Warung Bebas

Kamis, 13 Desember 2012

Melihat Statistik dan Ranking Twitter di Pengikut.com

Limit Komputer | Sekarang sudah hadir sebuah situs yang membantu pengguna untuk melihat statistik dan rangking twitter. situs yang bernama "Pengikut.com" merupakan sebuah situs direktori yang mampu melihat dengan lengkap statistik sebuah akun twitter dari awal sampai akhir.

Situs ini pun menggunakan bahasa indonesia, yang dapat mempermudah anda dalam melihat statistik dan rangking. Nah bagi yang berminat dapat mendaftarnya melalui Tautan di akhir artikel ini. soal biaya kalian tidak usah khawatir, sebab situs ini tidak memungut biaya sepeser pun alias gratis.

Dan apabila anda mendaftar di situs ini, maka anda akan mendapatkan fasilitas update statistik harian selama 3 bulan, syaratnya kalian harus memiliki follower twitter mencapai seribu.

Screenshot : 


Bagaimana dengan situsnya menarik bukan ? nah kalau menarik silahkan kunjungi situsnya di bawah ini :

http://pengikut.com/

Acceptance Rates and Impact Factors

For those of you who do publish at computer science conferences*:

1) On your CV/Biosketch/Website/etc. list-of-publications, do you include conference acceptance rates?

2) If you do, what  is the threshold for you to mention it? (e.g., 50%, 30%, 10% ?)

For those of you who don't publish at computer science conferences:

0) Hey, why aren't you publishing at CS conferences? We're cool people, and we start counting at zero.  

1) On your CV/Biosketch/Website/etc. list-of-publications, do you include journal impact factors?

2) If you do, what is the threshold for you to mention it? (e.g., do you list IFs for startup journals)?

And for anyone willing to share their field / subfield, I'd be interested to hear that as well. I'm planning to assemble this information into a longer post on the topic in a few weeks.

---
* This includes anything which has archival proceedings, like some workshops, symposia, summer/winter/fall/spring schools, etc. 

Is it Time to Re-write the Textbooks on Insulin and Obesity? Part II

A new paper published on December 6th in the journal Science once again tackles the question of whether elevated insulin drives the development of obesity (1).  Mice were generated that lack Jun kinases 1 and 2 specifically in immune cells, impairing their ability to produce inflammation while having very few off-target effects.  These mice do not become insulin resistant when placed on a fattening diet, and their insulin levels do not increase one iota.  Are they protected from obesity?  People who read the last post should know the answer already.
Read more »

Rainmeter - Aplikasi Memperindah Desktop dengan Gadget

Limit Komputer | Siapa sih yang ingin memalingkan wajahnya ketika melihat hal-hal yang indah ? nggak ada kan ?. lalu seandainya hal terindah tesebut tepat di depan mata, apakah  mata kita masih bisa berkedip ? saya yakin semuanya pada melotot, hehe. nah kalau itu terjadi pada windows anda, apa yang anda rasakan ? senang donk, hehe.

Sepenggal paragraf di atas, bukan untuk membahas seorang cewek atau panorama alam, melainkan membahas aplikasi memperindah desktop, yang saya rekomendasikan untuk anda sekalian. sebelumnya, kalian sudah pada tahu gk dengan aplikasinya ? Anda : "nggak tahu", Saya : "pengen tahu" ? silahkan lihat dulu screenshotnya di bawah ini :



Bagaimana aplikasi rekomendasi saya, keren kan ? 

Sebelum saya memberikan tautannya, saya ingin memberitahukan bahwa aplikasi yang saya sebut di atas itu bernama "Rainmeter"

Nah untuk memperolehnya kalian dapat mengunjungi situs resminya di bawah ini :



dengan adanya rainmeter maka kalian akan merasakan perubahan drastis pada windows terutama di desktop, menjadi lebih indah seindah-indahnya.

Pfizer's 13th Legal Settlement - Will it be Enough to End the Impunity?

It has been almost two months since we lasted noted misbehavior by giant global pharmaceutical firm Pfizer Inc. With little fanfare, however, a few small news items noted the corporation's latest legal settlements.

Deceptive Marketing of Protonix

The first settlement merited only a few paragraphs from Reuters.  The gist was:

Pfizer Inc will pay $55 million plus interest to settle charges that Wyeth promoted its acid reflux drug Protonix for unapproved uses and made unproven claims about the medicine, the U.S. Department of Justice said on Wednesday. 

The infractions took place between February 2000 and June 2001, long before the world's largest drugmaker acquired Wyeth in 2009 for $68 billion.

A report in the examiner explained that Wyeth did not merely go beyond the label in promoting Protonix, it went beyond the evidence.

Wyeth allegedly promoted Protonix as the 'best PPI for nighttime heartburn' even though there was never any clinical evidence that Protonix was more effective than any other PPI for nighttime heartburn. 

Furthermore, the charges were that systemic efforts to mislead were sanctioned by top management:

 The allegations in the complaint are that this superiority slogan was formulated at the highest levels of the company. Wyeth retained an outside market research firm, at the cost of tens of thousands of dollars, to ensure that sales representatives delivered that misleading superiority message.

Finally, the government asserted that Wyeth corrupted physicians' continuing medical education in the process:


Finally, the government alleges that Wyeth used continuing medical education (CME) programs to promote Protonix for unapproved uses. CME programs are sponsored by accredited independent providers, such as universities, nonprofit organizations, or specialty societies. Pharmaceutical companies are permitted to provide financial support for CME programs, but they are not permitted to use CME programs as promotional vehicles for off-label indications.

According to the complaint, Wyeth spent millions of dollars providing 'unrestricted educational grants' to CME providers, and these grants invariably included promises that Wyeth would not attempt to influence the content of the program in any way. Nevertheless, the government alleges that one of Wyeth’s core marketing tactics for Protonix was to use CME programs to drive off-label use of the drug. According to the complaint, the Protonix 'brand team' influenced virtually every aspect of these CME programs: program topics, speaker selection, organization, and content. In addition, the government alleges that Wyeth even insisted that the CME program materials use the same color and appearance as Protonix promotional materials–a tactic that Wyeth and the vendor called 'branducation.'

So it seemed that the company put on quite an effort to promote what we have called elsewhere pseudo-evidence based medicine, yet, like many other legal settlements involving large health care organizations, this one involved no penalties of any type against the people within the organization who authorized, directed, or implemented the bad behavior. 

 Misleading Marketing of Zyvox, Lyrica 

Another settlement, for a few dollars less, got even less attention.  Fox Business news did report this:

 Pfizer Inc. (PFE) agreed to pay a combined $42.9 million to North Carolina and 32 other states in a settlement of allegations that the drug maker used unfair and deceptive practices in the marketing of antibiotic Zyvox and nerve-pain medicine Lyrica.

I could find no detail about the sorts of deception allegedly involved in the news media.  What little more Fox provided did suggest that this case also involved pitching drugs in instances in which their use was unsupported by good evidence:

The states had alleged that Pfizer had marketed Zyvox as superior to another antibiotic in fighting certain types of infections, though there allegedly wasn't substantial evidence to support superior results for some uses that Pfizer claimed.

The states also alleged that Pfizer marketed Lyrica for some off-label, or unapproved, uses.
There was no hint that again any individual would suffer any negative consequences for this particular set of deceits either.

Avoiding Impunity as a Topic of Polite Discussion

We have discussed a seemingly endless parade of legal settlements by large health care organizations.  In almost none was there any consequence beyond a fine paid by the company, and sometimes a pledge that the company would thereafter behave better.  While these relatively small costs were diffused throughout the organizations, almost never did the people who authorized, directed, or implemented the bad behavior pay any price or suffer any penalty.  Thus we have opined again and again (e.g., most recently here) that these settlements have become just another cost of doing business, and have no power to deter future bad behavior.
In addition, we have noted not only have multiple organizations made such settlements, some organizations have settled again and again.  Yet even in the cases of these multiple organizational offenders, the individuals involved maintain their immunity from any negative consequences.  Thus these are examples of impunity.  
Transparency International declared 23 November, 2012, as the International Day to End Impunity, explained as follows:
At Transparency International we view impunity as getting away with bending the law, beating the system or escaping punishment. Impunity is anathema to the fight against corruption.

However, impunity is one of those concepts which never seems to be a subject of polite conversation in health care, or, as we say, it has become anechoic.  

Therefore, it is fascinating that while these two Pfizer settlements were announced almost simultaneously, each was discussed, such as it was, as if it occurred in a vacuum.  Moreover, it also seems that each settlement was crafted by law enforcers without any attention to the record of the company making the settlement.  Thus, any implications about impunity were avoided.

Pfizer's Multiple Ethical Opfenses

In fact, during the time we have been posting on Health Care Renewal, Pfizer has become one of the great repeat ethical offenders in the health care arena.  Its track record since the beginning of the 21st century, (with yello colored background below, compiled from this post), is remarkable.

In the beginning of the 21st century, according to the Philadelphia Inquirer, Pfizer made three major settlements,
October 2002: Pfizer and subsidiaries Warner-Lambert and Parke-Davis agreed to pay $49 million to settle allegations that the company fraudulently avoided paying fully rebates owed to the state and federal governments under the national Medicaid Rebate program for the cholesterol-lowering drug Lipitor.
May 2004: Pfizer agreed to pay $430 million to settle DOJ claims involving the off-label promotion of the epilepsy drug Neurontin by subsidiary Warner-Lambert. The promotions included flying doctors to lavish resorts and paying them hefty speakers' fees to tout the drug. The company said the activity took place years before it bought Warner-Lambert in 2000.
April 2007: Pfizer agreed to pay $34.7 million in fines to settle Department of Justice allegations that it improperly promoted the human growth hormone product Genotropin. The drugmaker's Pharmacia & Upjohn Co. subsidiary pleaded guilty to offering a kickback to a pharmacy-benefits manager to sell more of the drug.

Thereafter, Pfizer paid a $2.3 billion settlement in 2009 of civil and criminal allegations and a Pfizer subsidiary entered a guilty plea to charges it violated federal law regarding its marketing of Bextra (see post here).  Pfizer was involved in two other major cases from then to early 2010, including one in which a jury found the company guilty of violating the RICO (racketeer-influenced corrupt organization) statute (see post here).  The company was listed as one of the pharmaceutical "big four" companies in terms of defrauding the government (see post here).  Pfizer's Pharmacia subsidiary settled allegations that it inflated drugs costs paid by New York in early 2011 (see post here).   In March, 2011, a settlement was announced in a long-running class action case which involved allegations that another Pfizer subsidiary had exposed many people to asbestos (see this story in Bloomberg).  In October, 2011, Pfizer settled allegations that it illegally marketed bladder control drug Detrol (see this post). Finally, in August, 2012, Pfizer settled allegations that its subsidiaries bribed foreign (that is, with respect to the US) government officials, including government-employed doctors (see this post). 

By my count, the two current settlements would be numbers twelve and thirteen.  Of course, while I believe this list is accurate, it may be incomplete.

Since none of these posts involved any negative consequences for any individuals who authorized, directed, or implemented the bad behavior, or who profited from it, and none involved any changed in the leadership or organization of the company, this becomes an amazing record of the impunity of Pfizer leadership over time and space. 
Will Impunity Finally Lead to Outrage?

Impunity, though, is a concept that is beginning to command some attention.

The Brasilia Declaration which was published at the conclusion of the 15th International Anti-Corruption Conference (hosted by Transparency International) included:
it is clear we all face a common challenge in our work: impunity for those who abuse positions of power. 
If impunity is not stopped, we risk the dissolution of the very fabric of society and the rule of law, our trust in our politics and our hope for social justice.

Activists, businesspeople, politicians, public officials, journalists, academics, youth and citizens who gathered in Brasilia to discuss the threat of corruption made it clear that impunity undermines integrity everywhere.

Whether we are investing collective efforts and resources in fighting poverty, human rights violations, climate change or bailing out indebted economies, we need to give the people a reason to believe that impunity will be stopped.

While the two latest Pfizer settlements barely got media coverage, maybe a $1.9 billion dollar settlement in the US by international banking giant will get more attention.  The charges in this case were not merely deceiving some doctors and patients about drug efficacy and safety.  The company was accused of aiding money laundering by drug cartels, and facilitating rogue regimes get around international sanctions.  As the New York Times reported,

State and federal authorities decided against indicting HSBC in a money-laundering case over concerns that criminal charges could jeopardize one of the world’s largest banks and ultimately destabilize the global financial system.

Instead, HSBC announced on Tuesday that it had agreed to a record $1.92 billion settlement with authorities. The bank, which is based in Britain, faces accusations that it transferred billions of dollars for nations like Iran and enabled Mexican drug cartels to move money illegally through its American subsidiaries.

Unlike Pfizer's slow-motion impunity, this example got attention.  The Los Angeles Times noted,

The massive penalty still was not enough to appease some critics. No bank executives were charged as part of the investigation, leading some analysts to question the government's willingness to hold powerful Wall Street firms accountable.

'It's mind-boggling how they think you can have a financial system and allow this kind of impunity,' said William Black, a former banking regulator who aided federal prosecutors during the savings and loan crisis of the 1980s and 1990s. HSBC 'put the world at enormous risk.'

A NY Times editorial opened,

It is a dark day for the rule of law.   Federal and state authorities have not to indict HSBC, the London-based bank, on charges of vast and prolonged money laundering, for fear that criminal prosecution would topple the bank and, in the process, endanger the financial system.  They have also not charged any top HSBC banker in the case, though it boggles the mind that a bank could launder money as HSBC did without anyone in a position of authority making culpable decisions.

Clearly, the government has bought into the notion that too big to fail is too big to jail.  When prosecutors choose not to prosecute to the full extent of the law in a case as egregious as this, the law itself is diminished.  The deterrence that comes from the threat of criminal prosecution is weakened, if not lost.

So maybe this huge financial case will prove to be the straw that breaks impunity's back.  So I will close by quoting the end of the Brasilia Declaration, in the hope that a few people will take it to heart in the context of health care, as well as in finance.


To take this important struggle forward the international anti-corruption community should promote greater people engagement and find ways to provide greater security for anti-corruption activists.

Reducing impunity also requires independent and well-resourced judiciaries that are accountable to the people they serve.

We call on leaders everywhere to embrace not only transparency in public life but a culture of transparency leading to a participatory society in which leaders are accountable.

We call on the anti-corruption movement to support and protect the activists, whistleblowers and journalists who speak out against corruption, often at great risk.

It is up to all of us in government, business and society to embrace transparency so that it ensures full participation of all people, bringing us together to send a clear message: We are watching those who act with impunity and we will not let them get away with it.

Pennsylvania Patient Safety Authority: The Role of the Electronic Health Record in Patient Safety Events

The Pennsylvania Patient Safety Authority has released a report "The Role of the Electronic Health Record in Patient Safety Events."  A press release is at this link, and the full report in PDF is at this link.  In the report, the Pennsylvania Patient Safety Authority analyzed reports of EHR-related events from a state database of reported medical errors and identified several major themes.

The report was prepared with the assistance of Erin Sparnon, Senior Patient Safety Analyst the ECRI Institute near Philadelphia.  The ECRI Institute is an independent organization renowned for its safety testing of medical technologies and reporting on same, and that "researches the best approaches to improving the safety, quality, and cost-effectiveness of patient care."  I've mentioned it and its bylaws in this blog in the past as a model for independent, unbiased testing and reporting of healthcare techonlogies.

Regarding the Patient Safety Authority:


The Pennsylvania Patient Safety Authority was established under Act 13 of 2002, the Medical Care Availability and Reduction of Error ("Mcare") Act, as an independent state agency. It operates under an 11-member Board of Directors, six appointed by the Governor and four appointed by the Senate and House leadership. The eleventh member is a physician appointed by the Governor as Board Chair.  Current membership includes three physicians, three attorneys, three nurses, a pharmacist and a non-healthcare worker.

The Authority is charged with taking steps to reduce and eliminate medical errors by identifying problems and recommending solutions that promote patient safety in hospitals, ambulatory surgical facilities, birthing centers and certain abortion facilities. Under Act 13 of 2002, these facilities  must report what the Act defines as "Serious Events" and "Incidents" to the Authority.

The Authority maintains a database of serious events and incidents:

Consistent with Act 13 of 2002, the Authority developed the Pennsylvania Patient Safety Reporting System (PA-PSRS, pronounced "PAY-sirs"), a confidential web-based system that both receives and analyzes reports of what the Act calls Serious Events (actual occurrences) and Incidents (so-called "near-misses").

Cutting right to the chase, the paper's summary:

As adoption of health information technology solutions like electronic health records (EHRs) has increased across the United States, increasing attention is being paid to the safety and risk profile of these technologies. However, several groups have called out a lack of available safety data as a major challenge to assessing EHR safety, and this study was performed to inform the field about the types of EHR-related errors and problems reported to the Pennsylvania Patient Safety Authority and to serve as a basis for further study. Authority analysts queried the Pennsylvania Patient Safety Reporting System for reports related to EHR technologies and performed an exploratory analysis of 3,099 reports using a previously published classification structure specific to health information technology. The majority of EHR-related reports involved errors in human data entry, such as entry of “wrong” data or the failure to enter data, and a few reports indicated technical failures on the part of the EHR system. This may reflect the clinical mindset of frontline caregivers who report events to the Authority.

Results:

... Reported events were categorized by their reporter-selected harm score (see Table 1). Of the 3,099 EHR-related events, 2,763 (89%) were reported as “event, no harm” (e.g., an error did occur but there was no adverse outcome for the patient) [a risk best avoided to start with, because luck runs out eventually - ed.], and 320 (10%) were reported as “unsafe conditions,” which did not result in a harmful event. Fifteen reports involved temporary harm to the patient due to the following: entering wrong medication data (n = 6), administering the wrong medication (n = 3), ignoring a documented allergy (n = 2), failure to enter lab tests (n = 2), and failure to document (n = 2). Only one event report, related to a failure to properly document an allergy, involved significant harm.

A significant "study limitations" section was included that addressed: 

  • Issues regarding reporting statutes of the PA-PSRS errors database; 
  • lack of awareness of EHRs as a potential contributing factor to an error;
  • limitations of narrative reporting affecting both the types of reports queried and the tags applied (the study used textual data mining methodolgies);
  • query design of the study; and
  • the need for further refinement of the machine learning tool used in creating the working dataset, which may have missed relevant cases.

Some of these impediments to knowing the magnitude of extant HIT issues are also present in the 2008 Joint Commission Sentinel Events Alert on HIT, the 2010 FDA internal memorandum on HIT Safety, and the 2011 IOM report on the same topic.

(The IOM report specifically observed that the "barriers to generating evidence pose unacceptable risks to safety.") 

The major obstacle to this study in my view, though, was the nature of the dataset.  The database is for general reporting of medical errors, and it contains no specific fields or reminders about EHRs or the known ways in which they can contribute to, or cause, medical mistakes.  

The attempt was made, as acknowledged in the study, to glean information about EHR-related events from, in large part, textual analysis of narrative in the hopes that the reporter recognized the role of IT, and reported it using terms that could be detected by the search algorithms.  In other words, the data was not "purposed" for this type of study.  

It is axiomatic that one cannot find data that is simply not present, no matter how fancy the search algorithm.  Further, passive analysis of clinical IT risk/harms data in an industry where lack of knowledge of causation and misconceptions abound will produce only partial results that suggest further study is needed, and not give an indicator of just how incomplete the results are.

Thus, this cautionary statement was made in the new PA Patient Safety Authority report:

"Although the vast majority of EHR-related reports did not document actual harm to the patient, analysts believe that further study of EHR-related near misses and close calls is warranted as a proactive measure." 

My comments:

The report is welcome.

The most important part of the paper, I point out, is the “Limitations” section. FDA, IOM and others have made similar observations – we don’t know the true magnitude of the problem due to systematic limitations of the available data. 

Therefore, at best what is available must be deemed as risk management-relevant case reports, a “red flag” that could represent (using the words of FDA CDRH director Jeffrey Shuren regarding HIT safety), the tip of the iceberg.

It is imperative far more work be done in post-market surveillance as this technology is deployed nationally and internationally.  This is to ensure that good health IT (GHIT) prevails and bad health IT (BHIT) is either remediated or removed from the marketplace.  I had defined those in other writings as follows:

Good Health IT ("GHIT") is defined as IT that provides a good user experience, enhances cognitive function, puts essential information as effortlessly as possible into the physician’s hands, keeps eHealthinformation secure, protects patient privacy and facilitates better practice of medicine and better outcomes. 

Bad Health IT ("BHIT") is defined as IT that is ill-suited to purpose, hard to use, unreliable, loses data or provides incorrect data, causes cognitive overload, slows rather than facilitates users, lacks appropriate alerts, creates the need for hypervigilance (i.e., towards avoiding IT-related mishaps) that increases stress, is lacking in security, compromises patient privacy or otherwise demonstrates suboptimal design and/or implementation. 

An additional major factor that also contributes to lack of knowledge of EHR-related adverse events is hospital reporting non-compliance. For instance, I know of cases from my own legal consulting work and personal experience that I would have expected to appear in the database, but apparently do not.

But don’t take it from me alone. Here is PA Patient Safety Authority Board Member Cliff Rieders, Esq. on this.

From “Hospitals Are Not Reporting Errors as Required by Law, Phila. Inquirer”, pg. 4,http://articles.philly.com/2008-09-12/news/24991423_1_report-medical-mistakes-new-jersey-hospital-association-medication-safety:
  

... Hospitals don’t report serious events if patients have been warned of the possibility of them in consent forms, said Clifford Rieders, a trial lawyer and member of the Patient Safety Authority’s board.

He said he thought one reason many hospitals don’t want to report serious events is that the law also requires that patients be informed in writing within a week of such problems. So, if a hospital doesn’t report a problem, it doesn’t have to send the patient that letter. [Thus reducing risk of litigation, and, incidentally, potentially infringing on patients' rights to legal recourse - ed.]

Rieders says the agency has allowed hospitals to determine for themselves what constitutes a serious event and the agency has failed to come up with a solid definition in six years.

Fixing this “is not a priority,” he added.

This coincides with my own personal experience precisely.  In a case where my relative was permanently injured as a result of EHR-related medication error, and then died of the injuries, I never received the required report in writing from the hospital.  I also do not believe the case was reported to the Safety Authority, at least not as IT-related.

I suspect the true rates of EHR-related close calls, reversible injuries, permanent injuries and deaths is significantly higher than the limited data available suggests. That data is merely a red flag that much more education, stringent reporting requirements,  templates of known causes of error, and enforcement are needed.  (An April 2010  "thought experiment" on this issue I wrote about at "If The Benefits Of Healthcare IT Can Be Guesstimated, So Can And Should The Dangers" certainly suggested as much.)

Slides where I made those types of recommendations to the Patient Safety Authority, at a presentation I gave in July 2012 at their invitation, are at http://www.ischool.drexel.edu/faculty/ssilverstein/PA_patient_safety_Jul2012.ppt

A major concern I have is that the HIT industry will use this new report in a manner that ignores its limitations.

(Disclosure: I was an invited reviewer of this new PPSA report.)

-- SS 

Addendum Dec. 13:   

Also worth review is "Patient Safety Problems Associated with Heathcare Information Technology: an Analysis of Adverse Events Reported to the US Food and Drug Administration", Magrabi, Ong, Runciman, and Coiera, AMIA Annu Symp Proc. 2011.  

Data here came from FDA's voluntary (i.e., also tip of the iceberg) Manufacturer and User Facility Device Experience (MAUDE) database.  Ironically, the study was done in Australia using Australian grant funds.

-- SS




hello party people....i'm sorry i've been MIA this week....i don't have a great excuse....i wish i could say that i've been getting all of my christmas shopping done but that would be a lie.  i'm way behind and the thought that it's only a week and a half away is a little frightful!  are y'all ready?!!

*images courtesy of j crew, the coverteur, angie hranowsky, vogue

After December 22nd Saturday Morning Run


Day After the End of the World Run / Potluck

  • Run at Medway Trail at 8:00 as usual
  • Potluck brunch afterwards (9:30ish - ?
  • Robin Ashtons home just minutes from the trail head
  • 1698 Attawandaron Road
  • Pancakes and coffee provided by the Ashton clan
  • Please bring items for the potluck table (Tim Bits is cheating)
  • If the world does not in fact end on December 21, there is no Post-apocalypse 'rain date', sorry
  • RSVP robin_ashton@rogers.com

* Please bring a change of clothes so we don't stink the place up


BimaTRI - Aplikasi Pengingat Isi Ulang Kuota

Limit Komputer | Mendengar kata BimaTRI mungkin masih asing di telinga ? tapi kalau saya sebutkan kartu 3 (Tri), sudah pasti anda mengetahuinya ?. nah keduanya tersebut memiliki hubungan erat yang saling berdampingan, sebab BimaTRI sendiri merupakan aplikasi buatan tri yang terbaru.

Fungsi dari aplikasi ini sebenarnya dapat mengetahui sisa kuota agar tidak kehabisan secara tiba-tiba atau lebih cocoknya Pengingat isi ulang kuota. nah bagi anda pengguna tri, bersiap-siaplah untuk menggunakannya, karena aplikasi ini akan sangat membantu kalian dalam memberi rekomendasi paket yang sesuai kebutuhan. 



Fitur-fiturnya pun beragam, di antaranya :

1. Push Notification yang berfungsi untuk mengingat sisa kuota internet agar tidak kehabisan kuota secara tiba-tiba

2. Mempermudah isi ulang kuota melalui voucher atau online dengan kartu kredit.

3. Menampilkan informasi seputar kartu Tri kamu

4. Rekomendasi Paket sesuai kebutuhan

5. dan yang terakhir, memberi informasi aplikasi terkini yang berguna untuk aktvitas internetmu.


Bagaimana menurut kalian dengan aplikasinya, baguskan ? nah untuk mendapatkannya kalian bisa mengunjungi situs resminya di bawah ini :

7 Orang Indonesia Yang Mendunia



You'll Never Walk Alone - Hai sobat, bagaimana kabarnya hari ini? Semoga baik-baik saja. Kali ini aya akan berbagi informasi tentang  7 Orang Indonesia Yang Mendunia. Sebagai sebuah negara yang besar dan kaya raya, Indonesia di mata dunia lebih dikenal bukan karena prestasi yang membanggakan, melainkan karena berbagai image buruknya. Korupsi, kemiskinan, pengangguran dan berbagai konflik lainnya sudah bukan hal baru dan selalu terdengar dari negeri kita tercinta ini.
 
Namun siapa sangka, dari negeri yang telah ter-image buruk ini lahir anak bangsa berkualitas yang mampu mengangkat pamor Indonesia. Mereka mampu membuktikan diri bahwa mereka juga bisa berprestasi sehingga dikenal oleh dunia. Mereka adalah orang-orang Indonesia yang mendunia. Orang-orang Indonesia yang mampu mengangkat namanya di dunia internasional. Nah, siapa sajakah mereka ? berikut ini adalah 7 Orang Indonesia Yang Mendunia..

1. Paul Amron Yuwono
Menjadi perias di keluarga Presiden Obama mungkin hanyalah sebuah mimpi. Namun tidak bagi Paul Amron Yuwono. Pria Indonesia yang sejak umur 17 tahun sudah meninggalkan tanah air dan pergi ke Amerika Serikat ini pernah merasakannya, ketika dirinya dipercaya untuk merias Maya Sutoro – adik tiri Presiden Obama – saat akan hadir pada pelantikan kakaknya, Barrack Obama. Hal ini tentu sebuah kebanggaan tersendiri bagi Amron.

Sebuah pujian pun dilontarkan Obama setelah melihat hasil riasan Maya. Obama memuji Amron dengan mengatakan “terima kasih Amron, kamu sudah membuat adik saya terlihat sangat cantik”. Selain mendapat pujian dan bertemu langsung dengan Presiden Obama, Amron juga merupakan satu-satunya orang Indonesia yang bisa melihat langsung pelantikan Presiden Obama di Amerika. Ia juga satu-satunya orang Indonesia yang mendapatkan kartu akses untuk masuk ke semua area di gedung putih dengan pelayanan VVIP.

2. Sherina
Selain Anggun C. Sasmi dan Agnes Monica, Sherina ternyata juga membuat prestasi yang mendunia. Beberapa waktu lalu, Sherina diminta langsung oleh bintang laga terkenal Jackie Chan untuk menyanyi di sebuah acara amal yang digelar untuk membantu korban tsunami Jepang. Pada acara tersebut Sherina berkesempatan untuk tampil bersama dengan artis-artis dari Jepang, Korea, Hong Kong, Taiwan dan juga China.

Selain menyanyi, ternyata wanita berusia 21 tahun ini juga ditunjuk sebagai duta konferensi pemuda sedunia One Young World pada 2011 lalu di Zurich, Swiss. Pada kesempatan itu, Sherina membawakan sebuah lagu berjudul Sing Your Mind dengan iringan piano yang ia mainkan sendiri. Lagu hasil ciptaannya sendiri itu pun mendapat sambutan luar biasa dari para hadirin yang datang pada waktu itu.

3. Tex Saverio
Tex Saverio, satu lagi putra bangsa yang mendunia. Pemuda berusia 27 tahun yang akrab disapa Rio ini adalah seorang desainer muda berbakat. Ia berhasil memenangkan penghargaan pertamanya, Mercedes-Benz Asia Fashion Award ketika masih berusia 21 tahun. Tidak hanya itu, baru-baru ini Rio membuat sebuah prestasi yang membanggakan. Pasalnya, gaun hasil rancangannya yang Ia beri nama “La Glacon” telah dipakai oleh penyanyi sensasional Lady Gaga pada majalah Harper’s Bazaar tahun 2011.

Bahkan salah satu selebriti Blogger, Perez Hilton mengatakan di blognya bahwa Saverio sejajar dengan perancang terkemuka dunia Alexander McQueen. Sebenarnya, Rio tidak menyangka gaunnya akan dipakai oleh Lady Gaga. Awalnya Ia hanya diberi tahu bahwa gaunnya akan muncul di majalah Harper’s Bazaar, namun tidak menyangka jika yang akan memakainya adalah Lady Gaga. Begitu mengetahui Gaga yang memakai gaunnya, Ia begitu bangga dan gembira. Karena sudah sejak lama Rio menginginkan gaun rancangannya dipakai oleh sejumlah artis wanita dunia.

4. Chris Lesmana
Siapa sih yang tidak mengenal mobil Volkswagen alias VW. Mobil yang akrab disapa VW kodok ini, baru saja mengeluarkan VW Beetle dengan desain terbarunya. Namun siapa sangka, ternyata desain mobil ini dikerjakan oleh putra asli Indonesia bernama Chris Lesmana. Sejak 4 tahun lalu, desainer asal Bandung ini mendesain ulang wajah Beetle, dan hasil rancangannya itu digunakan sebagai dasar mobil Beetle terbaru ini.

Untuk mendesain mobil ini, Chris bekerja sama dengan desainer exterior, Frank Bruse. Di tangan Chris, mobil VW kodok ini dipercantik dengan atap yang lebih rendah, roda yang lebih besar dan interior yang sporty. Mobil ini pun dibuat lebih bundar dan condong serta lebih diperuntukkan bagi wanita.

5. Nancy Go
Nancy Go adalah seorang desainer tas yang mengambil aliran bergaya vintage, gaya tas yang tetap trendy sepanjang jaman. Berawal dari hobinya yang sangat suka dengan kerajinan tangan, Nancy mulai membuat proses pembuatan tas yang ia beri nama “Bagteria” ini di garasi rumahnya di daerah Jakarta Barat. Hingga ia akhirnya mempunyai karyawan sampai ratusan orang.

Dengan teknik rajut, sulam dan bahan unik lainnya seperti Kristal Swarovski, manik, payat, hingga emas dan perak, ia jahit secara satu persatu dengan tangan alias handmade. Karena itulah, tak heran hasil rancangan Nancy ini telah mendapat tempat di hati pecinta mode juga para selebriti dunia, seperti Paris Hilton, Emma Thompson, Anggun, juga putri Zara Phillips yang pernah terlihat memakai Bagteria untuk melengkapi penampilan mereka.

Kini produk buatan Nancy ini telah tersebar di 30 negara termasuk Italia, Prancis, Inggris, Amerika Serikat, Jepang, dan Kuwait. Bahkan di Eropa dan Amerika, merek Bagteria sudah dipadankan dengan merek sekaliber Louis Vuitton, Chanel, atau Christian Lacroix.

6. Pamela Halomoan
Setelah Rini Sugianto berhasil menjadi animator asal Indonesia yang membuat film animasi Tin-tin, kini hadir juga seorang illustrator muda bernama Pamela Halomoan. Di usianya yang baru 19 tahun, karya Pamela telah dinikmati masyarakat Singapura, Amerika, Inggris dan Turki. Tidak hanya itu, karakter yang Ia buat telah berhasil menarik perhatian banyak pengunjung saat dipamerkan di Singapore Game Toy Comic Convention.

Ribuan karakter telah dibuat oleh Pamela, namun salah satu karakter bernama “Wolly” yang membuat Pamela mendapat cukup perhatian. Wolly adalah salah satu karakter ciptaan Pamela yang digambarkan dengan muka seekor babi dengan mata setengah terbuka yang diikuti bentuk badan penggabungan dari beberapa hewan. Pameran pertama Pamela pun dilakukan di Papertoys Exhibition di Turki dan langsung mendapat perhatian dari pihak galeri.

7. Sri Mulyani Indrawati
Begitu banyak prestasi yang diukir oleh wanita kelahiran Bandar Lampung, 26 Agustus 1962 ini. Seperti diantaranya, sebagai menteri keuangan terbaik Asia tahun 2006 oleh Emerging Markets, sebagai wanita paling berpengaruh ke-23 di dunia versi majalah Forbes tahun 2008 dan juga sebagai wanita paling berpengaruh ke-2 di Indonesia versi majalah Globe Asia bulan Oktober 2007.

Awalnya ia dikenal sebagai pengamat ekonomi dan menjabat sebagai Kepala Lembaga Penyelidikan Ekonomi dan Masyarakat Fakultas Ekonomi Universitas Indonesia. Namanya semakin dikenal, ketika Sri Mulyani diangkat Presiden SBY sebagai menteri keuangan kabinet Indonesia Bersatu pada tahun 2005. Kemudian di tahun 2008, Ia juga menjabat pelaksana tugas Menteri Koordinator Bidang Perekonomian menggantikan Boediono.

Sebelum menjabat sebagai Menteri Keuangan, Sri sempat menjabat sebagai Menteri Negara Perencanaan Pembangunan Nasional dan juga kepala BAPPENAS. Hingga akhirnya di bulan Juli tahun 2010, Sri Mulyani mundur sebagai Menteri Keuangan dan kemudian resmi menjabat sebagai Direktur Pelaksana Bank Dunia yang membuat Sri Mulyani menjadi wanita sekaligus orang Indonesia pertama yang menjabat jabatan itu.

Namun, baru-baru ini nama Sri Mulyani kembali disebut-sebut sebagai salah satu calon kandidat terkuat Presiden Bank Dunia menggantikan pejabat yang sekarang yaitu Robert Zoellick. Hal ini terlihat pada saat pemungutan suara yang digelar di sebuah blog yaitu www.worldbankpresident.org, dimana Sri Mulyani memperoleh 13,078 suara atau 87% dari suara yang masuk sebanyak 15,049. Blog ini sendiri dibuat pada tahun 2005 lalu yang dibuat untuk memberikan pencerahan kepada publik dunia agar aktif mengusulkan calon presiden Bank Dunia. Dan di tahun ini, sudah ada beberapa nama calon kuat untuk menduduki posisi penting tersebut, termasuk Sri Mulyani.

Nah, itu tadi 7 Orang Indonesia Yang Mendunia. Ternyata orang Indonesia bisa juga kan bersaing di dunia internasional.


Sumber: www.pangkalanunik.com

Trik Memblokir Konten Porno di Mozilla Firefox

Limit Komputer | Mendengar kata porno, pasti terlintas di pikiran dengan hal-hal yang tabu, yang tidak wajib di ketahui bagi yang belum cukup umur, Seperti anak-anak dan remaja. namun seiring berkembangnya jaman, semua yang pertamanya tabu kini berubah menjadi biasa, termasuk konten porno.


Tentu ini sangat meresahkan orang tua yang memiliki buah hati yang hobi browsing, sebab takutnya akan terjerumus ke jurang yang menyesatkan. Nah untuk itu saya memberikan sebuah trik untuk memblokir konten porno di mozilla firefox dengan menggunakan Add-Ons FoxFilter, berikut ini :

1. Kunjungi https://addons.mozilla.org/en-us/firefox/addon/foxfilter/ 

2. Setelah terbuka, klik Continue to Download
3. Lalu klik Accept and Install

4. Setalah itu akan muncul Add-Ons Downloading, lalu tunggu sampai selesai

5. Setelah selesai maka akan muncul Software Installation dan klik Install Now

6. Setelah itu anda di minta untuk merestart firefox, maka klik Restart Now 

7. Maka Add-ons anti konten porno sudah terpasang di Firefox anda.

Selesai.  

 

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