.355, 95% 1.021-1.799), were significantly less likely to receive off unlicensed prescriptions as compare to reference age group. Male patients (OR 1.355, 95%CL 1.021-1.799) were significantly 1.3 times more exposed to receive unlicensed medicines compared to Abstract vii females. Neonatal patients of age 0 to 7 days (OR 1.631 (1.048-2.536) were also significantly 1.6 times more likely to receive off label medication as compared to patients of age 22 and above days. Of 420 patients admitted in pediatric intensive care units, the mean number of prescription per child was 4.13 ± 2.19, while 175 (41.66%) had sub-therapeutic doses and 54 (12.85%) had overdoses. Moreover, 74 (17.61%) patients had at least one DDI regardless of type of severity which were due to 41 interacting drug combinations leading to 156 DDIs. A total of 96 different drugs were prescribed 2453 times. Of these, 29.8% prescriptions were unlicensed from FDA and 42.27% were off label prescriptions. Dose (340, 32.79%) and indication (26.13%) was the highest reason for off label prescriptions. Multivariate regression analysis showed that patients receiving medications less than 5 (OR 0.280, 95%CL 0.137-0.570) were significantly less likely to receive off label prescriptions as compared to patients received 6 or more medications. In conclusion, prevalence of dosage errors and drug interactions was found to be higher in pediatric cardiology unit. A high prevalence of unlicensed and off label prescriptions was also observed in the present study which showed poor pediatric pharmacotherapy of our region. Increased number of prescribed drugs and infant age group were found to be significant predictors for unlicensed as well as for off label drug use. Unlicensed and off label drug use can also lead to adverse drug events. Therefore, to avoid exposing pediatrics to unnecessary risks, activities of health regularity agencies and perhaps, extra incentives are required to encourage the proper evidence based pediatric prescribing.
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81. Al-Takwir/The Wrapping Up

81. Al-Takwir/The Wrapping Up

I/We begin by the Blessed Name of Allah

The Immensely Merciful to all, The Infinitely Compassionate to everyone.

81:01
a. When the sun will be wrapped up and its radiation ceases,

81:02
a. and when the stars will fade away,

81:03
a. and when the mountains will be set to move and become scattered dust,

81:04
a. and when the pregnant she-camels will be abandoned by the herdsmen,

81:05
a. and when the wild beasts will be herded together,

81:06
a. and when the seas/oceans will be made to surge and swell into massive flooding,

81:07
a. and when the souls will be paired and joined with one’s deeds,

81:08
a. and when the female infant, buried alive, will be asked:

81:09
a. ‘for what sin/offence was she slain/buried alive?’

81:10
a. And when the pages/scrolls of deeds of every individual will be laid open/unrolled,

81:11
a. and when the celestial realm will be ripped off,

81:12
a. and when the Blazing Fire will be ignited and set ablaze,

Surah 81 * Al-Takwir 717

81:13
a. and when the Paradise will be brought close to those who would have merited it,

81:14
a. then every soul will know what it had presented for this time!

81:15
a. So I swear by those receding stars/planets,

81:16
a. the stars/planets withdrawing into themselves.

81:17
a. And the night as it recedes/close in,

81:18
a....

سند (مالک عن نافع عن ابن عمر)، محدثین اور مستشرقین کا نقطہ نظر

Abstract By preserving and narrating hadīth, a chain of narrators was started to maintain its authenticity. When the experts of hadīth realized that some unreliable transmitters might try to fabricate Hadīth, this work started more systematically. Even the chain gradually attained such importance that every Muhaddīth was concerned much about it. In the second century of  Hijra, when the teaching and learning of hadīth became the standard of honor and great respect, some people devoted their lives to this work. They travelled to many countries of world and obtained the knowledge of Hadīth from prominent scholars of their time. Experts of Asmā-ul-Rijāl awarded them the certificate of holding the highest position of trust and credibility. The chains having such trustworthy transmitters are considered to be of higher rank than others. Among such traditions there is also one "Mālik-an-Nāfi'-an-Ibn-e-Umar". Due to the reliability of its narrators, Imām Bukhāri and many other Muhaddithīn considered it as "golden chain". When some of the Orientalists started raising objections to the Prophetic Hadīth, they criticized the narrators of the Hadīth as well. Especially the narrators who were declared trustworthy and reliable by Muslim scholars. For this, they especially criticized Abu Hūraira from among the companions and Imām Zuhri among the Successors. The chain of hadīth, (Mālik an-Nāfi' an-Ibn e Umar) “golden chain” was also seriously criticized by Joseph Schacht and Juynboll etc. In this article, a comparative study of the viewpoints of the Muhaddithīn and the Orientalists regarding the chain “Mālik an-Nāfi' an-Ibn eUmar” is presented.

Evaluating Role of Plant Growth Promoting Rhizobacteria Pgpr to Increase Flower Production, Flower Periodicity and Essential Oil Contents in Rosa Damascena Mill.

The role of plant growth promoting rhizobacteria for improving yield and essential oil contents in Rosa damascena Mill. was evaluated in this study. Plant growth promoting rhizobacteria (PGPR) were isolated from the rhizosphere of Rosa damascena in first experiment, fifteen distinctive and fast growing rhizobacterial colonies (strains) were chosen to inoculate the Rosa cuttings by dipping in them. Results of the pot experiments revealed that most of the isolates showed growth promoting activities in Rosa cuttings except the isolates B5 which was proved to be growth limiting strain as it gave 20-40% less result for all parameters. All the other strains enhanced cutting growth characters up to 30- 60% compared to control. Strains LSI19, F6 and LC4 were proved to be superior strains in all growth attributes. Therefore, these three strains (LSI19, F6 and LC4) were selected for further studies. Three separate field experiments were laid out in factorial arrangement under randomized complete block design (RCBD) with four replications. Total eight inoculum combinations were made from three PGPR strains (alone and in different combination) for each experiment. Second experiment comprised of root application of eight combinations of PGPR treatments in the form of liquid inoculum along with zero, half of recommended and recommended dose of nitrogen and phosphorus. Maximum plant growth and production was observed in all PGPR treatments at NP @ 60 and 20 g/m2 only the stem diameter was found maximum when PGPR treatments were applied along with NP @ 30 and 10 g/m2. Combination of PGPR strains perform better than individual strains when applied at all three levels of nitrogen and phosphorus. Results regarding essential oil contents showed that PGPR combination of F6, LC4 and LSI19 at NP fertilization @ 30 and 10 g/m2 provided the highest concrete and absolute oil percentage but increasing levels of NP ultimately reduced oil contents. Third experiment comprised of foliar application of similar PGPR combinations, in which PGPR treatments were applied at three different growth stages (on new shoots after pruning, after flower bud formation and at flower burst). Results exhibited that plant growth and flower yield attained maximum values in triple inoculum of F6, LC4 and LSI19. Application of PGPR strains on new shoots after pruning (GS1) showed much better results regarding reproductive growth and flower yield than other growth stages while vegetative growth characters were enhanced by application of PGPR strains after flower bud formation (GS2). Last experiment was designed to assess the PGPR combinations by two methods of application (root and foliar). The results showed that plant growth, biomass of flowers, N contents in shoots and P contents in leaves and shoots were significantly improved by root application of PGPR strains while flower yield and N contents in leaves were improved with foliar application of PGPR strains. PGPR inoculation by different methods (root and foliar) significantly affected oil yield and chemical composition of essential oil. Overall results for all studies reflected that yield of Rosa damascena was enhanced with the application of PGPR inocula either single or in combination. However, co-inoculation performed better than individual inoculation.